U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

LOC101926956 uncharacterized LOC101926956 [ Homo sapiens (human) ]

Gene ID: 101926956, updated on 21-Mar-2023

Summary

Go to the top of the page Help
Gene symbol
LOC101926956
Gene description
uncharacterized LOC101926956
See related
Ensembl:ENSG00000253177
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
Biased expression in fat (RPKM 2.6), thyroid (RPKM 1.8) and 9 other tissues See more
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

Go to the top of the page Help
See LOC101926956 in Genome Data Viewer
Location:
8q22.1
Exon count:
4
Annotation release Status Assembly Chr Location
RS_2023_03 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (92668659..92683450)
RS_2023_03 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (93793594..93808359)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105375639 Neighboring gene Sharpr-MPRA regulatory region 14314 Neighboring gene uncharacterized LOC102724710 Neighboring gene uncharacterized LOC441369 Neighboring gene uncharacterized LOC124901978

Genomic regions, transcripts, and products

Go to the top of the page Help

Go to nucleotide: Graphics FASTA GenBank

Expression

Go to the top of the page Help
  • Project title: 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

Go to the top of the pageHelp

GeneRIFs: Gene References Into Functions

Phenotypes

Go to the top of the page Help

Review eQTL and phenotype association data in this region using PheGenI

Variation

Go to the top of the page Help

See studies and variants in dbVar

See Variation Viewer (GRCh38)

Genotypes

NCBI Reference Sequences (RefSeq)

Go to the top of the page Help

NEW Try the new Transcript table

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_03

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    92668659..92683450
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_928407.4 RNA Sequence

    Related
    ENST00000663356.1

  2. XR_928406.4 RNA Sequence

    Related
    ENST00000657155.1

  3. XR_928408.4 RNA Sequence

    Related
    ENST00000660470.1

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    93793594..93808359
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007079234.1 RNA Sequence

  2. XR_007079233.1 RNA Sequence

  3. XR_007079235.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Molecular Biology Databases