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RNU1-97P RNA, U1 small nuclear 97, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480182, updated on 10-Oct-2023

Summary

Official Symbol
RNU1-97Pprovided by HGNC
Official Full Name
RNA, U1 small nuclear 97, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48439
See related
Ensembl:ENSG00000252681 AllianceGenome:HGNC:48439
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:
Yq11.223
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (23740942..23741105, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (25121475..25121638)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (25887089..25887252, complement)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene XK related, Y-linked pseudogene 3 Neighboring gene USP9Y pseudogene 25 Neighboring gene USP9Y pseudogene 29 Neighboring gene RAB9A, member RAS oncogene family pseudogene 1 Neighboring gene trafficking protein particle complex 2 pseudogene 9

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_045417.1 

    Range
    101..264
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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_000024.10 Reference GRCh38.p14 Primary Assembly

    Range
    23740942..23741105 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060948.1 Alternate T2T-CHM13v2.0

    Range
    25121475..25121638
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)