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Symbol
Name
ID

Spns2
SPNS lysolipid transporter 2, sphingosine-1-phosphate
MGI:2384936

Phenotype annotations related to hearing/vestibular/ear

Darker colors indicate more annotations

Human Phenotypes	Sensorineural hearing impairment
Disease(s) Associated with SPNS2	Sensorineural hearing impairment
autosomal recessive nonsyndromic deafness 115

Mouse Phenotypes		abnormal auditory brainstem response
Availability	Mouse Genotype	abnormal auditory brainstem response
	Spns2^{tm1a(KOMP)Wtsi}/Spns2^{tm1a(KOMP)Wtsi}

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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