increased blood osmolality Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increase in the concentration of ions in the blood compared to the normal state (Mammalian Phenotype Ontology, MP_0008997)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008997
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Genes

13 gene mutations causing the increased blood osmolality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AQP1 aquaporin 1 (Colton blood group)
AQP2 aquaporin 2 (collecting duct)
AQP3 aquaporin 3 (Gill blood group)
ATP6V0A4 ATPase, H+ transporting, lysosomal V0 subunit a4
CLN3 ceroid-lipofuscinosis, neuronal 3
LOC102723475 putative uncharacterized protein LOC388820
PLA2G4A phospholipase A2, group IVA (cytosolic, calcium-dependent)
RLN1 relaxin 1
SLC2A2 solute carrier family 2 (facilitated glucose transporter), member 2
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
TRPV1 transient receptor potential cation channel, subfamily V, member 1
TRPV4 transient receptor potential cation channel, subfamily V, member 4
VAMP8 vesicle-associated membrane protein 8