TMEM237 (transmembrane protein 237)

2014-11-01  

Identity

HGNC
LOCATION
2q33.1
LOCUSID
ALIAS
ALS2CR4,JBTS14

Other Information

Locus ID:

NCBI: 65062
MIM: 614423
HGNC: 14432
Ensembl: ENSG00000155755

Variants:

dbSNP: 65062
ClinVar: 65062
TCGA: ENSG00000155755
COSMIC: TMEM237

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000155755ENST00000286196F8WE96
ENSG00000155755ENST00000409444Q96Q45
ENSG00000155755ENST00000409883Q96Q45
ENSG00000155755ENST00000432684F2Z329
ENSG00000155755ENST00000444047F2Z329
ENSG00000155755ENST00000621467A0A087WWU1

Expression (GTEx)

0
5
10
15
20
25
30
35

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
221526752011TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone.88
308929382019Identification of transmembrane protein 237 as a novel interactor with the intestinal riboflavin transporter-3 (RFVT-3): role in functionality and cell biology.1

Citation

Dessen P

TMEM237 (transmembrane protein 237)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/74901/tmem237