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Symbol
Name
ID
Ush1c
USH1 protein network component harmonin
MGI:1919338
Phenotype annotations related to vision/eye
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Iris hypopigmentation
Cataract
Rod-cone dystrophy
Abnormal electroretinogram
Undetectable electroretinogram
High hypermetropia
Nyctalopia
Hemianopia
Scotoma
Visual loss
Disease(s) Associated with USH1C
autosomal recessive nonsyndromic deafness 18A
Usher syndrome type 1
Usher syndrome type 1C

Mouse Phenotypes
vision/eye phenotype
retinal degeneration
abnormal electroretinogram waveform feature
Availability Mouse Genotype
Ush1cdfcr-3J/Ush1cdfcr-3J *
Ush1cdfcr/Ush1cdfcr
Ush1ctm1Xzl/Ush1ctm1Xzl *

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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last database update
03/13/2019
MGI 6.13
The Jackson Laboratory