SLC10A1

solute carrier family 10 member 1
OMIM: 182396, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Red SLC10A1 in Neonatal cholestasis Level 3: Liver disease Level 2: Gastroenterological disorders Version 1.26	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Emory Genetics Laboratory Phenotypes Sodium taurocholate cotransporting polypeptide deficiency

Panel

Reviews

Mode of inheritance

Details

Level 3: Liver disease
Level 2: Gastroenterological disorders
Version 1.26

review

BIALLELIC, autosomal or pseudoautosomal