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RNU7-193P RNA, U7 small nuclear 193 pseudogene [ Homo sapiens (human) ]

Gene ID: 106481804, updated on 10-Oct-2023

Summary

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Official Symbol
RNU7-193Pprovided by HGNC
Official Full Name
RNA, U7 small nuclear 193 pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:45727
See related
Ensembl:ENSG00000252532 AllianceGenome:HGNC:45727
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:
10q11.21
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (43458065..43458129)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (44339006..44339070)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (43953513..43953577)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2331 Neighboring gene H3K27ac hESC enhancer GRCh37_chr10:43916126-43916862 Neighboring gene long intergenic non-protein coding RNA 2916 Neighboring gene small nucleolar RNA, C/D box 3J Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3300 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2332 Neighboring gene zinc finger protein 487 Neighboring gene H3K27ac-H3K4me1 hESC enhancers GRCh37_chr10:43950240-43951128 and GRCh37_chr10:43951129-43952017 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr10:43953391-43953946 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr10:43959685-43960348 Neighboring gene zinc finger protein 12 pseudogene Neighboring gene NANOG hESC enhancer GRCh37_chr10:44039642-44040155 Neighboring gene zinc finger protein 239 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2334

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_045682.1 

    Range
    101..165
    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_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    43458065..43458129
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    44339006..44339070
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Other Literature Sources
Molecular Biology Databases