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LOC124903693 uncharacterized LOC124903693 [ Homo sapiens (human) ]

Gene ID: 124903693, updated on 27-Aug-2024

Summary

Gene symbol
LOC124903693
Gene description
uncharacterized LOC124903693
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 LOC124903693 in Genome Data Viewer
Location:
16q12.2
Exon count:
2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (55653106..55656113, complement)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene H3K4me1 hESC enhancer GRCh37_chr16:55536405-55536906 Neighboring gene matrix metallopeptidase 2 Neighboring gene lysophosphatidylcholine acyltransferase 2 Neighboring gene calpain small subunit 2 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:55633008-55633567 Neighboring gene Sharpr-MPRA regulatory region 3138 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr16:55690152-55690687 Neighboring gene solute carrier family 6 member 2 Neighboring gene uncharacterized LOC105371280 Neighboring gene carboxylesterase 1 pseudogene 2

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000016.10 Chromosome 16 Reference GRCh38.p14 Primary Assembly

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_000016.10 Reference GRCh38.p14 Primary Assembly

    Range
    55653106..55656113 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007065075.1 RNA Sequence