x-linked disease Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A monogenic disease that has_material_basis_in muations in genes on the X chromosome. (Human Disease Ontology, DOID_0050735)
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12 genes involed in the disease x-linked disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
CASK calcium/calmodulin-dependent serine protein kinase (MAGUK family)
FLNA filamin A, alpha
FMR1 fragile X mental retardation 1
MED12 mediator complex subunit 12
OCRL oculocerebrorenal syndrome of Lowe
PORCN porcupine homolog (Drosophila)
PRPS1 phosphoribosyl pyrophosphate synthetase 1
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter)
TAZ tafazzin
UPF3B UPF3 regulator of nonsense transcripts homolog B (yeast)
WAS Wiskott-Aldrich syndrome