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Protein Ontology report - voltage-gated potassium channel subunit KCNQ1 sequence variant 29 (human)
PR:000000838 -
http://purl.obolibrary.org/obo/PR_000000838
Annotations
Ontology Information
Show OBO stanza
/
PAF
/
GPI
PRO ID
PR:000000838
PRO name
voltage-gated potassium channel subunit KCNQ1 sequence variant 29 (human)
Synonyms
PRO-Short-label
:
EXACT:
hKCNQ1/var:29
PRO-proteoform-std
:
EXACT:
UniProtKB:P49747
, 21-70, 74-757
NARROW:
UniProtKB:P49747-1
, 21-70, 74-757
Definition
"A potassium voltage-gated channel subfamily KQT member 1 (human) that has a three-residue deletion at the positions equivalent to 71-73 of the amino acid sequence represented by
UniProtKB:P51787-1
. Example:
UniProtKB:P49747-1
, 21-70, 74-757." [PRO:CNA, PRO:DAN,
UniProtKB:P51787
]
PRO Category
organism-sequence
Parent
PR:P51787
potassium voltage-gated channel subfamily KQT member 1 (human)
Taxon
NCBITaxon:9606
Homo sapiens
Term Hierarchy
Visualization
DAG:
OLS:
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Related Cross References
Db identifiers
UniProtKB_VAR:VAR_009917
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Functional Annotation (PRO-centric view)
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GO Centric View
PRO Term
GO Annotation
Evidence
PR:000000838
hKCNQ1/var:29
UniProtKB:P49747, 21-70, 74-757 | UniProtKB:P49747-1, 21-70, 74-757
"A potassium voltage-gated channel subfamily KQT member 1 (human) that has a three-residue deletion at the positions equivalent to 71-73 of the amino acid sequence represented by UniProtKB:P51787-1. Example: UniProtKB:P49747-1, 21-70, 74-757." [PRO:CNA, PRO:DAN, UniProtKB:P51787]
associated_with_disease_progression
DO:2843
long QT syndrome
PMID:10511610