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WormBase Tree Display for Gene: RGD:1590969

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Name Class

RGD:1590969IdentityNameCGC_namePcdh15Inferred_automaticallyAGR_import
Public_namePcdh15
DB_infoDatabaseRGDid1590969
AGRcURIRGD:1590969
EnsEMBLENSEMBL_geneIDENSRNOG00000000606
UniProtUniProt_ACA0A8I5Y0L1
A0A8I6GK65
A0A8I6GEC2
A0A8I5ZYQ7
A0A8I6B3E0
A0A8I6AT55
A0A8I5ZTI9
A0A8I6A7Z6
F1LXN4
SpeciesRattus norvegicus
StatusLive
Gene_infoBiotypeSO:0001217
OrthologWBGene00000397Caenorhabditis elegansFrom_analysisHieranoid
Inparanoid
OrthoFinder
Structured_descriptionAutomated_descriptionPredicted to enable calcium ion binding activity. Involved in response to calcium ion. Predicted to be located in several cellular components, including extracellular space; photoreceptor outer segment; and stereocilium bundle. Predicted to be active in stereocilium. Human ortholog(s) of this gene implicated in Usher syndrome type 1D; Usher syndrome type 1F; and autosomal recessive nonsyndromic deafness 23. Orthologous to human PCDH15 (protocadherin related 15); PARTICIPATES IN auditory mechanotransduction pathway; retinitis pigmentosa pathway; INTERACTS WITH atrazine; bisphenol A; lidocaine.Inferred_automaticallyAGR_import