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    MAGED4B MAGE family member D4B [ Homo sapiens (human) ]

    Gene ID: 81557, updated on 28-Oct-2024

    Summary

    Official Symbol
    MAGED4Bprovided by HGNC
    Official Full Name
    MAGE family member D4Bprovided by HGNC
    Primary source
    HGNC:HGNC:22880
    See related
    Ensembl:ENSG00000187243 MIM:300765; AllianceGenome:HGNC:22880
    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
    Summary
    This gene is a member of the MAGED gene family. It is expressed only in brain and ovary, and some transcript variants of this gene are specifically expressed in glioma cells. This gene is clustered with other MAGED genes on chromosome Xp11. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, May 2011]
    Annotation information
    Note: There are two highly similar MAGED4 loci on the X chromosome. In June, 2007, the name of this locus was changed from MAGED4 to MAGED4B to conform to the annotation of the underlying clone. [20 Jun 2007]
    Expression
    Broad expression in brain (RPKM 32.3), endometrium (RPKM 13.7) and 14 other tissues See more
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    Genomic context

    See MAGED4B in Genome Data Viewer
    Location:
    Xp11.22
    Exon count:
    14
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (52061827..52069272, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (51333610..51341056, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (51804923..51812368, complement)

    Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene thiopurine S-methyltransferase pseudogene 3 Neighboring gene uncharacterized LOC105377208 Neighboring gene Putative uncharacterized protein FLJ39060 Neighboring gene small nucleolar RNA, H/ACA box 11E Neighboring gene uncharacterized LOC105377209 Neighboring gene small nucleolar RNA, H/ACA box 11D Neighboring gene MAGE family member D4 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:52004803-52005304 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:52005305-52005804

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Clone Names

    • MGC3210, KIAA1859, MGC88639

    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 biological_process ND
    No biological Data available
    more info
     
    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 cellular_component ND
    No biological Data available
    more info
     
    is_active_in nucleus IBA
    Inferred from Biological aspect of Ancestor
    more info
     

    General protein information

    Preferred Names
    melanoma-associated antigen D4
    Names
    MAGE-D4 antigen
    MAGE-E1 antigen
    melanoma antigen family D, 4B
    melanoma antigen family D4B

    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_029896.1 RefSeqGene

      Range
      5090..12446
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001242362.2NP_001229291.1  melanoma-associated antigen D4 isoform 3

      See identical proteins and their annotated locations for NP_001229291.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (4) contains a slightly longer 5' UTR as a result of using an alternate acceptor splice site at the 2nd exon, and an additional in-frame coding exon compared to variant 1. This results in a longer isoform (3) containing an internal protein segment not found in isoform 1.
      Source sequence(s)
      AC239585, BC001207
      Consensus CDS
      CCDS56602.1
      UniProtKB/Swiss-Prot
      Q96JG8
      Related
      ENSP00000421861.1, ENST00000485287.5
      Conserved Domains (2) summary
      pfam01454
      Location:420603
      MAGE; MAGE family
      pfam11321
      Location:250304
      DUF3123; Protein of unknown function (DUF3123)
    2. NM_030801.5NP_110428.2  melanoma-associated antigen D4 isoform 1

      See identical proteins and their annotated locations for NP_110428.2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) represents the predominant transcript, and encodes isoform 1. Variants 1 and 2 encode the same isoform.
      Source sequence(s)
      AB058762, BC001207
      Consensus CDS
      CCDS14338.1
      UniProtKB/Swiss-Prot
      A8K093, Q5HYN6, Q8WXW4, Q96JG8, Q9BQ84, Q9BVH1, Q9BYH3, Q9BYH4, Q9H217
      Related
      ENSP00000335385.5, ENST00000335504.10
      Conserved Domains (2) summary
      pfam01454
      Location:420587
      MAGE; MAGE family
      pfam11321
      Location:250304
      DUF3123; Protein of unknown function (DUF3123)
    3. NM_177535.3NP_803879.1  melanoma-associated antigen D4 isoform 1

      See identical proteins and their annotated locations for NP_803879.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2, also known as MAGE-E1a) has a slightly shorter 5' UTR compared to variant 1, as a result of using an alternate acceptor splice site at the 2nd exon. Variants 1 and 2 encode the same isoform (1).
      Source sequence(s)
      AB040527, AC239585, BC001207
      Consensus CDS
      CCDS14338.1
      UniProtKB/Swiss-Prot
      A8K093, Q5HYN6, Q8WXW4, Q96JG8, Q9BQ84, Q9BVH1, Q9BYH3, Q9BYH4, Q9H217
      Related
      ENSP00000423848.1, ENST00000497164.5
      Conserved Domains (2) summary
      pfam01454
      Location:420587
      MAGE; MAGE family
      pfam11321
      Location:250304
      DUF3123; Protein of unknown function (DUF3123)
    4. NM_177537.3NP_803881.1  melanoma-associated antigen D4 isoform 2

      See identical proteins and their annotated locations for NP_803881.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3, also known as MAGE-E1b) uses an alternate donor splice site at the penultimate exon compared to variant 1. This results in a frame-shift, early translation termination, and a shorter isoform (2) missing 2 aa from the C-terminus compared to isoform 1.
      Source sequence(s)
      AB040528, AC239585, BC001207
      Consensus CDS
      CCDS35281.1
      UniProtKB/Swiss-Prot
      Q96JG8
      Related
      ENSP00000353252.6, ENST00000360134.10
      Conserved Domains (2) summary
      pfam01454
      Location:420587
      MAGE; MAGE family
      pfam11321
      Location:250304
      DUF3123; Protein of unknown function (DUF3123)

    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
      52061827..52069272 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060947.1 Alternate T2T-CHM13v2.0

      Range
      51333610..51341056 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)