missing ribs Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A developmental anomaly with absence of one or more ribs. (Human Phenotype Ontology, HP_0000921)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000921
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Genes

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

Symbol Name
ATR ATR serine/threonine kinase
B3GALT6 UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
BMPER BMP binding endothelial regulator
FLNB filamin B, beta
HDAC6 histone deacetylase 6
KIAA0196 KIAA0196
LBR lamin B receptor
PTPN11 protein tyrosine phosphatase, non-receptor type 11
RNU4ATAC RNA, U4atac small nuclear (U12-dependent splicing)
ROR2 receptor tyrosine kinase-like orphan receptor 2
RPS19 ribosomal protein S19
SOX2 SRY (sex determining region Y)-box 2
SOX9 SRY (sex determining region Y)-box 9