absent ribs Gene Set

Dataset MPO Gene-Phenotype 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://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000151
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7 gene mutations causing the absent ribs phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AXIN1 axin 1
CDX1 caudal type homeobox 1
HOXB6 homeobox B6
MSGN1 mesogenin 1
RIPPLY2 ripply transcriptional repressor 2
UNCX UNC homeobox
WDR35 WD repeat domain 35