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LOC124902888 uncharacterized LOC124902888 [ Homo sapiens (human) ]

Gene ID: 124902888, updated on 10-Oct-2023

Summary

Gene symbol
LOC124902888
Gene description
uncharacterized LOC124902888
See related
Ensembl:ENSG00000256389
Gene type
ncRNA
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 LOC124902888 in Genome Data Viewer
Location:
12p12.3
Exon count:
2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (17589189..17615451)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene translocase of inner mitochondrial membrane 17B pseudogene 1 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_26433 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_26470 Neighboring gene VISTA enhancer hs605 Neighboring gene long intergenic non-protein coding RNA 2378 Neighboring gene uncharacterized LOC124902889 Neighboring gene VISTA enhancer hs579 Neighboring gene VISTA enhancer hs980 Neighboring gene microRNA 3974 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:18102760-18103303 Neighboring gene RERG like

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000012.12 Chromosome 12 Reference GRCh38.p14 Primary Assembly

NCBI Reference Sequences (RefSeq)

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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_000012.12 Reference GRCh38.p14 Primary Assembly

    Range
    17589189..17615451
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007063231.1 RNA Sequence

    Related
    ENST00000658328.1