Gene: TMEM151B ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 441151
Gene Symbol: TMEM151B
TMEM151B 		0.100 CausalMutation group CLINVAR Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies. 25058219 2014
Entrez Id: 441151
Gene Symbol: TMEM151B
TMEM151B 		0.100 CausalMutation group CLINVAR Novel (ovario) leukodystrophy related to AARS2 mutations. 24808023 2014
Entrez Id: 441151
Gene Symbol: TMEM151B
TMEM151B 		0.100 CausalMutation group CLINVAR Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing. 22277967 2012
Entrez Id: 441151
Gene Symbol: TMEM151B
TMEM151B 		0.100 CausalMutation group CLINVAR Exome sequencing identifies mitochondrial alanyl-tRNA synthetase mutations in infantile mitochondrial cardiomyopathy. 21549344 2011