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RNU6-499P RNA, U6 small nuclear 499, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479787, updated on 13-May-2022

Summary

Official Symbol
RNU6-499Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 499, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47462
See related
Ensembl:ENSG00000202485 AllianceGenome:HGNC:47462
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 RNU6-499P in Genome Data Viewer
Location:
4q21.22
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (82174547..82174653)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (85504082..85504188)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (83095700..83095806)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene nucleophosmin 1 pseudogene 41 Neighboring gene heterogeneous nuclear ribonucleoprotein A3 pseudogene 13 Neighboring gene uncharacterized LOC105377308 Neighboring gene bridging integrator 2 pseudogene 1 Neighboring gene vesicle associated membrane protein 9, 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_044246.1 

    Range
    101..207
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    82174547..82174653
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    85504082..85504188
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)