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RASSF10 Ras association domain family member 10 [ Homo sapiens (human) ]

Gene ID: 644943, updated on 22-May-2022

Summary

Official Symbol
RASSF10provided by HGNC
Official Full Name
Ras association domain family member 10provided by HGNC
Primary source
HGNC:HGNC:33984
See related
Ensembl:ENSG00000189431 MIM:614713; AllianceGenome:HGNC:33984
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
Summary
Predicted to be involved in positive regulation of neural precursor cell proliferation and positive regulation of neurogenesis. Predicted to be located in cytosol; microtubule organizing center; and spindle pole. [provided by Alliance of Genome Resources, Apr 2022]
Orthologs
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Genomic context

See RASSF10 in Genome Data Viewer
Location:
11p15.3
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (13009316..13012119)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (13101893..13104695)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (13030863..13033666)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 958 Neighboring gene RASSF10 divergent transcript Neighboring gene uncharacterized LOC105376558 Neighboring gene uncharacterized LOC124902635

Genomic regions, transcripts, and products

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Phenotypes

EBI GWAS Catalog

Description
Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
EBI GWAS Catalog

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Homology

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables protein binding IPI
Inferred from Physical Interaction
more info
PubMed 
Process Evidence Code Pubs
involved_in nervous system development IEA
Inferred from Electronic Annotation
more info
 
involved_in positive regulation of neural precursor cell proliferation ISS
Inferred from Sequence or Structural Similarity
more info
 
involved_in positive regulation of neurogenesis ISS
Inferred from Sequence or Structural Similarity
more info
 
involved_in signal transduction IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
located_in cytosol IEA
Inferred from Electronic Annotation
more info
 
located_in microtubule organizing center IEA
Inferred from Electronic Annotation
more info
 
located_in spindle pole IEA
Inferred from Electronic Annotation
more info
 

General protein information

Preferred Names
ras association domain-containing protein 10
Names
Ras association (RalGDS/AF-6) domain family (N-terminal) member 10

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_001080521.3NP_001073990.2  ras association domain-containing protein 10

    See identical proteins and their annotated locations for NP_001073990.2

    Status: VALIDATED

    Source sequence(s)
    AC084859, BX098487
    Consensus CDS
    CCDS44542.2
    UniProtKB/Swiss-Prot
    A6NK89
    Related
    ENSP00000485526.1, ENST00000529419.3
    Conserved Domains (1) summary
    cl00155
    Location:88132
    UBQ; Ubiquitin-like proteins

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000011.10 Reference GRCh38.p14 Primary Assembly

    Range
    13009316..13012119
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    13101893..13104695
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)