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RANP6 RAN pseudogene 6 [ Homo sapiens (human) ]

Gene ID: 100128266, updated on 2-Mar-2021

Summary

Official Symbol
RANP6provided by HGNC
Official Full Name
RAN pseudogene 6provided by HGNC
Primary source
HGNC:HGNC:39861
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 RANP6 in Genome Data Viewer
Location:
4q34.1
Annotation release Status Assembly Chr Location
109.20210226 current GRCh38.p13 (GCF_000001405.39) 4 NC_000004.12 (173633531..173634415, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (174554682..174555566, complement)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene HAND2 antisense RNA 1 Neighboring gene heart and neural crest derivatives expressed 2 Neighboring gene mortality factor 4 (pseudogene) Neighboring gene uncharacterized LOC107986203 Neighboring gene uncharacterized LOC105377543 Neighboring gene long intergenic non-protein coding RNA 2269

Genomic regions, transcripts, and products

Phenotypes

Associated conditions

Description Tests
Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene.
GeneReviews: Not available

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_022039.2 

    Range
    101..985
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210226

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000004.12 Reference GRCh38.p13 Primary Assembly

    Range
    173633531..173634415 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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