About   Help   FAQ
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
Export: Excel File
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/19/2024
MGI 6.24 		The Jackson Laboratory