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Search results 201 to 231 out of 231 for Mkrn3

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Type Details Score
Publication        
First Author: Marc Feuermann, Huaiyu Mi, Pascale Gaudet, Dustin Ebert, Anushya Muruganujan, Paul Thomas
Year: 2010
Title: Annotation inferences using phylogenetic trees
Publication      
First Author: Bairoch A
Year: 1999
Journal: Database Release
Title: SWISS-PROT Annotated protein sequence database
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and loading genome assembly coordinates from NCBI annotations
Publication      
First Author: Mouse Genome Informatics (MGI) and The National Center for Biotechnology Information (NCBI)
Year: 2010
Journal: Database Download
Title: Consensus CDS project
Publication      
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
Publication      
First Author: Mouse Genome Database and National Center for Biotechnology Information
Year: 2000
Journal: Database Release
Title: Entrez Gene Load
Publication      
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Gene 1.0 ST Array Platform
Publication      
First Author: Mouse Genome Informatics Group
Year: 2003
Journal: Database Procedure
Title: Automatic Encodes (AutoE) Reference
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome 430 2.0 Array Platform
Protein
Organism: Mus musculus/domesticus
Length: 248  
Fragment?: false
Interaction Experiment
Description: Mkrn3 functions as a novel ubiquitin E3 ligase to inhibit Nptx1 during puberty initiation.
Allele
Name: makorin, ring finger protein, 3; endonuclease-mediated mutation 1, Ronggui Hu
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
Publication
First Author: Liu H
Year: 2017
Journal: Oncotarget
Title: Mkrn3 functions as a novel ubiquitin E3 ligase to inhibit Nptx1 during puberty initiation.
Volume: 8
Issue: 49
Pages: 85102-85109
Genotype
Symbol: Mkrn3/Mkrn3<+>
Background: involves: C57BL/6
Zygosity: ht
Has Mutant Allele: true
DO Term
Allele
Name: transgene insertion 13F, R D Nicholls
Allele Type: Transgenic
Attribute String: Inserted expressed sequence
Allele  
Name: deletion, Chr 7, R D Nicholls13F; deletion, Chr 7, R D Nicholls 13F
Allele Type: Transgenic
Genotype
Symbol: Tg(Igh-Lmp2a)13FRdni/?
Background: involves: C57BL/6 * CD-1 * SJL
Zygosity: ot
Has Mutant Allele: true
Publication  
First Author: Stefan M
Year: 2005
Journal: BMC Genomics
Title: Genetic mapping of putative Chrna7 and Luzp2 neuronal transcriptional enhancers due to impact of a transgene-insertion and 6.8 Mb deletion in a mouse model of Prader-Willi and Angelman syndromes.
Volume: 6
Pages: 157
Genotype
Symbol: Del(7Herc2-Mkrn3)13FRdni/+
Background: involves: C57BL/6 * CD-1 * SJL
Zygosity: ht
Has Mutant Allele: true
Publication
First Author: Gabriel JM
Year: 1999
Journal: Proc Natl Acad Sci U S A
Title: A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes.
Volume: 96
Issue: 16
Pages: 9258-63
Publication
First Author: Stefan M
Year: 2005
Journal: Genomics
Title: A nonimprinted Prader-Willi Syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels.
Volume: 85
Issue: 5
Pages: 630-40
Publication
First Author: Ge Y
Year: 2002
Journal: Brain Res
Title: Anorexigenic melanocortin signaling in the hypothalamus is augmented in association with failure-to-thrive in a transgenic mouse model for Prader-Willi syndrome.
Volume: 957
Issue: 1
Pages: 42-5
Publication
First Author: Stefan M
Year: 2005
Journal: Endocrinology
Title: Hormonal and metabolic defects in a prader-willi syndrome mouse model with neonatal failure to thrive.
Volume: 146
Issue: 10
Pages: 4377-85
Publication
First Author: Nakagaki A
Year: 2018
Journal: Sci Rep
Title: Application of droplet digital PCR in the analysis of genome integration and organization of the transgene in BAC transgenic mice.
Volume: 8
Issue: 1
Pages: 6638
Publication
First Author: Dubose AJ
Year: 2011
Journal: Hum Mol Genet
Title: A new deletion refines the boundaries of the murine Prader-Willi syndrome imprinting center.
Volume: 20
Issue: 17
Pages: 3461-6
Publication
First Author: Bielinska B
Year: 2000
Journal: Nat Genet
Title: De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch.
Volume: 25
Issue: 1
Pages: 74-8
Publication
First Author: Resnick JL
Year: 2013
Journal: Mamm Genome
Title: Recommendations for the investigation of animal models of Prader-Willi syndrome.
Volume: 24
Issue: 5-6
Pages: 165-78
Publication
First Author: Rodriguez-Jato S
Year: 2013
Journal: PLoS One
Title: Regulatory elements associated with paternally-expressed genes in the imprinted murine Angelman/Prader-Willi syndrome domain.
Volume: 8
Issue: 2
Pages: e52390