Protein Ontology Report - hKCNQ4 PR:P56696 - http://purl.obolibrary.org/obo/PR_P56696

This page represents a class of proteins encompassing all the protein products of the KCNQ4 gene in human .

Ontology Information
PRO ID	PR:P56696 Show OBO stanza / PAF
PRO name	potassium voltage-gated channel subfamily KQT member 4 (human)
Synonyms	PRO-short-label: hKCNQ4 EXACT: KQT-like 4 (human); potassium channel subunit alpha KvLQT4 (human); voltage-gated potassium channel subunit Kv7.4 (human) Gene-based: KCNQ4
Definition	A voltage-gated potassium channel subunit KCNQ4 that is encoded in the genome of human. [PRO:CNA, UniProtKB:P56696]
PRO Category	organism-gene
Parent	PR:000000731 voltage-gated potassium channel subunit KCNQ4
Terms by PRO Category	Retrieve All terms OBO Stanza / PAF Organism-Specific Category Number of Terms organism-gene 1 organism-sequence 8 organism-modification 0
Term Hierarchy Visualization	DAG     OLS     Cytoscape

Related Cross References
DB identifiers	DTO:01100235, HGNC:6298, Reactome:R-HSA-977515, UniProtKB:P56696

Interactive Sequence View Select/align proteoforms across species

Protein Forms Display Category: All All organism-gene organism-sequence
PRO ID & Category Annotation Complex Name Short Label Definition & Comment

Functional Annotation PRO Centric View GO Centric View

PRO Term GO Annotation Evidence PR:000000923 hKCNQ4/var:L281S Leu-281, CHEBI:29999 associated_with_disease_progression DOID:0050564 autosomal dominant nonsyndromic deafness PMID:10571947 PR:000000922 hKCNQ4/var:G285S Gly-285, CHEBI:29999 associated_with_disease_progression DOID:0050564 autosomal dominant nonsyndromic deafness PMID:10025409 capable_of GO:0005249 voltage-gated potassium channel activity PMID:10025409 PR:000000921 hKCNQ4/var:L274H Leu-274, CHEBI:29979 associated_with_disease_progression DOID:0050564 autosomal dominant nonsyndromic deafness PMID:10925378 PR:000000920 hKCNQ4/var:G285C Gly-285, CHEBI:29950 associated_with_disease_progression DOID:0050564 autosomal dominant nonsyndromic deafness PMID:10369879 capable_of GO:0005249 voltage-gated potassium channel activity PMID:10369879 PR:000000925 hKCNQ4/var:G321S Gly-321, CHEBI:29999 associated_with_disease_progression DOID:0050564 autosomal dominant nonsyndromic deafness PMID:10369879 PR:000000924 hKCNQ4/var:W276S Trp-276, CHEBI:29999 associated_with_disease_progression DOID:0050564 autosomal dominant nonsyndromic deafness PMID:10369879

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