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RN7SL630P RNA, 7SL, cytoplasmic 630, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481094, updated on 25-Jan-2022

Summary

Official Symbol
RN7SL630Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 630, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46646
See related
Ensembl:ENSG00000264978 AllianceGenome:HGNC:46646
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 RN7SL630P in Genome Data Viewer
Location:
12q22
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (93831076..93831372)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (94224852..94225148)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene CASP2 and RIPK1 domain containing adaptor with death domain Neighboring gene CRADD antisense RNA 1 Neighboring gene Sharpr-MPRA regulatory region 9094 Neighboring gene uncharacterized LOC105369911 Neighboring gene uncharacterized LOC105369912 Neighboring gene RN7SK pseudogene 263

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_045861.1 

    Range
    101..397
    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_000012.12 Reference GRCh38.p13 Primary Assembly

    Range
    93831076..93831372
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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