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LOC100421793 tRNA methyltransferase 11 homolog (S. cerevisiae) pseudogene [ Homo sapiens (human) ]

Gene ID: 100421793, updated on 17-Jun-2024

Summary

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Gene symbol
LOC100421793
Gene description
tRNA methyltransferase 11 homolog (S. cerevisiae) 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 LOC100421793 in Genome Data Viewer
Location:
11q12.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (58072188..58073633, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (58021593..58023038, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (57839660..57841105, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene olfactory receptor family 9 subfamily Q member 1 Neighboring gene uncharacterized LOC124902674 Neighboring gene vomeronasal 2 receptor 9, pseudogene Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:57825504-57826184 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:57826185-57826864 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:57834537-57835036 Neighboring gene olfactory receptor family 9 subfamily L member 1 pseudogene Neighboring gene olfactory receptor family 9 subfamily I member 3 pseudogene

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_024359.2 

    Range
    101..1546
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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
    58072188..58073633 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    58021593..58023038 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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