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RNU6-1129P RNA, U6 small nuclear 1129, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481536, updated on 10-Oct-2023

Summary

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Official Symbol
RNU6-1129Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 1129, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48092
See related
Ensembl:ENSG00000251773 AllianceGenome:HGNC:48092
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

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Location:
3p12.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (86235321..86235424)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (86307186..86307289)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (86284471..86284574)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene cell adhesion molecule 2 Neighboring gene H3K27ac hESC enhancer GRCh37_chr3:86132353-86132853 Neighboring gene THAP domain containing 12 pseudogene 2 Neighboring gene small nucleolar RNA Z40 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr3:86224689-86225518 Neighboring gene uncharacterized LOC102723364 Neighboring gene RN7SK pseudogene 284 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr3:86529880-86531079 Neighboring gene long intergenic non-protein coding RNA 2070

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

General gene information

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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_043923.1 

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

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    86235321..86235424
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    86307186..86307289
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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