Entity Details

Primary name GAL
Entity type gene
Source Source Link

Details

PrimaryID51083
RefseqGeneNG_052785
SymbolGAL
Namegalanin and GMAP prepropeptide
Chromosome11
Location11q13.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-05-11
ModificationDate2021-06-20

Ontological Relatives

UniProt IDsGALA_HUMAN

GO terms

Show/Hide Table
GOName
GO:0004966 galanin receptor activity
GO:0005184 neuropeptide hormone activity
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0005794 Golgi apparatus
GO:0006954 inflammatory response
GO:0007186 G protein-coupled receptor signaling pathway
GO:0007218 neuropeptide signaling pathway
GO:0007631 feeding behavior
GO:0010737 protein kinase A signaling
GO:0019933 cAMP-mediated signaling
GO:0030073 insulin secretion
GO:0030141 secretory granule
GO:0031763 galanin receptor binding
GO:0031764 type 1 galanin receptor binding
GO:0031765 type 2 galanin receptor binding
GO:0031766 type 3 galanin receptor binding
GO:0031943 regulation of glucocorticoid metabolic process
GO:0032868 response to insulin
GO:0035902 response to immobilization stress
GO:0042493 response to drug
GO:0043025 neuronal cell body
GO:0043065 positive regulation of apoptotic process
GO:0043627 response to estrogen
GO:0045944 positive regulation of transcription by RNA polymerase II
GO:0050672 negative regulation of lymphocyte proliferation
GO:0051464 positive regulation of cortisol secretion
GO:0051795 positive regulation of timing of catagen
GO:1902608 positive regulation of large conductance calcium-activated potassium channel activity

Diseases

Show/Hide Table
Disease IDSourceNameDescription
616461 OMIMEpilepsy, familial temporal lobe, 8 (ETL8)A focal form of epilepsy characterized by recurrent seizures that arise from foci within the temporal lobe. Seizures are usually accompanied by sensory symptoms, most often auditory in nature. The disease is caused by variants affecting the gene represented in this entry.