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ST18 ST18 C2H2C-type zinc finger transcription factor [ Homo sapiens (human) ]

Gene ID: 9705, updated on 2-Nov-2024

Summary

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Official Symbol
ST18provided by HGNC
Official Full Name
ST18 C2H2C-type zinc finger transcription factorprovided by HGNC
Primary source
HGNC:HGNC:18695
See related
Ensembl:ENSG00000147488 MIM:617155; AllianceGenome:HGNC:18695
Gene type
protein coding
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
NZF3; NZF-3; ZNF387; ZC2H2C3; ZC2HC10
Summary
Enables RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in cytokine-mediated signaling pathway; negative regulation of cell population proliferation; and positive regulation of macromolecule metabolic process. Located in nucleus. Part of protein-DNA complex. [provided by Alliance of Genome Resources, Nov 2024]
Expression
Biased expression in brain (RPKM 3.7), stomach (RPKM 0.7) and 3 other tissues See more
Orthologs
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Genomic context

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See ST18 in Genome Data Viewer
Location:
8q11.23
Exon count:
36
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (52110838..52409879, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (52486561..52785956, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (53023398..53322439, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27339 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27340 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27341 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr8:52837590-52838789 Neighboring gene PCMTD1 divergent transcript Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19187 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27342 Neighboring gene uncharacterized LOC124901944 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27343 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:52959497-52959996 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:53013330-53014276 Neighboring gene uncharacterized LOC124901945 Neighboring gene uncharacterized LOC101929341 Neighboring gene ReSE screen-validated silencer GRCh37_chr8:53125987-53126195 Neighboring gene VISTA enhancer hs698 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_103338 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27344 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27345 Neighboring gene MPRA-validated peak7016 silencer Neighboring gene ribosomal protein L34 pseudogene 17 Neighboring gene ST18-FAM150A intergenic CAGE-defined low expression enhancer Neighboring gene MED14-independent group 3 enhancer GRCh37_chr8:53458378-53459577 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:53476246-53477222 Neighboring gene MPRA-validated peak7018 silencer Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr8:53512288-53512788 Neighboring gene ALK and LTK ligand 1 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr8:53541841-53542555 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr8:53566637-53567138 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr8:53567139-53567638 Neighboring gene RB1 inducible coiled-coil 1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19188 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19189 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19190 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19191

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Expression

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  • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

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Related articles in PubMed

  1. Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. Sarig O, et al. J Invest Dermatol, 2012 Jul. PMID 22437316
  2. ST18 affects cell-cell adhesion in pemphigus vulgaris in a tumour necrosis factor-α-dependent fashion. Assaf S, et al. Br J Dermatol, 2021 Jun. PMID 33205400
  3. ST18 Enhances PV-IgG-Induced Loss of Keratinocyte Cohesion in Parallel to Increased ERK Activation. Radeva MY, et al. Front Immunol, 2019. PMID 31057535, Free PMC Article
  4. High-resolution melting analysis to screen the ST18 gene functional risk variant for pemphigus vulgaris: The occasion to open a debate on its usefulness in clinical setting. De Bonis M, et al. Exp Mol Pathol, 2019 Jun. PMID 30926339
  5. Lack of association between the single nucleotide polymorphism of ST18 and pemphigus in Chinese population. Yue Z, et al. J Dermatol, 2014 Apr. PMID 24612320

See all (30) citations in PubMed

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. a Chinese population shows no remarkable association with the SNP rs2304365 in the region of ST18 and pemphigus, which suggests the relationship of ST18 and pemphigus may act in a population-specific manner
    Title: Lack of association between the single nucleotide polymorphism of ST18 and pemphigus in Chinese population.
  2. Up-regulation of ST18 in pemphigus vulgaris drives a self-amplifying p53-dependent pathomechanism resulting in decreased desmoglein 3 expression.
    Title: Up-regulation of ST18 in pemphigus vulgaris drives a self-amplifying p53-dependent pathomechanism resulting in decreased desmoglein 3 expression.
  3. Measurable Residual Disease Monitoring of SPAG6, ST18, PRAME, and XAGE1A Expression in Peripheral Blood May Detect Imminent Relapse in Childhood Acute Myeloid Leukemia.
    Title: Measurable Residual Disease Monitoring of SPAG6, ST18, PRAME, and XAGE1A Expression in Peripheral Blood May Detect Imminent Relapse in Childhood Acute Myeloid Leukemia.
  4. Genome-wide association study identifies susceptibility loci of brain atrophy to NFIA and ST18 in Alzheimer's disease.
    Title: Genome-wide association study identifies susceptibility loci of brain atrophy to NFIA and ST18 in Alzheimer's disease.
  5. ST18 affects cell-cell adhesion in pemphigus vulgaris in a tumour necrosis factor-alpha-dependent fashion.
    Title: ST18 affects cell-cell adhesion in pemphigus vulgaris in a tumour necrosis factor-α-dependent fashion.
  6. ST18 Enhances PV-IgG-Induced Loss of Keratinocyte Cohesion in Parallel to Increased ERK Activation.
    Title: ST18 Enhances PV-IgG-Induced Loss of Keratinocyte Cohesion in Parallel to Increased ERK Activation.
  7. The suppression of tumorigenicity 18 protein ST18 (ST18) -497-65050T>C polymorphisms (rs17315309) exhibit a very strong association in the pathogenesis of Pemphigus Vulgaris (PV) and could represent a new potential molecular target for the treatment of disease.
    Title: High-resolution melting analysis to screen the ST18 gene functional risk variant for pemphigus vulgaris: The occasion to open a debate on its usefulness in clinical setting.
  8. allele A in rs2304365 of ST18 may have a role in pemphigus in Iranian patients
    Title: The association between ST18 gene polymorphism and severe pemphigus disease among Iranian population.
  9. In this study, 2 of 8 (primary angle-closure glaucoma) PACG-associated loci were associated significantly with PACS status, the earliest stage in the angle-closure glaucoma disease course. The association of these PACG loci with PACS status suggests that these loci may confer susceptibility to a narrow angle configuration.
    Title: Evaluation of Primary Angle-Closure Glaucoma Susceptibility Loci in Patients with Early Stages of Angle-Closure Disease.
  10. the present findings indicate that ST18 may play a direct role in Pemphigus vulgaris (PV) and consequently represents a potential target for the treatment of this disease.
    Title: Identification of a Functional Risk Variant for Pemphigus Vulgaris in the ST18 Gene.
Submit: New GeneRIF Correction See all GeneRIFs (17)

Phenotypes

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Find tests for this gene in the NIH Genetic Testing Registry (GTR)

Review eQTL and phenotype association data in this region using PheGenI

EBI GWAS Catalog

Description
Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.
EBI GWAS Catalog

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Genotypes

Interactions

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Products Interactant Other Gene Complex Source Pubs Description

General gene information

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Markers

Homology

Clone Names

  • KIAA0535

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables DNA-binding transcription factor activity, RNA polymerase II-specific ISA
Inferred from Sequence Alignment
more info
  
enables RNA polymerase II cis-regulatory region sequence-specific DNA binding IDA
Inferred from Direct Assay
more info
 PubMed 
enables zinc ion binding IEA
Inferred from Electronic Annotation
more info
  
Process Evidence Code Pubs
involved_in interleukin-1-mediated signaling pathway IMP
Inferred from Mutant Phenotype
more info
 PubMed 
involved_in interleukin-6-mediated signaling pathway IMP
Inferred from Mutant Phenotype
more info
 PubMed 
involved_in negative regulation of cell population proliferation IDA
Inferred from Direct Assay
more info
 PubMed 
involved_in positive regulation of cysteine-type endopeptidase activity involved in apoptotic signaling pathway IMP
Inferred from Mutant Phenotype
more info
 PubMed 
involved_in positive regulation of transcription by RNA polymerase II IMP
Inferred from Mutant Phenotype
more info
 PubMed 
involved_in regulation of gene expression IBA
Inferred from Biological aspect of Ancestor
more info
  
involved_in tumor necrosis factor-mediated signaling pathway IMP
Inferred from Mutant Phenotype
more info
 PubMed 
Component Evidence Code Pubs
located_in chromatin ISA
Inferred from Sequence Alignment
more info
  
is_active_in nucleus IBA
Inferred from Biological aspect of Ancestor
more info
  
located_in nucleus IDA
Inferred from Direct Assay
more info
 PubMed 
part_of protein-DNA complex IDA
Inferred from Direct Assay
more info
 PubMed 

General protein information

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Preferred Names
suppression of tumorigenicity 18 protein
Names
ST18, C2H2C-type zinc finger
neural zinc finger transcription factor 3
suppression of tumorigenicity 18 (breast carcinoma) (zinc finger protein)
suppression of tumorigenicity 18, zinc finger
zinc finger protein 387

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

mRNA and Protein(s)

  1. NM_001352826.2 → NP_001339755.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915, AC103831
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  2. NM_001352827.2 → NP_001339756.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (3) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915, AC103831
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  3. NM_001352828.2 → NP_001339757.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (4) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915, AC103831
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Related
    ENSP00000514122.1, ENST00000699087.1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  4. NM_001352829.2 → NP_001339758.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (5) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915, AC103831
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  5. NM_001352830.2 → NP_001339759.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (6) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915, AC103831
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  6. NM_001352831.2 → NP_001339760.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (7) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915, AC103831
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Related
    ENSP00000508476.1, ENST00000693301.1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  7. NM_001352832.2 → NP_001339761.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (8) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915, AC103831
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  8. NM_001352833.2 → NP_001339762.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (9) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915, AC103831
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  9. NM_001352834.2 → NP_001339763.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (10) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915, AC103831
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  10. NM_001352835.2 → NP_001339764.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (11) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915, AC103831
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  11. NM_001352836.2 → NP_001339765.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (12) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915, AC103831
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  12. NM_001352837.2 → NP_001339766.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (13) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915, AC103831
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Related
    ENSP00000509475.1, ENST00000689386.1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  13. NM_001352838.2 → NP_001339767.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (14) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915, AC103831
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  14. NM_001352839.2 → NP_001339768.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (15) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  15. NM_001352840.2 → NP_001339769.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (16) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  16. NM_001352841.2 → NP_001339770.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (17) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  17. NM_001352842.2 → NP_001339771.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (18) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  18. NM_001352843.2 → NP_001339772.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (19) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  19. NM_001352844.2 → NP_001339773.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (20) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  20. NM_001352845.2 → NP_001339774.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (21) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  21. NM_001352846.2 → NP_001339775.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (22) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  22. NM_001352847.2 → NP_001339776.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (23) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  23. NM_001352848.2 → NP_001339777.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (24) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  24. NM_001352849.2 → NP_001339778.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (25) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  25. NM_001352850.2 → NP_001339779.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (26) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  26. NM_001352851.2 → NP_001339780.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (27) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  27. NM_001352852.2 → NP_001339781.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (28) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  28. NM_001352853.2 → NP_001339782.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (29) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  29. NM_001352854.2 → NP_001339783.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (30) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  30. NM_001352855.2 → NP_001339784.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (31) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  31. NM_001352856.2 → NP_001339785.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (32) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  32. NM_001352857.2 → NP_001339786.1  suppression of tumorigenicity 18 protein isoform a

    Status: VALIDATED

    Description
    Transcript Variant: This variant (33) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AC021915
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  33. NM_001352858.2 → NP_001339787.1  suppression of tumorigenicity 18 protein isoform c

    Status: VALIDATED

    Description
    Transcript Variant: This variant (43) encodes isoform c. Variants 43-45 all encode isoform c.
    Source sequence(s)
    AC021915, AC103831
    Conserved Domains (3) summary
    pfam01530
    Location:738 → 766
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:450 → 686
    MYT1; Myelin transcription factor 1
    cl25732
    Location:892 → 963
    SMC_N; RecF/RecN/SMC N terminal domain

  34. NM_001352859.2 → NP_001339788.1  suppression of tumorigenicity 18 protein isoform c

    Status: VALIDATED

    Description
    Transcript Variant: This variant (44) encodes isoform c. Variants 43-45 all encode isoform c.
    Source sequence(s)
    AC021915
    Conserved Domains (3) summary
    pfam01530
    Location:738 → 766
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:450 → 686
    MYT1; Myelin transcription factor 1
    cl25732
    Location:892 → 963
    SMC_N; RecF/RecN/SMC N terminal domain

  35. NM_001352860.2 → NP_001339789.1  suppression of tumorigenicity 18 protein isoform c

    Status: VALIDATED

    Description
    Transcript Variant: This variant (45) encodes isoform c. Variants 43-45 all encode isoform c.
    Source sequence(s)
    AC021915
    Conserved Domains (3) summary
    pfam01530
    Location:738 → 766
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:450 → 686
    MYT1; Myelin transcription factor 1
    cl25732
    Location:892 → 963
    SMC_N; RecF/RecN/SMC N terminal domain

  36. NM_001352861.2 → NP_001339790.1  suppression of tumorigenicity 18 protein isoform b

    Status: VALIDATED

    Description
    Transcript Variant: This variant (34) encodes isoform b. Variants 34-42 all encode isoform b.
    Source sequence(s)
    AC021915, AC103831
    Conserved Domains (3) summary
    pfam01530
    Location:732 → 760
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:444 → 680
    MYT1; Myelin transcription factor 1
    cl25732
    Location:886 → 957
    SMC_N; RecF/RecN/SMC N terminal domain

  37. NM_001352862.2 → NP_001339791.1  suppression of tumorigenicity 18 protein isoform b

    Status: VALIDATED

    Description
    Transcript Variant: This variant (35) encodes isoform b. Variants 34-42 all encode isoform b.
    Source sequence(s)
    AC021915, AC103831
    Conserved Domains (3) summary
    pfam01530
    Location:732 → 760
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:444 → 680
    MYT1; Myelin transcription factor 1
    cl25732
    Location:886 → 957
    SMC_N; RecF/RecN/SMC N terminal domain

  38. NM_001352863.2 → NP_001339792.1  suppression of tumorigenicity 18 protein isoform b

    Status: VALIDATED

    Description
    Transcript Variant: This variant (36) encodes isoform b. Variants 34-42 all encode isoform b.
    Source sequence(s)
    AC021915, AC103831
    Conserved Domains (3) summary
    pfam01530
    Location:732 → 760
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:444 → 680
    MYT1; Myelin transcription factor 1
    cl25732
    Location:886 → 957
    SMC_N; RecF/RecN/SMC N terminal domain

  39. NM_001352864.2 → NP_001339793.1  suppression of tumorigenicity 18 protein isoform b

    Status: VALIDATED

    Description
    Transcript Variant: This variant (37) encodes isoform b. Variants 34-42 all encode isoform b.
    Source sequence(s)
    AC021915
    Conserved Domains (3) summary
    pfam01530
    Location:732 → 760
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:444 → 680
    MYT1; Myelin transcription factor 1
    cl25732
    Location:886 → 957
    SMC_N; RecF/RecN/SMC N terminal domain

  40. NM_001352865.2 → NP_001339794.1  suppression of tumorigenicity 18 protein isoform b

    Status: VALIDATED

    Description
    Transcript Variant: This variant (38) encodes isoform b. Variants 34-42 all encode isoform b.
    Source sequence(s)
    AC021915
    Conserved Domains (3) summary
    pfam01530
    Location:732 → 760
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:444 → 680
    MYT1; Myelin transcription factor 1
    cl25732
    Location:886 → 957
    SMC_N; RecF/RecN/SMC N terminal domain

  41. NM_001352866.2 → NP_001339795.1  suppression of tumorigenicity 18 protein isoform b

    Status: VALIDATED

    Description
    Transcript Variant: This variant (39) encodes isoform b. Variants 34-42 all encode isoform b.
    Source sequence(s)
    AC021915
    Conserved Domains (3) summary
    pfam01530
    Location:732 → 760
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:444 → 680
    MYT1; Myelin transcription factor 1
    cl25732
    Location:886 → 957
    SMC_N; RecF/RecN/SMC N terminal domain

  42. NM_001352867.2 → NP_001339796.1  suppression of tumorigenicity 18 protein isoform b

    Status: VALIDATED

    Description
    Transcript Variant: This variant (40) encodes isoform b. Variants 34-42 all encode isoform b.
    Source sequence(s)
    AC021915
    Conserved Domains (3) summary
    pfam01530
    Location:732 → 760
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:444 → 680
    MYT1; Myelin transcription factor 1
    cl25732
    Location:886 → 957
    SMC_N; RecF/RecN/SMC N terminal domain

  43. NM_001352868.2 → NP_001339797.1  suppression of tumorigenicity 18 protein isoform b

    Status: VALIDATED

    Description
    Transcript Variant: This variant (41) encodes isoform b. Variants 34-42 all encode isoform b.
    Source sequence(s)
    AC021915
    Conserved Domains (3) summary
    pfam01530
    Location:732 → 760
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:444 → 680
    MYT1; Myelin transcription factor 1
    cl25732
    Location:886 → 957
    SMC_N; RecF/RecN/SMC N terminal domain

  44. NM_001352869.2 → NP_001339798.1  suppression of tumorigenicity 18 protein isoform b

    Status: VALIDATED

    Description
    Transcript Variant: This variant (42) encodes isoform b. Variants 46-51 all encode isoform b.
    Source sequence(s)
    AC021915
    Conserved Domains (3) summary
    pfam01530
    Location:732 → 760
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:444 → 680
    MYT1; Myelin transcription factor 1
    cl25732
    Location:886 → 957
    SMC_N; RecF/RecN/SMC N terminal domain

  45. NM_001352870.2 → NP_001339799.1  suppression of tumorigenicity 18 protein isoform d

    Status: VALIDATED

    Description
    Transcript Variant: This variant (46) encodes isoform d. Variants 46-51 all encode isoform d.
    Source sequence(s)
    AC021915, AC103831
    Conserved Domains (3) summary
    pfam01530
    Location:685 → 713
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 633
    MYT1; Myelin transcription factor 1
    cl25732
    Location:839 → 910
    SMC_N; RecF/RecN/SMC N terminal domain

  46. NM_001352871.2 → NP_001339800.1  suppression of tumorigenicity 18 protein isoform d

    Status: VALIDATED

    Description
    Transcript Variant: This variant (47) encodes isoform d. Variants 46-51 all encode isoform d.
    Source sequence(s)
    AC021915, AC103831
    Conserved Domains (3) summary
    pfam01530
    Location:685 → 713
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 633
    MYT1; Myelin transcription factor 1
    cl25732
    Location:839 → 910
    SMC_N; RecF/RecN/SMC N terminal domain

  47. NM_001352872.2 → NP_001339801.1  suppression of tumorigenicity 18 protein isoform d

    Status: VALIDATED

    Description
    Transcript Variant: This variant (48) encodes isoform d. Variants 34-42 all encode isoform d.
    Source sequence(s)
    AC021915, AC103831
    Conserved Domains (3) summary
    pfam01530
    Location:685 → 713
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 633
    MYT1; Myelin transcription factor 1
    cl25732
    Location:839 → 910
    SMC_N; RecF/RecN/SMC N terminal domain

  48. NM_001352873.2 → NP_001339802.1  suppression of tumorigenicity 18 protein isoform d

    Status: VALIDATED

    Description
    Transcript Variant: This variant (49) encodes isoform d. Variants 46-51 all encode isoform d.
    Source sequence(s)
    AC021915
    Conserved Domains (3) summary
    pfam01530
    Location:685 → 713
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 633
    MYT1; Myelin transcription factor 1
    cl25732
    Location:839 → 910
    SMC_N; RecF/RecN/SMC N terminal domain

  49. NM_001352874.2 → NP_001339803.1  suppression of tumorigenicity 18 protein isoform d

    Status: VALIDATED

    Description
    Transcript Variant: This variant (50) encodes isoform d. Variants 46-51 all encode isoform d.
    Source sequence(s)
    AC021915
    Conserved Domains (3) summary
    pfam01530
    Location:685 → 713
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 633
    MYT1; Myelin transcription factor 1
    cl25732
    Location:839 → 910
    SMC_N; RecF/RecN/SMC N terminal domain

  50. NM_001352875.2 → NP_001339804.1  suppression of tumorigenicity 18 protein isoform d

    Status: VALIDATED

    Description
    Transcript Variant: This variant (51) encodes isoform d. Variants 46-51 all encode isoform d.
    Source sequence(s)
    AC021915
    Conserved Domains (3) summary
    pfam01530
    Location:685 → 713
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 633
    MYT1; Myelin transcription factor 1
    cl25732
    Location:839 → 910
    SMC_N; RecF/RecN/SMC N terminal domain

  51. NM_001352876.2 → NP_001339805.1  suppression of tumorigenicity 18 protein isoform f

    Status: VALIDATED

    Source sequence(s)
    AC021915, AC103831
    Conserved Domains (3) summary
    pfam01530
    Location:421 → 449
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:215 → 369
    MYT1; Myelin transcription factor 1
    cl25732
    Location:575 → 646
    SMC_N; RecF/RecN/SMC N terminal domain

  52. NM_001352877.2 → NP_001339806.1  suppression of tumorigenicity 18 protein isoform e

    Status: VALIDATED

    Description
    Transcript Variant: This variant (52) encodes isoform e. Variants 52 and 53 both encode isoform e.
    Source sequence(s)
    AC021915, AC103831
    Conserved Domains (3) summary
    pfam01530
    Location:414 → 442
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:126 → 362
    MYT1; Myelin transcription factor 1
    cl25732
    Location:568 → 639
    SMC_N; RecF/RecN/SMC N terminal domain

  53. NM_001352878.2 → NP_001339807.1  suppression of tumorigenicity 18 protein isoform e

    Status: VALIDATED

    Description
    Transcript Variant: This variant (53) encodes isoform e. Variants 52 and 53 both encode isoform e.
    Source sequence(s)
    AC021915
    Conserved Domains (3) summary
    pfam01530
    Location:414 → 442
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:126 → 362
    MYT1; Myelin transcription factor 1
    cl25732
    Location:568 → 639
    SMC_N; RecF/RecN/SMC N terminal domain

  54. NM_001352879.1 → NP_001339808.1  suppression of tumorigenicity 18 protein isoform g

    Status: VALIDATED

    Description
    Transcript Variant: This variant (55) encodes isoform g. Variants 55-58 all encode isoform g.
    Source sequence(s)
    AC103831

  55. NM_001352880.1 → NP_001339809.1  suppression of tumorigenicity 18 protein isoform g

    Status: VALIDATED

    Description
    Transcript Variant: This variant (56) encodes isoform g. Variants 55-58 all encode isoform g.
    Source sequence(s)
    AC103831

  56. NM_001352881.1 → NP_001339810.1  suppression of tumorigenicity 18 protein isoform g

    Status: VALIDATED

    Description
    Transcript Variant: This variant (57) encodes isoform g. Variants 55-58 all encode isoform g.
    Source sequence(s)
    AC021915, AC103831

  57. NM_001352882.1 → NP_001339811.1  suppression of tumorigenicity 18 protein isoform g

    Status: VALIDATED

    Description
    Transcript Variant: This variant (58) encodes isoform g. Variants 55-58 all encode isoform g.
    Source sequence(s)
    AC103831

  58. NM_001352883.2 → NP_001339812.1  suppression of tumorigenicity 18 protein isoform h

    Status: VALIDATED

    Description
    Transcript Variant: This variant (59) encodes isoform h. Variants 59 and 60 both encode isoform h.
    Source sequence(s)
    AC103831
    Related
    ENST00000522102.5

  59. NM_001352884.2 → NP_001339813.1  suppression of tumorigenicity 18 protein isoform h

    Status: VALIDATED

    Description
    Transcript Variant: This variant (60) encodes isoform h. Variants 59 and 60 both encode isoform h.
    Source sequence(s)
    AC103831

  60. NM_014682.3 → NP_055497.1  suppression of tumorigenicity 18 protein isoform a

    See identical proteins and their annotated locations for NP_055497.1

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) encodes isoform a. Variants 1-33 all encode isoform a.
    Source sequence(s)
    AB011107, BC117147, BQ639545, DA288225
    Consensus CDS
    CCDS6149.1
    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Related
    ENSP00000276480.7, ENST00000276480.11
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

RNA

  1. NR_148195.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC021915, AC103831

  2. NR_148196.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC021915

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    52110838..52409879 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_047422485.1 → XP_047278441.1  suppression of tumorigenicity 18 protein isoform X2

  2. XM_047422486.1 → XP_047278442.1  suppression of tumorigenicity 18 protein isoform X2

  3. XM_047422487.1 → XP_047278443.1  suppression of tumorigenicity 18 protein isoform X2

  4. XM_024447349.2 → XP_024303117.1  suppression of tumorigenicity 18 protein isoform X1

    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  5. XM_047422484.1 → XP_047278440.1  suppression of tumorigenicity 18 protein isoform X1

    UniProtKB/Swiss-Prot
    O60284, Q17RY1

  6. XM_017014058.2 → XP_016869547.1  suppression of tumorigenicity 18 protein isoform X1

    UniProtKB/Swiss-Prot
    O60284, Q17RY1
    Conserved Domains (3) summary
    pfam01530
    Location:767 → 795
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:479 → 715
    MYT1; Myelin transcription factor 1
    cl25732
    Location:921 → 992
    SMC_N; RecF/RecN/SMC N terminal domain

  7. XM_024447350.2 → XP_024303118.1  suppression of tumorigenicity 18 protein isoform X3

    Conserved Domains (3) summary
    pfam01530
    Location:414 → 442
    zf-C2HC; Zinc finger, C2HC type
    pfam08474
    Location:126 → 362
    MYT1; Myelin transcription factor 1
    cl25732
    Location:568 → 639
    SMC_N; RecF/RecN/SMC N terminal domain

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    52486561..52785956 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_054361604.1 → XP_054217579.1  suppression of tumorigenicity 18 protein isoform X2

  2. XM_054361605.1 → XP_054217580.1  suppression of tumorigenicity 18 protein isoform X2

  3. XM_054361606.1 → XP_054217581.1  suppression of tumorigenicity 18 protein isoform X2

  4. XM_054361602.1 → XP_054217577.1  suppression of tumorigenicity 18 protein isoform X1

    UniProtKB/Swiss-Prot
    O60284, Q17RY1

  5. XM_054361601.1 → XP_054217576.1  suppression of tumorigenicity 18 protein isoform X1

    UniProtKB/Swiss-Prot
    O60284, Q17RY1

  6. XM_054361603.1 → XP_054217578.1  suppression of tumorigenicity 18 protein isoform X1

    UniProtKB/Swiss-Prot
    O60284, Q17RY1

  7. XM_054361607.1 → XP_054217582.1  suppression of tumorigenicity 18 protein isoform X3

Nucleotide Protein
Heading Accession and Version
Protein Accession Links
GenPept Link UniProtKB Link
O60284.1 GenPept UniProtKB/Swiss-Prot:O60284

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