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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Slc44a2
solute carrier family 44, member 2
MGI:1915932
12 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Slc44a2em1(IMPC)J/Slc44a2em1(IMPC)J
C57BL/6NJ-Slc44a2em1(IMPC)J/J
abnormal retina morphology J:211773
abnormal startle reflex J:211773
Slc44a2tm1.1Tec/Slc44a2tm1.1Tec
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL/J
no abnormal phenotype detected J:239440
Slc44a2tm1.2Tec/Slc44a2+
FVB.129(Cg)-Slc44a2tm1.2Tec
abnormal cochlear ganglion morphology J:239440
abnormal organ of Corti morphology J:239440
decreased cochlear outer hair cell number J:239440
increased or absent threshold for auditory brainstem response J:239440
Slc44a2tm1.2Tec/Slc44a2tm1.2Tec
FVB.129(Cg)-Slc44a2tm1.2Tec
abnormal cochlear ganglion morphology J:239440
abnormal organ of Corti morphology J:239440
abnormal tunnel of Corti morphology J:239440
decreased body size J:239440
decreased cochlear inner hair cell number J:239440
decreased cochlear outer hair cell number J:239440
increased or absent threshold for auditory brainstem response J:239440
increased susceptibility to age-related hearing loss J:239440
sensorineural hearing loss J:239440

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
06/12/2024
MGI 6.13
The Jackson Laboratory