Misplaced Pages

RAP1GAP2

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Protein-coding gene in the species Homo sapiens
RAP1GAP2
Identifiers
AliasesRAP1GAP2, GARNL4, RAP1GA3, RAP1 GTPase activating protein 2
External IDsMGI: 3028623; HomoloGene: 56695; GeneCards: RAP1GAP2; OMA:RAP1GAP2 - orthologs
Gene location (Human)
Chromosome 17 (human)
Chr.Chromosome 17 (human)
Chromosome 17 (human)Genomic location for RAP1GAP2Genomic location for RAP1GAP2
Band17p13.3Start2,755,705 bp
End3,037,741 bp
Gene location (Mouse)
Chromosome 11 (mouse)
Chr.Chromosome 11 (mouse)
Chromosome 11 (mouse)Genomic location for RAP1GAP2Genomic location for RAP1GAP2
Band11|11 B5Start74,274,182 bp
End74,501,741 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • Brodmann area 23

  • middle temporal gyrus

  • endothelial cell

  • superior frontal gyrus

  • right hemisphere of cerebellum

  • islet of Langerhans

  • postcentral gyrus

  • cerebellar vermis

  • entorhinal cortex

  • beta cell
Top expressed in
  • islet of Langerhans

  • primary motor cortex

  • medial vestibular nucleus

  • submandibular gland

  • prefrontal cortex

  • deep cerebellar nuclei

  • cingulate gyrus

  • pontine nuclei

  • dentate gyrus of hippocampal formation granule cell

  • epithelium of stomach
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

23108

380711

Ensembl

ENSG00000132359

ENSMUSG00000038807

UniProt

Q684P5

Q5SVL6

RefSeq (mRNA)

NM_001100398
NM_015085
NM_001330058

NM_001015046
NM_001364131
NM_001364132

RefSeq (protein)

NP_001093868
NP_001316987
NP_055900

NP_001015046
NP_001351060
NP_001351061
NP_001388587

Location (UCSC)Chr 17: 2.76 – 3.04 MbChr 11: 74.27 – 74.5 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

RAP1 GTPase activating protein 2 is a protein in humans that is encoded by the RAP1GAP2 gene.

This gene encodes a GTPase-activating protein that activates the small guanine-nucleotide-binding protein Rap1 in platelets. The protein interacts with synaptotagmin-like protein 1 and Rab27 and regulates secretion of dense granules from platelets at sites of endothelial damage. Multiple transcript variants encoding different isoforms have been found for this gene. .

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000132359Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000038807Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: RAP1 GTPase activating protein 2".

Further reading

Stub icon

This article on a gene on human chromosome 17 is a stub. You can help Misplaced Pages by expanding it.

Categories:
RAP1GAP2 Add topic