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LOC107985192 uncharacterized LOC107985192 [ Homo sapiens (human) ]

Gene ID: 107985192, updated on 4-Mar-2025

Summary

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Gene symbol
LOC107985192
Gene description
uncharacterized LOC107985192
Gene type
ncRNA
RefSeq status
MODEL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Low expression observed in reference dataset See more
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Genomic context

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See LOC107985192 in Genome Data Viewer
Location:
1p12
Exon count:
2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (119248203..119255941, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (119261426..119269171, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene tryptophanyl tRNA synthetase 2, mitochondrial Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1590 Neighboring gene RPS3A pseudogene 12 Neighboring gene WARS2 antisense RNA 1 Neighboring gene ribosomal protein L6 pseudogene 2 Neighboring gene small nucleolar RNA U13 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1591 Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:119836037-119836616 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr1:119836617-119837196 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr1:119837197-119837776 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr1:119868596-119869458 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:119869459-119870319 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:119870320-119871181 Neighboring gene long intergenic non-protein coding RNA 1780 Neighboring gene RNA, U1 small nuclear 75, pseudogene

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Expression

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  • Project title: Tissue-specific circular RNA induction during human fetal development
  • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
  • BioProject: PRJNA270632
  • Publication: PMID 26076956
  • Analysis date: Mon Apr 2 22:54:59 2018

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

Variation

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See studies and variants in dbVar

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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    119248203..119255941 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_001738199.2 RNA Sequence

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    119261426..119269171 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007070574.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

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