Genomics England
GMS Panels
Panels
Genes and Entities
SLC25A36
solute carrier family 25 member 36
OMIM:
616149
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Panel
Mode of inheritance
Details
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Mitochondrial disorders
Component of the following Super Panels:
- Childhood onset leukodystrophy
Signed-off version 8.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Hyperinsulinemic hypoglycemia, familial, 8, OMIM:620211