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RNU6-957P RNA, U6 small nuclear 957, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479989, updated on 1-Jun-2020

Summary

Official Symbol
RNU6-957Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 957, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47920
See related
Ensembl:ENSG00000200522
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 RNU6-957P in Genome Data Viewer
Location:
6q21
Annotation release Status Assembly Chr Location
109.20200522 current GRCh38.p13 (GCF_000001405.39) 6 NC_000006.12 (110722250..110722348, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene cyclin dependent kinase 19 Neighboring gene phosphoethanolamine/phosphocholine phosphatase 1 pseudogene Neighboring gene ribosomal protein S20 pseudogene 18 Neighboring gene adenosylmethionine decarboxylase 1 Neighboring gene small nucleolar RNA, H/ACA box 40C Neighboring gene RNA, U6 small nuclear 1115, pseudogene

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000006.12 Chromosome 6 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_045600.1 

    Range
    101..199
    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_000006.12 Reference GRCh38.p13 Primary Assembly

    Range
    110722250..110722348 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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