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    LOC100533710 mannosidase alpha class 1B member 1 pseudogene [ Homo sapiens (human) ]

    Gene ID: 100533710, updated on 17-Jun-2024

    Summary

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    Gene symbol
    LOC100533710
    Gene description
    mannosidase alpha class 1B member 1 pseudogene
    Gene type
    pseudo
    RefSeq status
    INFERRED
    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 LOC100533710 in Genome Data Viewer
    Location:
    11p12
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (43063631..43064856, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (43218870..43220095, complement)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (43085181..43086406, complement)

    Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene ReSE screen-validated silencer GRCh37_chr11:42243924-42244178 Neighboring gene long intergenic non-protein coding RNA 2740 Neighboring gene uncharacterized LOC105376642 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:42548059-42548559 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr11:42617353-42617887 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr11:42898020-42898550 Neighboring gene uncharacterized LOC124902662 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:43121800-43122300 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 4639 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:43233497-43234097 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:43234098-43234697 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:43290423-43290924 Neighboring gene heterogeneous nuclear ribonucleoprotein K pseudogene 3

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    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.

    Genomic

    1. NG_028802.1 

      Range
      101..1326
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      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000011.10 Reference GRCh38.p14 Primary Assembly

      Range
      43063631..43064856 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060935.1 Alternate T2T-CHM13v2.0

      Range
      43218870..43220095 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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