Version 5.4
Homo sapiens Gene: SMCR5
Summary
InnateDB Gene IDBG-301758.4
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SMCR5
Gene Name Smith-Magenis syndrome chromosome region, candidate 5 (non-protein coding)
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000226746
Encoded Proteins
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary Currently no Entrez Summary Available. You might want to check the Summary Sections of the Orthologs.
Gene Information
Type antisense
Genomic Location Chromosome 17:17776686-17779529
Strand Reverse strand
Band p11.2
Transcripts
ENST00000543475
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Orthologs
No orthologs found for this gene
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene 140771
UniGene Hs.352643
RefSeq
HUGO HGNC:17918
OMIM
CCDS
HPRD
IMGT
EMBL
GenPept
RNA Seq Atlas 140771

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