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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Ndp
Norrie disease (pseudoglioma) (human)
MGI:102570
31 phenotypes from 3 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Ndptm1Lex/Y
involves: 129S5/SvEvBrd
abnormal retina vasculature morphology J:154863
blood vessel congestion J:154863
increased vascular permeability J:154863
Ndptm1Lex/Ndptm1Lex
involves: 129S5/SvEvBrd
abnormal retina vasculature morphology J:154863
blood vessel congestion J:154863
increased vascular permeability J:154863
Ndptm1Wbrg/Y
involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1
abnormal cochlear ganglion morphology J:77024
abnormal retina vasculature morphology J:77024
abnormal stria vascularis vasculature morphology J:77024
abnormal strial intermediate cell morphology J:77024
absent strial marginal cells J:77024
normal behavior/neurological phenotype J:77024
cochlear ganglion degeneration J:77024
cochlear inner hair cell degeneration J:77024
cochlear outer hair cell degeneration J:77024
deafness J:77024
increased or absent threshold for auditory brainstem response J:77024
increased susceptibility to age-related hearing loss J:77024
sensorineural hearing loss J:77024
stria vascularis degeneration J:77024
type I spiral ligament fibrocyte degeneration J:77024
Ndptm1Wbrg/Y
involves: 129P2/OlaHsd * C57BL/6
abnormal retina inner nuclear layer morphology J:30902
abnormal retina outer nuclear layer morphology J:30902
abnormal retina outer plexiform layer morphology J:30902
abnormal retina photoreceptor layer morphology J:30902
abnormal retina pigmentation J:30902
abnormal vitreous body morphology J:30902
decreased retina photoreceptor cell number J:30902
disorganized retina ganglion layer J:30902
disorganized retina layers J:30902
photoreceptor outer segment degeneration J:30902
vitreous body deposition J:30902
Ndptm1Wbrg/Ndp+
involves: 129P2/OlaHsd * C57BL/6
normal vision/eye phenotype J:30902
Ndptm1Wbrg/Ndptm1Wbrg
involves: 129P2/OlaHsd * C57BL/6
normal reproductive system phenotype J:115734
Ndptm2Nat/Ndp+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal brain vasculature morphology J:154020
abnormal retina vasculature morphology J:154020

Contributing Projects:
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
The Jackson Laboratory