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RN7SL98P RNA, 7SL, cytoplasmic 98, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479259, updated on 10-Oct-2023

Summary

Official Symbol
RN7SL98Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 98, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46114
See related
Ensembl:ENSG00000240613 AllianceGenome:HGNC:46114
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

Location:
9p22.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (15525782..15526081, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (15537688..15537987, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (15525780..15526079, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene small nuclear RNA activating complex polypeptide 3 Neighboring gene PC4 and SRSF1 interacting protein 1 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:15510081-15511034 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:15511035-15511987 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr9:15512640-15513258 Neighboring gene thymosin beta-11-like Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:15532576-15533116 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:15533117-15533656 Neighboring gene ferritin heavy chain 1 pseudogene 12 Neighboring gene RNA, U6 small nuclear 246, pseudogene

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.

Genomic

  1. NG_045721.1 

    Range
    101..400
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

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_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    15525782..15526081 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    15537688..15537987 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)