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RNU6-743P RNA, U6 small nuclear 743, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480605, updated on 17-Sep-2024

Summary

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Official Symbol
RNU6-743Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 743, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47706
See related
Ensembl:ENSG00000201021 AllianceGenome:HGNC:47706
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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See RNU6-743P in Genome Data Viewer
Location:
20q13.11
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 20 NC_000020.11 (43405473..43405568)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 20 NC_060944.1 (45138704..45138799)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 20 NC_000020.10 (42034113..42034208)

Chromosome 20 - NC_000020.11Genomic Context describing neighboring genes Neighboring gene peptidylprolyl isomerase A pseudogene 21 Neighboring gene small Cajal body-specific RNA 15 Neighboring gene NANOG hESC enhancer GRCh37_chr20:41948123-41948641 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 12923 Neighboring gene eukaryotic translation initiation factor 4E binding protein 2 pseudogene 1 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 17900 Neighboring gene ReSE screen-validated silencer GRCh37_chr20:42072831-42073022 Neighboring gene ReSE screen-validated silencer GRCh37_chr20:42073753-42073955 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 17901 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:42086334-42087281 Neighboring gene serine and arginine rich splicing factor 6

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_044655.1 

    Range
    101..196
    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_000020.11 Reference GRCh38.p14 Primary Assembly

    Range
    43405473..43405568
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060944.1 Alternate T2T-CHM13v2.0

    Range
    45138704..45138799
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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