Misplaced Pages

RASGRP2

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
RASGRP2
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

2MA2

Identifiers
AliasesRASGRP2, CALDAG-GEFI, CDC25L, RAS guanyl releasing protein 2
External IDsOMIM: 605577; MGI: 1333849; HomoloGene: 4250; GeneCards: RASGRP2; OMA:RASGRP2 - orthologs
Gene location (Human)
Chromosome 11 (human)
Chr.Chromosome 11 (human)
Chromosome 11 (human)Genomic location for RASGRP2Genomic location for RASGRP2
Band11q13.1Start64,726,911 bp
End64,745,456 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • granulocyte

  • spleen

  • monocyte

  • apex of heart

  • right coronary artery

  • popliteal artery

  • blood

  • tibial arteries

  • lymph node

  • left coronary artery
    n/a
More reference expression data
BioGPS


More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

10235

19395

Ensembl

ENSG00000068831

ENSMUSG00000032946

UniProt

Q7LDG7

Q9QUG9

RefSeq (mRNA)

NM_001098670
NM_001098671
NM_005825
NM_153819
NM_001318398

NM_011242

RefSeq (protein)

NP_001092140
NP_001092141
NP_001305327
NP_722541

NP_035372
NP_001351991
NP_001351992

Location (UCSC)Chr 11: 64.73 – 64.75 Mbn/a
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

RAS guanyl-releasing protein 2 is a protein that in humans is encoded by the RASGRP2 gene.

The protein encoded by this gene is a brain-enriched nucleotide exchange factor that contains an N-terminal GEF domain, 2 tandem repeats of EF-hand calcium-binding motifs, and a C-terminal diacylglycerol/phorbol ester-binding domain. This protein can activate small GTPases, including RAS and RAP1/RAS3. The nucleotide exchange activity of this protein can be stimulated by calcium and diacylglycerol. Two alternatively spliced transcript variants of this gene, encoding distinct isoforms, have been reported.

Clinical significance

Mutations in RASGRP2 are associated with severe bleeding.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000068831Ensembl, May 2017
  2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. Kawasaki H, Springett GM, Toki S, Canales JJ, Harlan P, Blumenstiel JP, Chen EJ, Bany IA, Mochizuki N, Ashbacher A, Matsuda M, Housman DE, Graybiel AM (Nov 1998). "A Rap guanine nucleotide exchange factor enriched highly in the basal ganglia". Proc Natl Acad Sci U S A. 95 (22): 13278–83. Bibcode:1998PNAS...9513278K. doi:10.1073/pnas.95.22.13278. PMC 23782. PMID 9789079.
  5. ^ "Entrez Gene: RASGRP2 RAS guanyl releasing protein 2 (calcium and DAG-regulated)".
  6. Canault, M; Ghalloussi, D; Grosdidier, C; Guinier, M; Perret, C; Chelghoum, N; Germain, M; Raslova, H; Peiretti, F; Morange, P. E.; Saut, N; Pillois, X; Nurden, A. T.; Cambien, F; Pierres, A; Van Den Berg, T. K.; Kuijpers, T. W.; Alessi, M. C.; Tregouet, D. A. (2014). "Human CalDAG-GEFI gene (RASGRP2) mutation affects platelet function and causes severe bleeding". Journal of Experimental Medicine. 211 (7): 1349–62. doi:10.1084/jem.20130477. PMC 4076591. PMID 24958846.

Further reading

External links


Stub icon

This article on a gene on human chromosome 11 is a stub. You can help Misplaced Pages by expanding it.

Categories: