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LOC105377843 uncharacterized LOC105377843 [ Homo sapiens (human) ]

Gene ID: 105377843, updated on 17-Sep-2024

Summary

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Gene symbol
LOC105377843
Gene description
uncharacterized LOC105377843
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 LOC105377843 in Genome Data Viewer
Location:
6q12
Exon count:
3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (67282677..67301037, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (68439029..68457358, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107986540 Neighboring gene ReSE screen-validated silencer GRCh37_chr6:67768818-67768993 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_94183 Neighboring gene small nucleolar RNA SNORD65 Neighboring gene uncharacterized LOC105377842 Neighboring gene MPRA-validated peak5869 silencer Neighboring gene MED14-independent group 3 enhancer GRCh37_chr6:68055308-68056507 Neighboring gene SH3 domain binding protein 4 pseudogene Neighboring gene RNA, 5S ribosomal pseudogene 208

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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    67282677..67301037 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_942660.1 RNA Sequence

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    68439029..68457358 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007077403.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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Molecular Biology Databases
Research Materials