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PRDX3P4 peroxiredoxin 3 pseudogene 4 [ Homo sapiens (human) ]

Gene ID: 100418955, updated on 10-Dec-2024

Summary

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Official Symbol
PRDX3P4provided by HGNC
Official Full Name
peroxiredoxin 3 pseudogene 4provided by HGNC
Primary source
HGNC:HGNC:44643
See related
AllianceGenome:HGNC:44643
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 PRDX3P4 in Genome Data Viewer
Location:
3p14.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (64174378..64175347)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (64217963..64218931)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (64160054..64161023)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene PRICKLE2 antisense RNA 1 Neighboring gene long intergenic non-protein coding RNA 994 Neighboring gene PRICKLE2 antisense RNA 2 Neighboring gene prickle planar cell polarity protein 2 Neighboring gene Sharpr-MPRA regulatory region 15033 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:64142501-64143002 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:64143003-64143503 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:64149309-64149810 Neighboring gene PRICKLE2 antisense RNA 3 Neighboring gene Sharpr-MPRA regulatory region 502 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:64224596-64225354 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:64330481-64331062 Neighboring gene PRICKLE2 divergent transcript Neighboring gene uncharacterized LOC105377123

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_025701.2 

    Range
    101..1070
    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_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    64174378..64175347
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    64217963..64218931
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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