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Symbol
Name
ID

Slc12a2
solute carrier family 12, member 2
MGI:101924

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Schizophrenia	Global developmental delay	Motor delay
Disease(s) Associated with SLC12A2
autosomal dominant nonsyndromic deafness 78

Mouse Phenotypes		absent cochlear hair cells	decreased cochlear inner hair cell number	decreased cochlear outer hair cell number	abnormal cochlear inner hair cell morphology	abnormal cranial ganglia morphology
Availability	Mouse Genotype	absent cochlear hair cells	decreased cochlear inner hair cell number	decreased cochlear outer hair cell number	abnormal cochlear inner hair cell morphology	abnormal cranial ganglia morphology
	Slc12a2^sy-ns/Slc12a2^sy-ns
	Slc12a2^tm1Dlp/Slc12a2^tm1Dlp
	Slc12a2^tm1Ges/Slc12a2^tm1Ges
	Slc12a2^tm2Bhk/Slc12a2^tm2Bhk

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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