failure of initiation of embryo turning Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description failure to begin the axial rotation of the germ layers of the embryo during the primitive streak/early somite stage (Mammalian Phenotype Ontology, MP_0004180)
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43 gene mutations causing the failure of initiation of embryo turning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALG13 ALG13, UDP-N-acetylglucosaminyltransferase subunit
ANKRD11 ankyrin repeat domain 11
CRB2 crumbs family member 2
CUBN cubilin (intrinsic factor-cobalamin receptor)
DAP3 death associated protein 3
DLG3 discs, large homolog 3 (Drosophila)
DNMT1 DNA (cytosine-5-)-methyltransferase 1
DYNC2LI1 dynein, cytoplasmic 2, light intermediate chain 1
ENPP2 ectonucleotide pyrophosphatase/phosphodiesterase 2
FLRT3 fibronectin leucine rich transmembrane protein 3
FN1 fibronectin 1
FOXF1 forkhead box F1
FURIN furin (paired basic amino acid cleaving enzyme)
HGS hepatocyte growth factor-regulated tyrosine kinase substrate
HUS1 HUS1 checkpoint homolog (S. pombe)
IFT57 intraflagellar transport 57
KDM6A lysine (K)-specific demethylase 6A
MESP1 mesoderm posterior basic helix-loop-helix transcription factor 1
NR6A1 nuclear receptor subfamily 6, group A, member 1
NUMB numb homolog (Drosophila)
PDGFRA platelet-derived growth factor receptor, alpha polypeptide
POGLUT1 protein O-glucosyltransferase 1
POLG2 polymerase (DNA directed), gamma 2, accessory subunit
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
PSMD4 proteasome (prosome, macropain) 26S subunit, non-ATPase, 4
PTEN phosphatase and tensin homolog
PTK2 protein tyrosine kinase 2
PTPN11 protein tyrosine phosphatase, non-receptor type 11
PTPN12 protein tyrosine phosphatase, non-receptor type 12
RBL2 retinoblastoma-like 2
RNF111 ring finger protein 111
RPS6KA6 ribosomal protein S6 kinase, 90kDa, polypeptide 6
RTTN rotatin
SLC31A1 solute carrier family 31 (copper transporter), member 1
SLC34A2 solute carrier family 34 (type II sodium/phosphate cotransporter), member 2
SMAD5 SMAD family member 5
SOX17 SRY (sex determining region Y)-box 17
SRD5A3 steroid 5 alpha-reductase 3
STK11 serine/threonine kinase 11
TXNRD1 thioredoxin reductase 1
USP9X ubiquitin specific peptidase 9, X-linked
WASL Wiskott-Aldrich syndrome-like
ZFAT zinc finger and AT hook domain containing