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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Alg10
ALG10 alpha-1,2-glucosyltransferase
MGI:2146159
8 phenotypes from 1 allele in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Alg10nse5/Alg10nse5
129S6.B6-Alg10nse5
abnormal cochlear outer hair cell morphology J:209766
absent cochlear microphonics J:209766
absent distortion product otoacoustic emissions J:209766
cochlear outer hair cell degeneration J:209766
deafness J:209766
decreased cochlear outer hair cell number J:209766
normal hearing/vestibular/ear phenotype J:209766
increased or absent threshold for auditory brainstem response J:209766
Alg10nse5/Alg10nse5
involves: C57BL/6J
deafness J:85113

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
03/18/2025
MGI 6.24
The Jackson Laboratory