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Protein Ontology Report - KCNQ4

PR:000000731 - http://purl.obolibrary.org/obo/PR_000000731
Ontology Information
PRO ID PR:000000731 Show OBO stanza / PAF
PRO name voltage-gated potassium channel subunit KCNQ4
Synonyms
PRO-short-label: KCNQ4
EXACT: KQT-like 4; potassium channel subunit alpha KvLQT4; voltage-gated potassium channel subunit Kv7.4
Definition A voltage-gated potassium channel subunit KQT that is a translation product of the human KCNQ4 gene or a 1:1 ortholog thereof. [PRO:CNA]
PRO Category gene
Parent PR:000000684 voltage-gated potassium channel subunit KQT
Terms by PRO Category Retrieve All terms OBO Stanza / PAF
Organism-Independent Organism-Specific
Category Number of Terms Category Number of Terms
gene 1 organism-gene 2
sequence 2 organism-sequence 8
modification 0 organism-modification 0
union 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: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
PR:Q9JK97
mKCNQ4
participates_in GO:0042472 inner ear morphogenesis PMID:16437162
participates_in GO:0007605 sensory perception of sound PMID:16437162
Biological Process GO Term Protein Forms & Complexes Evidence
GO:0042472 inner ear morphogenesis PR:Q9JK97 mKCNQ4

PMID:16437162
GO:0007605 sensory perception of sound PR:Q9JK97 mKCNQ4

PMID:16437162

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