decreased alcohol consumption Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description less than normal consumption of alcohol (Mammalian Phenotype Ontology, MP_0003546)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003546
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Genes

12 gene mutations causing the decreased alcohol consumption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALDH2 aldehyde dehydrogenase 2 family (mitochondrial)
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
DRD2 dopamine receptor D2
DRD3 dopamine receptor D3
GNAS GNAS complex locus
GRIA3 glutamate receptor, ionotropic, AMPA 3
GRIN1 glutamate receptor, ionotropic, N-methyl D-aspartate 1
GRM5 glutamate receptor, metabotropic 5
SLC18A2 solute carrier family 18 (vesicular monoamine transporter), member 2