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    CG31693 uncharacterized protein [ Drosophila melanogaster (fruit fly) ]

    Gene ID: 318887, updated on 9-Dec-2024

    Summary

    Official Symbol
    CG31693provided by FlyBase
    Official Full Name
    uncharacterized proteinprovided by FlyBase
    Primary source
    FLYBASE:FBgn0051693
    Locus tag
    Dmel_CG31693
    See related
    AllianceGenome:FB:FBgn0051693
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Drosophila melanogaster
    Lineage
    Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Diptera; Brachycera; Muscomorpha; Ephydroidea; Drosophilidae; Drosophila; Sophophora
    Also known as
    BcDNA:GH25177; Dmel\CG31693
    Summary
    Predicted to enable monoatomic ion transmembrane transporter activity. Predicted to be involved in transmembrane transport. Predicted to be located in membrane. Is expressed in adult head. Human ortholog(s) of this gene implicated in actinic keratosis; oculocutaneous albinism type II; pigmentation disease; skin cancer (multiple); and squamous cell carcinoma. Orthologous to human OCA2 (OCA2 melanosomal transmembrane protein). [provided by Alliance of Genome Resources, Dec 2024]
    Orthologs
    NEW
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    Genomic context

    See CG31693 in Genome Data Viewer
    Location:
    40D3-40D3; 2-54 cM
    Exon count:
    2
    Annotation release Status Assembly Chr Location
    Release 6.54 current Release 6 plus ISO1 MT (GCF_000001215.4) 2L NT_033779.5 (22015190..22017334)
    Release 5.57 previous assembly Release 5 (GCF_000001215.2) 2L NT_033779.4 (22015190..22017334)

    Chromosome 2L - NT_033779.5Genomic Context describing neighboring genes Neighboring gene uncharacterized protein Neighboring gene long non-coding RNA:CR44916 Neighboring gene long non-coding RNA:CR33987 Neighboring gene tiptop Neighboring gene long non-coding RNA:CR45335

    Genomic regions, transcripts, and products

    General gene information

    • Annotated by Drosophila Heterochromatin Genome Project, Lawrence Berkeley National Lab, http://www.dhgp.org

    Gene Ontology Provided by FlyBase

    Function Evidence Code Pubs
    enables monoatomic ion transmembrane transporter activity ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    Process Evidence Code Pubs
    involved_in transmembrane transport IEA
    Inferred from Electronic Annotation
    more info
     
    Component Evidence Code Pubs
    located_in membrane IEA
    Inferred from Electronic Annotation
    more info
     
    located_in membrane ISS
    Inferred from Sequence or Structural Similarity
    more info
     

    General protein information

    Preferred Names
    uncharacterized protein
    Names
    CG31693-PA
    CG31693-PB

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    Genome Annotation

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference assembly

    Genomic

    1. NT_033779.5 Reference assembly

      Range
      22015190..22017334
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_165402.3NP_724369.2  uncharacterized protein Dmel_CG31693, isoform A [Drosophila melanogaster]

      See identical proteins and their annotated locations for NP_724369.2

      Status: REVIEWED

      UniProtKB/TrEMBL
      Q7KRS1, Q8T0L2
      Conserved Domains (2) summary
      COG1055
      Location:196675
      ArsB; Na+/H+ antiporter NhaD or related arsenite permease [Inorganic ion transport and metabolism]
      cd01116
      Location:205674
      P_permease; Permease P (pink-eyed dilution). Mutations in the human melanosomal P gene were responsible for classic phenotype of oculocutaneous albinism type 2 (OCA2). Although the precise function of the P protein is unknown, it was predicted to regulate the ...
    2. NM_001038844.2NP_001033933.1  uncharacterized protein Dmel_CG31693, isoform B [Drosophila melanogaster]

      See identical proteins and their annotated locations for NP_001033933.1

      Status: REVIEWED

      UniProtKB/TrEMBL
      Q2PDP2, Q8T0L2
      Conserved Domains (2) summary
      COG1055
      Location:115594
      ArsB; Na+/H+ antiporter NhaD or related arsenite permease [Inorganic ion transport and metabolism]
      cd01116
      Location:124593
      P_permease; Permease P (pink-eyed dilution). Mutations in the human melanosomal P gene were responsible for classic phenotype of oculocutaneous albinism type 2 (OCA2). Although the precise function of the P protein is unknown, it was predicted to regulate the ...