FB2026_03 , released September 17, 2026
Human Disease Model Report: alcohol, response to, UNC13A-related
Open Close
General Information
Name
alcohol, response to, UNC13A-related
FlyBase ID
FBhh0000703
OMIM
Overview

In experiments in mouse and rat, orthologs of UNC13A have emerged as having roles in alcohol use and response. UNC13A (Unc-13 Homolog A) encodes a member of the UNC13 family; genes in this family are involved in neurotransmitter release and synaptic vesicle maturation. There is a single orthologous gene in Drosophila, unc-13, for which RNAi-targeting constructs and alleles caused by insertional mutagenesis have been generated. Dmel\unc-13 is also orthologous to UNC13B and UNC13C in human.

None of the human UNC13 genes has been introduced into flies. A tagged wild-type version of the rat ortholog of UNC13A, Rnor\Unc13a, has been introduced; pan-neuronal expression of Rnor\Unc13a is able to suppress the increase in ethanol self-administration observed for a Dmel\unc-13 loss-of-function mutation.

The more extreme loss-of-function mutations of Dmel\unc-13 are lethal as homozygotes; embryos exhibit with defects in neurophysiology and synaptic vesicles. Adults heterozygous for a loss-of-function mutation exhibit a significant increase in ethanol self-administration.

[updated Jan. 2018 by FlyBase; FBrf0222196]

Disease Summary Information
Parent Disease Summary: alcohol use disorder, susceptibility to (fly models overview)
Symptoms and phenotype

Alcoholism can be defined as persistence of excessive drinking over a long period of time despite adverse health effects and disruption of social relations (Morozova et al., 2014; pubmed:24395673).

The 2013 Diagnostic and Statistical Manual of Mental Disorders (DSM) combined the two former categorizations of abnormal alcohol use (alcohol abuse and alcohol dependence) into one diagnosis: alcohol use disorder. The severity of an individual's AUD is broken into classifications: mild, moderate, or severe. "Alcoholism" is a non-medical term often used to describe a severe form of alcohol use disorder. (https://www.therecoveryvillage.com/recovery-blog/alcoholism-alcohol-use-disorder-whats-difference/)

Excessive alcohol consumption is associated with increased risk of different types of cancer, higher cardiovascular disease mortality, birth defects, liver diseases, and neuropsychiatric disorders (Morozova et al., 2014; pubmed:24395673).

Alcoholism is a multifactorial, genetically influenced disorder. [from MIM:103780; 2017.12.19]

Specific Disease Summary: alcohol, response to, UNC13A-related
OMIM report
Human gene(s) implicated
Symptoms and phenotype
Genetics
Cellular phenotype and pathology
Molecular information

UNC13A encodes a protein involved in neurotransmitter release by acting in synaptic vesicle priming prior to vesicle fusion; it is essential for synaptic vesicle maturation. [Gene Cards, UNC13A; 2018.01.18]

External links
Disease synonyms
AUD susceptibility, UNC13A-related
Search term: alcohol use disorder
Ortholog Information
Human gene(s) in FlyBase
    Human gene (HGNC)
    D. melanogaster ortholog (based on DIOPT)
    Comments on ortholog(s)

    Many to one (3 human to 1 Drosophila). The other human genes are UNC13B and UNC13C.

    Other mammalian ortholog(s) used
    D. melanogaster Gene Information (1)
    Gene Snapshot
    unc-13 (unc-13) encodes a protein involved in synaptic vesicle exocytosis. [Date last reviewed: 2019-09-19]
    Gene Groups / Pathways
      Comments on ortholog(s)

      Moderate-scoring ortholog of human UNC13A, UNC13B and UNC13C (1 Drosophila to 3 human). Dmel\unc-13 shares 50% identity and 64% similarity with the human UNC13A gene.

      Orthologs and Alignments from DRSC
      DIOPT - DRSC Integrative Ortholog Prediction Tool - Click the link below to search for orthologs in Humans
      Other Genes Used: Viral, Bacterial, Synthetic (0)
        Summary of Physical Interactions (6 groups)
        protein-protein
        Interacting group
        Assay
        References
        far western blotting, tag visualisation, lambda phage display, pull down, anti tag western blot
        anti tag coimmunoprecipitation, peptide massfingerprinting
        Alleles Reported to Model Human Disease (Disease Ontology) (5 alleles)
        Models Based on Experimental Evidence ( 3 )
        Modifiers Based on Experimental Evidence ( 1 )
        Allele
        Disease
        Interaction
        References
        Models Based on Experimental Evidence ( 0 )
        Allele
        Disease
        Evidence
        References
        Modifiers Based on Experimental Evidence ( 2 )
        Allele
        Disease
        Interaction
        References
        Alleles Representing Disease-Implicated Variants
        Genetic Tools, Stocks and Reagents
        Sources of Stocks
        Contact lab of origin for a reagent not available from a public stock center.
        Bloomington Stock Center Disease Page
        Related mammalian, viral, bacterial, or synthetic transgenes
        Allele
        Transgene
        Publicly Available Stocks
        Selected Drosophila transgenes
        Allele
        Transgene
        Publicly Available Stocks
        RNAi constructs available
        Allele
        Transgene
        Publicly Available Stocks
        Selected Drosophila classical alleles
        Allele
        Allele class
        Mutagen
        Publicly Available Stocks
        loss of function allele
        P-element activity
        References (5)