Format

Send to:

Choose Destination

RN7SL448P RNA, 7SL, cytoplasmic 448, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481843, updated on 23-Nov-2021

Summary

Official Symbol
RN7SL448Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 448, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46464
See related
Ensembl:ENSG00000264322
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See RN7SL448P in Genome Data Viewer
Location:
17q23.2
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 17 NC_000017.11 (60899891..60900185)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (58977252..58977546)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene BCAS3 microtubule associated cell migration factor Neighboring gene keratin 18 pseudogene 61 Neighboring gene high mobility group nucleosome binding domain 1 pseudogene 28 Neighboring gene ribosomal protein L23a pseudogene 74 Neighboring gene uncharacterized LOC107984992

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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_045801.1 

    Range
    101..395
    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_000017.11 Reference GRCh38.p13 Primary Assembly

    Range
    60899891..60900185
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Support Center