Abnormality Of The Rib Cage Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A morphological anomaly of the rib cage. (Human Phenotype Ontology, HP_0001547)
External Link https://www.disgenet.org/browser/0/1/0/C4025763
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Genes

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

Symbol Name
AR androgen receptor
EFNB1 ephrin-B1
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
GNPTG N-acetylglucosamine-1-phosphate transferase, gamma subunit
IGF1R insulin-like growth factor 1 receptor
MAN2B1 mannosidase, alpha, class 2B, member 1
MED12 mediator complex subunit 12
MGAT2 mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase
NEB nebulin
NOTCH3 notch 3
OFD1 oral-facial-digital syndrome 1
PIEZO2 piezo-type mechanosensitive ion channel component 2
PQBP1 polyglutamine binding protein 1
SELENON selenoprotein N
TNNT1 troponin T type 1 (skeletal, slow)
TRPV4 transient receptor potential cation channel, subfamily V, member 4