Chromosome Disorders Gene Set

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

26 genes associated with the Chromosome Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
APOB apolipoprotein B
CHRNA2 cholinergic receptor, nicotinic, alpha 2 (neuronal)
CYP2B6 cytochrome P450, family 2, subfamily B, polypeptide 6
DMPK dystrophia myotonica-protein kinase
DUX4 double homeobox 4
FGFR1 fibroblast growth factor receptor 1
GATA4 GATA binding protein 4
GJB3 gap junction protein, beta 3, 31kDa
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone)
GNRHR gonadotropin-releasing hormone receptor
GSTM1 glutathione S-transferase mu 1
GSTP1 glutathione S-transferase pi 1
GSTT1 glutathione S-transferase theta 1
KISS1R KISS1 receptor
KL klotho
LDLR low density lipoprotein receptor
NRXN1 neurexin 1
NSMF NMDA receptor synaptonuclear signaling and neuronal migration factor
PARK7 parkinson protein 7
PDE1A phosphodiesterase 1A, calmodulin-dependent
PPP1R1C protein phosphatase 1, regulatory (inhibitor) subunit 1C
PSEN1 presenilin 1
SOX7 SRY (sex determining region Y)-box 7
TARDBP TAR DNA binding protein
TLR2 toll-like receptor 2
TPH1 tryptophan hydroxylase 1