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LOC101929881 uncharacterized LOC101929881 [ Homo sapiens (human) ]

Gene ID: 101929881, updated on 12-Sep-2024

Summary

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Gene symbol
LOC101929881
Gene description
uncharacterized LOC101929881
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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See LOC101929881 in Genome Data Viewer
Location:
chromosome: 8
Exon count:
3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (34228995..34242757, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (34500239..34514099, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (34086513..34100275, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105379364 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_103242 Neighboring gene MPRA-validated peak6990 silencer Neighboring gene VISTA enhancer hs1715 Neighboring gene CYCS pseudogene 3 Neighboring gene uncharacterized LOC105379366 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:34072823-34073322 Neighboring gene ribosomal protein L10a pseudogene 3 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_103270 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_103276 Neighboring gene long intergenic non-protein coding RNA 1288 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr8:34714442-34715641 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:34717375-34718364

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

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 Variation Viewer (GRCh37.p13)

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

RNA

  1. NR_189603.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC087855

  2. NR_189604.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC087855

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_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    34228995..34242757 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    34500239..34514099 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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Molecular Biology Databases
Research Materials