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RNU6-1266P RNA, U6 small nuclear 1266, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480118, updated on 12-Oct-2019

Summary

Official Symbol
RNU6-1266Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 1266, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48229
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 RNU6-1266P in Genome Data Viewer
Location:
10q22.3
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 10 NC_000010.11 (77776952..77777055, complement)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene zinc finger protein 532 pseudogene Neighboring gene RBBP6 pseudogene 1 Neighboring gene inosine monophosphate dehydrogenase 1 pseudogene 5 Neighboring gene discs large MAGUK scaffold protein 5 Neighboring gene uncharacterized LOC101929347

Genomic regions, transcripts, and products

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_044865.1 

    Range
    101..204
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000010.11 Reference GRCh38.p13 Primary Assembly

    Range
    77776952..77777055 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p13 ALT_REF_LOCI_1

Genomic

  1. NT_187580.1 Reference GRCh38.p13 ALT_REF_LOCI_1

    Range
    15644..15747 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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