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RNU6-1000P RNA, U6 small nuclear 1000, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481496, updated on 13-May-2022

Summary

Official Symbol
RNU6-1000Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 1000, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47963
See related
Ensembl:ENSG00000212368 AllianceGenome:HGNC:47963
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See RNU6-1000P in Genome Data Viewer
Location:
4q21.1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (76356610..76356715, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (79697338..79697443, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (77277763..77277868, complement)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene FAM47E-STBD1 readthrough Neighboring gene starch binding domain 1 Neighboring gene coiled-coil domain containing 158 Neighboring gene sorting nexin 5 pseudogene 1 Neighboring gene small nucleolar RNA SNORD50 Neighboring gene ribosomal protein L36a pseudogene 18

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

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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_045517.1 

    Range
    101..206
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    76356610..76356715 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    79697338..79697443 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)