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    MAGEE2 MAGE family member E2 [ Homo sapiens (human) ]

    Gene ID: 139599, updated on 27-Nov-2024

    Summary

    Official Symbol
    MAGEE2provided by HGNC
    Official Full Name
    MAGE family member E2provided by HGNC
    Primary source
    HGNC:HGNC:24935
    See related
    Ensembl:ENSG00000186675 MIM:300760; AllianceGenome:HGNC:24935
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    HCA3
    Summary
    This gene encodes a member of the E subfamily of MAGE (melanoma antigen-encoding gene) gene family. The gene is intronless and the encoded protein has two of the MAGE domains which are characteristic of MAGE family proteins. [provided by RefSeq, Sep 2011]
    Orthologs
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    Genomic context

    See MAGEE2 in Genome Data Viewer
    Location:
    Xq13.3
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (75782987..75785254, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (74216673..74218940, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (75002822..75005089, complement)

    Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107985664 Neighboring gene BRAF pseudogene 1 Neighboring gene tetratricopeptide repeat domain 3 pseudogene 1 Neighboring gene Sharpr-MPRA regulatory region 1365 Neighboring gene secretion associated Ras related GTPase 1A pseudogene 4 Neighboring gene FOXN3 pseudogene 2

    Genomic regions, transcripts, and products

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Clone Names

    • MGC138154

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in negative regulation of transcription by RNA polymerase II IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    Component Evidence Code Pubs
    is_active_in nucleus IBA
    Inferred from Biological aspect of Ancestor
    more info
     

    General protein information

    Preferred Names
    melanoma-associated antigen E2
    Names
    MAGE-E2 antigen
    hepatocellular carcinoma-associated protein 3
    hepatocellular carcinoma-associated protein HCA3
    melanoma antigen family E, 2
    melanoma antigen family E2

    NCBI Reference Sequences (RefSeq)

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    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    Genomic

    1. NG_021324.1 RefSeqGene

      Range
      4991..7258
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_138703.5NP_619648.1  melanoma-associated antigen E2

      See identical proteins and their annotated locations for NP_619648.1

      Status: REVIEWED

      Source sequence(s)
      AK094624, AL391495, DA793762
      Consensus CDS
      CCDS14431.1
      UniProtKB/Swiss-Prot
      Q5JSI5, Q8TD90
      Related
      ENSP00000362457.2, ENST00000373359.4
      Conserved Domains (1) summary
      pfam01454
      Location:124264
      MAGE; MAGE family

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000023.11 Reference GRCh38.p14 Primary Assembly

      Range
      75782987..75785254 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060947.1 Alternate T2T-CHM13v2.0

      Range
      74216673..74218940 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)