abnormal embryonic tissue physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly in any of the tissues of the embryo proper (Mammalian Phenotype Ontology, MP_0008932)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008932
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Genes

81 gene mutations causing the abnormal embryonic tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AATF apoptosis antagonizing transcription factor
ADAMTS20 ADAM metallopeptidase with thrombospondin type 1 motif, 20
AHCTF1 AT hook containing transcription factor 1
ALDH1A2 aldehyde dehydrogenase 1 family, member A2
BICC1 BicC family RNA binding protein 1
CAPNS1 calpain, small subunit 1
CDH1 cadherin 1, type 1, E-cadherin (epithelial)
CDK7 cyclin-dependent kinase 7
CDK8 cyclin-dependent kinase 8
CDX2 caudal type homeobox 2
CFL1 cofilin 1 (non-muscle)
CHD7 chromodomain helicase DNA binding protein 7
CHORDC1 cysteine and histidine-rich domain (CHORD) containing 1
CHRD chordin
COPS5 COP9 signalosome subunit 5
DAB2 Dab, mitogen-responsive phosphoprotein, homolog 2 (Drosophila)
DAD1 defender against cell death 1
DDX11 DEAD/H (Asp-Glu-Ala-Asp/His) box helicase 11
DIDO1 death inducer-obliterator 1
DMBT1 deleted in malignant brain tumors 1
DNAH11 dynein, axonemal, heavy chain 11
EEF2 eukaryotic translation elongation factor 2
EFNB1 ephrin-B1
EFNB2 ephrin-B2
ERBB2 erb-b2 receptor tyrosine kinase 2
ERBB3 erb-b2 receptor tyrosine kinase 3
EXT1 exostosin glycosyltransferase 1
FGF8 fibroblast growth factor 8 (androgen-induced)
FGFR1 fibroblast growth factor receptor 1
FOLR1 folate receptor 1 (adult)
FOXI3 forkhead box I3
FOXJ1 forkhead box J1
GBX2 gastrulation brain homeobox 2
GINS1 GINS complex subunit 1 (Psf1 homolog)
GINS4 GINS complex subunit 4 (Sld5 homolog)
HIF1A hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)
HOXA1 homeobox A1
HSPA5 heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa)
INVS inversin
JUN jun proto-oncogene
KAT8 K(lysine) acetyltransferase 8
KIF11 kinesin family member 11
KIF3A kinesin family member 3A
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
MAD2L1 MAD2 mitotic arrest deficient-like 1 (yeast)
MED12 mediator complex subunit 12
MKS1 Meckel syndrome, type 1
NANOG Nanog homeobox
NBN nibrin
NCAPG2 non-SMC condensin II complex, subunit G2
NLE1 notchless homolog 1 (Drosophila)
NOTO notochord homeobox
NRG1 neuregulin 1
NUSAP1 nucleolar and spindle associated protein 1
ODC1 ornithine decarboxylase 1
OVOL2 ovo-like zinc finger 2
PAX3 paired box 3
PDPK1 3-phosphoinositide dependent protein kinase 1
PHOX2B paired-like homeobox 2b
PIFO primary cilia formation
PRPF19 pre-mRNA processing factor 19
PTPMT1 protein tyrosine phosphatase, mitochondrial 1
RBM19 RNA binding motif protein 19
RET ret proto-oncogene
RIPPLY3 ripply transcriptional repressor 3
SEMA3C sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C
SMARCA5 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 5
SMARCB1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
SOX10 SRY (sex determining region Y)-box 10
TAF10 TAF10 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 30kDa
TBX1 T-box 1
TCOF1 Treacher Collins-Franceschetti syndrome 1
TERF1 telomeric repeat binding factor (NIMA-interacting) 1
TGS1 trimethylguanosine synthase 1
UBA3 ubiquitin-like modifier activating enzyme 3
UBE2I ubiquitin-conjugating enzyme E2I
UBR2 ubiquitin protein ligase E3 component n-recognin 2
VCL vinculin
XAB2 XPA binding protein 2
ZEB2 zinc finger E-box binding homeobox 2
ZPR1 ZPR1 zinc finger