|
Symbol Name ID |
Snx14
sorting nexin 14 MGI:2155664 |
| Darker colors indicate more annotations |
| Human Phenotypes | Spasticity |
Cerebral cortical atrophy |
Cerebellar hypoplasia |
Cerebellar atrophy |
Ataxia |
Apraxia |
Babinski sign |
Absent speech |
Delayed speech and language development |
Delayed early-childhood social milestone development |
Autistic behavior |
Intellectual disability |
Hyporeflexia |
Inability to walk |
Global developmental delay |
Delayed fine motor development |
Delayed gross motor development |
Delayed ability to sit |
Seizure |
| Disease(s) Associated with SNX14 | |||||||||||||||||||
| autosomal recessive spinocerebellar ataxia 20 |
| Mouse Phenotypes | decreased prepulse inhibition |
|
| 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 05/07/2024 MGI 6.23 |
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