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LOC124907979 uncharacterized LOC124907979 [ Homo sapiens (human) ]

Gene ID: 124907979, updated on 22-Oct-2024

Summary

Gene symbol
LOC124907979
Gene description
uncharacterized LOC124907979
See related
Ensembl:ENSG00000309139
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 LOC124907979 in Genome Data Viewer
Location:
2q35
Exon count:
2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (216856397..216857777)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene IGFBP5 antisense RNA 1 Neighboring gene fatty acid binding protein 5 pseudogene 14 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr2:217706511-217707710 Neighboring gene uncharacterized LOC124907978 Neighboring gene uncharacterized LOC124906118 Neighboring gene transition protein 1

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000002.12 Chromosome 2 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_000002.12 Reference GRCh38.p14 Primary Assembly

    Range
    216856397..216857777
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007088084.1 RNA Sequence

    Related
    ENST00000839000.1