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LOC105370286 uncharacterized LOC105370286 [ Homo sapiens (human) ]

Gene ID: 105370286, updated on 10-Dec-2024

Summary

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Gene symbol
LOC105370286
Gene description
uncharacterized LOC105370286
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 LOC105370286 in Genome Data Viewer
Location:
13q31.1
Exon count:
7
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (83720131..83817725, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (82952922..83050526, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr13:83473788-83474433 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr13:83474434-83475078 Neighboring gene glycogenin 1 pseudogene 2 Neighboring gene RNA, U6 small nuclear 67, pseudogene Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr13:84091305-84092504 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr13:84407388-84407977 Neighboring gene SLIT and NTRK like family member 1 Neighboring gene VENT homeobox pseudogene 2

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_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    83720131..83817725 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_942129.2 RNA Sequence

  2. XR_001749945.1 RNA Sequence

  3. XR_001749947.1 RNA Sequence

  4. XR_001749948.1 RNA Sequence

  5. XR_001749946.1 RNA Sequence

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    82952922..83050526 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007083966.1 RNA Sequence

  2. XR_007083965.1 RNA Sequence

  3. XR_007083968.1 RNA Sequence

  4. XR_007083969.1 RNA Sequence

  5. XR_007083967.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

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