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RNU6-1100P RNA, U6 small nuclear 1100, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480049, updated on 11-Jun-2021

Summary

Official Symbol
RNU6-1100Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 1100, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48063
See related
Ensembl:ENSG00000222623
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 RNU6-1100P in Genome Data Viewer
Location:
1p36.33
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) 1 NC_000001.11 (157784..157887, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (157784..157887, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC100996442 Neighboring gene septin 14 pseudogene 18 Neighboring gene uncharacterized LOC729737 Neighboring gene capicua transcriptional repressor pseudogene 27 Neighboring gene general transcription factor IIi pseudogene 10 Neighboring gene DEAD/H-box helicase 11 like 17 (pseudogene) Neighboring gene WAS protein family homolog 9, pseudogene

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_045795.1 

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

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000001.11 Reference GRCh38.p13 Primary Assembly

    Range
    157784..157887 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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