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Symbol Name ID |
Marveld2
MARVEL (membrane-associating) domain containing 2 MGI:2446166 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Prelingual sensorineural hearing impairment |
| Disease(s) Associated with MARVELD2 | |
| autosomal recessive nonsyndromic deafness 49 |
| Mouse Phenotypes | hearing/vestibular/ear phenotype |
abnormal ear morphology |
cochlear inner hair cell degeneration |
cochlear outer hair cell degeneration |
cochlear hair cell degeneration |
abnormal organ of Corti morphology |
abnormal stria vascularis morphology |
thin stria vascularis |
abnormal utricular macula morphology |
abnormal auditory brainstem response |
increased or absent threshold for auditory brainstem response |
abnormal distortion product otoacoustic emission |
deafness |
syndromic hearing loss |
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| Availability | Mouse Genotype | ||||||||||||||
| Marveld2tm1.1Sria/Marveld2tm1.1Sria | * | ||||||||||||||
| Marveld2tm1b(EUCOMM)Wtsi/Marveld2tm1b(EUCOMM)Wtsi | |||||||||||||||
| Marveld2tm1Sats/Marveld2tm1Sats | |||||||||||||||
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 04/23/2024 MGI 6.23 |
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