umbilical hernia Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	A intestinal disease characterized by the protrusion by part of the intestine though an opening in the abdominal muscles. (Human Disease Ontology, DOID_0060321)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010146
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Genes

10 gene mutations causing the umbilical hernia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
BMP5	bone morphogenetic protein 5
COL27A1	collagen, type XXVII, alpha 1
GAD1	glutamate decarboxylase 1 (brain, 67kDa)
GPC3	glypican 3
IFT27	intraflagellar transport 27
LRP2	low density lipoprotein receptor-related protein 2
NBEA	neurobeachin
NPRL3	nitrogen permease regulator-like 3 (S. cerevisiae)
SLC32A1	solute carrier family 32 (GABA vesicular transporter), member 1
TP63	tumor protein p63