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MAGEB6B MAGE family member B6B [ Homo sapiens (human) ]

Gene ID: 392433, updated on 11-Jun-2021

Summary

Official Symbol
MAGEB6Bprovided by HGNC
Official Full Name
MAGE family member B6Bprovided by HGNC
Primary source
HGNC:HGNC:28824
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
MAGEB6P1
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Genomic context

See MAGEB6B in Genome Data Viewer
Location:
Xp21.3
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (26160526..26162413)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (26178643..26180530)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107985707 Neighboring gene MAGE family member B18 Neighboring gene MAGE family member B3 pseudogene Neighboring gene MAGE family member B6

Genomic regions, transcripts, and products

General gene information

Other Names

  • MAGE family member B6 pseudogene 1
  • melanoma antigen family B, 6 pseudogene 1
  • melanoma antigen family B, 6B pseudogene
  • melanoma antigen family B6 pseudogene 1

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_008389.2 

    Range
    101..1988
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    26160526..26162413
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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