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Protein Ontology report - cystic fibrosis transmembrane conductance regulator (human)
PR:P13569 - http://purl.obolibrary.org/obo/PR_P13569
 
  Protein Forms  Annotations      
Ontology Information Show OBO stanza / PAF / GPI
  PRO ID
PR:P13569   
  PRO namecystic 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 Categoryorganism-gene 
  ParentPR:000001044 cystic fibrosis transmembrane conductance regulator
PR:000029067 Homo sapiens protein
  Gene TemplateHGNC:1884 CFTR (human)
  TaxonNCBITaxon:9606 Homo sapiens
  Terms by PRO Category
Organism-Independent Organism-Specific
         Category          Number of Terms          Category          Number of Terms
         Gene0                                                  Organism-Gene 1                                        
         Sequence0                                                  Organism-Sequence 5                                        
         Modification0                                                  Organism-Modification 5                                        
  Term Hierarchy
  Visualization
DAG: OLS:
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Related Cross References

  Db identifiers
UniProtKB:P13569
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Protein Forms  Switch to Extended View   

Category  
PRO Form Name
Short Name
Ann. Has Annotation?

comp. In Complex?
organism-gene


PR:P13569 cystic fibrosis transmembrane conductance regulator (human)
hCFTR

organism-sequence


PR:000063429 cystic fibrosis transmembrane conductance regulator sequence variant N1303K (human)
hCFTR/var:N1303K

organism-sequence


PR:000063523 cystic fibrosis transmembrane conductance regulator sequence variant G551D (human)
hCFTR/var:G551D

organism-sequence


PR:P13569-1 cystic fibrosis transmembrane conductance regulator isoform 1 (human)
hCFTR/iso:1

organism-modification


PR:000036593 cftr isoform 1 N-glycosylated 1 (human)
hCFTR/iso:1/NGlyco:1

organism-modification


PR:000036594 cftr isoform 1 phosphorylated 1 (human)
hCFTR/iso:1/Phos:1
Yes
organism-modification


PR:000036595 cftr isoform 1 phosphorylated 2 (human)
hCFTR/iso:1/Phos:2

organism-sequence


PR:P13569-2 cystic fibrosis transmembrane conductance regulator isoform 2 (human)
hCFTR/iso:2

organism-sequence


PR:P13569-3 cystic fibrosis transmembrane conductance regulator isoform 3 (human)
hCFTR/iso:3
Yes
organism-modification


PR:000046699 cystic fibrosis transmembrane conductance regulator ubiquitinated form (human)
hCFTR/UbiqLys+

organism-modification


PR:000079746 cystic fibrosis transmembrane conductance regulator phosphorylated 1 (human)
hCFTR/Phos:1

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Functional Annotation (PRO-centric view) Switch to GO Centric View   
PRO Term GO Annotation Evidence
PR:000036594 hCFTR/iso:1/Phos:1
Example: UniProtKB:P13569-1, Ser-737/Ser-768/Ser-795/Ser-813, MOD:00046		 enablesGO:0005260 intracellularly ATP-gated chloride channel activity PMID:1716180
GO:0005260 intracellularly ATP-gated chloride channel activity PMID:1716180
PR:P13569-3 hCFTR/iso:3 associated_with_disease_progressionDO:1485 cystic fibrosis PMID:12913074