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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Slc12a7
solute carrier family 12, member 7
MGI:1342283
16 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Slc12a7em1(IMPC)Bay/Slc12a7em1(IMPC)Bay
C57BL/6N-Slc12a7em1(IMPC)Bay/BayMmucd
preweaning lethality, incomplete penetrance J:211773
Slc12a7mpc264H/Slc12a7mpc264H
involves: BALB/c * C3H/HeH * C57BL/6J
deafness J:234901
Slc12a7tm1Tjj/Slc12a7tm1Tjj
involves: 129/Sv * C57BL/6
abnormal inner ear morphology J:76136
absent cochlear outer hair cells J:76136
absent organ of Corti J:76136
absent pinna reflex J:76136
normal behavior/neurological phenotype J:76136
cochlear ganglion degeneration J:76136
cochlear outer hair cell degeneration J:76136
deafness J:76136
decreased body weight J:76136
impaired hearing J:76136
increased or absent threshold for auditory brainstem response J:76136
increased urine pH J:76136
organ of Corti degeneration J:76136
renal tubular acidosis J:76136
normal vision/eye phenotype J:76136

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
04/16/2024
MGI 6.23
The Jackson Laboratory