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RN7SKP216 RN7SK pseudogene 216 [ Homo sapiens (human) ]

Gene ID: 106479190, updated on 11-Jun-2021

Summary

Official Symbol
RN7SKP216provided by HGNC
Official Full Name
RN7SK pseudogene 216provided by HGNC
Primary source
HGNC:HGNC:45940
See related
Ensembl:ENSG00000222982
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 RN7SKP216 in Genome Data Viewer
Location:
12q24.21
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (114504876..114505187, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (114942681..114942992, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene T-box transcription factor 5 Neighboring gene uncharacterized LOC105369998 Neighboring gene CRE16 enhancer upstream of TBX5 Neighboring gene TBX5 antisense RNA 1 Neighboring gene osteoclast stimulating factor 1 pseudogene 1 Neighboring gene TBX3 antisense RNA 1 Neighboring gene T-box transcription factor 3

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_043612.1 

    Range
    101..412
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

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
    114504876..114505187 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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