|
Symbol Name ID |
Gja1
gap junction protein, alpha 1 MGI:95713 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormality of the ear |
Conductive hearing impairment |
Mixed hearing impairment |
Abnormal pinna morphology |
Large earlobe |
Low-set ears |
Protruding ear |
Hearing impairment |
Unilateral deafness |
| Disease(s) Associated with GJA1 | |||||||||
| autosomal recessive craniometaphyseal dysplasia | |||||||||
| erythrokeratodermia variabilis | |||||||||
| oculodentodigital dysplasia | |||||||||
| palmoplantar keratoderma and congenital alopecia 1 |
| Mouse Phenotypes | hearing/vestibular/ear phenotype |
decreased tympanic ring size |
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| Availability | Mouse Genotype | ||
| Gja1tm1Kdr/Gja1tm1Kdr | |||
| Gja1M1Jrt/Gja1+ | * | ||
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 05/21/2024 MGI 6.23 |
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