About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Ush1c
USH1 protein network component harmonin
MGI:1919338
55 phenotypes from 8 alleles in 10 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Ush1cdfcr-2J/Ush1cdfcr-2J
B6;129S4
abnormal inner hair cell stereociliary bundle morphology J:85400
abnormal outer hair cell stereociliary bundle morphology J:85400
circling J:85400
cochlear inner hair cell degeneration J:85400
cochlear outer hair cell degeneration J:85400
deafness J:85400
head tossing J:85400
impaired balance J:85400
increased or absent threshold for auditory brainstem response J:85400
vestibular hair cell degeneration J:85400
Ush1cdfcr-3J/Ush1cdfcr-3J
STOCK Ush1cdfcr-3J/J
circling J:147859
deafness J:147859
head bobbing J:147859
normal vision/eye phenotype J:147859
Ush1cdfcr/Ush1cdfcr
involves: BALB/cByJ
abnormal inner hair cell stereociliary bundle morphology J:85400
abnormal outer hair cell stereociliary bundle morphology J:85400
circling J:85400
cochlear inner hair cell degeneration J:85400
cochlear outer hair cell degeneration J:85400
deafness J:85400
head tossing J:85400
impaired balance J:85400
increased or absent threshold for auditory brainstem response J:85400
retinal degeneration J:85400
vestibular hair cell degeneration J:85400
Ush1cdfcr/Ush1cdfcr
involves: BALB/cBySmn * C57BL/6 * CB17
abnormal cochlear hair bundle tip links morphology J:157359
abnormal hair cell mechanoelectric transduction J:157359
cochlear ganglion degeneration J:157359
deafness J:157359
increased or absent threshold for auditory brainstem response J:157359
organ of Corti degeneration J:157359
Ush1ctm1.1Mull/Ush1ctm1.1Mull
involves: 129S/SvEv * C57BL/6 * SJL
abnormal cochlear hair cell stereociliary bundle morphology J:157359
circling J:157359
deafness J:157359
head tossing J:157359
increased or absent threshold for auditory brainstem response J:157359
Ush1ctm1.1Ugds/Ush1ctm1.1Ugds
involves: 129S2/SvPas
abnormal cochlear hair cell inter-stereocilial links morphology J:135991
abnormal cochlear outer hair cell morphology J:158897
abnormal inner hair cell stereociliary bundle morphology J:135991
abnormal orientation of cochlear hair cell stereociliary bundles J:135991
abnormal outer hair cell stereociliary bundle morphology J:135991, J:141421, J:158897
Ush1ctm1a(KOMP)Wtsi/Ush1ctm1a(KOMP)Wtsi
C57BL/6N-Ush1ctm1a(KOMP)Wtsi/Wtsi
absent pinna reflex J:211773
decreased body length J:211773
decreased circulating amylase level J:211773
decreased circulating cholesterol level J:211773
decreased circulating glucose level J:211773
decreased circulating HDL cholesterol level J:211773
decreased circulating insulin level J:211773
decreased circulating potassium level J:211773
decreased circulating triglyceride level J:211773
decreased grip strength J:211773
decreased total body fat amount J:211773
impaired righting response J:211773
improved glucose tolerance J:211773
increased bone mineral content J:211773
increased circulating chloride level J:211773
increased circulating sodium level J:211773
increased lean body mass J:211773
increased mean platelet volume J:211773
increased or absent threshold for auditory brainstem response J:211773
increased rib number J:211773
limb grasping J:211773
stereotypic behavior J:211773
trunk curl J:211773
Ush1ctm1Bkts/Ush1ctm1Bkts
involves: 129S6/SvEvTac * C57BL/6J * FVB/N
absent pinna reflex J:118248
circling J:118248
head tossing J:118248
hyperactivity J:118248
normal reproductive system phenotype J:118248
Ush1ctm1Xzl/Ush1c+
B6.129-Ush1ctm1Xzl
increased or absent threshold for auditory brainstem response J:183898
Ush1ctm1Xzl/Ush1ctm1Xzl
B6.129-Ush1ctm1Xzl
abnormal cochlear hair cell morphology J:158047
abnormal cochlear outer hair cell morphology J:158047
abnormal electroretinogram waveform feature J:158047
abnormal orientation of inner hair cell stereociliary bundles J:158047
abnormal orientation of outer hair cell stereociliary bundles J:158047
abnormal outer hair cell stereociliary bundle morphology J:158047
circling J:158047
deafness J:158047
head tossing J:158047
hyperactivity J:158047
impaired swimming J:158047
increased or absent threshold for auditory brainstem response J:158047
normal vision/eye phenotype J:158047
Ush1ctm1Xzl/Ush1ctm1Xzl
involves: 129S1/Sv * 129X1/SvJ
abnormal colon morphology J:212327
abnormal enterocyte morphology J:212327
abnormal intestinal epithelium morphology J:212327
abnormal small intestine morphology J:212327
decreased small intestinal microvillus size J:212327

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
10/09/2018
MGI 6.12
The Jackson Laboratory