Slc44a2 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc44a2
solute carrier family 44, member 2
MGI:1915932

11 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc44a2^em1(IMPC)J/Slc44a2^em1(IMPC)J C57BL/6NJ-Slc44a2^em1(IMPC)J/J	abnormal startle reflex	J:211773
Slc44a2^tm1.1Tec/Slc44a2^tm1.1Tec involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL/J	no abnormal phenotype detected	J:239440
Slc44a2^tm1.2Tec/Slc44a2⁺ FVB.129(Cg)-Slc44a2^tm1.2Tec	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
Slc44a2^tm1.2Tec/Slc44a2^tm1.2Tec FVB.129(Cg)-Slc44a2^tm1.2Tec	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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