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Documentation
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 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
PR:000029067
Homo sapiens protein
Gene Template
HGNC:1884
CFTR (human)
Taxon
NCBITaxon:9606
Homo sapiens
Terms by PRO Category
Organism-Independent
Organism-Specific
Category
Number of Terms
Category
Number of Terms
Gene
0
Organism-Gene
1
Sequence
0
Organism-Sequence
5
Modification
0
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 (GO-centric view)
Switch to
PRO Centric View
Disease Associated GO Term
Protein Forms & Complexes
Evidence
DO:1485
cystic fibrosis
PR:P13569-3
hCFTR/iso:3
PMID:12913074
Molecular Function GO Term
Protein Forms & Complexes
Evidence
GO:0005260
intracellularly ATP-gated chloride channel activity
PR:000036594
hCFTR/iso:1/Phos:1
PMID:1716180
PR:000036594
hCFTR/iso:1/Phos:1
PMID:1716180
PR:000036594
hCFTR/iso:1/Phos:1
PMID:1716180
PR:000036594
hCFTR/iso:1/Phos:1
PMID:1716180
PR:000036594
hCFTR/iso:1/Phos:1
PMID:1716180
PR:000036594
hCFTR/iso:1/Phos:1
PMID:1716180
PR:000036594
hCFTR/iso:1/Phos:1
PMID:1716180
PR:000036594
hCFTR/iso:1/Phos:1
PMID:1716180
PR:000036594
hCFTR/iso:1/Phos:1
PMID:1716180
PR:000036594
hCFTR/iso:1/Phos:1
PMID:1716180
PR:000036594
hCFTR/iso:1/Phos:1
PMID:1716180
PR:000036594
hCFTR/iso:1/Phos:1
PMID:1716180
PR:000036594
hCFTR/iso:1/Phos:1
PMID:1716180
PR:000036594
hCFTR/iso:1/Phos:1
PMID:1716180
PR:000036594
hCFTR/iso:1/Phos:1
PMID:1716180
PR:000036594
hCFTR/iso:1/Phos:1
PMID:1716180
