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    MTMR9P1 MTMR9 pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 132542984, updated on 28-Oct-2024

    Summary

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    Official Symbol
    MTMR9P1provided by HGNC
    Official Full Name
    MTMR9 pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:56931
    See related
    Ensembl:ENSG00000218337 AllianceGenome:HGNC:56931
    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 MTMR9P1 in Genome Data Viewer
    Location:
    6p12.3
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (49077712..49078038, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (48919690..48920016, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (49045349..49045675, complement)

    Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107986602 Neighboring gene MPRA-validated peak5834 silencer Neighboring gene NANOG hESC enhancer GRCh37_chr6:48732670-48733267 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr6:48794410-48795609 Neighboring gene PRR11 pseudogene 1 Neighboring gene piggyBac transposable element derived 4 pseudogene Neighboring gene uncharacterized LOC124901478

    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 Variation Viewer (GRCh37.p13)

    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_241857.1 

      Range
      101..427
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      GenBank, FASTA, Sequence Viewer (Graphics)

    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_000006.12 Reference GRCh38.p14 Primary Assembly

      Range
      49077712..49078038 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060930.1 Alternate T2T-CHM13v2.0

      Range
      48919690..48920016 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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