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RNU6-799P RNA, U6 small nuclear 799, pseudogene [ Homo sapiens (human) ]

Gene ID: 107105254, updated on 1-Jun-2020

Summary

Official Symbol
RNU6-799Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 799, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47762
See related
Ensembl:ENSG00000200437
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

See RNU6-799P in Genome Data Viewer
Location:
17p12
Annotation release Status Assembly Chr Location
109.20200522 current GRCh38.p13 (GCF_000001405.39) 17 NC_000017.11 (15311346..15311452)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105371547 Neighboring gene peripheral myelin protein 22 Neighboring gene microRNA 4731 Neighboring gene tektin 3 Neighboring gene RNA, 7SL, cytoplasmic 792, pseudogene Neighboring gene TVP23C-CDRT4 readthrough Neighboring gene CMT1A duplicated region transcript 4 Neighboring gene ribosomal protein L9 pseudogene 2

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000017.11 Chromosome 17 Reference GRCh38.p13 Primary Assembly

NCBI Reference Sequences (RefSeq)

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_046572.1 

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

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000017.11 Reference GRCh38.p13 Primary Assembly

    Range
    15311346..15311452
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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