sideroblastic anemia with spinocerebellar ataxia Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [LS]. (Human Disease Ontology, DOID_0060064)
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23 genes co-occuring with the disease sideroblastic anemia with spinocerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
GOT1 glutamic-oxaloacetic transaminase 1, soluble 1.54539
GOT2 glutamic-oxaloacetic transaminase 2, mitochondrial 1.5115
MDH2 malate dehydrogenase 2, NAD (mitochondrial) 1.0362
SORD sorbitol dehydrogenase 0.876148
BPIFA1 BPI fold containing family A, member 1 0.852402
GATM glycine amidinotransferase (L-arginine:glycine amidinotransferase) 0.832329
GGT1 gamma-glutamyltransferase 1 0.793771
ABAT 4-aminobutyrate aminotransferase 0.74761
GGT2 gamma-glutamyltransferase 2 0.738271
TDO2 tryptophan 2,3-dioxygenase 0.65288
PIK3C2A phosphatidylinositol-4-phosphate 3-kinase, catalytic subunit type 2 alpha 0.62885
ALPPL2 alkaline phosphatase, placental-like 2 0.621008
ALPP alkaline phosphatase, placental 0.620617
ALPL alkaline phosphatase, liver/bone/kidney 0.620226
IDH2 isocitrate dehydrogenase 2 (NADP+), mitochondrial 0.590948
TKT transketolase 0.498085
MDH1 malate dehydrogenase 1, NAD (soluble) 0.402318
SERPINA7 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 7 0.354868
LDHA lactate dehydrogenase A 0.34384
TAT tyrosine aminotransferase 0.270108
ACPP acid phosphatase, prostate 0.254888
HK1 hexokinase 1 0.236312
IDH1 isocitrate dehydrogenase 1 (NADP+), soluble 0.199681