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RNY1P9 RNY1 pseudogene 9 [ Homo sapiens (human) ]

Gene ID: 100874358, updated on 20-Mar-2020

Summary

Official Symbol
RNY1P9provided by HGNC
Official Full Name
RNY1 pseudogene 9provided by HGNC
Primary source
HGNC:HGNC:41481
See related
Ensembl:ENSG00000255156
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
RNYP1; KLHL22-IT1

Genomic context

See RNY1P9 in Genome Data Viewer
Location:
22q11.21
Annotation release Status Assembly Chr Location
109.20200228 current GRCh38.p13 (GCF_000001405.39) 22 NC_000022.11 (20475194..20475311, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107985588 Neighboring gene kelch like family member 22 Neighboring gene kelch like family member 12 pseudogene Neighboring gene RNA, 7SL, cytoplasmic 812, pseudogene Neighboring gene keratin 18 pseudogene 5

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000022.11 Chromosome 22 Reference GRCh38.p13 Primary Assembly

General gene information

Other Names

  • KLHL22 intronic transcript 1 (non-protein coding)
  • RNA, Ro-associated Y, pseudogene 1
  • RNA, Ro-associated Y1 pseudogene 9

NCBI Reference Sequences (RefSeq)

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_033992.1 

    Range
    101..218
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000022.11 Reference GRCh38.p13 Primary Assembly

    Range
    20475194..20475311 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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