enlarged allantois Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increased size of the fetal membrane which contributes to the formation of the umbilical cord and placental blood vessels (Mammalian Phenotype Ontology, MP_0004556)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004556
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Genes

15 gene mutations causing the enlarged allantois phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BRCA2 breast cancer 2, early onset
CHRD chordin
CSK c-src tyrosine kinase
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
HAND1 heart and neural crest derivatives expressed 1
HIRA histone cell cycle regulator
HSD17B12 hydroxysteroid (17-beta) dehydrogenase 12
MIXL1 Mix paired-like homeobox
NR6A1 nuclear receptor subfamily 6, group A, member 1
PPAP2B phosphatidic acid phosphatase type 2B
PTEN phosphatase and tensin homolog
PTK2 protein tyrosine kinase 2
RAPGEF2 Rap guanine nucleotide exchange factor (GEF) 2
RTEL1 regulator of telomere elongation helicase 1