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RNU6-99P RNA, U6 small nuclear 99, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479610, updated on 10-Oct-2023

Summary

Official Symbol
RNU6-99Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 99, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47062
See related
Ensembl:ENSG00000201591 AllianceGenome:HGNC:47062
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:
11p12
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (39261107..39261213)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (39407689..39407795)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (39282657..39282763)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC101928563 Neighboring gene ribosomal protein L18 pseudogene 8 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:39463923-39464422 Neighboring gene uncharacterized LOC107984362 Neighboring gene uncharacterized LOC105376636

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_044892.1 

    Range
    101..207
    Download
    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_000011.10 Reference GRCh38.p14 Primary Assembly

    Range
    39261107..39261213
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    39407689..39407795
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)