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Search results 1301 to 1400 out of 8285 for C2

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Type Details Score
Publication
17726579 | -
First Author: Chen C
Year: 2007
Journal: Cancer Metastasis Rev
Title: The Nedd4-like family of E3 ubiquitin ligases and cancer.
Volume: 26
Issue: 3-4
Pages: 587-604
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Publication
18223681 | -
First Author: Li Y
Year: 2008
Journal: Oncogene
Title: A novel HECT-type E3 ubiquitin protein ligase NEDL1 enhances the p53-mediated apoptotic cell death in its catalytic activity-independent manner.
Volume: 27
Issue: 26
Pages: 3700-9
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Publication
12890487 | -
First Author: Miyazaki K
Year: 2003
Journal: Biochem Biophys Res Commun
Title: A novel HECT-type E3 ubiquitin ligase, NEDL2, stabilizes p73 and enhances its transcriptional activity.
Volume: 308
Issue: 1
Pages: 106-13
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Protein Domain
IPR037795 | C2_HECW
Type: Domain
Description: HECW1 (HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1), also known as NEDL1, is an HECT-type E3 ubiquitin protein ligase highly expressed in favorable neuroblastomas []. NEDL1 is thought to normally function in the quality control of cellular proteins by eliminating misfolded proteins. This is thought to be accomplished via a mechanism analogous to that of ER-associated degradation by forming tight complexes and aggregating misfolded proteins that have escaped ubiquitin-mediated degradation []. NEDL1 is thought to stimulate p53-mediated apoptosis [].NEDL1 shares large homology and structure with NEDL2, including a C2 domain at the N terminus, two WW domains in the middle of the protein, and a HECT domain at the C terminus []. NEDL2 regulates the stability of p73 []and functions as a regulator of the metaphase to anaphase transition [].This entry represents the C2 domain of NEDL1 and NEDL2.
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Not Specified Targeted Library C2 (Nagy) C57BL/6N Not Specified
Creator: Not Specified
Vector Type: Not Specified
Vector: Not Specified
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Gene trapped
Name: CMHD Gene trapped Library C2 (Tcp) C57BL/6N pPT1
Creator: CMHD
Vector Type: Not Specified
Vector: pPT1
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Wellcome Trust Sanger Institute Targeted Library C2 (Nagy) C57BL/6N L1L2_gt0
Creator: Wellcome Trust Sanger Institute
Vector Type: Not Specified
Vector: L1L2_gt0
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Cell Line Derivation
Cell Line Derivation
 
Derivation Type: Endonuclease-mediated
Name: Not Specified Endonuclease-mediated Library C2 (Nagy) C57BL/6NCrl Not Specified
Creator: Not Specified
Vector: Not Specified
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Not Specified Targeted Library C2 (Tcp) C57BL/6N Not Specified
Creator: Not Specified
Vector Type: Not Specified
Vector: Not Specified
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Endonuclease-mediated
Name: Not Specified Endonuclease-mediated Library C2 (Nagy) C57BL/6NTac Not Specified
Creator: Not Specified
Vector Type: Not Specified
Vector: Not Specified
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Spontaneous
Name: Not Specified Spontaneous Library C2 (Nagy) C57BL/6N Not Specified
Creator: Not Specified
Vector Type: Not Specified
Vector: Not Specified
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Transposon induced
Name: Not Specified Transposon induced Library C2 (Nagy) C57BL/6N Not Specified
Creator: Not Specified
Vector Type: Not Specified
Vector: Not Specified
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Cell Line Derivation
Cell Line Derivation
Derivation Type: QTL
Name: Not Specified QTL Library C2 (Nagy) C57BL/6N Not Specified
Creator: Not Specified
Vector Type: Not Specified
Vector: Not Specified
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Cell Line Derivation
Cell Line Derivation
 
Name: Not Specified Not Applicable Library C2 (Nagy) C57BL/6N Not Specified
Creator: Not Specified
Vector Type: Not Specified
Vector: Not Specified
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Not Specified
Name: Not Specified Not Specified Library C2 (Nagy) C57BL/6N Not Specified
Creator: Not Specified
Vector Type: Not Specified
Vector: Not Specified
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Gene trapped
Name: Not Specified Gene trapped Library C2 (Nagy) C57BL/6N Not Specified
Creator: Not Specified
Vector Type: Not Specified
Vector: Not Specified
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Radiation induced
Name: Not Specified Radiation induced Library C2 (Nagy) C57BL/6N Not Specified
Creator: Not Specified
Vector Type: Not Specified
Vector: Not Specified
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Transgenic
Name: Not Specified Transgenic Library C2 (Nagy) C57BL/6N Not Specified
Creator: Not Specified
Vector Type: Not Specified
Vector: Not Specified
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Wellcome Trust Sanger Institute Targeted Library C2 (Nagy) C57BL/6N L1L2_Bact_P
Creator: Wellcome Trust Sanger Institute
Vector Type: Not Specified
Vector: L1L2_Bact_P
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Wellcome Trust Sanger Institute Targeted Library C2 (Nagy) C57BL/6N L1L2_Pgk_P
Creator: Wellcome Trust Sanger Institute
Vector Type: Not Specified
Vector: L1L2_Pgk_P
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Wellcome Trust Sanger Institute Targeted Library C2 (Nagy) C57BL/6N L1L2_Pgk_PM
Creator: Wellcome Trust Sanger Institute
Vector Type: Not Specified
Vector: L1L2_Pgk_PM
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Wellcome Trust Sanger Institute Targeted Library C2 (Nagy) C57BL/6N L1L2_gt1
Creator: Wellcome Trust Sanger Institute
Vector Type: Not Specified
Vector: L1L2_gt1
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Wellcome Trust Sanger Institute Targeted Library C2 (Nagy) C57BL/6N L1L2_gt2
Creator: Wellcome Trust Sanger Institute
Vector Type: Not Specified
Vector: L1L2_gt2
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Wellcome Trust Sanger Institute Targeted Library C2 (Nagy) C57BL/6N L1L2_gtk
Creator: Wellcome Trust Sanger Institute
Vector Type: Not Specified
Vector: L1L2_gtk
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Wellcome Trust Sanger Institute Targeted Library C2 (Nagy) C57BL/6N L1L2_st0
Creator: Wellcome Trust Sanger Institute
Vector Type: Not Specified
Vector: L1L2_st0
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Wellcome Trust Sanger Institute Targeted Library C2 (Nagy) C57BL/6N L1L2_st1
Creator: Wellcome Trust Sanger Institute
Vector Type: Not Specified
Vector: L1L2_st1
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Wellcome Trust Sanger Institute Targeted Library C2 (Nagy) C57BL/6N L1L2_st2
Creator: Wellcome Trust Sanger Institute
Vector Type: Not Specified
Vector: L1L2_st2
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: University of California, Davis Targeted Library C2 (Nagy) C57BL/6N L1L2_Bact_P
Creator: University of California, Davis
Vector Type: Not Specified
Vector: L1L2_Bact_P
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: University of California, Davis Targeted Library C2 (Nagy) C57BL/6N L1L2_Pgk_P
Creator: University of California, Davis
Vector Type: Not Specified
Vector: L1L2_Pgk_P
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: University of California, Davis Targeted Library C2 (Nagy) C57BL/6N L1L2_Pgk_PM
Creator: University of California, Davis
Vector Type: Not Specified
Vector: L1L2_Pgk_PM
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: University of California, Davis Targeted Library C2 (Nagy) C57BL/6N L1L2_gt0
Creator: University of California, Davis
Vector Type: Not Specified
Vector: L1L2_gt0
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: University of California, Davis Targeted Library C2 (Nagy) C57BL/6N L1L2_gt1
Creator: University of California, Davis
Vector Type: Not Specified
Vector: L1L2_gt1
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: University of California, Davis Targeted Library C2 (Nagy) C57BL/6N L1L2_gt2
Creator: University of California, Davis
Vector Type: Not Specified
Vector: L1L2_gt2
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: University of California, Davis Targeted Library C2 (Nagy) C57BL/6N L1L2_gtk
Creator: University of California, Davis
Vector Type: Not Specified
Vector: L1L2_gtk
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: University of California, Davis Targeted Library C2 (Nagy) C57BL/6N L1L2_st0
Creator: University of California, Davis
Vector Type: Not Specified
Vector: L1L2_st0
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: University of California, Davis Targeted Library C2 (Nagy) C57BL/6N L1L2_st1
Creator: University of California, Davis
Vector Type: Not Specified
Vector: L1L2_st1
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: University of California, Davis Targeted Library C2 (Nagy) C57BL/6N L1L2_st2
Creator: University of California, Davis
Vector Type: Not Specified
Vector: L1L2_st2
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Helmholtz Zentrum Muenchen GmbH Targeted Library C2 (Nagy) C57BL/6N L1L2_Bact_P
Creator: Helmholtz Zentrum Muenchen GmbH
Vector Type: Not Specified
Vector: L1L2_Bact_P
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Helmholtz Zentrum Muenchen GmbH Targeted Library C2 (Nagy) C57BL/6N L1L2_Pgk_P
Creator: Helmholtz Zentrum Muenchen GmbH
Vector Type: Not Specified
Vector: L1L2_Pgk_P
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Helmholtz Zentrum Muenchen GmbH Targeted Library C2 (Nagy) C57BL/6N L1L2_Pgk_PM
Creator: Helmholtz Zentrum Muenchen GmbH
Vector Type: Not Specified
Vector: L1L2_Pgk_PM
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Helmholtz Zentrum Muenchen GmbH Targeted Library C2 (Nagy) C57BL/6N L1L2_gt0
Creator: Helmholtz Zentrum Muenchen GmbH
Vector Type: Not Specified
Vector: L1L2_gt0
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Helmholtz Zentrum Muenchen GmbH Targeted Library C2 (Nagy) C57BL/6N L1L2_gt1
Creator: Helmholtz Zentrum Muenchen GmbH
Vector Type: Not Specified
Vector: L1L2_gt1
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Helmholtz Zentrum Muenchen GmbH Targeted Library C2 (Nagy) C57BL/6N L1L2_gt2
Creator: Helmholtz Zentrum Muenchen GmbH
Vector Type: Not Specified
Vector: L1L2_gt2
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Helmholtz Zentrum Muenchen GmbH Targeted Library C2 (Nagy) C57BL/6N L1L2_gtk
Creator: Helmholtz Zentrum Muenchen GmbH
Vector Type: Not Specified
Vector: L1L2_gtk
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Helmholtz Zentrum Muenchen GmbH Targeted Library C2 (Nagy) C57BL/6N L1L2_st0
Creator: Helmholtz Zentrum Muenchen GmbH
Vector Type: Not Specified
Vector: L1L2_st0
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Helmholtz Zentrum Muenchen GmbH Targeted Library C2 (Nagy) C57BL/6N L1L2_st1
Creator: Helmholtz Zentrum Muenchen GmbH
Vector Type: Not Specified
Vector: L1L2_st1
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Targeted
Name: Helmholtz Zentrum Muenchen GmbH Targeted Library C2 (Nagy) C57BL/6N L1L2_st2
Creator: Helmholtz Zentrum Muenchen GmbH
Vector Type: Not Specified
Vector: L1L2_st2
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Cell Line Derivation
Cell Line Derivation
Derivation Type: Endonuclease-mediated
Name: Not Specified Endonuclease-mediated Library C2 (Tcp) C57BL/6N Not Specified
Creator: Not Specified
Vector Type: Not Specified
Vector: Not Specified
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Publication
15049706 | -
First Author: Schulz TA
Year: 2004
Journal: Biochemistry
Title: The tricalbin C2 domains: lipid-binding properties of a novel, synaptotagmin-like yeast protein family.
Volume: 43
Issue: 13
Pages: 3987-95
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Protein Coding Gene
MGI:2685817 | Hecw2
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGI:2385166 | Slc35c2
Type: protein_coding_gene
Organism: mouse, laboratory
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DO Term
DOID:0060295 | complement component 2 deficiency
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DO Term
DOID:0110026 | age related macular degeneration 14
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Ontology Term
- | Glycolate pathway
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GO Term
GO:0071021 | U2-type post-spliceosomal complex
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GO Term
GO:0071022 | U12-type post-spliceosomal complex
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Publication
11395408 | -
 
First Author: Maehama T
Year: 2001
Journal: Annu Rev Biochem
Title: PTEN and myotubularin: novel phosphoinositide phosphatases.
Volume: 70
Pages: 247-79
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Publication
11858936 | -
First Author: Leslie NR
Year: 2002
Journal: Cell Signal
Title: PTEN: The down side of PI 3-kinase signalling.
Volume: 14
Issue: 4
Pages: 285-95
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Publication
29552027 | J:262467
 
First Author: Zamarbide M
Year: 2018
Journal: Front Genet
Title: Loss of the Intellectual Disability and Autism Gene Cc2d1a and Its Homolog Cc2d1b Differentially Affect Spatial Memory, Anxiety, and Hyperactivity.
Volume: 9
Pages: 65
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Publication
30732858 | J:280260
First Author: Zamarbide M
Year: 2019
Journal: Biol Psychiatry
Title: Male-Specific cAMP Signaling in the Hippocampus Controls Spatial Memory Deficits in a Mouse Model of Autism and Intellectual Disability.
Volume: 85
Issue: 9
Pages: 760-768
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Publication
7791877 | J:26068
First Author: Li C
Year: 1995
Journal: Nature
Title: Ca(2+)-dependent and -independent activities of neural and non-neural synaptotagmins.
Volume: 375
Issue: 6532
Pages: 594-9
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Interaction Experiment
Chazot PL (1997)
Description: Biochemical evidence for the existence of a pool of unassembled C2 exon-containing NR1 subunits of the mammalian forebrain NMDA receptor.
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Publication
17510957 | -
First Author: Jiménez JL
Year: 2007
Journal: Proteins
Title: Beta-strand recombination in tricalbin evolution and the origin of synaptotagmin-like C2 domains.
Volume: 68
Issue: 3
Pages: 770-8
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Publication
14713287 | -
First Author: Rickman C
Year: 2004
Journal: Biochem J
Title: Comparative analysis of tandem C2 domains from the mammalian synaptotagmin family.
Volume: 378
Issue: Pt 2
Pages: 681-6
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Publication
11371549 | -
First Author: Fukuda M
Year: 2001
Journal: J Biol Chem
Title: The C2A domain of double C2 protein gamma contains a functional nuclear localization signal.
Volume: 276
Issue: 27
Pages: 24441-4
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Publication
34070186 | J:307361
 
First Author: Brücher VC
Year: 2021
Journal: Int J Mol Sci
Title: Lack of WWC2 Protein Leads to Aberrant Angiogenesis in Postnatal Mice.
Volume: 22
Issue: 10
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Publication
518534 | J:6249
First Author: Holmes RS
Year: 1979
Journal: Biochem Genet
Title: Genetics and ontogeny of alcohol dehydrogenase isozymes in the mouse: evidence for a cis-acting regulator gene (Adt-i) controlling C2 isozyme expression in reproductive tissues and close linkage of Adh-3 and Adt-i on chromosome 3.
Volume: 17
Issue: 5-6
Pages: 461-72
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Protein
Q8C5G6
Organism: Mus musculus/domesticus
Length: 220  
Fragment?: false
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Protein Domain
IPR037808 | C2_Dock-C
Type: Domain
Description: DOCK family members are evolutionarily conserved guanine nucleotide exchange factors (GEFs) for Rho-family GTPases []. DOCK proteins are required during several cellular processes, such as cell motility and phagocytosis. The N-terminal SH3 domain of the DOCK proteins functions as an inhibitor of GEF, which can be relieved upon its binding to the ELMO1-3 adaptor proteins, after their binding to active RhoG at the plasma membrane [, ]. DOCK family proteins are categorised into four subfamilies based on their sequence homology: DOCK-A subfamily (DOCK1/180, 2, 5), DOCK-B subfamily (DOCK3, 4), DOCK-C subfamily (DOCK6, 7, 8), DOCK-D subfamily (DOCK9, 10, 11) []. This entry represents the C2 domain found in the Dock-C members. In addition to the C2 domain (also known as DHR-1 domain) and the DHR-2 domain, Dock-C members contain a functionally uncharacterised domain upstream of the C2 domain. DHR-2 has the catalytic activity for Rac and/or Cdc42, but is structurally unrelated to the DH domain. The C2/DHR-1 domains of Dock1 (also known as Dock180) and Dock4 have been shown to bind phosphatidylinositol-3, 4, 5-triphosphate (PtdIns(3,4,5)P3) [, , ].
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Protein Domain
IPR037809 | C2_Dock-D
Type: Domain
Description: DOCK family members are evolutionarily conserved guanine nucleotide exchange factors (GEFs) for Rho-family GTPases []. DOCK proteins are required during several cellular processes, such as cell motility and phagocytosis. The N-terminal SH3 domain of the DOCK proteins functions as an inhibitor of GEF, which can be relieved upon its binding to the ELMO1-3 adaptor proteins, after their binding to active RhoG at the plasma membrane [, ]. DOCK family proteins are categorised into four subfamilies based on their sequence homology: DOCK-A subfamily (DOCK1/180, 2, 5), DOCK-B subfamily (DOCK3, 4), DOCK-C subfamily (DOCK6, 7, 8), DOCK-D subfamily (DOCK9, 10, 11) []. This entry represents the C2 domain of the Dock-D members. In addition to the C2 domain (also known as the DHR-1 domain) and the DHR-2, Dock-D members contain a functionally uncharacterised domain and a PH domain upstream of the C2 domain. DHR-2 has the catalytic activity for Rac and/or Cdc42, but is structurally unrelated to the DH domain. The C2/DHR-1 domains of Dock1 (also known as Dock180) and Dock4 have been shown to bind phosphatidylinositol-3, 4, 5-triphosphate (PtdIns(3,4,5)P3). The PH domain broadly binds to phospholipids and is thought to be involved in targeting the plasma membrane [, , ].
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Protein Domain
IPR037811 | C2_Dock-B
Type: Domain
Description: DOCK family members are evolutionarily conserved guanine nucleotide exchange factors (GEFs) for Rho-family GTPases []. DOCK proteins are required during several cellular processes, such as cell motility and phagocytosis. The N-terminal SH3 domain of the DOCK proteins functions as an inhibitor of GEF, which can be relieved upon its binding to the ELMO1-3 adaptor proteins, after their binding to active RhoG at the plasma membrane [, ]. DOCK family proteins are categorised into four subfamilies based on their sequence homology: DOCK-A subfamily (DOCK1/180, 2, 5), DOCK-B subfamily (DOCK3, 4), DOCK-C subfamily (DOCK6, 7, 8), DOCK-D subfamily (DOCK9, 10, 11) []. This entry represents the C2 domain of the Dock-B members. Most of these members have been shown to be GEFs specific for Rac, although Dock4 has also been shown to interact indirectly with the Ras family GTPase Rap1, probably through Rap regulatory proteins. In addition to the C2 domain (also known as DHR-1 domain) and the DHR-2 domain, Dock-B members contain a SH3 domain upstream of the C2 domain and a proline-rich region downstream. DHR-2 has the catalytic activity for Rac and/or Cdc42, but is structurally unrelated to the DH domain. The C2/DHR-1 domains of Dock1 (also known as Dock180) and Dock4 have been shown to bind phosphatidylinositol-3, 4, 5-triphosphate (PtdIns(3,4,5)P3)[, , ].
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Protein
Q768S4
Organism: Mus musculus/domesticus
Length: 302  
Fragment?: false
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Protein
Q9EPW0
Organism: Mus musculus/domesticus
Length: 939  
Fragment?: false
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Protein
Q6P1Y8
Organism: Mus musculus/domesticus
Length: 924  
Fragment?: false
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Protein
E9PVM3
Organism: Mus musculus/domesticus
Length: 941  
Fragment?: false
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Protein
D3YUL8
Organism: Mus musculus/domesticus
Length: 972  
Fragment?: false
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Protein
A7MCT9
Organism: Mus musculus/domesticus
Length: 308  
Fragment?: false
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Protein
Q1A6V1
Organism: Mus musculus/domesticus
Length: 927  
Fragment?: false
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Protein
Q1A6U9
Organism: Mus musculus/domesticus
Length: 941  
Fragment?: false
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Protein
F6V2U0
Organism: Mus musculus/domesticus
Length: 939  
Fragment?: false
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Protein
E9Q9A0
Organism: Mus musculus/domesticus
Length: 938  
Fragment?: false
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Protein
D3Z230
Organism: Mus musculus/domesticus
Length: 977  
Fragment?: false
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Protein
D3YUD3
Organism: Mus musculus/domesticus
Length: 954  
Fragment?: false
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Protein
E9PVM1
Organism: Mus musculus/domesticus
Length: 927  
Fragment?: false
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Protein
Q3UEQ1
Organism: Mus musculus/domesticus
Length: 890  
Fragment?: false
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Protein
Q3URI3
Organism: Mus musculus/domesticus
Length: 818  
Fragment?: true
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Publication
35429439 | J:325475
First Author: Qi S
Year: 2022
Journal: Mol Cell
Title: WWC proteins mediate LATS1/2 activation by Hippo kinases and imply a tumor suppression strategy.
Volume: 82
Issue: 10
Pages: 1850-1864.e7
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Protein
Q3ULW6
Organism: Mus musculus/domesticus
Length: 985  
Fragment?: false
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Protein
D3YU68
Organism: Mus musculus/domesticus
Length: 730  
Fragment?: false
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Protein
A0A0R4J0H2
Organism: Mus musculus/domesticus
Length: 731  
Fragment?: false
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Protein
A0A1L1SR74
Organism: Mus musculus/domesticus
Length: 950  
Fragment?: false
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Protein
E9QQ55
Organism: Mus musculus/domesticus
Length: 985  
Fragment?: false
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Protein
A0A087WPN8
Organism: Mus musculus/domesticus
Length: 149  
Fragment?: true
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Publication
29101244 | J:251143
First Author: Vahid-Ansari F
Year: 2017
Journal: J Neurosci
Title: Abrogated Freud-1/Cc2d1a Repression of 5-HT1A Autoreceptors Induces Fluoxetine-Resistant Anxiety/Depression-Like Behavior.
Volume: 37
Issue: 49
Pages: 11967-11978
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Protein
A0A087WRC5
Organism: Mus musculus/domesticus
Length: 198  
Fragment?: true
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GXD Expression
GXD Expression
Probe: MGI:5435874
Assay Type: Immunohistochemistry
Annotation Date: 2012-09-27
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1707420
Pattern: Regionally restricted
Stage: TS20
Assay Id: MGI:5436318
Age: embryonic day 12.5
Image: 2D
Note: Expression is present in GABAergic neurons derived from the c2 domain.
Specimen Label: 2D
Detected: true
Specimen Num: 1
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GXD Expression
GXD Expression
Probe: MGI:1341780
Assay Type: Immunohistochemistry
Annotation Date: 2012-09-27
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1707420
Pattern: Regionally restricted
Stage: TS20
Assay Id: MGI:5436319
Age: embryonic day 12.5
Image: 2C
Note: Expression is present in GABAergic neurons derived from the c2 domain.
Specimen Label: 2C
Detected: true
Specimen Num: 1
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GXD Expression
GXD Expression
Probe: MGI:1341780
Assay Type: Immunohistochemistry
Annotation Date: 2012-09-27
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1707420
Pattern: Regionally restricted
Stage: TS20
Assay Id: MGI:5436403
Age: embryonic day 12.5
Image: 2C
Note: Expression is present in GABAergic neurons derived from the c2 domain.
Specimen Label: 2C
Detected: true
Specimen Num: 1
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Protein Coding Gene
MGP_CAROLIEiJ_G0019836 | -
Type: protein_coding_gene
Organism: Mus caroli
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Protein Coding Gene
MGP_CAROLIEiJ_G0029302 | -
Type: protein_coding_gene
Organism: Mus caroli
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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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