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USP9YP9 USP9Y pseudogene 9 [ Homo sapiens (human) ]

Gene ID: 100421220, updated on 17-Sep-2024

Summary

Official Symbol
USP9YP9provided by HGNC
Official Full Name
USP9Y pseudogene 9provided by HGNC
Primary source
HGNC:HGNC:38435
See related
AllianceGenome:HGNC:38435
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 USP9YP9 in Genome Data Viewer
Location:
Yq11.23
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (25730010..25733452, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (26542417..26545856, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (27876157..27879599, complement)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene RNA, U1 small nuclear 107, pseudogene Neighboring gene USP9Y pseudogene 30 Neighboring gene testis expressed transcript, Y-linked 3 Neighboring gene USP9Y pseudogene 19 Neighboring gene XK related, Y-linked pseudogene 5

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_021931.1 

    Range
    101..3543
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000024.10 Reference GRCh38.p14 Primary Assembly

    Range
    25730010..25733452 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060948.1 Alternate T2T-CHM13v2.0

    Range
    26542417..26545856 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)