Mus musculus Gene: Tmem237
Summary
InnateDB Gene IDBG-157797.7
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Tmem237
Gene Name transmembrane protein 237
Synonyms
Species Mus musculus
Ensembl Gene ENSMUSG00000038079
Encoded Proteins
amyotrophic lateral sclerosis 2 (juvenile) chromosome region, candidate 4
amyotrophic lateral sclerosis 2 (juvenile) chromosome region, candidate 4
transmembrane protein 237
transmembrane protein 237
transmembrane protein 237
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 ENSG00000155755:
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 1:59100590-59120408
Strand Reverse strand
Band C1.3
Transcripts
ENSMUST00000094917 ENSMUSP00000092522
ENSMUST00000087475 ENSMUSP00000084745
ENSMUST00000186794 ENSMUSP00000139823
ENSMUST00000190014 ENSMUSP00000140134
ENSMUST00000185951
ENSMUST00000186395 ENSMUSP00000140461
ENSMUST00000186820
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 2 interaction(s) predicted by orthology.
Predicted by orthology
Total 2 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003674 molecular_function
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
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt Q3V0J1
TrEMBL
UniProt Splice Variant
Entrez Gene 381259
UniGene Mm.261275 Mm.415906
RefSeq NM_001033449 NM_001037812 XM_006496096 XM_006496097
OMIM
CCDS CCDS14983 CCDS14984
HPRD
IMGT
MGI ID MGI:2138365
MGI Symbol Tmem237
EMBL AC133162 AK133112 AK167733 BC147243 BC147244
GenPept AAI47244 AAI47245 BAE21513 BAE39774
RNA Seq Atlas 381259