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LOC105375721 uncharacterized LOC105375721 [ Homo sapiens (human) ]

Gene ID: 105375721, updated on 4-Mar-2025

Summary

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Gene symbol
LOC105375721
Gene description
uncharacterized LOC105375721
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 LOC105375721 in Genome Data Viewer
Location:
8q24.11
Exon count:
12
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (117610897..117732139, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (118741728..118860541, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105375716 Neighboring gene uncharacterized LOC105375717 Neighboring gene NANOG hESC enhancer GRCh37_chr8:118369992-118370493 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr8:118400318-118401517 Neighboring gene ribosomal protein S10 pseudogene 16 Neighboring gene mediator complex subunit 30 Neighboring gene uncharacterized LOC107986970 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:118824531-118825096 Neighboring gene Sharpr-MPRA regulatory region 14285 Neighboring gene EXT1 intron enhancer-blocking element 8-1-1 Neighboring gene exostosin glycosyltransferase 1 Neighboring gene small nucleolar RNA, C/D box 168

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Expression

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  • Project title: Tissue-specific circular RNA induction during human fetal development
  • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
  • BioProject: PRJNA270632
  • Publication: PMID 26076956
  • Analysis date: Mon Apr 2 22:54:59 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

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_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    117610897..117732139 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007061069.1 RNA Sequence

  2. XR_001746050.1 RNA Sequence

  3. XR_001746049.1 RNA Sequence

  4. XR_001746046.1 RNA Sequence

  5. XR_007061071.1 RNA Sequence

  6. XR_007061070.1 RNA Sequence

  7. XR_001746048.2 RNA Sequence

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    118741728..118860541 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007079370.1 RNA Sequence

  2. XR_007079369.1 RNA Sequence

  3. XR_007079365.1 RNA Sequence

  4. XR_007079367.1 RNA Sequence

  5. XR_007079366.1 RNA Sequence

  6. XR_007079371.1 RNA Sequence

  7. XR_007079368.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

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