Version 5.4
Homo sapiens Gene: SMPX
Summary
InnateDB Gene IDBG-51362.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SMPX
Gene Name small muscle protein, X-linked
Synonyms DFN6; DFNX4
Species Homo sapiens
Ensembl Gene ENSG00000091482
Encoded Proteins
IDBP-51364
small muscle protein, X-linked
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a small protein that has no known functional domains. Mutations in this gene are a cause of X-linked deafness-4, and the encoded protein may play a role in the maintenance of inner ear cells subjected to mechanical stress. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2011]
Gene Information
Type Protein coding
Genomic Location Chromosome X:21705972-21758163
Strand Reverse strand
Band p22.12
Transcripts
ENST00000379494 ENSP00000368808
ENST00000494525
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
Biological Process
GO:0006941 striated muscle contraction
Cellular Component
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005927 muscle tendon junction
GO:0031430 M band
GO:0043034 costamere
GO:0043292 contractile fiber
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
ENSMUSG00000041476
View Gene Order
ENSBTAG00000015204
Not yet available
Cross-References
SwissProt Q9UHP9
TrEMBL A0A024RBY1
UniProt Splice Variant
Entrez Gene 23676
UniGene Hs.86492
RefSeq NM_014332
HUGO HGNC:11122
OMIM 300226
CCDS CCDS14200
HPRD
IMGT
EMBL AF129505 AJ250584 AK312134 AL772370 BC005948 CH471074
GenPept AAF19343 AAH05948 BAG35070 CAC08492 CAH71012 EAW98980 EAW98981
RNA Seq Atlas 23676

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