Congenital Fusion Of Ribs Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0265695
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Genes

36 genes associated with the disease Congenital Fusion Of Ribs in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACTB actin, beta
ANKRD11 ankyrin repeat domain 11
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
COG1 component of oligomeric golgi complex 1
CPLX1 complexin 1
CTBP1 C-terminal binding protein 1
DLL3 delta-like 3 (Drosophila)
FGFRL1 fibroblast growth factor receptor-like 1
FOXO1 forkhead box O1
GABRD gamma-aminobutyric acid (GABA) A receptor, delta
GLI3 GLI family zinc finger 3
HES7 hes family bHLH transcription factor 7
KCNAB2 potassium channel, voltage gated subfamily A regulatory beta subunit 2
LETM1 leucine zipper-EF-hand containing transmembrane protein 1
LFNG LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
MAP3K7 mitogen-activated protein kinase kinase kinase 7
MESP2 mesoderm posterior basic helix-loop-helix transcription factor 2
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
NELFA negative elongation factor complex member A
NSD2 nuclear receptor binding SET domain protein 2
NXN nucleoredoxin
PRDM16 PR domain containing 16
PTCH1 patched 1
PTCH2 patched 2
RECQL4 RecQ protein-like 4
RERE arginine-glutamic acid dipeptide (RE) repeats
RIPPLY2 ripply transcriptional repressor 2
ROR2 receptor tyrosine kinase-like orphan receptor 2
SIM1 single-minded family bHLH transcription factor 1
SIX6 SIX homeobox 6
SKI SKI proto-oncogene
SON SON DNA binding protein
SOX2 SRY (sex determining region Y)-box 2
SUFU suppressor of fused homolog (Drosophila)
TBX2 T-box 2
TMCO1 transmembrane and coiled-coil domains 1