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LOC100996756 uncharacterized LOC100996756 [ Homo sapiens (human) ]

Gene ID: 100996756, updated on 27-Aug-2024

Summary

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Gene symbol
LOC100996756
Gene description
uncharacterized LOC100996756
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
Ubiquitous expression in bone marrow (RPKM 5.7), prostate (RPKM 4.4) and 25 other tissues See more
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Genomic context

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Location:
1q21.1
Exon count:
2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (146386547..146388089)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (148420292..148421498, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene SEC22 homolog B4, pseudogene Neighboring gene tRNA-Asn (anticodon GTT) 24-1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1276 Neighboring gene U1 spliceosomal RNA Neighboring gene uncharacterized LOC112268274 Neighboring gene U1 spliceosomal RNA Neighboring gene uncharacterized LOC105371235 Neighboring gene uncharacterized LOC124904407

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

See Variation Viewer (GRCh38)

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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    146386547..146388089
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_159169.5 RNA Sequence

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    148420292..148421498 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007070654.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

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