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RNU6-74P RNA, U6 small nuclear 74, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480752, updated on 20-Mar-2020

Summary

Official Symbol
RNU6-74Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 74, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:42564
See related
Ensembl:ENSG00000206962
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
RNU6-74

Genomic context

See RNU6-74P in Genome Data Viewer
Location:
13q14.11
Annotation release Status Assembly Chr Location
109.20200228 current GRCh38.p13 (GCF_000001405.39) 13 NC_000013.11 (41905118..41905223)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene von Willebrand factor A domain containing 8 Neighboring gene FOXA motif-containing MPRA enhancer 169 Neighboring gene RNA, 7SL, cytoplasmic 515, pseudogene Neighboring gene lysyl-tRNA synthetase 1 pseudogene 1 Neighboring gene uncharacterized LOC105370176 Neighboring gene VWA8 antisense RNA 1 (head to head)

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000013.11 Chromosome 13 Reference GRCh38.p13 Primary Assembly

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_043811.1 

    Range
    101..206
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000013.11 Reference GRCh38.p13 Primary Assembly

    Range
    41905118..41905223
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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