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Symbol Name ID |
Ank
progressive ankylosis MGI:3045421 |
| Darker colors indicate more annotations |
| Human Phenotypes | Mixed hearing impairment |
| Disease(s) Associated with ANKH | |
| autosomal dominant craniometaphyseal dysplasia |
| Mouse Phenotypes | abnormal middle ear ossicle morphology |
fusion of middle ear ossicles |
incudomalleolar fusion |
abnormal auditory bulla morphology |
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| Availability | Mouse Genotype | ||||
| Anktm1.1Ejr/Anktm1.1Ejr | |||||
| Anktm1.1Kng/Anktm1.1Kng | |||||
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 04/09/2024 MGI 6.23 |
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