abnormal placenta weight Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any change in the weight of the organ of metabolic interchange between fetus and mother (Mammalian Phenotype Ontology, MP_0004257)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004257
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31 gene mutations causing the abnormal placenta weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADM adrenomedullin
AKT1 v-akt murine thymoma viral oncogene homolog 1
ALKBH1 alkB, alkylation repair homolog 1 (E. coli)
CBS cystathionine-beta-synthase
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CELF1 CUGBP, Elav-like family member 1
ESX1 ESX homeobox 1
FBXW8 F-box and WD repeat domain containing 8
FOS FBJ murine osteosarcoma viral oncogene homolog
GHR growth hormone receptor
GJB5 gap junction protein, beta 5, 31.1kDa
GPC3 glypican 3
GRB10 growth factor receptor-bound protein 10
H19 H19, imprinted maternally expressed transcript (non-protein coding)
IGF2 insulin-like growth factor 2
IGF2BP1 insulin-like growth factor 2 mRNA binding protein 1
IGF2R insulin-like growth factor 2 receptor
LLGL2 lethal giant larvae homolog 2 (Drosophila)
MEG3 maternally expressed 3 (non-protein coding)
MEST mesoderm specific transcript
NRK Nik related kinase
PGF placental growth factor
PHLDA2 pleckstrin homology-like domain, family A, member 2
PLAC1 placenta-specific 1
PLK2 polo-like kinase 2
PON3 paraoxonase 3
PTP4A2 protein tyrosine phosphatase type IVA, member 2
RAF1 Raf-1 proto-oncogene, serine/threonine kinase
RTL1 retrotransposon-like 1
SSR3 signal sequence receptor, gamma (translocon-associated protein gamma)
UTF1 undifferentiated embryonic cell transcription factor 1