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RN7SKP51 RN7SK pseudogene 51 [ Homo sapiens (human) ]

Gene ID: 106479117, updated on 17-Sep-2024

Summary

Official Symbol
RN7SKP51provided by HGNC
Official Full Name
RN7SK pseudogene 51provided by HGNC
Primary source
HGNC:HGNC:45775
See related
Ensembl:ENSG00000222713 AllianceGenome:HGNC:45775
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 RN7SKP51 in Genome Data Viewer
Location:
6q22.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (117301455..117301758)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (118485366..118485669)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (117622618..117622921)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene vestigial like family member 2 Neighboring gene ROS proto-oncogene 1, receptor tyrosine kinase Neighboring gene RN7SK pseudogene 18 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_88320 Neighboring gene RAP1B pseudogene 3 Neighboring gene RNA, U6 small nuclear 253, 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_043006.1 

    Range
    101..404
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    117301455..117301758
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    118485366..118485669
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)