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Protein Ontology Report - hKCNV2

PR:Q8TDN2 - http://purl.obolibrary.org/obo/PR_Q8TDN2
This page represents a class of proteins encompassing all the protein products of the KCNV2 gene in human.
Ontology Information
PRO ID PR:Q8TDN2 Show OBO stanza / PAF
PRO name potassium voltage-gated channel subfamily V member 2 (human)
Synonyms
PRO-short-label: EXACT: hKCNV2
Gene-based: RELATED: KCNV2
Other: EXACT: voltage-gated potassium channel subunit Kv8.2 (human)
Definition A voltage-gated potassium channel KCNV2 that is encoded in the genome of human. [PRO:CNA, UniProtKB:Q8TDN2]
PRO Category organism-gene
Parent PR:000000726 voltage-gated potassium channel KCNV2
Gene Template HGNC:19698 KCNV2
Taxon NCBITaxon:9606 Homo sapiens
Terms by PRO Category Retrieve All terms OBO Stanza / PAF
Organism-Specific
Category Number of Terms
organism-gene 1
organism-sequence 7
organism-modification 0
Term Hierarchy Visualization DAG     OLS     Cytoscape


Interactive Sequence View Select/align proteoforms across species

Protein Forms
PRO ID & Category Annotation Complex Name Short Label Definition & Comment

Functional Annotation
PRO Term GO Annotation Evidence
PR:000000803
hKCNV2/var:G459D
Gly-459, CHEBI:29958
associated_with_disease_progression DOID:0050795 cone dystrophy PMID:16909397
PR:000000804
hKCNV2/var:A259V
Ala-259, CHEBI:30015
associated_with_disease_progression DOID:0050795 cone dystrophy PMID:16909397
PR:000000805
hKCNV2/var:L126Q
Leu-126, CHEBI:30011
associated_with_disease_progression DOID:0050795 cone dystrophy PMID:16909397
PR:000000806
hKCNV2/var:4
associated_with_disease_progression DOID:0050795 cone dystrophy PMID:16909397
PR:000000807
hKCNV2/var:S256W
Ser-256, CHEBI:29954
associated_with_disease_progression DOID:0050795 cone dystrophy PMID:16909397
PR:000000808
hKCNV2/var:W188C
Trp-188, CHEBI:29950
associated_with_disease_progression DOID:0050795 cone dystrophy PMID:16909397
PR:000000726
KCNV2
enables GO:0015459 potassium channel regulator activity PANTHER:PTHR11537:SF40

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