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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Ercc8
excision repaiross-complementing rodent repair deficiency, complementation group 8
MGI:1919241
17 phenotypes from 2 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Ercc8em1(IMPC)H/Ercc8em1(IMPC)H
C57BL/6N-Ercc8em1(IMPC)H/H
abnormal locomotor behavior J:211773
increased circulating cholesterol level J:211773
increased circulating HDL cholesterol level J:211773
Ercc8tm1Jhjh/Ercc8tm1Jhjh
B6J.129P2-Ercc8tm1Jhjh
cochlear inner hair cell degeneration J:219993
cochlear outer hair cell degeneration J:219993
decreased distortion product otoacoustic emission amplitude J:219993
impaired hearing J:219993
increased or absent threshold for auditory brainstem response J:219993
Ercc8tm1Jhjh/Ercc8tm1Jhjh
involves: 129P2/OlaHsd * C57BL/6J
abnormal DNA repair J:74959
astrocytosis J:179808
increased cellular sensitivity to ultraviolet irradiation J:74959
increased incidence of tumors by UV-induction J:74959
increased sensitivity to skin irradiation J:74959
microgliosis J:179808
photophobia J:74959
retina photoreceptor degeneration J:74959
skin photosensitivity J:74959

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
11/19/2024
MGI 6.24
The Jackson Laboratory