Possible mitochondrial disorder - nuclear genes
Gene: SLC25A40

SLC25A40 (solute carrier family 25 member 40)
EnsemblGeneIds (GRCh38): ENSG00000075303
EnsemblGeneIds (GRCh37): ENSG00000075303
OMIM: 610821, Gene2Phenotype
SLC25A40 is in 3 panels

2 reviews

Ivone Leong (Genomics England Curator)

Red List (low evidence)

Initial gene list and info collated by Carl Fratter (Oxford University Hospitals NHS Trust) January 2019 on behalf of the GMS Mitochondrial specialist test group.
Created: 4 Feb 2019, 1:36 p.m.

Mode of inheritance
Unknown

Phenotypes
No OMIM phenotype

Created: 4 Feb 2019, 1:36 p.m.

Panel version: 0.5

Shamima Rahman (UCL Institute of Child Health)

I don't know

Created: 8 Feb 2016, 10:34 a.m.

Panel version: Imported from Mitochondrial disorders panel version 0.37

Details

Mode of Inheritance

Unknown

Sources

NHS GMS
Expert Review Red

Phenotypes

No OMIM phenotype

OMIM

610821

Clinvar variants

Variants in SLC25A40

Penetrance

None

Panels with this gene

History Filter Activity

4 Feb 2019, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set Phenotypes

Ivone Leong (Genomics England Curator)

gene: SLC25A40 was added gene: SLC25A40 was added to Possible mitochondrial disorder - nuclear genes. Sources: Expert Review Red,NHS GMS Mode of inheritance for gene: SLC25A40 was set to Unknown Phenotypes for gene: SLC25A40 were set to No OMIM phenotype

Possible mitochondrial disorder - nuclear genes Gene: SLC25A40