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RN7SKP80 RN7SK pseudogene 80 [ Homo sapiens (human) ]

Gene ID: 106479130, updated on 13-May-2022

Summary

Official Symbol
RN7SKP80provided by HGNC
Official Full Name
RN7SK pseudogene 80provided by HGNC
Primary source
HGNC:HGNC:45804
See related
Ensembl:ENSG00000202058 AllianceGenome:HGNC:45804
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

See RN7SKP80 in Genome Data Viewer
Location:
22q13.2
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (42565062..42565329, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (43045927..43046194, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (42961068..42961335, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene serine hydrolase like (pseudogene) Neighboring gene ribosomal RNA processing 7 homolog A Neighboring gene uncharacterized LOC124900479 Neighboring gene Sharpr-MPRA regulatory region 9885 Neighboring gene serine hydrolase like 2 Neighboring gene RNA, U6 small nuclear 513, pseudogene Neighboring gene ribosomal RNA processing 7 homolog B, 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_045320.1 

    Range
    101..368
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    GenBank, FASTA, Sequence Viewer (Graphics)

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_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    42565062..42565329 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    43045927..43046194 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)