Homo sapiens Protein: ASCC1 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-77843.7 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | ASCC1 | ||||||||||||||||||
Protein Name | activating signal cointegrator 1 complex subunit 1 | ||||||||||||||||||
Synonyms | |||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000320461 | ||||||||||||||||||
InnateDB Gene | IDBG-77835 (ASCC1) | ||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||
Function | Enhances NF-kappa-B, SRF and AP1 transactivation. In cells responding to gastrin-activated paracrine signals, it is involved in the induction of SERPINB2 expression by gastrin. {ECO:0000269PubMed:19074642}. | ||||||||||||||||||
Subcellular Localization | Cytoplasm. | ||||||||||||||||||
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=The gene represented in this entry may be involved in disease pathogenesis. | ||||||||||||||||||
Tissue Specificity | Ubiquitous. | ||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 6 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||
PDB ID | |||||||||||||||||||
InterPro |
IPR004087
K Homology domain IPR004088 K Homology domain, type 1 IPR009097 RNA ligase/cyclic nucleotide phosphodiesterase IPR009210 Predicted eukaryotic LigT IPR019510 Protein kinase A anchor protein, nuclear localisation signal domain |
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PFAM |
PF00013
PF13014 PF10469 |
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PRINTS | |||||||||||||||||||
PIRSF |
PIRSF027019
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SMART |
SM00322
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TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | Q8N9N2 | ||||||||||||||||||
PhosphoSite | PhosphoSite-Q8N9N2 | ||||||||||||||||||
TrEMBL | F5H874 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 51008 | ||||||||||||||||||
UniGene | Hs.607176 | ||||||||||||||||||
RefSeq | XP_006717939 | ||||||||||||||||||
HUGO | HGNC:24268 | ||||||||||||||||||
OMIM | 614215 | ||||||||||||||||||
CCDS | CCDS31219 | ||||||||||||||||||
HPRD | |||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AC022392 AF132952 AK023436 AK094170 AL607035 AY013290 BC012291 CH471083 | ||||||||||||||||||
GenPept | AAD27727 AAG45476 AAH12291 BAC04299 BAG51193 CAI15907 CAI15908 EAW54444 EAW54445 | ||||||||||||||||||