Format

Send to:

Choose Destination

RNU6-837P RNA, U6 small nuclear 837, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479936, updated on 1-Jun-2020

Summary

Official Symbol
RNU6-837Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 837, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47800
See related
Ensembl:ENSG00000212358
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 RNU6-837P in Genome Data Viewer
Location:
12p12.3
Annotation release Status Assembly Chr Location
109.20200522 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (17071398..17071505, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene eukaryotic translation elongation factor 1 alpha 1 pseudogene 16 Neighboring gene VISTA enhancer hs1532 Neighboring gene ribosomal protein L7 pseudogene 40 Neighboring gene VISTA enhancer hs993

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000012.12 Chromosome 12 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_043439.1 

    Range
    101..208
    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_000012.12 Reference GRCh38.p13 Primary Assembly

    Range
    17071398..17071505 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Support Center