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RN7SKP63 RN7SK pseudogene 63 [ Homo sapiens (human) ]

Gene ID: 106479123, updated on 13-May-2022

Summary

Official Symbol
RN7SKP63provided by HGNC
Official Full Name
RN7SK pseudogene 63provided by HGNC
Primary source
HGNC:HGNC:45787
See related
AllianceGenome:HGNC:45787
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 RN7SKP63 in Genome Data Viewer
Location:
22q11.21
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (21389191..21389428)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (21958884..21959121, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (21743480..21743717)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene family with sequence similarity 246 member A Neighboring gene sushi domain containing 2 pseudogene 1 Neighboring gene RIMS binding protein 3B Neighboring gene small Cajal body-specific RNA 18 Neighboring gene small Cajal body-specific RNA 17

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_045295.1 

    Range
    101..338
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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
    21389191..21389428
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    21958884..21959121 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)