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RNU7-10P RNA, U7 small nuclear 10 pseudogene [ Homo sapiens (human) ]

Gene ID: 100147758, updated on 13-May-2022

Summary

Official Symbol
RNU7-10Pprovided by HGNC
Official Full Name
RNA, U7 small nuclear 10 pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:34106
See related
Ensembl:ENSG00000271841 AllianceGenome:HGNC:34106
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
U7.10
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Genomic context

See RNU7-10P in Genome Data Viewer
Location:
3p24.3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (17664967..17665024)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (17667522..17667579)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (17706459..17706516)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene TBC1 domain family member 5 Neighboring gene Sharpr-MPRA regulatory region 9690 Neighboring gene ribosomal protein L31 pseudogene 19 Neighboring gene tRNA-Cys (anticodon GCA) 25-1 Neighboring gene uncharacterized LOC105376975

Genomic regions, transcripts, and products

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_007597.1 

    Range
    101..158
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    17664967..17665024
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    17667522..17667579
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)