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    RBMY2EP RNA binding motif protein Y-linked family 2 member E, pseudogene [ Homo sapiens (human) ]

    Gene ID: 159125, updated on 10-Dec-2024

    Summary

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    Official Symbol
    RBMY2EPprovided by HGNC
    Official Full Name
    RNA binding motif protein Y-linked family 2 member E, pseudogeneprovided by HGNC
    Primary source
    HGNC:HGNC:23890
    See related
    AllianceGenome:HGNC:23890
    Gene type
    pseudo
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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    Genomic context

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    See RBMY2EP in Genome Data Viewer
    Location:
    Yq11.223
    Exon count:
    5
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (21395148..21401562, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (22270410..22276824, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (23557034..23563448, complement)

    Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107987346 Neighboring gene uncharacterized LOC107987347 Neighboring gene RNA binding motif protein Y-linked family 2 member S, pseudogene Neighboring gene PRORY Y-linked lncRNA Neighboring gene RNA binding motif protein Y-linked family 2 member T, pseudogene Neighboring gene testis specific protein Y-linked 14, pseudogene

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    Related articles in PubMed

    1. Multiple functional copies of the RBM gene family, a spermatogenesis candidate on the human Y chromosome. Chai NN, et al. Genomics, 1997 Oct 15. PMID 9344660
    2. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes. Skaletsky H, et al. Nature, 2003 Jun 19. PMID 12815422

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Review eQTL and phenotype association data in this region using PheGenI

    Variation

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    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    General gene information

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    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.

    RNA

    1. NR_001574.2 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC010086, U94388

    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_000024.10 Reference GRCh38.p14 Primary Assembly

      Range
      21395148..21401562 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060948.1 Alternate T2T-CHM13v2.0

      Range
      22270410..22276824 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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