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LOC107984982 uncharacterized LOC107984982 [ Homo sapiens (human) ]

Gene ID: 107984982, updated on 17-Sep-2024

Summary

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Gene symbol
LOC107984982
Gene description
uncharacterized LOC107984982
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 LOC107984982 in Genome Data Viewer
Location:
17q22
Exon count:
3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (53746972..53748876, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (54622211..54624115, complement)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene tubulin beta 6 class V pseudogene Neighboring gene phosphatidylinositol 4-kinase type 2 alpha pseudogene Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr17:51532575-51533558 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr17:51693716-51694915 Neighboring gene H3K27ac hESC enhancer GRCh37_chr17:51707755-51708255 Neighboring gene MPRA-validated peak2897 silencer Neighboring gene ribosomal protein S2 pseudogene 48 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:51868774-51869274 Neighboring gene uncharacterized LOC124904030

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 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

Genotypes

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_000017.11 Reference GRCh38.p14 Primary Assembly

    Range
    53746972..53748876 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_001753060.1 RNA Sequence

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060941.1 Alternate T2T-CHM13v2.0

    Range
    54622211..54624115 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007087691.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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