abnormal chorioallantoic fusion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the process by which a highly vascularized extra-embryonic fetal membrane is formed by fusion of the chorion and allantois; in most mammals, the chorioallantois constitutes the fetal portion of the placenta (Mammalian Phenotype Ontology, MP_0002824)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002824
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Genes

65 gene mutations causing the abnormal chorioallantoic fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABI1 abl-interactor 1
CCDC160 coiled-coil domain containing 160
CCNF cyclin F
CDX2 caudal type homeobox 2
CHM choroideremia (Rab escort protein 1)
CHMP5 charged multivesicular body protein 5
CRB2 crumbs family member 2
CYR61 cysteine-rich, angiogenic inducer, 61
DAD1 defender against cell death 1
DDX11 DEAD/H (Asp-Glu-Ala-Asp/His) box helicase 11
DNAJB6 DnaJ (Hsp40) homolog, subfamily B, member 6
DNMT3L DNA (cytosine-5-)-methyltransferase 3-like
DPH3 diphthamide biosynthesis 3
ENPP2 ectonucleotide pyrophosphatase/phosphodiesterase 2
EPB41L5 erythrocyte membrane protein band 4.1 like 5
ERF Ets2 repressor factor
ESRRB estrogen-related receptor beta
FGFR2 fibroblast growth factor receptor 2
FN1 fibronectin 1
FOXF1 forkhead box F1
FURIN furin (paired basic amino acid cleaving enzyme)
GRB2 growth factor receptor-bound protein 2
GTF2I general transcription factor IIi
GTF2IRD1 GTF2I repeat domain containing 1
HAND1 heart and neural crest derivatives expressed 1
HGS hepatocyte growth factor-regulated tyrosine kinase substrate
HIRA histone cell cycle regulator
HNRNPU heterogeneous nuclear ribonucleoprotein U (scaffold attachment factor A)
HUS1 HUS1 checkpoint homolog (S. pombe)
IPMK inositol polyphosphate multikinase
ITGA4 integrin, alpha 4 (antigen CD49D, alpha 4 subunit of VLA-4 receptor)
ITGB1 integrin, beta 1 (fibronectin receptor, beta polypeptide, antigen CD29 includes MDF2, MSK12)
ITGB8 integrin, beta 8
KAT7 K(lysine) acetyltransferase 7
LDB1 LIM domain binding 1
LEFTY2 left-right determination factor 2
MIB1 mindbomb E3 ubiquitin protein ligase 1
MPI mannose phosphate isomerase
NCKAP1 NCK-associated protein 1
NR6A1 nuclear receptor subfamily 6, group A, member 1
PAXIP1 PAX interacting (with transcription-activation domain) protein 1
PNPLA6 patatin-like phospholipase domain containing 6
PPAP2B phosphatidic acid phosphatase type 2B
PTEN phosphatase and tensin homolog
PTK2 protein tyrosine kinase 2
RPS6KA6 ribosomal protein S6 kinase, 90kDa, polypeptide 6
RTEL1 regulator of telomere elongation helicase 1
SETD2 SET domain containing 2
SLC34A2 solute carrier family 34 (type II sodium/phosphate cotransporter), member 2
SMAD1 SMAD family member 1
SMAD2 SMAD family member 2
SMAD5 SMAD family member 5
SS18 synovial sarcoma translocation, chromosome 18
STK11 serine/threonine kinase 11
TBX4 T-box 4
TENM4 teneurin transmembrane protein 4
TGFB1 transforming growth factor, beta 1
TMED2 transmembrane emp24 domain trafficking protein 2
TPT1 tumor protein, translationally-controlled 1
UBR5 ubiquitin protein ligase E3 component n-recognin 5
USP9X ubiquitin specific peptidase 9, X-linked
VCAM1 vascular cell adhesion molecule 1
VPS26A vacuolar protein sorting 26 homolog A (S. pombe)
WNT7B wingless-type MMTV integration site family, member 7B
ZFP36L1 ZFP36 ring finger protein-like 1