ENSMUSG00000025169


Mus musculus

Features
Gene ID: ENSMUSG00000025169
  
Biological name :Ogfod3
  
Synonyms : 2-oxoglutarate and iron-dependent oxygenase domain-containing protein 3 / Ogfod3 / Q9D136
  
Possible biological names infered from orthology : 2-oxoglutarate and iron dependent oxygenase domain containing 3 / Q6PK18
  
Species: Mus musculus
  
Chr. number: 11
Strand: -1
Band: E2
Gene start: 121177591
Gene end: 121204711
  
Corresponding Affymetrix probe sets: 10394082 (MoGene1.0st)   1418331_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000026169
NCBI entrez gene - 66179     See in Manteia.
MGI - MGI:1913429
RefSeq - NM_025402
RefSeq Peptide - NP_079678
swissprot - Q9D136
Ensembl - ENSMUSG00000025169
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 zgc:195081ENSDARG00000078481Danio rerio
 OGFOD3ENSGALG00000001618Gallus gallus
 OGFOD3ENSG00000181396Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
No match


Protein motifs (from Interpro)
Interpro ID Name
 IPR005123  Oxoglutarate/iron-dependent dioxygenase
 IPR006620  Prolyl 4-hydroxylase, alpha subunit


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0055114 oxidation-reduction process IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 molecular_functionGO:0003674 molecular_function ND
 molecular_functionGO:0005506 iron ion binding IEA
 molecular_functionGO:0016491 oxidoreductase activity IEA
 molecular_functionGO:0016705 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen IEA
 molecular_functionGO:0031418 L-ascorbic acid binding IEA
 molecular_functionGO:0046872 metal ion binding IEA
 molecular_functionGO:0051213 dioxygenase activity IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0001399 hyperactivity "general restlessness or excessive movement; more frequent movement from one place to another" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409, J:57125]
Show

Allelic Composition: Plcl1tm2.1Matk/Plcl1tm2.1Matk
Genetic Background: FVB.Cg-Plcl1tm2.1Matk

 MP:0001523 impaired righting response "reduced ability or greater amount of time needed to recover from supine position" [J:25565]
Show

Allelic Composition: Ltatm1.1(KOMP)Vlcg/Ltatm1.1(KOMP)Vlcg
Genetic Background: C57BL/6N-Ltatm1.1(KOMP)Vlcg/Ucd

 MP:0011967 increased or absent threshold for auditory brainstem response "increase in the value at which one or more sound frequencies or broadband clicks first elicits a recordable response generated by electrical activity of neurons in the ascending auditory system, or complete lack of a recordable response at any frequency or broadband click" [MGI:csmith]
Show

Allelic Composition: Plcl1tm2.1Matk/Plcl1tm2.1Matk
Genetic Background: FVB.Cg-Plcl1tm2.1Matk

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

0 s.

 
External programs and data are copyrighted by and are the property of their respective authors.
The Manteia system, data and analyses are provided "as is" with no warranties, expressed or implied as to capabilities or accuracy. User assumes the entire risk as to the results and performance of the software, data and documentation


                   

© Olivier Tassy / Olivier Pourquie 2007-2025
contact: otassy@igbmc.fr