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NPAP1P7 nuclear pore associated protein 1 pseudogene 7 [ Homo sapiens (human) ]

Gene ID: 107161163, updated on 10-Oct-2023

Summary

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Official Symbol
NPAP1P7provided by HGNC
Official Full Name
nuclear pore associated protein 1 pseudogene 7provided by HGNC
Primary source
HGNC:HGNC:51473
See related
AllianceGenome:HGNC:51473
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:
9q22.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (87824927..87825963)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (99978477..99979513)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (90439842..90440878)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene cathepsin L family member 3, pseudogene Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr9:90407204-90408403 Neighboring gene Sharpr-MPRA regulatory region 3109 Neighboring gene death associated protein kinase 1 pseudogene Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:90415146-90415646 Neighboring gene ELF2 pseudogene 3 Neighboring gene fructose-bisphosphatase 2 pseudogene 1 Neighboring gene uncharacterized LOC112267903 Neighboring gene cathepsin L pseudogene 8

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)

General gene information

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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_046704.1 

    Range
    101..1137
    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_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    87824927..87825963
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    99978477..99979513
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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