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RNU6-712P RNA, U6 small nuclear 712, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481404, updated on 10-Oct-2023

Summary

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Official Symbol
RNU6-712Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 712, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47675
See related
Ensembl:ENSG00000222490 AllianceGenome:HGNC:47675
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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Location:
3p11.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (90184634..90184733)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (90261231..90261330)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (90233784..90233883)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene MT-CO1 pseudogene 6 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:89867784-89868284 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr3:89880545-89881744 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:90007237-90007836 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr3:90013784-90014983 Neighboring gene small nucleolar RNA U3 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr3:90130041-90130845 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr3:90131977-90132854 Neighboring gene H3K27ac hESC enhancer GRCh37_chr3:90132855-90133730 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr3:90191642-90192254 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:90226998-90227498 Neighboring gene protein S (beta) pseudogene Neighboring gene heat shock protein family E (Hsp10) member 1 pseudogene 19

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)

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_044913.1 

    Range
    101..200
    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_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    90184634..90184733
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    90261231..90261330
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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