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NAP1L4P3 nucleosome assembly protein 1 like 4 pseudogene 3 [ Homo sapiens (human) ]

Gene ID: 730174, updated on 17-Sep-2024

Summary

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Official Symbol
NAP1L4P3provided by HGNC
Official Full Name
nucleosome assembly protein 1 like 4 pseudogene 3provided by HGNC
Primary source
HGNC:HGNC:39738
See related
Ensembl:ENSG00000234145 AllianceGenome:HGNC:39738
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 NAP1L4P3 in Genome Data Viewer
Location:
13q14.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (47763559..47764572)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (46983893..46984906)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (48337694..48338707)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr13:48046529-48047210 Neighboring gene RNA, 7SL, cytoplasmic 700, pseudogene Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr13:48095470-48096669 Neighboring gene uncharacterized LOC105370196 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr13:48355836-48356352 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr13:48356353-48356869 Neighboring gene ribosomal protein L27a pseudogene 8 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr13:48387787-48388329 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr13:48431764-48432963 Neighboring gene long intergenic non-protein coding RNA 562

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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Markers

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_021968.1 

    Range
    101..1114
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    47763559..47764572
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    46983893..46984906
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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