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Protein Ontology Report - hCFTR

PR:P13569 - http://purl.obolibrary.org/obo/PR_P13569
This page represents a class of proteins encompassing all the protein products of the CFTR gene in human.
Ontology Information
PRO ID PR:P13569 Show OBO stanza / PAF
PRO name cystic fibrosis transmembrane conductance regulator (human)
Synonyms
PRO-short-label: EXACT: hCFTR
Gene-based: RELATED: ABCC7 | CFTR
Other: EXACT: ATP-binding cassette sub-family C member 7 (human) | cAMP-dependent chloride channel (human) | channel conductance-controlling ATPase (human)
Definition A cystic fibrosis transmembrane conductance regulator that is encoded in the genome of human. [PRO:CNA, UniProtKB:P13569]
PRO Category organism-gene
Parent PR:000001044 cystic fibrosis transmembrane conductance regulator
Gene Template HGNC:1884 CFTR
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 3
organism-modification 4
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:P13569-3
hCFTR/iso:3
associated_with_disease_progression DOID:1485 cystic fibrosis PMID:12913074
PR:000036594
hCFTR/iso:1/Phos:1
Ser-737/Ser-768/Ser-795/Ser-813, MOD:00046
enables GO:0005260 intracellularly ATP-gated chloride channel activity PMID:14602047
enables GO:0005260 intracellularly ATP-gated chloride channel activity PMID:1716180

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