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UHRF2P1 ubiquitin like with PHD and ring finger domains 2 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 260337, updated on 10-Oct-2023

Summary

Official Symbol
UHRF2P1provided by HGNC
Official Full Name
ubiquitin like with PHD and ring finger domains 2 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:39565
See related
AllianceGenome:HGNC:39565
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

Location:
Xq13.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (74105279..74108818)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (72538819..72542358)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (73325114..73328653)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene JPX transcript, XIST activator Neighboring gene FTX transcript, XIST regulator Neighboring gene SHISA5 pseudogene 2 Neighboring gene AARSD1 pseudogene 1 Neighboring gene DEAD-box helicase 3 pseudogene 1 Neighboring gene DEAD-box helicase 3 pseudogene 2 Neighboring gene makorin ring finger protein 5, 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_002342.6 

    Range
    101..3640
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    74105279..74108818
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    72538819..72542358
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)