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RNU4-32P RNA, U4 small nuclear 32, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479572, updated on 25-Jan-2022

Summary

Official Symbol
RNU4-32Pprovided by HGNC
Official Full Name
RNA, U4 small nuclear 32, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46968
See related
Ensembl:ENSG00000200274 AllianceGenome:HGNC:46968
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 RNU4-32P in Genome Data Viewer
Location:
12q24.11
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (109567975..109568115, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (110005780..110005920, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene potassium channel tetramerization domain containing 10 Neighboring gene ubiquitin protein ligase E3B Neighboring gene metabolism of cobalamin associated B Neighboring gene mevalonate kinase Neighboring gene RN7SK pseudogene 250

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_044581.1 

    Range
    101..241
    Download
    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
    109567975..109568115 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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