pale placenta Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description placenta lacking normal reddish coloration, often refers to bloodless condition (Mammalian Phenotype Ontology, MP_0004266)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004266
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Genes

11 gene mutations causing the pale placenta phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALKBH1 alkB, alkylation repair homolog 1 (E. coli)
CAPN2 calpain 2, (m/II) large subunit
CUL4B cullin 4B
CYR61 cysteine-rich, angiogenic inducer, 61
FGFRL1 fibroblast growth factor receptor-like 1
FZR1 fizzy/cell division cycle 20 related 1 (Drosophila)
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
MECOM MDS1 and EVI1 complex locus
MET MET proto-oncogene, receptor tyrosine kinase
PAK4 p21 protein (Cdc42/Rac)-activated kinase 4
SLC20A1 solute carrier family 20 (phosphate transporter), member 1