Entity Details

Primary name CNPY3_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9BT09
EntryNameCNPY3_HUMAN
FullNameProtein canopy homolog 3
TaxID9606
Evidenceevidence at protein level
Length278
SequenceStatuscomplete
DateCreated2008-01-15
DateModified2021-06-02

Ontological Relatives

GenesCNPY3

GO terms

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GOName
GO:0002224 toll-like receptor signaling pathway
GO:0005102 signaling receptor binding
GO:0005788 endoplasmic reticulum lumen
GO:0045087 innate immune response

Subcellular Location

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Subcellular Location
Endoplasmic reticulum

Domains

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DomainNameCategoryType
IPR021852 Domain of unknown function DUF3456DomainDomain

Diseases

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Disease IDSourceNameDescription
617929 OMIMDevelopmental and epileptic encephalopathy 60 (DEE60)A form of epileptic encephalopathy, a heterogeneous group of severe childhood onset epilepsies characterized by refractory seizures, neurodevelopmental impairment, and poor prognosis. Development is normal prior to seizure onset, after which cognitive and motor delays become apparent. DEE60 is an autosomal recessive condition characterized by onset of seizures in the first months of life. The disease is caused by variants affecting the gene represented in this entry.