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RNU6-72P RNA, U6 small nuclear 72, pseudogene [ Homo sapiens (human) ]

Gene ID: 100873775, updated on 17-Sep-2024

Summary

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Official Symbol
RNU6-72Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 72, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:42562
See related
AllianceGenome:HGNC:42562
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
RNU6-72
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Genomic context

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See RNU6-72P in Genome Data Viewer
Location:
13q31.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (85584748..85584853, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (84830665..84830770, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (86158883..86158988, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105370292 Neighboring gene long intergenic non-protein coding RNA 351 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr13:86006193-86006693 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr13:86182343-86182998 Neighboring gene NANOG hESC enhancer GRCh37_chr13:86193480-86193991 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr13:86238925-86240124 Neighboring gene SLIT and NTRK like family member 6 Neighboring gene ReSE screen-validated silencer GRCh37_chr13:86428461-86428657 Neighboring gene Sharpr-MPRA regulatory region 1723 Neighboring gene MOB kinase activator 1A pseudogene 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_043299.1 

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

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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
    85584748..85584853 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    84830665..84830770 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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