Chromosome Disorders Gene Set
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
|
