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RNU6-623P RNA, U6 small nuclear 623, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481378, updated on 12-Oct-2019

Summary

Official Symbol
RNU6-623Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 623, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47586
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

See RNU6-623P in Genome Data Viewer
Location:
17q23.2
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 17 NC_000017.11 (60662333..60662437, complement)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene splicing factor 3B subunit 6 pseudogene Neighboring gene amyloid beta precursor protein binding protein 2 Neighboring gene long intergenic non-protein coding RNA 1999 Neighboring gene ribosomal protein SA pseudogene 66 Neighboring gene protein phosphatase, Mg2+/Mn2+ dependent 1D Neighboring gene RNA, 7SL, cytoplasmic 606, pseudogene Neighboring gene ribosomal protein L36a pseudogene 46 Neighboring gene BCAS3 microtubule associated cell migration factor

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

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_044695.1 

    Range
    101..205
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000017.11 Reference GRCh38.p13 Primary Assembly

    Range
    60662333..60662437 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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