SFXN4 Chromosome 10

Sideroflexin 4
19 variants 19 Health Risk

Upload your DNA to see your personal genotypes for variants in SFXN4.

What This Gene Does
This gene encodes a member of the sideroflexin family. The encoded protein is a transmembrane protein of the inner mitochondrial membrane, and is required for mitochondrial respiratory homeostasis and erythropoiesis. Mutations in this gene are associated with mitochondriopathy and macrocytic anemia. Alternatively spliced transcript variants have been found in this gene. [provided by RefSeq, Jan 2014]
Gene Info
Gene Group
"Mitochondrial respiratory chain complex assembly factors|Solute carrier family 56, sideroflexins"
Locus Type
gene with protein product
Location
10q26.11
Ensembl
ENSG00000183605
Associated Conditions (2)
Inborn genetic diseases
Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome
Key Variants
All Variants (19)
RSID Category Clinical Significance Conditions
RS1254398721 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS151157939 Health Risk Conflicting classifications of pathogenicity Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome, Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome
RS200465740 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS368065380 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS749944766 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS754192985 Health Risk Conflicting classifications of pathogenicity
RS977248748 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS762968127 Health Risk Likely pathogenic
RS781171561 Health Risk Likely pathogenic
RS1156283736 Health Risk Pathogenic Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome, Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome
RS1380193482 Health Risk Pathogenic Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome, Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome
RS147648163 Health Risk Pathogenic
RS1554886159 Health Risk Pathogenic Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome, Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome
RS2133612740 Health Risk Pathogenic Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome, Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome
RS2493890591 Health Risk Pathogenic
RS398124642 Health Risk Pathogenic Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome, Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome
RS1589625048 Health Risk Pathogenic/Likely pathogenic Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome, Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome
RS367932369 Health Risk Pathogenic/Likely pathogenic Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome, Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome
RS756173225 Health Risk Pathogenic/Likely pathogenic Inborn genetic diseases, Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome, Inborn genetic diseases
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