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KNOP1P2 lysine rich nucleolar protein 1 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 100420898, updated on 25-Jan-2022

Summary

Official Symbol
KNOP1P2provided by HGNC
Official Full Name
lysine rich nucleolar protein 1 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:48920
See related
Ensembl:ENSG00000270429 AllianceGenome:HGNC:48920
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 KNOP1P2 in Genome Data Viewer
Location:
12q12
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (45880950..45882268, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (46274733..46276051, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene AT-rich interaction domain 2 Neighboring gene uncharacterized LOC105369745 Neighboring gene RNA, 7SL, cytoplasmic 246, pseudogene Neighboring gene SR-related CTD associated factor 11 Neighboring gene ribosomal protein L13a pseudogene 21

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_024004.1 

    Range
    101..1419
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000012.12 Reference GRCh38.p13 Primary Assembly

    Range
    45880950..45882268 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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