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RNU6-1128P RNA, U6 small nuclear 1128, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480062, updated on 13-May-2022

Summary

Official Symbol
RNU6-1128Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 1128, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48091
See related
Ensembl:ENSG00000199695 AllianceGenome:HGNC:48091
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 RNU6-1128P in Genome Data Viewer
Location:
22q12.2
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (31222759..31222848, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (31686325..31686414, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (31618745..31618834, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene microRNA 3928 Neighboring gene ring finger protein 185 Neighboring gene origin of replication in RNF185 Neighboring gene LIM domain kinase 2 Neighboring gene protein phosphatase 1 regulatory inhibitor subunit 14B pseudogene 1 Neighboring gene phosphoinositide-3-kinase interacting protein 1

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_045159.1 

    Range
    101..190
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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_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    31222759..31222848 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    31686325..31686414 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)