abnormal proximal-distal axis patterning Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the formation or development of a body structure, often a limb, in relation to the structure's proximity to the trunk or point of origin (Mammalian Phenotype Ontology, MP_0001705)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001705
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11 gene mutations causing the abnormal proximal-distal axis patterning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARC activity-regulated cytoskeleton-associated protein
ATAD3A ATPase family, AAA domain containing 3A
BPTF bromodomain PHD finger transcription factor
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
CYP26B1 cytochrome P450, family 26, subfamily B, polypeptide 1
FOXD3 forkhead box D3
MAPK1 mitogen-activated protein kinase 1
PBX1 pre-B-cell leukemia homeobox 1
PRKCI protein kinase C, iota
SMAD2 SMAD family member 2
SMAD4 SMAD family member 4