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RNU6-67P RNA, U6 small nuclear 67, pseudogene [ Homo sapiens (human) ]

Gene ID: 100873771, updated on 10-Oct-2023

Summary

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Official Symbol
RNU6-67Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 67, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:42557
See related
Ensembl:ENSG00000222791 AllianceGenome:HGNC:42557
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
RNU6-67
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Genomic context

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Location:
13q31.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (83298071..83298167, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (82531220..82531316, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (83872206..83872302, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124903242 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr13:83473788-83474433 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr13:83474434-83475078 Neighboring gene glycogenin 1 pseudogene 2 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr13:84091305-84092504 Neighboring gene uncharacterized LOC105370286 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr13:84407388-84407977 Neighboring gene SLIT and NTRK like family member 1

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)

See Variation Viewer (GRCh38)

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_043266.1 

    Range
    101..197
    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_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    83298071..83298167 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    82531220..82531316 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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