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Symbol Name ID |
Rab3gap2
RAB3 GTPase activating protein subunit 2 MGI:1916043 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcornea |
Cataract |
Developmental cataract |
Optic atrophy |
Deeply set eye |
Hypotelorism |
Microphthalmia |
Undetectable visual evoked potentials |
Strabismus |
| Disease(s) Associated with RAB3GAP2 | |||||||||
| Martsolf syndrome | |||||||||
| Warburg micro syndrome 2 |
| Mouse Phenotypes | abnormal optic disk morphology |
narrow eye opening |
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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 04/23/2024 MGI 6.23 |
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