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LOC105370449 uncharacterized LOC105370449 [ Homo sapiens (human) ]

Gene ID: 105370449, updated on 17-Sep-2024

Summary

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Gene symbol
LOC105370449
Gene description
uncharacterized LOC105370449
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 LOC105370449 in Genome Data Viewer
Location:
14q13.1
Exon count:
5
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 14 NC_000014.9 (34544089..34557252, complement)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene E2F associated phosphoprotein Neighboring gene Sharpr-MPRA regulatory region 9667 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:35008110-35009034 Neighboring gene uncharacterized LOC105370447 Neighboring gene uncharacterized LOC112268123 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:35015659-35016230 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:35016231-35016802 Neighboring gene ReSE screen-validated silencer GRCh37_chr14:35022516-35022692 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:35024749-35025306 Neighboring gene RNA, U1 small nuclear 27, pseudogene Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:35025307-35025864 Neighboring gene RNA, U1 small nuclear 28, pseudogene Neighboring gene sorting nexin 6 Neighboring gene ribosomal protein S19 pseudogene 3 Neighboring gene Sharpr-MPRA regulatory region 6350 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5666 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 8255 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:35117872-35118710 Neighboring gene ReSE screen-validated silencer GRCh37_chr14:35121050-35121268 Neighboring gene RNA, U6 small nuclear 1261, pseudogene

Genomic regions, transcripts, and products

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Genomic Sequence:
NC_000014.9 Chromosome 14 Reference GRCh38.p14 Primary Assembly

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_000014.9 Reference GRCh38.p14 Primary Assembly

    Range
    34544089..34557252 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007064114.1 RNA Sequence

  2. XR_943742.4 RNA Sequence

  3. XR_001750946.3 RNA Sequence

Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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