Gene: TMEM237 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 65062
Gene Symbol: TMEM237
TMEM237 		0.510 GermlineCausalMutation disease ORPHANET Our study, the largest comprehensive molecular series on JS, provides independent confirmation of the recently reported TCTN1, TMEM237, and C5ORF42 as bona fide JS disease genes, and expands the allelic heterogeneity of this disease. 22693042 2012
Entrez Id: 65062
Gene Symbol: TMEM237
TMEM237 		0.510 GermlineCausalMutation disease ORPHANET TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone. 22152675 2011
Entrez Id: 65062
Gene Symbol: TMEM237
TMEM237 		0.510 GeneticVariation disease BEFREE TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone. 22152675 2011
Entrez Id: 65062
Gene Symbol: TMEM237
TMEM237 		0.510 Biomarker disease GENOMICS_ENGLAND TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone. 22152675 2011