Bos taurus Gene: SELENBP1
Summary
InnateDB Gene IDBG-633107.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SELENBP1
Gene Name Selenium-binding protein 1
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000008091
Encoded Proteins
Selenium-binding protein 1
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000143416:
This gene encodes a member of the selenium-binding protein family. Selenium is an essential nutrient that exhibits potent anticarcinogenic properties, and deficiency of selenium may cause certain neurologic diseases. The effects of selenium in preventing cancer and neurologic diseases may be mediated by selenium-binding proteins, and decreased expression of this gene may be associated with several types of cancer. The encoded protein may play a selenium-dependent role in ubiquitination/deubiquitination-mediated protein degradation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Apr 2012]
Gene Information
Type Protein coding
Genomic Location Chromosome 3:19484700-19493477
Strand Forward strand
Band
Transcripts
ENSBTAT00000010644 ENSBTAP00000010644
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 20 interaction(s) predicted by orthology.
Predicted by orthology
Total 20 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0008430 selenium binding
Biological Process
GO:0006810 transport
GO:0015031 protein transport
Cellular Component
GO:0005615 extracellular space
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0016020 membrane
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Cross-References
SwissProt Q2KJ32
TrEMBL
UniProt Splice Variant
Entrez Gene 510154
UniGene Bt.33139
RefSeq NM_001046048 XM_005203869
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL BC105545
GenPept AAI05546
RNA Seq Atlas 510154