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SLC25A46

solute carrier family 25 member 46

HCNC Approved Symbol
SLC25A46 (HGNC:25198)
Genomic Coordinates
5:110,738,145 - 110,765,157 (5q22.1)
Synonyms
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Neuropathy, hereditary motor and sensory, type VIB
616505AR
Pontocerebellar hypoplasia, type 1E
619303AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the SLC25A46 gene.

Frequently observed phenotypes

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

No Results