InnateDB Protein
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IDBP-31719.5
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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CTHRC1
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Protein Name
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collagen triple helix repeat containing 1
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Synonyms
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000330523
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InnateDB Gene
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IDBG-31717 (CTHRC1)
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Protein Structure
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Function |
May act as a negative regulator of collagen matrix deposition. {ECO:0000250}.
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Subcellular Localization |
Secreted, extracellular space, extracellular matrix {ECO:0000250}.
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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.
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Tissue Specificity |
Isoform 1 is expressed in calcified atherosclerotic plaque and chondrocyte-like cells. {ECO:0000269PubMed:15618538}.
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Comments |
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Number of Interactions
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This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
Experimentally validated |
Total |
2
[view]
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Protein-Protein |
2
[view]
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Protein-DNA |
0
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Protein-RNA |
0
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DNA-DNA |
0
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RNA-RNA |
0
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DNA-RNA |
0
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Molecular Function |
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Biological Process |
GO:0016477
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cell migration
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GO:0032092
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positive regulation of protein binding
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GO:0033690
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positive regulation of osteoblast proliferation
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GO:0043932
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ossification involved in bone remodeling
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GO:0045669
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positive regulation of osteoblast differentiation
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GO:0060071
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Wnt signaling pathway, planar cell polarity pathway
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GO:0060122
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inner ear receptor stereocilium organization
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GO:0090090
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negative regulation of canonical Wnt signaling pathway
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GO:0090103
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cochlea morphogenesis
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GO:0090177
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establishment of planar polarity involved in neural tube closure
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Cellular Component |
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PDB ID |
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InterPro |
IPR008160
Collagen triple helix repeat
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PFAM |
PF01391
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PRINTS |
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PIRSF |
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SMART |
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TIGRFAMs |
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Modification |
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SwissProt |
Q96CG8
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PhosphoSite |
PhosphoSite-Q96CG8
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TrEMBL |
E5RK99
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UniProt Splice Variant |
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Entrez Gene |
115908
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UniGene |
Hs.405614
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RefSeq |
NP_612464
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HUGO |
HGNC:18831
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OMIM |
610635
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CCDS |
CCDS6299
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HPRD |
16772
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IMGT |
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EMBL |
AC012213
AC069351
AF395488
AY136825
AY358914
BC014245
CH471060
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GenPept |
AAH14245
AAN15749
AAO17919
AAQ89273
EAW91876
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