Format

Send to:

Choose Destination

RNU6-1052P RNA, U6 small nuclear 1052, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480028, updated on 12-Oct-2019

Summary

Official Symbol
RNU6-1052Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 1052, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48015
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 RNU6-1052P in Genome Data Viewer
Location:
7p11.2
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 7 NC_000007.14 (56402070..56402173, complement)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene putative uncharacterized protein FLJ44672 Neighboring gene uncharacterized LOC105375292 Neighboring gene uncharacterized LOC101930109 Neighboring gene ankyrin repeat domain 26 pseudogene Neighboring gene zinc finger protein 430 pseudogene

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000007.14 Chromosome 7 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_044137.1 

    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_000007.14 Reference GRCh38.p13 Primary Assembly

    Range
    56402070..56402173 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Support Center