Symbol Name ID |
Snx14
sorting nexin 14 MGI:2155664 |
Darker colors indicate more annotations |
Human Phenotypes | Delayed early-childhood social milestone development |
Autistic behavior |
Disease(s) Associated with SNX14 | ||
autosomal recessive spinocerebellar ataxia 20 |
Mouse Phenotypes | increased exploration in new environment |
increased grip strength |
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Availability | Mouse Genotype | ||
Snx14em1(IMPC)H/Snx14+ |
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 09/03/2024 MGI 6.24 |
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