fetal bleb Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description presence of subepidermal blister-like structures on the skin, often on the head, formed during embryonic development and usually filled with blood (Mammalian Phenotype Ontology, MP_0008856)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008856
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Genes

5 gene mutations causing the fetal bleb phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CRIM1 cysteine rich transmembrane BMP regulator 1 (chordin-like)
FH fumarate hydratase
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
PDGFRA platelet-derived growth factor receptor, alpha polypeptide