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RANP7 RAN pseudogene 7 [ Homo sapiens (human) ]

Gene ID: 100874192, updated on 10-Oct-2023

Summary

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Official Symbol
RANP7provided by HGNC
Official Full Name
RAN pseudogene 7provided by HGNC
Primary source
HGNC:HGNC:39862
See related
AllianceGenome:HGNC:39862
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

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Location:
3p24.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (22904653..22905338)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (22909501..22910186)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (22946144..22946829)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene FCRL4 pseudogene 1 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:22843155-22843752 Neighboring gene RRBP1 pseudogene 2 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:22967452-22967952 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_68424 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19586 Neighboring gene ReSE screen-validated silencer GRCh37_chr3:23004270-23004480 Neighboring gene spalt like transcription factor 4 pseudogene 5 Neighboring gene H3K27ac hESC enhancer GRCh37_chr3:23077142-23077642 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_68455 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr3:23109558-23110259 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 14137 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19587 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19588 Neighboring gene RPL24 pseudogene 7

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Other Names

  • RAN, member RAS oncogene family pseudogene 7

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_032365.2 

    Range
    101..786
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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
    22904653..22905338
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    22909501..22910186
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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