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LOC107986667 uncharacterized LOC107986667 [ Homo sapiens (human) ]

Gene ID: 107986667, updated on 17-Sep-2024

Summary

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Gene symbol
LOC107986667
Gene description
uncharacterized LOC107986667
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 LOC107986667 in Genome Data Viewer
Location:
6q27
Exon count:
4
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (164437574..164527702)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (165802371..165892468)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105378109 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr6:164757982-164759181 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr6:164764686-164765488 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr6:164765489-164766289 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr6:164800638-164801837 Neighboring gene uncharacterized LOC105379712 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 25426 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:165129011-165129555 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_91179 Neighboring gene melanoma-associated transcript 6 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_91213 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_91215 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr6:165591001-165592200 Neighboring gene uncharacterized LOC124901500

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Expression

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  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    164437574..164527702
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_001744460.3 RNA Sequence

  2. XR_001744458.2 RNA Sequence

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    165802371..165892468
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007077487.1 RNA Sequence

  2. XR_007077486.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

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