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LOC124902899 uncharacterized LOC124902899 [ Homo sapiens (human) ]

Gene ID: 124902899, updated on 10-Oct-2023

Summary

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Gene symbol
LOC124902899
Gene description
uncharacterized LOC124902899
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

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See LOC124902899 in Genome Data Viewer
Location:
12p12.1
Exon count:
2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (25215551..25219874)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene inositol 1,4,5-triphosphate receptor associated 2 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_26664 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:25288649-25289148 Neighboring gene dynein axonemal intermediate chain 7 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr12:25321883-25322516 Neighboring gene ReSE screen-validated silencer GRCh37_chr12:25323195-25323341 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 6115 Neighboring gene electron transfer flavoprotein regulatory factor 1 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_26705 Neighboring gene KRAS proto-oncogene, GTPase Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 4293 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 4294 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 6116 Neighboring gene NFE2L2 motif-containing MPRA enhancer 301/302 Neighboring gene uncharacterized LOC105369701 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr12:25517951-25518546 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:25522046-25522546 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:25522547-25523047 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:25538426-25539295 Neighboring gene RNA, U4 small nuclear 67, pseudogene

Genomic regions, transcripts, and products

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

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

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
    25215551..25219874
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007063246.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

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