Symbol Name ID |
Slc12a7
solute carrier family 12, member 7 MGI:1342283 |
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 |
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 12/10/2024 MGI 6.24 |
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