rostral body truncation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description rostral part of body truncated; typically with the caudal portion of the body relatively normal (Mammalian Phenotype Ontology, MP_0012157)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012157
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Genes

18 gene mutations causing the rostral body truncation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APC adenomatous polyposis coli
CNBP CCHC-type zinc finger, nucleic acid binding protein
DKK1 dickkopf WNT signaling pathway inhibitor 1
FLRT3 fibronectin leucine rich transmembrane protein 3
FOXA2 forkhead box A2
GDF3 growth differentiation factor 3
HHEX hematopoietically expressed homeobox
KMT2B lysine (K)-specific methyltransferase 2B
LDB1 LIM domain binding 1
LIAS lipoic acid synthetase
NODAL nodal growth differentiation factor
OTX2 orthodenticle homeobox 2
PPAP2B phosphatidic acid phosphatase type 2B
SMAD1 SMAD family member 1
SMAD2 SMAD family member 2
SMAD4 SMAD family member 4
TCF7L1 transcription factor 7-like 1 (T-cell specific, HMG-box)
TDGF1 teratocarcinoma-derived growth factor 1