| Primary Identifier | MGI:1333857 | Organism | mouse, laboratory |
| Chromosome | 16 | NCBI Gene Number | 12549 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0) Enables GTPase activator activity and SH3 domain binding activity. Acts upstream of or within small GTPase-mediated signal transduction. Located in lamellipodium. Is expressed in several structures, including 1st branchial arch; central nervous system; heart; retina layer; and surface ectoderm. Human ortholog(s) of this gene implicated in Adams-Oliver syndrome and coronary artery disease. Orthologous to human ARHGAP31 (Rho GTPase activating protein 31). PHENOTYPE: Mice homozygous for a knock-out allele exhibit partial lethality during fetal growth through weaning and abnormal vascular development associated with subcutaneous edema and hemorrhages, pale meninges and liver, and reduced VEGF-mediated capillary sprouting from aortic ring explants. [provided by MGI curators] |
Features --> Cross References
Canonical gene --> CDSs in specific strains.
Canonical gene --> Exons in specific strains
Canonical gene --> Strain-specific IDs, biotypes, and locations
Canonical gene --> Transcripts in specific strains.
Features --> Overlapping features
