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LOC107984714 uncharacterized LOC107984714 [ Homo sapiens (human) ]

Gene ID: 107984714, updated on 22-Oct-2024

Summary

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Gene symbol
LOC107984714
Gene description
uncharacterized LOC107984714
See related
Ensembl:ENSG00000261632
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 LOC107984714 in Genome Data Viewer
Location:
15q23
Exon count:
9
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 15 NC_000015.10 (71972207..72036764)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 15 NC_060939.1 (69791120..69855690)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene myosin IXA Neighboring gene RNA, 5S ribosomal pseudogene 399 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9707 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9708 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9709 Neighboring gene uncharacterized LOC107984713 Neighboring gene ReSE screen-validated silencer GRCh37_chr15:72323133-72323348 Neighboring gene eukaryotic translation initiation factor 5A2 pseudogene 1 Neighboring gene RNA, U2 small nuclear 65, pseudogene

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_000015.10 Reference GRCh38.p14 Primary Assembly

    Range
    71972207..72036764
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_001751798.3 RNA Sequence

  2. XR_007064705.1 RNA Sequence

  3. XR_001751797.2 RNA Sequence

    Related
    ENST00000819064.1

  4. XR_001751796.2 RNA Sequence

  5. XR_007064704.1 RNA Sequence

  6. XR_007064702.1 RNA Sequence

  7. XR_007064703.1 RNA Sequence

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060939.1 Alternate T2T-CHM13v2.0

    Range
    69791120..69855690
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007085680.1 RNA Sequence

  2. XR_007085681.1 RNA Sequence

  3. XR_007085679.1 RNA Sequence

  4. XR_007085677.1 RNA Sequence

  5. XR_007085678.1 RNA Sequence

  6. XR_007085676.1 RNA Sequence

  7. XR_007085674.1 RNA Sequence

  8. XR_007085675.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

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