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LOC105371199 uncharacterized LOC105371199 [ Homo sapiens (human) ]

Gene ID: 105371199, updated on 17-Sep-2024

Summary

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Gene symbol
LOC105371199
Gene description
uncharacterized LOC105371199
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
Restricted expression toward skin (RPKM 2.4) See more
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Genomic context

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See LOC105371199 in Genome Data Viewer
Location:
16p11.1
Exon count:
4
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (35319031..35327711, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (38801215..38809907)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene chromosome 2 open reading frame 69 pseudogene 5 Neighboring gene uncharacterized LOC124903768 Neighboring gene uncharacterized LOC105371198 Neighboring gene FSHD region gene 2 family member H, pseudogene Neighboring gene retinoic acid receptor responder 2 pseudogene 9 Neighboring gene angiogenic factor with G-patch and FHA domains 1 pseudogene 9

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_000016.10 Reference GRCh38.p14 Primary Assembly

    Range
    35319031..35327711 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_942154.1 RNA Sequence

  2. XR_942153.1 RNA Sequence

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060940.1 Alternate T2T-CHM13v2.0

    Range
    38801215..38809907
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007086658.1 RNA Sequence

  2. XR_007086659.1 RNA Sequence

  3. XR_007086657.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

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