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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Eps8l2
EPS8-like 2
MGI:2138828
20 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Eps8l2tm1b(EUCOMM)Wtsi/Eps8l2tm1b(EUCOMM)Wtsi
C57BL/6N-Eps8l2tm1b(EUCOMM)Wtsi/H
abnormal ear morphology J:211773
abnormal snout morphology J:211773
abnormal startle reflex J:211773
decreased circulating fructosamine level J:211773
decreased circulating serum albumin level J:211773
decreased prepulse inhibition J:211773
decreased startle reflex J:211773
increased circulating alkaline phosphatase level J:211773
Eps8l2tm1Wma/Eps8l2tm1Wma
B6.129P2-Eps8l2tm1Wma
abnormal auditory brainstem response J:200669
abnormal auditory summating potential J:200669
abnormal cochlear hair cell morphology J:200669
abnormal cochlear hair cell stereociliary bundle morphology J:200669
abnormal distortion product otoacoustic emission J:200669
abnormal hearing electrophysiology J:200669
abnormal vestibular system physiology J:200669
decreased cochlear nerve compound action potential J:200669
decreased inner hair cell stereocilia number J:200669
impaired hearing J:200669
increased or absent threshold for auditory brainstem response J:200669
short cochlear hair cell stereocilia J:200669

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
03/31/2020
MGI 6.15
The Jackson Laboratory