abnormal alcohol consumption Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description aberrant behavioral-related or physiological-related intake of alcohol into the body (Mammalian Phenotype Ontology, MP_0001425)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001425
Similar Terms
Downloads & Tools

Genes

28 gene mutations causing the abnormal 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
CCR5 chemokine (C-C motif) receptor 5 (gene/pseudogene)
CRHR1 corticotropin releasing hormone receptor 1
DRD2 dopamine receptor D2
DRD3 dopamine receptor D3
EPS8 epidermal growth factor receptor pathway substrate 8
FAAH fatty acid amide hydrolase
GNAS GNAS complex locus
GPR26 G protein-coupled receptor 26
GRIA3 glutamate receptor, ionotropic, AMPA 3
GRIN1 glutamate receptor, ionotropic, N-methyl D-aspartate 1
GRM5 glutamate receptor, metabotropic 5
NOS1 nitric oxide synthase 1 (neuronal)
NPY1R neuropeptide Y receptor Y1
NPY2R neuropeptide Y receptor Y2
POMC proopiomelanocortin
PPP1R1B protein phosphatase 1, regulatory (inhibitor) subunit 1B
PRKCG protein kinase C, gamma
SLC18A2 solute carrier family 18 (vesicular monoamine transporter), member 2
SLC29A1 solute carrier family 29 (equilibrative nucleoside transporter), member 1
SLC6A1 solute carrier family 6 (neurotransmitter transporter), member 1
TAOK2 TAO kinase 2
TRPV1 transient receptor potential cation channel, subfamily V, member 1
UNC79 unc-79 homolog (C. elegans)