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Symbol
Name
ID
Xpnpep3
X-prolyl aminopeptidase 3, mitochondrial
MGI:2445217
Phenotype annotations related to hearing/vestibular/ear
Darker colors indicate more annotations
Human Phenotypes
Sensorineural hearing impairment
Disease(s) Associated with XPNPEP3
nephronophthisis-like nephropathy 1

Mouse Phenotypes
abnormal auditory brainstem response
Availability Mouse Genotype
Xpnpep3tm1.1(KOMP)Vlcg/Xpnpep3+

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
04/16/2024
MGI 6.23
The Jackson Laboratory