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RNU6-630P RNA, U6 small nuclear 630, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481380, updated on 10-Oct-2023

Summary

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Official Symbol
RNU6-630Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 630, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47593
See related
Ensembl:ENSG00000212560 AllianceGenome:HGNC:47593
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:
Xp11.4
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (42139425..42139530, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (41544346..41544451, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (41998678..41998783, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene calcium/calmodulin dependent serine protein kinase Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20778 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20779 Neighboring gene RNA, U6 small nuclear 202, pseudogene Neighboring gene MED14-independent group 3 enhancer GRCh37_chrX:41944854-41946053 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20780 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29562 Neighboring gene ATP5MC2 pseudogene 4 Neighboring gene RNA, U6 small nuclear 1124, pseudogene Neighboring gene H3K4me1 hESC enhancers GRCh37_chrX:42201990-42202490 and GRCh37_chrX:42202491-42202991 Neighboring gene H3K27ac hESC enhancer GRCh37_chrX:42325954-42326454 Neighboring gene H3K27ac hESC enhancer GRCh37_chrX:42333231-42333767 Neighboring gene ribosomal biogenesis factor-like

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_044714.1 

    Range
    101..206
    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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    42139425..42139530 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    41544346..41544451 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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