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RNU1-142P RNA, U1 small nuclear 142, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480197, updated on 10-Oct-2023

Summary

Official Symbol
RNU1-142Pprovided by HGNC
Official Full Name
RNA, U1 small nuclear 142, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48484
See related
Ensembl:ENSG00000252491 AllianceGenome:HGNC:48484
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:
Xp21.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (26790142..26790286)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (26377440..26377584)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (26808259..26808403)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene ribosomal protein L7 pseudogene 58 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chrX:26773077-26773647 Neighboring gene high mobility group AT-hook 1 pseudogene 1 Neighboring gene uncharacterized LOC124905231 Neighboring gene uncharacterized LOC105373150 Neighboring gene AMZ2 pseudogene 3

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_043475.1 

    Range
    101..245
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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
    26790142..26790286
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    26377440..26377584
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    GenBank, FASTA, Sequence Viewer (Graphics)