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Symbol Name ID |
Rab3gap2
RAB3 GTPase activating protein subunit 2 MGI:1916043 |
| Darker colors indicate more annotations |
| Human Phenotypes | Low anterior hairline |
Low posterior hairline |
Brachycephaly |
Micrognathia |
Hypoplasia of the maxilla |
Malar flattening |
Microcephaly |
Secondary microcephaly |
Midface retrusion |
Everted lower lip vermilion |
Long philtrum |
Short philtrum |
High palate |
Furrowed tongue |
Tooth malposition |
Broad nasal tip |
Depressed nasal bridge |
Prominent nasal bridge |
Short nose |
Downslanted palpebral fissures |
Epicanthus |
| Disease(s) Associated with RAB3GAP2 | |||||||||||||||||||||
| Martsolf syndrome | |||||||||||||||||||||
| Warburg micro syndrome 2 |
| Mouse Phenotypes | abnormal snout morphology |
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| Availability | Mouse Genotype | |
| Rab3gap2tm1b(KOMP)Wtsi/Rab3gap2tm1b(KOMP)Wtsi | ||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/16/2024 MGI 6.23 |
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