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RNU6-1205P RNA, U6 small nuclear 1205, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480093, updated on 10-Oct-2023

Summary

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Official Symbol
RNU6-1205Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 1205, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48168
See related
Ensembl:ENSG00000200495 AllianceGenome:HGNC:48168
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:
1q44
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (248912692..248912793, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (248351319..248351420, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (249206891..249206992, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:249167279-249168120 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2053 Neighboring gene tRNA-Leu (anticodon CAA) 4-1 Neighboring gene tRNA-Glu (anticodon CTC) 2-1 Neighboring gene piggyBac transposable element derived 2 Neighboring gene CRISPRi-validated cis-regulatory element chr1.12988 Neighboring gene CRISPRi-validated cis-regulatory element chr1.12989 Neighboring gene Sharpr-MPRA regulatory region 4184 Neighboring gene ReSE screen-validated silencer GRCh37_chr1:249190071-249190253 Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:249200064-249200985 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2056 Neighboring gene ribosomal protein L23a pseudogene 25

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_044653.1 

    Range
    101..202
    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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    248912692..248912793 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    248351319..248351420 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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