decreased fluid intake Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduction in the total amount of fluid taken in over time when compared to the normal state (Mammalian Phenotype Ontology, MP_0011942)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011942
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Genes

26 gene mutations causing the decreased fluid intake phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADM adrenomedullin
ALDH2 aldehyde dehydrogenase 2 family (mitochondrial)
APLNR apelin receptor
BRS3 bombesin-like receptor 3
CACNA1B calcium channel, voltage-dependent, N type, alpha 1B subunit
CCL13 chemokine (C-C motif) ligand 13
CCL3L3 chemokine (C-C motif) ligand 3-like 3
CCR2 chemokine (C-C motif) receptor 2
CISD2 CDGSH iron sulfur domain 2
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
DRD2 dopamine receptor D2
DRD3 dopamine receptor D3
GABRA5 gamma-aminobutyric acid (GABA) A receptor, alpha 5
GNAS GNAS complex locus
GRIA3 glutamate receptor, ionotropic, AMPA 3
GRIN1 glutamate receptor, ionotropic, N-methyl D-aspartate 1
GRM5 glutamate receptor, metabotropic 5
HNF4G hepatocyte nuclear factor 4, gamma
MMP17 matrix metallopeptidase 17 (membrane-inserted)
MYH1 myosin, heavy chain 1, skeletal muscle, adult
PHOSPHO1 phosphatase, orphan 1
PTGER1 prostaglandin E receptor 1 (subtype EP1), 42kDa
SLC18A2 solute carrier family 18 (vesicular monoamine transporter), member 2
TRIB2 tribbles pseudokinase 2
TRPV1 transient receptor potential cation channel, subfamily V, member 1
TRPV4 transient receptor potential cation channel, subfamily V, member 4