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RNU6-1013P RNA, U6 small nuclear 1013, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480012, updated on 10-Oct-2023

Summary

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Official Symbol
RNU6-1013Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 1013, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47976
See related
Ensembl:ENSG00000206907 AllianceGenome:HGNC:47976
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:
9q31.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (111839828..111839934)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (124011187..124011293)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (114602108..114602214)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene shortage in chiasmata 1 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_105998 Neighboring gene uncharacterized LOC124902249 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_106030 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr9:114630592-114631111 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:114637095-114637945 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:114648577-114649405 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:114658545-114659128 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20185 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28799 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28800 Neighboring gene UDP-glucose ceramide glucosyltransferase Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20186 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28801 Neighboring gene uncharacterized LOC124902250 Neighboring gene microRNA 4668

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_044005.1 

    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_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    111839828..111839934
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    124011187..124011293
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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