Symbol Name ID |
Prkd1
protein kinase D1 MGI:99879 |
Age | E1 | E1.5 | E2 | E2.5 | E3.5 | E8.5 | E9.5 | E10.5 | E11.5 | E12.5 | E13.5 | E14.5 | E15 | E15.5 | E16 | E16.5 | E17.5 | E18.5 | P |
In situ RNA (section) | 2 | 1 | |||||||||||||||||
Immunohistochemistry (whole mount) | 1 | 1 | 1 | 1 | |||||||||||||||
In situ RNA (whole mount) | 1 | 1 | |||||||||||||||||
Western blot | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 2 | 1 | 1 | 1 | 1 | 1 | ||||||
RT-PCR | 1 | 1 | 1 | 1 | 1 | 1 | 2 | 3 | 1 | 1 | 1 | 1 | 2 | 3 |
Prkd1 protein kinase D1 (Synonyms: Pkcm, PKD1, Prkcm) | |
Results | Reference |
1* | J:313619 Bedogni F, Hevner RF, Cell-Type-Specific Gene Expression in Developing Mouse Neocortex: Intermediate Progenitors Implicated in Axon Development. Front Mol Neurosci. 2021;14:686034 |
9 | J:87315 Cogram P, Hynes A, Dunlevy LP, Greene ND, Copp AJ, Specific isoforms of protein kinase C are essential for prevention of folate-resistant neural tube defects by inositol. Hum Mol Genet. 2004 Jan 1;13(1):7-14 |
1 | J:108241 Desai J, Shannon ME, Johnson MD, Ruff DW, Hughes LA, Kerley MK, Carpenter DA, Johnson DK, Rinchik EM, Culiat CT, Nell1-deficient mice have reduced expression of extracellular matrix proteins causing cranial and vertebral defects. Hum Mol Genet. 2006 Apr 15;15(8):1329-41 |
3* | J:46439 Freeman TC, Dixon AK, Campbell EA, Tait TM, Richardson PJ, Rice KM, Maslen GL, Metcalfe AD, Streuli CH, Bentley DR, Expression Mapping of Mouse Genes. MGI Direct Data Submission. 1998; |
2 | J:346070 Godoy-Corchuelo JM, Ali Z, Brito Armas JM, Martins-Bach AB, Garcia-Toledo I, Fernandez-Beltran LC, Lopez-Carbonero JI, Bascunana P, Spring S, Jimenez-Coca I, Munoz de Bustillo Alfaro RA, Sanchez-Barrena MJ, Nair RR, Nieman BJ, Lerch JP, Miller KL, Ozdinler HP, Fisher EMC, Cunningham TJ, Acevedo-Arozena A, Corrochano S, TDP-43-M323K causes abnormal brain development and progressive cognitive and motor deficits associated with mislocalised and increased levels of TDP-43. Neurobiol Dis. 2024 Feb 15;193:106437 |
3* | J:165681 Hall JA, Ribich S, Christoffolete MA, Simovic G, Correa-Medina M, Patti ME, Bianco AC, Absence of thyroid hormone activation during development underlies a permanent defect in adaptive thermogenesis. Endocrinology. 2010 Sep;151(9):4573-82 |
1* | J:234970 Kalyani R, Lee JY, Min H, Yoon H, Kim MH, Genes Frequently Coexpressed with Hoxc8 Provide Insight into the Discovery of Target Genes. Mol Cells. 2016 May 31;39(5):395-402 |
8* | J:105949 Oster H, Abraham D, Leitges M, Expression of the protein kinase D (PKD) family during mouse embryogenesis. Gene Expr Patterns. 2006 Apr;6(4):400-8 |
13* | J:63657 Pauken CM, Capco DG, The expression and stage-specific localization of protein kinase C isotypes during mouse preimplantation development. Dev Biol. 2000 Jul 15;223(2):411-21 |
2* | J:347799 Waheed-Ullah Q, Wilsdon A, Abbad A, Rochette S, Bu'Lock F, Hitz MP, Dombrowsky G, Cuello F, Brook JD, Loughna S, Effect of deletion of the protein kinase PRKD1 on development of the mouse embryonic heart. J Anat. 2024 Feb 28; |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 12/17/2024 MGI 6.24 |
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