The TMEM237 gene homepage

This database is one of the "Eye disease" gene variant databases.
General information
Gene symbol TMEM237
Gene name transmembrane protein 237
Chromosome 2
Chromosomal band q33
Imprinted Unknown
Genomic reference NG_032049.1
Transcript reference NM_001044385.2
Exon/intron information NM_001044385.2 exon/intron table
Associated with diseases ID, JBTS14
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Lijia Huang
Total number of public variants reported 74
Unique public DNA variants reported 39
Individuals with public variants 103
Hidden variants 4
Download all this gene's data Download all data
Notes This database is one of the "Eye disease" gene variant databases..
Establishment of the database was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement No 200754 - the GEN2PHEN project.
Date created January 31, 2012
Date last updated February 26, 2024
Version TMEM237:240226

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_001044385.2.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/TMEM237
HGNC 14432
Entrez Gene 65062
PubMed articles TMEM237
OMIM - Gene 614423
OMIM - Diseases JBTS14 (Joubert syndrome, type 14 (JBTS-14))
HGMD TMEM237
GeneCards TMEM237
GeneTests TMEM237
Orphanet TMEM237


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00024092 2 transcript variant 1 NM_001044385.2 NP_001037850.1 74


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