Homo sapiens Protein: CTHRC1
Summary
InnateDB Protein IDBP-31719.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CTHRC1
Protein Name collagen triple helix repeat containing 1
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000330523
InnateDB Gene IDBG-31717 (CTHRC1)
Protein Structure
UniProt Annotation
Function May act as a negative regulator of collagen matrix deposition. {ECO:0000250}.
Subcellular Localization Secreted, extracellular space, extracellular matrix {ECO:0000250}.
Disease Associations Barrett esophagus (BE) [MIM:614266]: A condition characterized by a metaplastic change in which normal esophageal squamous epithelium is replaced by a columnar and intestinal-type epithelium. Patients with Barrett esophagus have an increased risk of esophageal adenocarcinoma. The main cause of Barrett esophagus is gastroesophageal reflux. The retrograde movement of acid and bile salts from the stomach into the esophagus causes prolonged injury to the esophageal epithelium and induces chronic esophagitis, which in turn is believed to trigger the pathologic changes. {ECO:0000269PubMed:21791690}. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry.
Tissue Specificity Isoform 1 is expressed in calcified atherosclerotic plaque and chondrocyte-like cells. {ECO:0000269PubMed:15618538}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
Experimentally validated
Total 2 [view]
Protein-Protein 2 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005109 frizzled binding
GO:0005515 protein binding
GO:0017147 Wnt-protein binding
Biological Process
GO:0016477 cell migration
GO:0032092 positive regulation of protein binding
GO:0033690 positive regulation of osteoblast proliferation
GO:0043932 ossification involved in bone remodeling
GO:0045669 positive regulation of osteoblast differentiation
GO:0060071 Wnt signaling pathway, planar cell polarity pathway
GO:0060122 inner ear receptor stereocilium organization
GO:0090090 negative regulation of canonical Wnt signaling pathway
GO:0090103 cochlea morphogenesis
GO:0090177 establishment of planar polarity involved in neural tube closure
Cellular Component
GO:0005578 proteinaceous extracellular matrix
GO:0005581 collagen trimer
GO:0005615 extracellular space
GO:0005737 cytoplasm
GO:0031012 extracellular matrix
Protein Structure and Domains
PDB ID
InterPro IPR008160 Collagen triple helix repeat
PFAM PF01391
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q96CG8
PhosphoSite PhosphoSite-Q96CG8
TrEMBL E5RK99
UniProt Splice Variant
Entrez Gene 115908
UniGene Hs.405614
RefSeq NP_612464
HUGO HGNC:18831
OMIM 610635
CCDS CCDS6299
HPRD 16772
IMGT
EMBL AC012213 AC069351 AF395488 AY136825 AY358914 BC014245 CH471060
GenPept AAH14245 AAN15749 AAO17919 AAQ89273 EAW91876