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Symbol Name ID |
Vwa1
von Willebrand factor A domain containing 1 MGI:2179729 |
| Darker colors indicate more annotations |
| Human Phenotypes | Tongue fasciculations |
Motor axonal neuropathy |
Hyporeflexia |
Impaired tactile sensation |
Paresthesia |
| Disease(s) Associated with VWA1 | |||||
| autosomal recessive distal hereditary motor neuronopathy 7 |
| Mouse Phenotypes | abnormal nervous system morphology |
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| Availability | Mouse Genotype | |
| Vwa1tm1Jfba/Vwa1tm1Jfba | ||
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 07/14/2026 MGI 6.24 |
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