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RN7SKP169 RN7SK pseudogene 169 [ Homo sapiens (human) ]

Gene ID: 106480886, updated on 28-Sep-2022

Summary

Official Symbol
RN7SKP169provided by HGNC
Official Full Name
RN7SK pseudogene 169provided by HGNC
Primary source
HGNC:HGNC:45893
See related
Ensembl:ENSG00000223056 AllianceGenome:HGNC:45893
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 RN7SKP169 in Genome Data Viewer
Location:
22q12.1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (25963983..25964273, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (26426242..26426532, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (26359949..26360239, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 2919 Neighboring gene myosin XVIIIB Neighboring gene MYO18B antisense RNA 1 Neighboring gene uncharacterized LOC102724801 Neighboring gene uncharacterized LOC105372971 Neighboring gene long intergenic non-protein coding RNA 2559

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_044867.1 

    Range
    101..391
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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
    25963983..25964273 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    26426242..26426532 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)