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SLC25A42

solute carrier family 25 member 42

HCNC Approved Symbol
SLC25A42 (HGNC:28380)
Genomic Coordinates
19:19,063,994 - 19,113,030 (19p13.11)
Synonyms
MGC26694
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression
618416AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the SLC25A42 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results