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LOC105376043 uncharacterized LOC105376043 [ Homo sapiens (human) ]

Gene ID: 105376043, updated on 17-Sep-2024

Summary

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Gene symbol
LOC105376043
Gene description
uncharacterized LOC105376043
Gene type
ncRNA
RefSeq status
VALIDATED
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 LOC105376043 in Genome Data Viewer
Location:
9p13.1
Exon count:
4
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (38848549..38873649)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (38848546..38873646)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:38687515-38688496 Neighboring gene uncharacterized LOC124902156 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:38688497-38689479 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:38689480-38690461 Neighboring gene family with sequence similarity 240 member B Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:38733012-38733512 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr9:38767852-38769051 Neighboring gene uncharacterized LOC105376044 Neighboring gene uncharacterized LOC124902157 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr9:40134136-40134683

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 variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

Genotypes

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

RNA

  1. NR_188596.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL845311

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_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    38848549..38873649
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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