EGLN2 egl-9 family hypoxia inducible factor 2 [Macaca mulatta (Rhesus monkey)] - Gene

Summary

Gene symbol: EGLN2
Gene description: egl-9 family hypoxia inducible factor 2
See related: Ensembl:ENSMMUG00000063422
Gene type: protein coding
RefSeq status: PROVISIONAL
Organism: Macaca mulatta
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Cercopithecidae; Cercopithecinae; Macaca
Annotation information: Annotation category: partial on reference assembly
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Genomic context

Location:: chromosome: 19

Exon count:: 5

Annotation release	Status	Assembly	Chr	Location
103	current	Mmul_10 (GCF_003339765.1)	19 Unlocalized Scaffold	NW_021160367.1 (36818..44778)
102	previous assembly	Mmul_8.0.1 (GCF_000772875.2)	19	NC_027911.1 (36565739..36573700)

NW_021160367.1 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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General gene information

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Markers

SHGC-64133 (e-PCR)
- UniSTS:53779

RH93347 (e-PCR)
- UniSTS:84676

Gene Ontology Provided by RefSeq

Function	Evidence Code	Pubs
enables L-ascorbic acid binding	IEA Inferred from Electronic Annotation more info	PubMed
enables ferrous iron binding	IEA Inferred from Electronic Annotation more info	PubMed
enables peptidyl-proline 4-dioxygenase activity	IEA Inferred from Electronic Annotation more info	PubMed

Process	Evidence Code	Pubs
involved_in cellular response to hypoxia	IEA Inferred from Electronic Annotation more info	PubMed
involved_in peptidyl-proline hydroxylation to 4-hydroxy-L-proline	IEA Inferred from Electronic Annotation more info	PubMed

Component	Evidence Code	Pubs
located_in cytoplasm	IEA Inferred from Electronic Annotation more info	PubMed
located_in nucleus	IEA Inferred from Electronic Annotation more info	PubMed

General protein information

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Preferred Names: egl nine homolog 2

NP_001248020.1

EC 1.14.11.29

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.