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Symbol Name ID |
Nr2f1
nuclear receptor subfamily 2, group F, member 1 MGI:1352451 |
| Darker colors indicate more annotations |
| Human Phenotypes | Prominent antihelix |
Uplifted earlobe |
Abnormal helix morphology |
Darwin tubercle of helix |
Protruding ear |
Hearing impairment |
| Disease(s) Associated with NR2F1 | ||||||
| Bosch-Boonstra-Schaaf optic atrophy syndrome |
| Mouse Phenotypes | abnormal organ of Corti supporting cell differentiation |
abnormal cochlear hair cell development |
abnormal cochlear sensory epithelium morphology |
increased cochlear hair cell number |
increased cochlear inner hair cell number |
increased cochlear outer hair cell number |
abnormal orientation of inner hair cell stereociliary bundles |
abnormal orientation of outer hair cell stereociliary bundles |
increased Deiters cell number |
short scala media |
abnormal hearing physiology |
abnormal auditory brainstem response |
increased or absent threshold for auditory brainstem response |
impaired hearing |
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| Availability | Mouse Genotype | ||||||||||||||
| Nr2f1tm1Mjts/Nr2f1tm1Mjts | |||||||||||||||
| Nr2f1tm1.1(KOMP)Mbp/Nr2f1+ | |||||||||||||||
| Nr2f1tm1Mjts/Nr2f1+ | |||||||||||||||
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 04/30/2024 MGI 6.23 |
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