split xiphoid process 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:0004678
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Genes

13 gene mutations causing the split xiphoid process phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMP4 bone morphogenetic protein 4
CHUK conserved helix-loop-helix ubiquitous kinase
COL27A1 collagen, type XXVII, alpha 1
DPPA4 developmental pluripotency associated 4
DVL3 dishevelled segment polarity protein 3
FGFR2 fibroblast growth factor receptor 2
GPC3 glypican 3
HOXC8 homeobox C8
IRF6 interferon regulatory factor 6
NXN nucleoredoxin
SEMA3A sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A
SMARCAD1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1
TAPT1 transmembrane anterior posterior transformation 1