x-linked sideroblastic anemia with 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. [SN]. (Human Disease Ontology, DOID_0050554)
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Genes

13 genes co-occuring with the disease x-linked sideroblastic anemia with ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
ABCB7 ATP-binding cassette, sub-family B (MDR/TAP), member 7 2.69442
HSCB HscB mitochondrial iron-sulfur cluster co-chaperone 1.77586
FXN frataxin 1.51106
ACO1 aconitase 1, soluble 1.09797
ALAS1 5'-aminolevulinate synthase 1 0.937874
TTPA tocopherol (alpha) transfer protein 0.918436
ACO2 aconitase 2, mitochondrial 0.741517
PGK1 phosphoglycerate kinase 1 0.691094
CS citrate synthase 0.614747
RARS arginyl-tRNA synthetase 0.60069
FTH1 ferritin, heavy polypeptide 1 0.442042
FTL ferritin, light polypeptide 0.442042
CDSN corneodesmosin 0.168854