SLC25A10

solute carrier family 25 member 10
OMIM: 606794, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Red SLC25A10 in Mitochondrial disorders Level 3: Mitochondrial Level 2: Metabolic disorders Version 4.168 Latest signed off version: v4.0 (22 Mar 2023) Component of the following Super Panels: Childhood onset leukodystrophy	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert list Phenotypes ?Mitochondrial DNA depletion syndrome 19, OMIM:618972

Panel

Reviews

Mode of inheritance

Details

Red SLC25A10 in Mitochondrial disorders

Level 3: Mitochondrial
Level 2: Metabolic disorders
Version 4.168
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

Childhood onset leukodystrophy

review

BIALLELIC, autosomal or pseudoautosomal

Sources

Expert list

Phenotypes

?Mitochondrial DNA depletion syndrome 19, OMIM:618972