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RNU6-205P RNA, U6 small nuclear 205, pseudogene [ Homo sapiens (human) ]

Gene ID: 106633815, updated on 10-Oct-2023

Summary

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Official Symbol
RNU6-205Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 205, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47168
See related
Ensembl:ENSG00000212160 AllianceGenome:HGNC:47168
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 RNU6-205P in Genome Data Viewer
Location:
4q25
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (110278185..110278291)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (113580590..113580696)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (111199341..111199447)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124900759 Neighboring gene heat shock factor binding protein 1 pseudogene 2 Neighboring gene RNF14 pseudogene 2 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 21816 Neighboring gene zinc finger BED-type containing 1 pseudogene 1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 15629 Neighboring gene Sharpr-MPRA regulatory region 5470 Neighboring gene uncharacterized LOC105377362 Neighboring gene RPL7L1 pseudogene 13

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_042885.1 

    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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    110278185..110278291
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    113580590..113580696
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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