Abnormality Of The Ribs Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An anomaly of the rib. (Human Phenotype Ontology, HP_0000772)
External Link https://www.disgenet.org/browser/0/1/0/C1842083
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Genes

69 genes associated with the disease Abnormality Of The Ribs in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ANTXR2 anthrax toxin receptor 2
APC adenomatous polyposis coli
BANF1 barrier to autointegration factor 1
CDC45 cell division cycle 45
CDC6 cell division cycle 6
CDT1 chromatin licensing and DNA replication factor 1
CEP120 centrosomal protein 120kDa
CHD7 chromodomain helicase DNA binding protein 7
CHRM3 cholinergic receptor, muscarinic 3
CLCN7 chloride channel, voltage-sensitive 7
COG1 component of oligomeric golgi complex 1
DACT1 dishevelled-binding antagonist of beta-catenin 1
DDRGK1 DDRGK domain containing 1
DHCR7 7-dehydrocholesterol reductase
DMRT2 doublesex and mab-3 related transcription factor 2
DONSON downstream neighbor of SON
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1
DYNC2LI1 dynein, cytoplasmic 2, light intermediate chain 1
FERMT1 fermitin family member 1
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FLNA filamin A, alpha
FLNB filamin B, beta
GDF3 growth differentiation factor 3
GDF6 growth differentiation factor 6
GLE1 GLE1 RNA export mediator
GMNN geminin, DNA replication inhibitor
GPC3 glypican 3
GPC4 glypican 4
GPX4 glutathione peroxidase 4
HAAO 3-hydroxyanthranilate 3,4-dioxygenase
HOXD13 homeobox D13
HSPG2 heparan sulfate proteoglycan 2
IDUA iduronidase, alpha-L-
IFT140 intraflagellar transport 140
IFT172 intraflagellar transport 172
IFT80 intraflagellar transport 80
IRF6 interferon regulatory factor 6
JAG1 jagged 1
LRP4 low density lipoprotein receptor-related protein 4
LRP5 low density lipoprotein receptor-related protein 5
MBTPS2 membrane-bound transcription factor peptidase, site 2
MEOX1 mesenchyme homeobox 1
MYF5 myogenic factor 5
OCRL oculocerebrorenal syndrome of Lowe
ORC1 origin recognition complex, subunit 1
ORC4 origin recognition complex, subunit 4
ORC6 origin recognition complex, subunit 6
P4HB prolyl 4-hydroxylase, beta polypeptide
PCYT1A phosphate cytidylyltransferase 1, choline, alpha
PTCH1 patched 1
PTCH2 patched 2
RUNX2 runt-related transcription factor 2
SALL1 spalt-like transcription factor 1
SEC24D SEC24 family member D
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SMAD4 SMAD family member 4
SNX10 sorting nexin 10
SON SON DNA binding protein
SOST sclerostin
TBX5 T-box 5
TCIRG1 T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
TNFSF11 tumor necrosis factor (ligand) superfamily, member 11
TRPV4 transient receptor potential cation channel, subfamily V, member 4
TTC21B tetratricopeptide repeat domain 21B
WDR19 WD repeat domain 19
WDR34 WD repeat domain 34
WDR60 WD repeat domain 60