Symbol Name ID |
Xpnpep3
X-prolyl aminopeptidase 3, mitochondrial MGI:2445217 |
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 |
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Availability | Mouse Genotype | |
Xpnpep3tm1.1(KOMP)Vlcg/Xpnpep3+ |
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 |
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