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STMN3 stathmin 3 [ Homo sapiens (human) ]

Gene ID: 50861, updated on 9-Jul-2017
Official Symbol
STMN3provided by HGNC
Official Full Name
stathmin 3provided by HGNC
Primary source
HGNC:HGNC:15926
See related
Ensembl:ENSG00000197457 MIM:608362; Vega:OTTHUMG00000032985
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
SCLIP
Summary
This gene encodes a protein which is a member of the stathmin protein family. Members of this protein family form a complex with tubulins at a ratio of 2 tubulins for each stathmin protein. Microtubules require the ordered assembly of alpha- and beta-tubulins, and formation of a complex with stathmin disrupts microtubule formation and function. A pseudogene of this gene is located on chromosome 22. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]
Orthologs
Location:
20q13.33
Exon count:
6
Annotation release Status Assembly Chr Location
108 current GRCh38.p7 (GCF_000001405.33) 20 NC_000020.11 (63639705..63653610, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 20 NC_000020.10 (62271058..62284963, complement)

Chromosome 20 - NC_000020.11Genomic Context describing neighboring genes Neighboring gene glucocorticoid modulatory element binding protein 2 Neighboring gene melanoma highly expressed competing endogenous lncRNA for miR-425 and miR-489 Neighboring gene uncharacterized LOC105372726 Neighboring gene RTEL1-TNFRSF6B readthrough (NMD candidate) Neighboring gene regulator of telomere elongation helicase 1 Neighboring gene TNF receptor superfamily member 6b Neighboring gene ADP ribosylation factor related protein 1

  • 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 Jun 15 11:32:44 2016

GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

NHGRI GWAS Catalog

Description
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.
NHGRI GWA Catalog
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.
NHGRI GWA Catalog
Products Interactant Other Gene Complex Source Pubs Description

Homology

Gene Ontology Provided by GOA

Function Evidence Code Pubs
protein domain specific binding ISS
Inferred from Sequence or Structural Similarity
more info
 
tubulin binding IBA
Inferred from Biological aspect of Ancestor
more info
 
Process Evidence Code Pubs
cytoplasmic microtubule organization ISS
Inferred from Sequence or Structural Similarity
more info
 
microtubule depolymerization IBA
Inferred from Biological aspect of Ancestor
more info
 
negative regulation of Rac protein signal transduction ISS
Inferred from Sequence or Structural Similarity
more info
 
nervous system development TAS
Traceable Author Statement
more info
PubMed 
neuron projection development IBA
Inferred from Biological aspect of Ancestor
more info
 
neuron projection development ISS
Inferred from Sequence or Structural Similarity
more info
 
regulation of GTPase activity ISS
Inferred from Sequence or Structural Similarity
more info
 
regulation of cytoskeleton organization IBA
Inferred from Biological aspect of Ancestor
more info
 
regulation of cytoskeleton organization ISS
Inferred from Sequence or Structural Similarity
more info
 
regulation of microtubule polymerization or depolymerization IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
Golgi apparatus IEA
Inferred from Electronic Annotation
more info
 
axon IEA
Inferred from Electronic Annotation
more info
 
cytoplasm IBA
Inferred from Biological aspect of Ancestor
more info
 
cytoplasm ISS
Inferred from Sequence or Structural Similarity
more info
 
growth cone IEA
Inferred from Electronic Annotation
more info
 
neuron projection IBA
Inferred from Biological aspect of Ancestor
more info
 
Preferred Names
stathmin-3
Names
SCG10-like protein
stathmin-like 3

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_001276310.1NP_001263239.1  stathmin-3 isoform 2

    See identical proteins and their annotated locations for NP_001263239.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (2) contains an alternate 5' exon and uses a downstream start codon, compared to variant 1. The resulting protein (isoform 2) is shorter and has a distinct N-terminus compared to isoform 1.
    Source sequence(s)
    AK298903, AL353715
    Consensus CDS
    CCDS63330.1
    UniProtKB/Swiss-Prot
    Q9NZ72
    Related
    ENSP00000439840.1, ENST00000540534.5
    Conserved Domains (1) summary
    pfam00836
    Location:32163
    Stathmin; Stathmin family
  2. NM_015894.3NP_056978.2  stathmin-3 isoform 1

    See identical proteins and their annotated locations for NP_056978.2

    Status: REVIEWED

    Description
    Transcript Variant: This variant (1) encodes the longest protein (isoform 1).
    Source sequence(s)
    AK131326, BC009381, BC056873, BQ703411, BX449528, DA161621, DA181040, DB564475
    Consensus CDS
    CCDS13529.1
    UniProtKB/Swiss-Prot
    Q9NZ72
    Related
    ENSP00000359070.1, OTTHUMP00000031570, ENST00000370053.2, OTTHUMT00000080163
    Conserved Domains (1) summary
    pfam00836
    Location:43174
    Stathmin; Stathmin family

RNA

  1. NR_075070.1 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (3) uses an alternate splice site in an internal exon compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AK310010, AL353715

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 108 details...Open this link in a new tab

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

Reference GRCh38.p7 Primary Assembly

Genomic

  1. NC_000020.11 Reference GRCh38.p7 Primary Assembly

    Range
    63639705..63653610 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate CHM1_1.1

Genomic

  1. NC_018931.2 Alternate CHM1_1.1

    Range
    62172106..62186629 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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