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RN7SKP124 RN7SK pseudogene 124 [ Homo sapiens (human) ]

Gene ID: 106480871, updated on 21-Mar-2023

Summary

Official Symbol
RN7SKP124provided by HGNC
Official Full Name
RN7SK pseudogene 124provided by HGNC
Primary source
HGNC:HGNC:45848
See related
AllianceGenome:HGNC:45848
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 RN7SKP124 in Genome Data Viewer
Location:
3q23
Annotation release Status Assembly Chr Location
RS_2023_03 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (139584206..139584445, complement)
RS_2023_03 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (142331636..142331875, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (139303048..139303287, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene COPB2 divergent transcript Neighboring gene Sharpr-MPRA regulatory region 7279 Neighboring gene retinol binding protein 1 Neighboring gene nicotinamide nucleotide adenylyltransferase 3 Neighboring gene DTWD1 pseudogene 1 Neighboring gene RNA, 7SL, cytoplasmic 724, pseudogene Neighboring gene Sharpr-MPRA regulatory region 1318

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_045964.1 

    Range
    101..340
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_03

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    139584206..139584445 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    142331636..142331875 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)