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Search results 6101 to 6200 out of 8285 for C2

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Type Details Score
Publication
7689224 | J:14165
First Author: Kaestner KH
Year: 1993
Journal: Proc Natl Acad Sci U S A
Title: Six members of the mouse forkhead gene family are developmentally regulated.
Volume: 90
Issue: 16
Pages: 7628-31
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Publication
9106663 | J:39636
First Author: Winnier GE
Year: 1997
Journal: Genes Dev
Title: The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo.
Volume: 11
Issue: 7
Pages: 926-40
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Publication
26138476 | J:239652
First Author: Cajigas I
Year: 2015
Journal: Development
Title: Evf2 lncRNA/BRG1/DLX1 interactions reveal RNA-dependent inhibition of chromatin remodeling.
Volume: 142
Issue: 15
Pages: 2641-52
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Publication
24590274 | J:209628
First Author: Brouillard P
Year: 2014
Journal: J Clin Invest
Title: Genetics of lymphatic anomalies.
Volume: 124
Issue: 3
Pages: 898-904
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Publication
27771509 | J:256746
First Author: Wang X
Year: 2017
Journal: Biochim Biophys Acta
Title: A mouse model of aniridia reveals the in vivo downstream targets of Pax6 driving iris and ciliary body development in the eye.
Volume: 1863
Issue: 1
Pages: 60-67
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Publication
14512019 | J:85739
First Author: Rice R
Year: 2003
Journal: Dev Biol
Title: Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4.
Volume: 262
Issue: 1
Pages: 75-87
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Publication
9425147 | J:46220
First Author: Ruiz-Lozano P
Year: 1998
Journal: Development
Title: Energy deprivation and a deficiency in downstream metabolic target genes during the onset of embryonic heart failure in RXRalpha-/- embryos.
Volume: 125
Issue: 3
Pages: 533-44
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Publication
20960542 | J:166528
First Author: Zacharias AL
Year: 2010
Journal: Dev Dyn
Title: Canonical Wnt/β-catenin signaling is required for maintenance but not activation of Pitx2 expression in neural crest during eye development.
Volume: 239
Issue: 12
Pages: 3215-25
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Publication
28754980 | J:270967
First Author: Kodo K
Year: 2017
Journal: Sci Rep
Title: Regulation of Sema3c and the Interaction between Cardiac Neural Crest and Second Heart Field during Outflow Tract Development.
Volume: 7
Issue: 1
Pages: 6771
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Publication
33667029 | J:308975
First Author: Takenoshita M
Year: 2021
Journal: Dev Dyn
Title: Cell lineage- and expression-based inference of the roles of forkhead box transcription factor Foxc2 in craniofacial development.
Volume: 250
Issue: 8
Pages: 1125-1139
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Publication
22012621 | J:177488
First Author: Srinivasan RS
Year: 2011
Journal: Genes Dev
Title: Prox1 dosage controls the number of lymphatic endothelial cell progenitors and the formation of the lymphovenous valves.
Volume: 25
Issue: 20
Pages: 2187-97
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Publication
26214525 | J:225799
First Author: Kazenwadel J
Year: 2015
Journal: J Clin Invest
Title: GATA2 is required for lymphatic vessel valve development and maintenance.
Volume: 125
Issue: 8
Pages: 2979-94
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Publication
21076395 | J:167523
First Author: Jagani Z
Year: 2010
Journal: Nat Med
Title: Loss of the tumor suppressor Snf5 leads to aberrant activation of the Hedgehog-Gli pathway.
Volume: 16
Issue: 12
Pages: 1429-33
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Publication
30482854 | J:269498
First Author: Nonomura K
Year: 2018
Journal: Proc Natl Acad Sci U S A
Title: Mechanically activated ion channel PIEZO1 is required for lymphatic valve formation.
Volume: 115
Issue: 50
Pages: 12817-12822
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Publication
12223415 | J:78685
First Author: Frank DU
Year: 2002
Journal: Development
Title: An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome.
Volume: 129
Issue: 19
Pages: 4591-603
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Publication
10886375 | J:77612
First Author: Akazawa H
Year: 2000
Journal: Genes Cells
Title: Targeted disruption of the homeobox transcription factor Bapx1 results in lethal skeletal dysplasia with asplenia and gastroduodenal malformation.
Volume: 5
Issue: 6
Pages: 499-513
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Publication
15210844 | J:93243
First Author: Ishimori N
Year: 2004
Journal: J Lipid Res
Title: Quantitative trait loci that determine plasma lipids and obesity in C57BL/6J and 129S1/SvImJ inbred mice.
Volume: 45
Issue: 9
Pages: 1624-32
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Publication
11528125 | J:71031
First Author: Akeson EC
Year: 2001
Journal: Cytogenet Cell Genet
Title: Ts65Dn -- localization of the translocation breakpoint and trisomic gene content in a mouse model for Down syndrome.
Volume: 93
Issue: 3-4
Pages: 270-6
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Publication
33750945 | J:304565
First Author: Bi-Lin KW
Year: 2021
Journal: PLoS Genet
Title: Critical role of the BAF chromatin remodeling complex during murine neural crest development.
Volume: 17
Issue: 3
Pages: e1009446
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Publication
26839363 | J:240081
First Author: Mayeuf-Louchart A
Year: 2016
Journal: Development
Title: Endothelial cell specification in the somite is compromised in Pax3-positive progenitors of Foxc1/2 conditional mutants, with loss of forelimb myogenesis.
Volume: 143
Issue: 5
Pages: 872-9
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Publication
28705793 | J:269234
First Author: Pujol F
Year: 2017
Journal: Arterioscler Thromb Vasc Biol
Title: Dachsous1-Fat4 Signaling Controls Endothelial Cell Polarization During Lymphatic Valve Morphogenesis-Brief Report.
Volume: 37
Issue: 9
Pages: 1732-1735
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Publication
23741013 | J:201783
First Author: Levet S
Year: 2013
Journal: Blood
Title: Bone morphogenetic protein 9 (BMP9) controls lymphatic vessel maturation and valve formation.
Volume: 122
Issue: 4
Pages: 598-607
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Publication
25082981 | J:215770
First Author: Poulain M
Year: 2014
Journal: Mol Hum Reprod
Title: Involvement of doublesex and mab-3-related transcription factors in human female germ cell development demonstrated by xenograft and interference RNA strategies.
Volume: 20
Issue: 10
Pages: 960-71
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Publication
28506991 | J:311497
First Author: Everson JL
Year: 2017
Journal: Development
Title: Sonic hedgehog regulation of Foxf2 promotes cranial neural crest mesenchyme proliferation and is disrupted in cleft lip morphogenesis.
Volume: 144
Issue: 11
Pages: 2082-2091
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Publication
22036572 | J:178686
First Author: Yao J
Year: 2011
Journal: Cell
Title: Doc2 is a Ca2+ sensor required for asynchronous neurotransmitter release.
Volume: 147
Issue: 3
Pages: 666-77
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Publication
21835308 | -
First Author: Doi H
Year: 2011
Journal: Am J Hum Genet
Title: Exome sequencing reveals a homozygous SYT14 mutation in adult-onset, autosomal-recessive spinocerebellar ataxia with psychomotor retardation.
Volume: 89
Issue: 2
Pages: 320-7
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Protein
Q8BL96
Organism: Mus musculus/domesticus
Length: 306  
Fragment?: true
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Protein
A0A0A6YWI3
Organism: Mus musculus/domesticus
Length: 77  
Fragment?: false
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Publication
15947782 | -
First Author: Zhu Y
Year: 2005
Journal: EMBO Rep
Title: Crystal structure of a polyphosphate kinase and its implications for polyphosphate synthesis.
Volume: 6
Issue: 7
Pages: 681-7
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Publication
14745138 | -
First Author: Izumi T
Year: 2003
Journal: Cell Struct Funct
Title: The roles of Rab27 and its effectors in the regulated secretory pathways.
Volume: 28
Issue: 5
Pages: 465-74
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Publication
16376304 | -
First Author: Herrero-Turrión MJ
Year: 2006
Journal: Biochem Biophys Res Commun
Title: Cloning and genomic characterization of sytdep, a new synaptotagmin XIV-related gene.
Volume: 340
Issue: 2
Pages: 386-94
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Publication
15990870 | -
First Author: Gottschalk A
Year: 2005
Journal: EMBO J
Title: Identification and characterization of novel nicotinic receptor-associated proteins in Caenorhabditis elegans.
Volume: 24
Issue: 14
Pages: 2566-78
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Publication
27484220 | -
First Author: Zou B
Year: 2016
Journal: Genome
Title: Identification and analysis of copine/BONZAI proteins among evolutionarily diverse plant species.
Volume: 59
Issue: 8
Pages: 565-73
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Publication
10074452 | -
First Author: Lockyer PJ
Year: 1999
Journal: Curr Biol
Title: Identification of the ras GTPase-activating protein GAP1(m) as a phosphatidylinositol-3,4,5-trisphosphate-binding protein in vivo.
Volume: 9
Issue: 5
Pages: 265-8
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Protein Domain
IPR030536 | Doc2g
Type: Family
Description: This entry represents double C2-like domain-containing protein gamma (Doc2g). The Doc2 (double C2) family members Doc2a and Doc2b are characterised by an N-terminal Munc13-1 interacting domain, and two C2 domains that interact with Ca(2+) and phospholipid at the C terminus. In contrast, the C2 domains of Doc2g impair Ca(2+)-dependent phospholipid binding activity. The Ca2+-independent C2A domain of Doc2g seems to have a nuclear localisation function []. Doc2g may also function as an effector for Munc13-1, and it may be involved in the regulation of vesicular trafficking [].
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Protein Domain
IPR003172 | ML_dom
Type: Domain
Description: The MD-2-related lipid-recognition (ML) domain is implicated in lipid recognition, particularly in the recognition of pathogen related products. It has an immunoglobulin-likeβ-sandwich fold similar to that of E-set Ig domains. This domain is present in proteins from plants, animals and fungi, including the following proteins:Epididymal secretory protein E1 (also known as Niemann-Pick C2 protein - Npc2), which is known to bind cholesterol. Niemann-Pick disease type C2 is a fatal hereditary disease characterised by accumulation of low-density lipoprotein-derived cholesterol in lysosomes [].House-dust mite allergen proteins such as Der f 2 from Dermatophagoides farinae and Der p 2 from Dermatophagoides pteronyssinus [].
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Publication
10508505 | J:57764
First Author: Bittner RE
Year: 1999
Journal: Nat Genet
Title: Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B.
Volume: 23
Issue: 2
Pages: 141-2
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Publication
17420270 | J:119974
First Author: Crozat K
Year: 2007
Journal: J Exp Med
Title: Jinx, an MCMV susceptibility phenotype caused by disruption of Unc13d: a mouse model of type 3 familial hemophagocytic lymphohistiocytosis.
Volume: 204
Issue: 4
Pages: 853-63
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Publication
11891182 | J:75304
First Author: Kostek CA
Year: 2002
Journal: Am J Pathol
Title: Up-regulation of MHC class I expression accompanies but is not required for spontaneous myopathy in dysferlin-deficient SJL/J mice.
Volume: 160
Issue: 3
Pages: 833-9
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Strain
MGI:5825075 | B10.SJL-Dysf<im>
Attribute String: spontaneous mutation, congenic, mutant strain
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Strain
MGI:4430877 | B10.SJL-Dysf<im>/AwaJ
Attribute String: congenic, deletion, mutant strain, spontaneous mutation
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Publication
26112643 | J:328065
First Author: Rubi L
Year: 2015
Journal: Cell Physiol Biochem
Title: Proper Voltage-Dependent Ion Channel Function in Dysferlin-Deficient Cardiomyocytes.
Volume: 36
Issue: 3
Pages: 1049-58
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Publication
16288871 | J:106591
First Author: von der Hagen M
Year: 2005
Journal: Neuromuscul Disord
Title: The differential gene expression profiles of proximal and distal muscle groups are altered in pre-pathological dysferlin-deficient mice.
Volume: 15
Issue: 12
Pages: 863-77
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Publication
31218594 | J:294421
First Author: Ishiba R
Year: 2019
Journal: J Mol Histol
Title: Faster regeneration associated to high expression of Fam65b and Hdac6 in dysferlin-deficient mouse.
Volume: 50
Issue: 4
Pages: 375-387
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Publication
16314532 | J:103754
First Author: Harada K
Year: 2005
Journal: Mol Cell Biol
Title: The class II phosphoinositide 3-kinase C2beta is not essential for epidermal differentiation.
Volume: 25
Issue: 24
Pages: 11122-30
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Publication
23418460 | J:199416
First Author: Mito T
Year: 2013
Journal: PLoS One
Title: Mitochondrial DNA mutations in mutator mice confer respiration defects and B-cell lymphoma development.
Volume: 8
Issue: 2
Pages: e55789
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Strain
MGI:6144458 | STOCK Pax3<tm1Mrc>/Nci
Attribute String: mutant stock, targeted mutation
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Strain
MGI:3822367 | B6;129-Syngap1<tm1Rlh>/J
Attribute String: targeted mutation, mutant stock
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Publication
12598599 | J:97391
First Author: Kim JH
Year: 2003
Journal: J Neurosci
Title: The role of synaptic GTPase-activating protein in neuronal development and synaptic plasticity.
Volume: 23
Issue: 4
Pages: 1119-24
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Publication
23785156 | J:199642
First Author: Clement JP
Year: 2013
Journal: J Neurosci
Title: SYNGAP1 links the maturation rate of excitatory synapses to the duration of critical-period synaptic plasticity.
Volume: 33
Issue: 25
Pages: 10447-52
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Publication
19145222 | J:194146
First Author: Guo X
Year: 2009
Journal: Neuropsychopharmacology
Title: Reduced expression of the NMDA receptor-interacting protein SynGAP causes behavioral abnormalities that model symptoms of Schizophrenia.
Volume: 34
Issue: 7
Pages: 1659-72
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Publication
27827368 | J:242720
 
First Author: Berryer MH
Year: 2016
Journal: Nat Commun
Title: Decrease of SYNGAP1 in GABAergic cells impairs inhibitory synapse connectivity, synaptic inhibition and cognitive function.
Volume: 7
Pages: 13340
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Publication
37595758 | J:340773
     
First Author: Dettmer-Monaco V
Year: 2023
Journal: J Allergy Clin Immunol
Title: Gene editing of hematopoietic stem cells restores T-cell response in familial hemophagocytic lymphohistiocytosis.
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Publication
27079884 | J:247079
First Author: Crescente M
Year: 2016
Journal: Arterioscler Thromb Vasc Biol
Title: Intracellular Trafficking, Localization, and Mobilization of Platelet-Borne Thiol Isomerases.
Volume: 36
Issue: 6
Pages: 1164-73
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Publication
25511702 | J:220366
First Author: Mito T
Year: 2015
Journal: Biochem Biophys Res Commun
Title: Transmitochondrial mito-miceΔ and mtDNA mutator mice, but not aged mice, share the same spectrum of musculoskeletal disorders.
Volume: 456
Issue: 4
Pages: 933-7
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Allele
Hprt1<tm79(Ple7-EGFP)Ems> | MGI:5303437
Name: hypoxanthine phosphoribosyltransferase 1; targeted mutation 79, Elizabeth M Simpson
Allele Type: Targeted
Attribute String: Reporter
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Allele
Hprt1<tm80(Ple9-EGFP/cre)Ems> | MGI:5303438
Name: hypoxanthine phosphoribosyltransferase 1; targeted mutation 80, Elizabeth M Simpson
Allele Type: Targeted
Attribute String: Recombinase, Reporter
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Allele
Tg(TcraB4,TcrbB4)#Wrh | MGI:6508112
Name: transgene insertion, William R Heath
Allele Type: Transgenic
Attribute String: Inserted expressed sequence
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Genotype
Genotype
Symbol: Pax3/Pax3
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Dysf/Dysf
Background: involves: SJL
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Syngap1/Syngap1
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Syngap1/Syngap1<+>
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Zygosity: ht
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Notch2/Notch2<+> Tg(Tyr-cre)2Lru/?
Background: involves: 129/Sv * BALB/c * C57BL/6 * DBA/2
Zygosity: cn
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Notch2/Notch2 Tg(Tyr-cre)2Lru/?
Background: involves: 129/Sv * BALB/c * C57BL/6 * DBA/2
Zygosity: cn
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Notch2/Notch2 Tg(Mx1-cre)1Cgn/?
Background: involves: BALB/c * C57BL/6 * CBA
Zygosity: cn
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Tcra/Tcra Tg(Mx1-cre)1Cgn/?
Background: involves: 129S7/SvEvBrd * C57BL/6 * CBA
Zygosity: cn
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Syngap1/Syngap1<+>
Background: involves: 129S1/Sv * 129X1/SvJ
Zygosity: ht
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Syngap1/Syngap1
Background: involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6J
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Syngap1/Syngap1<+>
Background: involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6J
Zygosity: ht
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Tcra/Tcra Tg(Mx1-cre)1Cgn/?
Background: involves: C57BL/6 * CBA
Zygosity: cn
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Dysf/Dysf
Background: B10.SJL-Dysf
Zygosity: hm
Has Mutant Allele: true
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Publication
10440375 | J:56513
First Author: Augustin I
Year: 1999
Journal: Nature
Title: Munc13-1 is essential for fusion competence of glutamatergic synaptic vesicles.
Volume: 400
Issue: 6743
Pages: 457-61
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Publication
12070347 | J:77339
First Author: Varoqueaux F
Year: 2002
Journal: Proc Natl Acad Sci U S A
Title: Total arrest of spontaneous and evoked synaptic transmission but normal synaptogenesis in the absence of Munc13-mediated vesicle priming.
Volume: 99
Issue: 13
Pages: 9037-42
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Publication
11150314 | J:66984
First Author: Augustin I
Year: 2001
Journal: J Neurosci
Title: The cerebellum-specific Munc13 isoform Munc13-3 regulates cerebellar synaptic transmission and motor learning in mice.
Volume: 21
Issue: 1
Pages: 10-7
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Publication
9697857 | -
First Author: Betz A
Year: 1998
Journal: Neuron
Title: Munc13-1 is a presynaptic phorbol ester receptor that enhances neurotransmitter release.
Volume: 21
Issue: 1
Pages: 123-36
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Publication
11566361 | J:71776
First Author: Wiedemann M
Year: 2001
Journal: Biochim Biophys Acta
Title: The mouse Fgfrl1 gene coding for a novel FGF receptor-like protein.
Volume: 1520
Issue: 3
Pages: 247-50
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Publication
8674531 | J:33425
First Author: Perez M
Year: 1996
Journal: FEBS Lett
Title: Zfp60, a mouse zinc finger gene expressed transiently during in vitro muscle differentiation.
Volume: 387
Issue: 2-3
Pages: 117-21
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Publication
- | J:27505
 
First Author: Evans EP
Year: 1988
Journal: Mouse News Lett
Title: A large deletion at the Sl locus
Volume: 81
Pages: 66
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Publication
30333125 | J:266995
First Author: Miyatake Y
Year: 2018
Journal: J Immunol
Title: Myoferlin-Mediated Lysosomal Exocytosis Regulates Cytotoxicity by Phagocytes.
Volume: 201
Issue: 10
Pages: 3051-3057
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Publication
10488064 | J:57874
First Author: Duncan RR
Year: 1999
Journal: J Biol Chem
Title: Transient, phorbol ester-induced DOC2-Munc13 interactions in vivo.
Volume: 274
Issue: 39
Pages: 27347-50
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Publication
11125141 | J:127190
First Author: Naureckiene S
Year: 2000
Journal: Science
Title: Identification of HE1 as the second gene of Niemann-Pick C disease.
Volume: 290
Issue: 5500
Pages: 2298-301
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Publication
24070258 | J:205001
First Author: Traore DA
Year: 2013
Journal: Biochem J
Title: Defining the interaction of perforin with calcium and the phospholipid membrane.
Volume: 456
Issue: 3
Pages: 323-35
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Protein Coding Gene
MGI:1926250 | Doc2g
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_CAROLIEiJ_G0022482 | -
Type: protein_coding_gene
Organism: Mus caroli
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Protein Coding Gene
MGP_129S1SvImJ_G0024639 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_AJ_G0024607 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_AKRJ_G0024578 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_BALBcJ_G0024605 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_C3HHeJ_G0024373 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGI_C57BL6J_1926250 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_C57BL6NJ_G0025053 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_CASTEiJ_G0023845 | -
Type: protein_coding_gene
Organism: mouse, laboratory
•
•
•
•
•
Protein Coding Gene
MGP_CBAJ_G0024344 | -
Type: protein_coding_gene
Organism: mouse, laboratory
•
•
•
•
•
Protein Coding Gene
MGP_DBA2J_G0024472 | -
Type: protein_coding_gene
Organism: mouse, laboratory
•
•
•
•
•
Protein Coding Gene
MGP_FVBNJ_G0024439 | -
Type: protein_coding_gene
Organism: mouse, laboratory
•
•
•
•
•
Protein Coding Gene
MGP_LPJ_G0024559 | -
Type: protein_coding_gene
Organism: mouse, laboratory
•
•
•
•
•
Protein Coding Gene
MGP_NODShiLtJ_G0024470 | -
Type: protein_coding_gene
Organism: mouse, laboratory
•
•
•
•
•
Protein Coding Gene
MGP_NZOHlLtJ_G0025101 | -
Type: protein_coding_gene
Organism: mouse, laboratory
•
•
•
•
•
Protein Coding Gene
MGP_PWKPhJ_G0023592 | -
Type: protein_coding_gene
Organism: mouse, laboratory
•
•
•
•
•
Protein Coding Gene
MGP_WSBEiJ_G0023908 | -
Type: protein_coding_gene
Organism: mouse, laboratory
•
•
•
•
•




MouseMine is a collaboration between MGI at The Jackson Laboratory and the InterMine project at the Cambridge Systems Biology Centre. MouseMine is funded through a grant from the NIH/NHGRI.The Jackson Laboratory makes no representation about the suitability or accuracy of this software or data for any purpose, and makes no warranties, either express or implied, including merchantability and fitness for a particular purpose or that the use of this software or data will not infringe any third party patents, copyrights, trademarks, or other rights. the software and data are provided "as is". This software and data are provided to enhance knowledge and encourage progress in the scientific community and are to be used only for research and educational purposes. Any reproduction or use for commercial purpose is prohibited without the prior express written permission of the Jackson Laboratory.

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