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RNU6-1317P RNA, U6 small nuclear 1317, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481596, updated on 10-Oct-2023

Summary

Official Symbol
RNU6-1317Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 1317, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48280
See related
Ensembl:ENSG00000201452 AllianceGenome:HGNC:48280
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

Location:
3q26.31
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (175767558..175767661)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (178562538..178562641)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (175485346..175485449)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene N-acetylated alpha-linked acidic dipeptidase like 2 Neighboring gene small nucleolar RNA U13 Neighboring gene NAALADL2 antisense RNA 1 Neighboring gene UBE2V1 pseudogene 2 Neighboring gene uncharacterized LOC124909459 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr3:175540382-175540932

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_045827.1 

    Range
    101..204
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    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
    175767558..175767661
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    178562538..178562641
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    GenBank, FASTA, Sequence Viewer (Graphics)