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LOC112577592 uncharacterized LOC112577592 [ Homo sapiens (human) ]

Gene ID: 112577592, updated on 15-Mar-2024

Summary

Gene symbol
LOC112577592
Gene description
uncharacterized LOC112577592
See related
Ensembl:ENSG00000286126
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Orthologs
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Genomic context

See LOC112577592 in Genome Data Viewer
Location:
18p11.23
Exon count:
2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 18 NC_000018.10 (7455842..7461135, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 18 NC_060942.1 (7619097..7624393, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 18 NC_000018.9 (7455840..7461133, complement)

Chromosome 18 - NC_000018.10Genomic Context describing neighboring genes Neighboring gene small nucleolar RNA SNORA48 Neighboring gene uncharacterized LOC105371975 Neighboring gene ReSE screen-validated silencer GRCh37_chr18:7347954-7348125 Neighboring gene ReSE screen-validated silencer GRCh37_chr18:7429686-7429920 Neighboring gene uncharacterized LOC105371976 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 9270 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr18:7577695-7578451 Neighboring gene protein tyrosine phosphatase receptor type M Neighboring gene MED14-independent group 3 enhancer GRCh37_chr18:7727774-7728973 Neighboring gene NANOG hESC enhancer GRCh37_chr18:7734824-7735325 Neighboring gene uncharacterized LOC124904242

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_172881.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AP001095
    Related
    ENST00000651113.1

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_000018.10 Reference GRCh38.p14 Primary Assembly

    Range
    7455842..7461135 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060942.1 Alternate T2T-CHM13v2.0

    Range
    7619097..7624393 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001364581.1: Suppressed sequence

    Description
    NM_001364581.1: This RefSeq was removed because it is now thought that this gene does not encode a protein.