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RNU6-1100P RNA, U6 small nuclear 1100, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480049, updated on 17-Sep-2024

Summary

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Official Symbol
RNU6-1100Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 1100, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48063
See related
Ensembl:ENSG00000222623 AllianceGenome:HGNC:48063
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 RNU6-1100P in Genome Data Viewer
Location:
1p36.33
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (157784..157887, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (157784..157887, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124900384 Neighboring gene septin 14 pseudogene 18 Neighboring gene capicua transcriptional repressor pseudogene 27 Neighboring gene uncharacterized LOC729737 Neighboring gene general transcription factor IIi pseudogene 10 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:172206-172706 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:172707-173207 Neighboring gene uncharacterized LOC124903814

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_045795.1 

    Range
    101..204
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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
    157784..157887 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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