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LOC124904126 uncharacterized LOC124904126 [ Homo sapiens (human) ]

Gene ID: 124904126, updated on 27-Aug-2024

Summary

Gene symbol
LOC124904126
Gene description
uncharacterized LOC124904126
Gene type
pseudo
RefSeq status
MODEL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See LOC124904126 in Genome Data Viewer
Location:
17p12
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (15237785..15237881, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (15143793..15143889, complement)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107984976 Neighboring gene uncharacterized LOC105371547 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr17:15083139-15084083 Neighboring gene peripheral myelin protein 22 Neighboring gene microRNA 4731 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 8211 Neighboring gene uncharacterized LOC124903931

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

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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_000017.11 Reference GRCh38.p14 Primary Assembly

    Range
    15237785..15237881 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060941.1 Alternate T2T-CHM13v2.0

    Range
    15143793..15143889 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)