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RNU1-148P RNA, U1 small nuclear 148, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481635, updated on 17-Sep-2024

Summary

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Official Symbol
RNU1-148Pprovided by HGNC
Official Full Name
RNA, U1 small nuclear 148, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48490
See related
Ensembl:ENSG00000207201 AllianceGenome:HGNC:48490
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 RNU1-148P in Genome Data Viewer
Location:
8p21.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (24076997..24077158, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (24352067..24352228, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (23934510..23934671, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124900262 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr8:23747587-23748786 Neighboring gene uncharacterized LOC107986931 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:23775304-23775840 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:23775841-23776377 Neighboring gene ReSE screen-validated silencer GRCh37_chr8:23778915-23779185 Neighboring gene stanniocalcin 1 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:23836477-23837459 Neighboring gene Sharpr-MPRA regulatory region 10080 Neighboring gene uncharacterized LOC105379328 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:23963874-23964511 Neighboring gene MPRA-validated peak6951 silencer Neighboring gene ADAM7, ADAMDEC1 and ADAM28 antisense RNA 1 Neighboring gene ADAM metallopeptidase domain 28

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_044706.1 

    Range
    101..262
    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_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    24076997..24077158 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    24352067..24352228 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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