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LOC105370338 uncharacterized LOC105370338 [ Homo sapiens (human) ]

Gene ID: 105370338, updated on 17-Sep-2024

Summary

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Gene symbol
LOC105370338
Gene description
uncharacterized LOC105370338
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 LOC105370338 in Genome Data Viewer
Location:
13q33.1
Exon count:
4
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (103290969..103306424)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (102508997..102524514)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene methyltransferase like 21E, pseudogene Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7973 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7974 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7975 Neighboring gene solute carrier family 10 member 2 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7976 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr13:104003539-104004232 Neighboring gene uncharacterized LOC105370339 Neighboring gene NANOG hESC enhancer GRCh37_chr13:104049244-104049745 Neighboring gene long intergenic non-protein coding RNA 1309

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_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    103290969..103306424
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_931687.1 RNA Sequence

  2. XR_931686.1 RNA Sequence

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    102508997..102524514
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007083646.1 RNA Sequence

  2. XR_007083645.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

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