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LOC101929007 uncharacterized LOC101929007 [ Homo sapiens (human) ]

Gene ID: 101929007, updated on 17-Jun-2024

Summary

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Gene symbol
LOC101929007
Gene description
uncharacterized LOC101929007
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
Broad expression in bone marrow (RPKM 1.8), testis (RPKM 1.6) and 19 other tissues See more
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Genomic context

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See LOC101929007 in Genome Data Viewer
Location:
19p12
Exon count:
6
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 19 NC_000019.10 (21569902..21594675, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 19 NC_060943.1 (21708389..21733154, complement)

Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene zinc finger protein 429 Neighboring gene BCL2 interacting protein 3 pseudogene 26 Neighboring gene H3K27ac hESC enhancer GRCh37_chr19:21734180-21734961 Neighboring gene uncharacterized LOC124904670 Neighboring gene uncharacterized LOC105372323 Neighboring gene Sharpr-MPRA regulatory region 12513 Neighboring gene zinc finger protein 100-like Neighboring gene metadherin pseudogene 3

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
  • 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)

Genotypes

NCBI Reference Sequences (RefSeq)

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RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000019.10 Reference GRCh38.p14 Primary Assembly

    Range
    21569902..21594675 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007067176.1 RNA Sequence

  2. XR_002958421.2 RNA Sequence

  3. XR_007067177.1 RNA Sequence

  4. XR_007067179.1 RNA Sequence

  5. XR_001754041.3 RNA Sequence

  6. XR_007067178.1 RNA Sequence

  7. XR_007067180.1 RNA Sequence

  8. XR_001754044.3 RNA Sequence

  9. XR_007067174.1 RNA Sequence

  10. XR_002958423.2 RNA Sequence

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060943.1 Alternate T2T-CHM13v2.0

    Range
    21708389..21733154 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007088978.1 RNA Sequence

  2. XR_007088977.1 RNA Sequence

  3. XR_007088979.1 RNA Sequence

  4. XR_007088980.1 RNA Sequence

  5. XR_007088982.1 RNA Sequence

  6. XR_007088981.1 RNA Sequence

  7. XR_007088983.1 RNA Sequence

  8. XR_007088975.1 RNA Sequence

  9. XR_007088976.1 RNA Sequence

Nucleotide Protein
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