Gene: TRIM36 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55521
Gene Symbol: TRIM36
TRIM36 		0.610 GeneticVariation disease BEFREE In this study, we employed whole-exome sequencing and identified a homozygous missense mutation c.1522C > A (p.Pro508Thr) in the TRIM36 gene as the cause of autosomal recessive APH in an Indian family. 28087737 2017
Entrez Id: 55521
Gene Symbol: TRIM36
TRIM36 		0.610 GeneticVariation disease UNIPROT A homozygous mutation in TRIM36 causes autosomal recessive anencephaly in an Indian family. 28087737 2017
Entrez Id: 55521
Gene Symbol: TRIM36
TRIM36 		0.610 Biomarker disease CTD_human
Entrez Id: 55521
Gene Symbol: TRIM36
TRIM36 		0.610 Biomarker disease HPO