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PTGER4P2 prostaglandin E receptor 4 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 5736, updated on 12-Oct-2019

Summary

Official Symbol
PTGER4P2provided by HGNC
Official Full Name
prostaglandin E receptor 4 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:9598
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

See PTGER4P2 in Genome Data Viewer
Location:
9q13
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 9 NC_000009.12 (62843789..62844171)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 1410 Neighboring gene RNA, 5S ribosomal pseudogene 283 Neighboring gene PTGER4P2-CDK2AP2P2 readthrough, transcribed pseudogene Neighboring gene uncharacterized LOC100132249 Neighboring gene cyclin dependent kinase 2 associated protein 2 pseudogene 2 Neighboring gene myosin VB pseudogene 2 Neighboring gene lncRNA negative regulator of fibroblast-like synoviocyte migration, SYNCRIP interacting

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000009.12 Chromosome 9 Reference GRCh38.p13 Primary Assembly

NCBI Reference Sequences (RefSeq)

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_046646.1 

    Range
    101..483
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000009.12 Reference GRCh38.p13 Primary Assembly

    Range
    62843789..62844171
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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