Version 5.4
Bos taurus Gene: REP15
Summary
InnateDB Gene IDBG-648397.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol REP15
Gene Name Uncharacterized protein
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000022083
Encoded Proteins
IDBP-701145
RAB15 effector protein
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 ENSG00000174236:
REP15 is a binding partner of the RAB GTPase family member RAB15 that facilitates transferrin receptor (TFRC; MIM 190010) recycling from the endocytic recycling compartment (Strick and Elferink, 2005 [PubMed 16195351]).[supplied by OMIM, Mar 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 5:82539065-82539763
Strand Reverse strand
Band
Transcripts
ENSBTAT00000029688 ENSBTAP00000029686
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:0005515 protein binding
Biological Process
GO:0001881 receptor recycling
GO:0033572 transferrin transport
Cellular Component
GO:0010008 endosome membrane
GO:0048471 perinuclear region of cytoplasm
GO:0055037 recycling endosome
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
ENSG00000174236
View Gene Order
ENSMUSG00000040121
View Gene Order
Cross-References
SwissProt
TrEMBL F1MSH7
UniProt Splice Variant
Entrez Gene 614599
UniGene
RefSeq XM_005198367 XM_005206922
HUGO HGNC:33748
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02014000
GenPept
RNA Seq Atlas 614599

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