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LOC105378782 uncharacterized LOC105378782 [ Homo sapiens (human) ]

Gene ID: 105378782, updated on 17-Sep-2024

Summary

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Gene symbol
LOC105378782
Gene description
uncharacterized LOC105378782
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 LOC105378782 in Genome Data Viewer
Location:
1p31.3
Exon count:
3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (68293251..68305568)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (68170652..68182974)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene ribosomal protein S7 pseudogene 4 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr1:68742024-68742651 Neighboring gene NANOG hESC enhancer GRCh37_chr1:68743733-68744317 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:68755969-68756470 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:68759281-68760159 Neighboring gene cytochrome c oxidase subunit 6B1 pseudogene 7 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:68760160-68761038 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:68761039-68761917 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr1:68849743-68850942 Neighboring gene elongin C pseudogene 18 Neighboring gene uncharacterized LOC124904198 Neighboring gene retinoid isomerohydrolase RPE65

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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    68293251..68305568
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_947476.3 RNA Sequence

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    68170652..68182974
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007070321.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

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