Homo sapiens Gene: TMEM38B
Summary
InnateDB Gene IDBG-79728.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol TMEM38B
Gene Name transmembrane protein 38B
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000095209
Encoded Proteins
transmembrane protein 38B
transmembrane protein 38B
transmembrane protein 38B
transmembrane protein 38B
transmembrane protein 38B
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes an intracellular monovalent cation channel that functions in maintenance of intracellular calcium release. Mutations in this gene may be associated with autosomal recessive osteogenesis. [provided by RefSeq, Oct 2012]
Gene Information
Type Protein coding
Genomic Location Chromosome 9:105694544-105776612
Strand Forward strand
Band q31.2
Transcripts
ENST00000374692 ENSP00000363824
ENST00000374688 ENSP00000363820
ENST00000434214 ENSP00000403026
ENST00000435034 ENSP00000410800
ENST00000451560 ENSP00000416680
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
Experimentally validated
Total 2 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 1 [view]
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005261 cation channel activity
GO:0005267 potassium channel activity
Biological Process
GO:0015672 monovalent inorganic cation transport
GO:0071805 potassium ion transmembrane transport
Cellular Component
GO:0005634 nucleus
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0031965 nuclear membrane
GO:0033017 sarcoplasmic reticulum membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.411925 Hs.597568 Hs.610338 Hs.706182 Hs.741980
RefSeq NM_018112 XM_005252075 XM_005252078
HUGO
OMIM
CCDS CCDS6768
HPRD 15538
IMGT
EMBL
GenPept
RNA Seq Atlas