Version 5.4
Homo sapiens Protein: FAM132A
Summary
InnateDB Protein IDBP-84748.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol FAM132A
Protein Name family with sequence similarity 132, member A
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000329137
InnateDB Gene IDBG-84746 (FAM132A)
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.
Gene Ontology

Molecular Function
Accession GO Term
GO:0005179 hormone activity
GO:0005515 protein binding
Biological Process
GO:0010906 regulation of glucose metabolic process
GO:0035774 positive regulation of insulin secretion involved in cellular response to glucose stimulus
GO:0045721 negative regulation of gluconeogenesis
GO:0046324 regulation of glucose import
GO:0046326 positive regulation of glucose import
GO:0046628 positive regulation of insulin receptor signaling pathway
GO:0050728 negative regulation of inflammatory response
GO:0051897 positive regulation of protein kinase B signaling
Cellular Component
GO:0005576 extracellular region
GO:0005615 extracellular space
Protein Structure and Domains
PDB ID
InterPro IPR008983 Tumour necrosis factor-like domain
PFAM
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q5T7M4
PhosphoSite PhosphoSite-
TrEMBL
UniProt Splice Variant
Entrez Gene 388581
UniGene Hs.197613
RefSeq NP_001014980
HUGO HGNC:32308
OMIM
CCDS CCDS30554
HPRD
IMGT
EMBL AL162741 BC089443
GenPept AAH89443 CAI23256

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