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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Rp1l1
retinitis pigmentosa 1 homolog like 1
MGI:2384303
8 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Rp1l1tm1Jnz/Rp1l1tm1Jnz
involves: 129S7/SvEvBrd
abnormal cone electrophysiology J:151463
abnormal photoreceptor outer segment morphology J:151463
abnormal retina morphology J:151463
abnormal rod electrophysiology J:151463
decreased retina photoreceptor cell number J:151463
retina rod cell degeneration J:151463
short photoreceptor outer segment J:151463
thin retina outer nuclear layer J:151463

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
04/23/2024
MGI 6.23
The Jackson Laboratory