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 |
|
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 08/02/2024 MGI 6.24 |
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