U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

RNU4-66P RNA, U4 small nuclear 66, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479588, updated on 10-Oct-2023

Summary

Go to the top of the page Help
Official Symbol
RNU4-66Pprovided by HGNC
Official Full Name
RNA, U4 small nuclear 66, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47002
See related
Ensembl:ENSG00000202069 AllianceGenome:HGNC:47002
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

Go to the top of the page Help
See RNU4-66P in Genome Data Viewer
Location:
6q13
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (71652474..71652611, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (72833496..72833633, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (72362177..72362314, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_94343 Neighboring gene NGRN pseudogene 2 Neighboring gene keratin 19 pseudogene 1 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr6:72478705-72479904 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:72541212-72542010 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:72542011-72542808 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 17327 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 17328 Neighboring gene regulating synaptic membrane exocytosis 1 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 24736 Neighboring gene forkhead box H1 pseudogene Neighboring gene uncharacterized LOC107986611

Genomic regions, transcripts, and products

Go to the top of the page Help

Go to nucleotide: Graphics FASTA GenBank

Bibliography

Go to the top of the pageHelp

GeneRIFs: Gene References Into Functions

Phenotypes

Go to the top of the page Help

Review eQTL and phenotype association data in this region using PheGenI

Variation

Go to the top of the page Help

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

General gene information

Go to the top of the page Help

NCBI Reference Sequences (RefSeq)

Go to the top of the page Help

NEW Try the new Transcript table

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_044710.1 

    Range
    101..238
    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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    71652474..71652611 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    72833496..72833633 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Molecular Biology Databases