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RN7SL229P RNA, 7SL, cytoplasmic 229, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479305, updated on 23-Nov-2021

Summary

Official Symbol
RN7SL229Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 229, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46245
See related
Ensembl:ENSG00000242811
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

See RN7SL229P in Genome Data Viewer
Location:
3q26.33
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 3 NC_000003.12 (180736405..180736703, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (180454193..180454491, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene tetratricopeptide repeat domain 14 Neighboring gene coiled-coil domain containing 39 Neighboring gene uncharacterized LOC101928882 Neighboring gene VISTA enhancer hs258 Neighboring gene VISTA enhancer hs655 Neighboring gene ring finger protein 13 pseudogene

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_045869.1 

    Range
    101..399
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p13 Primary Assembly

    Range
    180736405..180736703 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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