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LOC100131496 uncharacterized LOC100131496 [ Homo sapiens (human) ]

Gene ID: 100131496, updated on 13-May-2022

Summary

Gene symbol
LOC100131496
Gene description
uncharacterized LOC100131496
See related
Ensembl:ENSG00000267882
Gene type
ncRNA
RefSeq status
PREDICTED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See LOC100131496 in Genome Data Viewer
Location:
20q13.12
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 20 NC_000020.11 (47318502..47320754)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 20 NC_060944.1 (49056783..49059035)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 20 NC_000020.10 (45947246..45949498)

Chromosome 20 - NC_000020.11Genomic Context describing neighboring genes Neighboring gene EYA transcriptional coactivator and phosphatase 2 Neighboring gene Sharpr-MPRA regulatory region 12423 Neighboring gene Sharpr-MPRA regulatory region 5760 Neighboring gene zinc finger MYND-type containing 8 Neighboring gene uncharacterized LOC101927377 Neighboring gene Sharpr-MPRA regulatory region 8686

Genomic regions, transcripts, and products

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_024594.1 RNA Sequence

    Status: PREDICTED

    Source sequence(s)
    AI198948, AK056171
    Related
    ENST00000599904.2

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000020.11 Reference GRCh38.p14 Primary Assembly

    Range
    47318502..47320754
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060944.1 Alternate T2T-CHM13v2.0

    Range
    49056783..49059035
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)