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NAP1L4P2 nucleosome assembly protein 1 like 4 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 100874319, updated on 10-Oct-2023

Summary

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Official Symbol
NAP1L4P2provided by HGNC
Official Full Name
nucleosome assembly protein 1 like 4 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:39739
See related
AllianceGenome:HGNC:39739
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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See NAP1L4P2 in Genome Data Viewer
Location:
Xq22.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (106466780..106467366, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (104902721..104903307, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (105710010..105710596, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene PWWP domain containing 3B Neighboring gene CSGALNACT2 pseudogene 2 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29827 Neighboring gene serpin family A member 7 pseudogene 1 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29828 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29829 Neighboring gene microRNA 548an Neighboring gene RPA1 related single stranded DNA binding protein, X-linked

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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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_032355.1 

    Range
    101..687
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    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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    106466780..106467366 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    104902721..104903307 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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