abnormal amniotic fluid composition Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any alteration in the expected chemical makeup of the watery liquid within the amnion that surrounds and cushions a growing fetus; normally, early in gestation, amniotic fluid is similar to maternal plasma, mainly water with electrolytes, and later in gestation, proteins, carbohydrates, lipids, phospholipids originating from the lungs, fetal cells, and urea are deposited in the fluid (Mammalian Phenotype Ontology, MP_0012172)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012172
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Genes

6 gene mutations causing the abnormal amniotic fluid composition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
HSD11B1 hydroxysteroid (11-beta) dehydrogenase 1
PKD1 polycystic kidney disease 1 (autosomal dominant)
PKD2 polycystic kidney disease 2 (autosomal dominant)
SLC25A19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
SLC5A3 solute carrier family 5 (sodium/myo-inositol cotransporter), member 3
SULT1E1 sulfotransferase family 1E, estrogen-preferring, member 1