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LOC101927314 uncharacterized LOC101927314 [ Homo sapiens (human) ]

Gene ID: 101927314, updated on 23-Nov-2021

Summary

Gene symbol
LOC101927314
Gene description
uncharacterized LOC101927314
See related
Ensembl:ENSG00000271860
Gene type
ncRNA
RefSeq status
VALIDATED
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

See LOC101927314 in Genome Data Viewer
Location:
6q16.1
Exon count:
5
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 6 NC_000006.12 (97305586..97708917)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (97753462..98156793)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene kelch like family member 32 Neighboring gene VISTA enhancer hs676 Neighboring gene MMS22 like, DNA repair protein Neighboring gene VISTA enhancer hs978 Neighboring gene uncharacterized LOC105377909 Neighboring gene VISTA enhancer hs1564 Neighboring gene uncharacterized LOC107986627 Neighboring gene VISTA enhancer hs1035 Neighboring gene VISTA enhancer hs282 Neighboring gene VISTA enhancer hs1220 Neighboring gene VISTA enhancer hs567

Genomic regions, transcripts, and products

Expression

  • 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

Phenotypes

Associated conditions

Description Tests
Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients.
GeneReviews: Not available

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

RNA

  1. NR_110757.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AK091365, AL080316, AL353679, H05806
    Related
    ENST00000433637.2

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000006.12 Reference GRCh38.p13 Primary Assembly

    Range
    97305586..97708917
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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