abnormal ventral body wall morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the anterior portion of a human body or the lower surface of an animal body comprised of ectoderm and mesoderm layers that encloses the body cavity (Mammalian Phenotype Ontology, MP_0003384)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003384
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20 gene mutations causing the abnormal ventral body wall morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALDH1A2 aldehyde dehydrogenase 1 family, member A2
BMP4 bone morphogenetic protein 4
CALR calreticulin
FENDRR FOXF1 adjacent non-coding developmental regulatory RNA
FLRT3 fibronectin leucine rich transmembrane protein 3
FURIN furin (paired basic amino acid cleaving enzyme)
GPC3 glypican 3
HIC1 hypermethylated in cancer 1
HOXB4 homeobox B4
MAB21L2 mab-21-like 2 (C. elegans)
NR6A1 nuclear receptor subfamily 6, group A, member 1
PITX2 paired-like homeodomain 2
PORCN porcupine homolog (Drosophila)
SMAD1 SMAD family member 1
SMAD5 SMAD family member 5
SRD5A3 steroid 5 alpha-reductase 3
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TP63 tumor protein p63
VANGL2 VANGL planar cell polarity protein 2
YAP1 Yes-associated protein 1