Genetic Diseases, X-Linked Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

20 genes associated with the Genetic Diseases, X-Linked phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
BTK Bruton agammaglobulinemia tyrosine kinase
CEP290 centrosomal protein 290kDa
CLCN5 chloride channel, voltage-sensitive 5
FRMD7 FERM domain containing 7
GJB1 gap junction protein, beta 1, 32kDa
GLRA1 glycine receptor, alpha 1
GLRB glycine receptor, beta
IQCB1 IQ motif containing B1
IRAK1 interleukin-1 receptor-associated kinase 1
MECP2 methyl CpG binding protein 2
NOD2 nucleotide-binding oligomerization domain containing 2
PGAM4 phosphoglycerate mutase family member 4
RHO rhodopsin
RP2 retinitis pigmentosa 2 (X-linked recessive)
RPGR retinitis pigmentosa GTPase regulator
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1
RPGRIP1L RPGRIP1-like
SLC6A5 solute carrier family 6 (neurotransmitter transporter), member 5
TLR7 toll-like receptor 7
TMEM27 transmembrane protein 27