herniated abdominal wall Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000757
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Genes

19 gene mutations causing the herniated abdominal wall phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AEBP1 AE binding protein 1
ALX4 ALX homeobox 4
BMP1 bone morphogenetic protein 1
BMP2 bone morphogenetic protein 2
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CYP26A1 cytochrome P450, family 26, subfamily A, polypeptide 1
EFEMP1 EGF containing fibulin-like extracellular matrix protein 1
GLI3 GLI family zinc finger 3
GRHL2 grainyhead-like 2 (Drosophila)
LRP1 low density lipoprotein receptor-related protein 1
MEGF8 multiple EGF-like-domains 8
NUAK1 NUAK family, SNF1-like kinase, 1
PDGFRA platelet-derived growth factor receptor, alpha polypeptide
PITX2 paired-like homeodomain 2
RPL38 ribosomal protein L38
SCRIB scribbled planar cell polarity protein
SEC24B SEC24 family member B
SLC27A4 solute carrier family 27 (fatty acid transporter), member 4
TP63 tumor protein p63