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Symbol Name ID |
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| Synonyms | CdGAP, mKIAA1204 | ||||||||||||||||
| Feature Type | protein coding gene | ||||||||||||||||
| Genetic Map | |||||||||||||||||
| Sequence Map |
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Mammalian homology |
human;
rat;
cattle;
chimpanzee;
dog, domestic
(Mammalian Orthology) Comparative Map (Mouse/Human Arhgap31 ± 2 cM)
Gene Tree: Arhgap31 |
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Humanortholog |
ARHGAP31 Rho GTPase activating protein 31
NCBI Gene ID 57514 Human Synonyms: AOS1, CDGAP Human Chr3:119013220-119138323 bp, + strand Reference GRCh37.p2 Primary Assembly Human Diseases Associated with Human ARHGAP31 (1) | ||||||||||||||||
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Alleles and phenotypes |
All alleles(3) :
Targeted(3)
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Gene Ontology (GO) classifications |
All GO classifications: (10 annotations)
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| Expression |
Literature Summary: (2 records) Data Summary: Results (30) Tissues (18) Images (17) Theiler Stages: 15, 17, 19, 20, 22, 24, 26, 28
External Resources: Allen Institute GEO ArrayExpress |
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Molecular reagents |
All nucleic(18)
Genomic(1)
cDNA(16)
Primer pair(1)
Microarray probesets(7) |
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Other database links |
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| Sequences |
All sequences(45) RefSeq(2) UniProt(2) |
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| Polymorphisms | SNPs(487 from dbSNP Build 128) | ||||||||||||||||
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Protein-related information |
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| References |
(Earliest) J:50532
Lamarche-Vane N, et al., CdGAP, a novel proline-rich GTPase-activating protein for Cdc42 and Rac. J Biol Chem. 1998 Oct 30;273(44):29172-7 (Latest) J:177944 Southgate L, et al., Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies. Am J Hum Genet. 2011 May 13;88(5):574-85 All references(41) |
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Other accession IDs |
MGI:1923377, MGI:2146575 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 04/03/2013 MGI 5.12 |
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