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RNU6-38P RNA, U6 small nuclear 38, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480709, updated on 10-Oct-2023

Summary

Official Symbol
RNU6-38Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 38, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:34282
See related
Ensembl:ENSG00000206812 AllianceGenome:HGNC:34282
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
RNU6-38
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Genomic context

Location:
13q22.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (75109587..75109692)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (74333244..74333349)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (75683724..75683829)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene RIO kinase 3 pseudogene 1 Neighboring gene uncharacterized LOC107984620 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr13:75709394-75710593 Neighboring gene signal sequence receptor subunit 1 pseudogene 2 Neighboring gene CTAGE family member 11, pseudogene

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_043476.1 

    Range
    101..206
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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_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    75109587..75109692
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    74333244..74333349
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)