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RNU6-742P RNA, U6 small nuclear 742, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481414, updated on 10-Dec-2024

Summary

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Official Symbol
RNU6-742Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 742, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47705
See related
Ensembl:ENSG00000202159 AllianceGenome:HGNC:47705
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 RNU6-742P in Genome Data Viewer
Location:
18q21.31
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 18 NC_000018.10 (57755394..57755494)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 18 NC_060942.1 (57955689..57955789)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 18 NC_000018.9 (55422626..55422726)

Chromosome 18 - NC_000018.10Genomic Context describing neighboring genes Neighboring gene ATPase phospholipid transporting 8B1 Neighboring gene tRNA-Gly (anticodon TCC) 6-1 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr18:55360919-55362118 Neighboring gene MPRA-validated peak3164 silencer Neighboring gene H3K27ac hESC enhancer GRCh37_chr18:55366253-55366936 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr18:55380387-55380889 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr18:55386192-55386760 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr18:55386761-55387329 Neighboring gene uncharacterized LOC105372141 Neighboring gene H3K27ac hESC enhancer GRCh37_chr18:55404555-55405056 Neighboring gene H3K27ac hESC enhancer GRCh37_chr18:55405057-55405556 Neighboring gene uncharacterized LOC124904310 Neighboring gene mitochondrial ribosomal protein S17 pseudogene 7 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr18:55443057-55444256

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_042951.1 

    Range
    101..201
    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_000018.10 Reference GRCh38.p14 Primary Assembly

    Range
    57755394..57755494
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060942.1 Alternate T2T-CHM13v2.0

    Range
    57955689..57955789
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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