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RNU6-637P RNA, U6 small nuclear 637, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479848, updated on 10-Oct-2023

Summary

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Official Symbol
RNU6-637Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 637, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47600
See related
Ensembl:ENSG00000206777 AllianceGenome:HGNC:47600
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:
3q26.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (169720187..169720293, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (172504138..172504244, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (169437975..169438081, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene MDS1 and EVI1 complex locus Neighboring gene uncharacterized LOC124906301 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr3:169378582-169379302 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 14873 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:169384421-169384937 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr3:169386901-169387402 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 20782 Neighboring gene telomerase RNA component (TERC) promoter Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 3:169486144 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 20783 Neighboring gene succinate dehydrogenase complex subunit D pseudogene 3 Neighboring gene actin related protein T3 Neighboring gene telomerase RNA component

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_044744.1 

    Range
    101..207
    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
    169720187..169720293 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    172504138..172504244 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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