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C19orf84 chromosome 19 open reading frame 84 [ Homo sapiens (human) ]

Gene ID: 147646, updated on 23-Nov-2021

Summary

Official Symbol
C19orf84provided by HGNC
Official Full Name
chromosome 19 open reading frame 84provided by HGNC
Primary source
HGNC:HGNC:27112
See related
Ensembl:ENSG00000262874
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
Expression
Restricted expression toward testis (RPKM 8.4) See more
Orthologs
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Genomic context

See C19orf84 in Genome Data Viewer
Location:
19q13.41
Exon count:
2
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 19 NC_000019.10 (51388289..51390591, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (51891543..51893845, complement)

Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene natural killer cell granule protein 7 Neighboring gene lens intrinsic membrane protein 2 Neighboring gene LIM2 and SIGLEC10 antisense RNA 1 Neighboring gene nucleolar protein interacting with the FHA domain of MKI67 pseudogene 6 Neighboring gene sialic acid binding Ig like lectin 10 Neighboring gene SIGLEC10 antisense RNA 1

Genomic regions, transcripts, and products

Expression

  • Project title: 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

General protein information

Preferred Names
uncharacterized protein C19orf84

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_001193623.2NP_001180552.1  uncharacterized protein C19orf84

    See identical proteins and their annotated locations for NP_001180552.1

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) encodes the supported protein.
    Source sequence(s)
    AC008750, BC043532
    Consensus CDS
    CCDS58676.1
    UniProtKB/Swiss-Prot
    I3L1E1
    Related
    ENSP00000458772.1, ENST00000574814.2
    Conserved Domains (1) summary
    PLN02205
    Location:4590
    PLN02205; alpha,alpha-trehalose-phosphate synthase [UDP-forming]

RNA

  1. NR_126530.2 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) uses an alternate splice site in the 5' terminal exon, compared to variant 1. This variant is represented as non-coding because the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AC008750, BC043532, BC143997

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000019.10 Reference GRCh38.p13 Primary Assembly

    Range
    51388289..51390591 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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