Homo sapiens Gene: TMEM237
Summary
InnateDB Gene IDBG-78719.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol TMEM237
Gene Name transmembrane protein 237
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000155755
Encoded Proteins
transmembrane protein 237
transmembrane protein 237
transmembrane protein 237
transmembrane protein 237
transmembrane protein 237
transmembrane protein 237
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The protein encoded by this gene is a tetraspanin protein that is thought to be involved in WNT signaling. Defects in this gene are a cause of Joubert syndrome-14. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]
Gene Information
Type Protein coding
Genomic Location Chromosome 2:201620184-201643570
Strand Reverse strand
Band q33.1
Transcripts
ENST00000286196 ENSP00000286196
ENST00000409883 ENSP00000386264
ENST00000409444 ENSP00000387203
ENST00000432684 ENSP00000413230
ENST00000444047 ENSP00000402681
ENST00000495329
ENST00000471318
ENST00000466641
ENST00000466839
ENST00000489550
ENST00000480124
ENST00000463205
ENST00000621467 ENSP00000480508
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 5 experimentally validated interaction(s) in this database.
Experimentally validated
Total 5 [view]
Protein-Protein 5 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
GO:0030111 regulation of Wnt signaling pathway
GO:0042384 cilium assembly
Cellular Component
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0035869 ciliary transition zone
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.12319
RefSeq NM_001044385 NM_152388
HUGO
OMIM
CCDS CCDS46489 CCDS46490
HPRD 12448
IMGT
EMBL
GenPept
RNA Seq Atlas