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LOC101928495 uncharacterized LOC101928495 [ Homo sapiens (human) ]

Gene ID: 101928495, updated on 10-Oct-2023

Summary

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Gene symbol
LOC101928495
Gene description
uncharacterized LOC101928495
See related
Ensembl:ENSG00000237208
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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Location:
Xq25
Exon count:
3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (126109762..126115562)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (124422468..124428268)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (125243745..125249545)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene FBLIM1 pseudogene 1 Neighboring gene uncharacterized LOC124905212 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:124522665-124523229 Neighboring gene H3K27ac hESC enhancer GRCh37_chrX:124525724-124526468 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chrX:124527213-124527957 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:124527958-124528701 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:124913288-124914246 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:124960324-124960824 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:125243268-125243822 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:125299194-125299694 Neighboring gene uncharacterized LOC107985648 Neighboring gene DDB1 and CUL4 associated factor 12 like 2

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 variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Genotypes

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_110409.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL445072
    Related
    ENST00000438994.1

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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    126109762..126115562
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    124422468..124428268
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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Molecular Biology Databases