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RNU6-1145P RNA, U6 small nuclear 1145, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481541, updated on 10-Oct-2023

Summary

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Official Symbol
RNU6-1145Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 1145, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48108
See related
Ensembl:ENSG00000206973 AllianceGenome:HGNC:48108
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 RNU6-1145P in Genome Data Viewer
Location:
2p15
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (61605616..61605721)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (61611656..61611761)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (61832751..61832856)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene proteasome 26S subunit, non-ATPase 12 pseudogene Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr2:61809253-61809844 Neighboring gene H3K27ac hESC enhancer GRCh37_chr2:61823834-61824398 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr2:61824963-61825528 Neighboring gene ribosomal protein S29 pseudogene 10 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 15834 Neighboring gene MPRA-validated peak3721 silencer Neighboring gene ATAC-STARR-seq lymphoblastoid active region 15835 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11531 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:61922999-61923614 Neighboring gene ribosomal protein L14 pseudogene Neighboring gene uncharacterized LOC107985767 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 15836

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_043959.1 

    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_000002.12 Reference GRCh38.p14 Primary Assembly

    Range
    61605616..61605721
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    61611656..61611761
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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