thin ribs Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Ribs with a reduced diameter. (Human Phenotype Ontology, HP_0000883)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000883
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Genes

18 genes associated with the thin ribs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CHRNA1 cholinergic receptor, nicotinic, alpha 1 (muscle)
CHRND cholinergic receptor, nicotinic, delta (muscle)
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
COL11A1 collagen, type XI, alpha 1
COL2A1 collagen, type II, alpha 1
DNM2 dynamin 2
DOK7 docking protein 7
HDAC6 histone deacetylase 6
LIFR leukemia inhibitory factor receptor alpha
ORC1 origin recognition complex, subunit 1
P3H1 prolyl 3-hydroxylase 1
RAPSN receptor-associated protein of the synapse
SCARF2 scavenger receptor class F, member 2
SERPINH1 serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1)
SKI SKI proto-oncogene
SOX9 SRY (sex determining region Y)-box 9
TBCE tubulin folding cofactor E
WNT1 wingless-type MMTV integration site family, member 1