Version 5.4
Bos taurus Protein: RECS1
Summary
InnateDB Protein IDBP-696390.2
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol RECS1
Protein Name transmembrane BAX inhibitor motif-containing protein 1
Synonyms RECS1;
Species Bos taurus
Ensembl Protein ENSBTAP00000005137
InnateDB Gene IDBG-643802 (RECS1)
Protein Structure
UniProt Annotation
Function
Subcellular Localization
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 2 interaction(s) predicted by orthology.
Predicted by orthology
Total 2 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005123 death receptor binding
Biological Process
GO:0090005 negative regulation of establishment of protein localization to plasma membrane
GO:1902042 negative regulation of extrinsic apoptotic signaling pathway via death domain receptors
GO:1902045 negative regulation of Fas signaling pathway
Cellular Component
GO:0005765 lysosomal membrane
GO:0005794 Golgi apparatus
GO:0010008 endosome membrane
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0070062 extracellular vesicular exosome
Protein Structure and Domains
PDB ID
InterPro IPR006214 Bax inhibitor 1-related
PFAM PF01027
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt
PhosphoSite PhosphoSite-
TrEMBL Q6QRN7
UniProt Splice Variant
Entrez Gene 404134
UniGene Bt.6989
RefSeq NP_991367
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL AY528248 BC116018 BC142530 BT025369 DAAA02005929
GenPept AAI16019 AAI42531 AAS20596 ABF57325

If you use InnateDB for your research, please cite the following publication:

Breuer et al., InnateDB: systems biology of innate immunity and beyond - recent updates and continuing curation. Nucl. Acids Res. (2013) 41 (D1) 

InnateDB is being developed jointly by the Brinkman Laboratory (Simon Fraser University, British Columbia, Canada), the Hancock Laboratory (University of British Columbia, Vancouver, British Columbia) and the Lynn EMBL Australia Group (South Australian Health & Medical Research Institute and Flinders University, Adelaide, Australia).

Funding is currently provided by Allergen and EMBL Australia. Previous funding has been provided by Genome Canada, the Foundation for the National Institutes of Health through the Grand Challenges in Global Health initiative and by Teagasc. InnateDB curated interactions are licensed under the Design Science License. All other data is licensed under the terms of the originating database. Contact: innatedb-mail@sfu.ca