Symbol Name ID |
Evc2
EvC ciliary complex subunit 2 MGI:1915775 |
Age | E7 | E9.5 | E10 | E10.5 | E11 | E11.5 | E12.5 | E13.5 | E14.5 | E15 | E15.5 | E16.5 | E17 | E17.5 | E18.5 | P |
Immunohistochemistry (section) | 1 | 1 | 1 | 1 | 3 | 1 | 1 | |||||||||
In situ RNA (section) | 1 | 1 | 1 | 2 | 1 | 1 | 1 | 2 | ||||||||
In situ RNA (whole mount) | 1 | |||||||||||||||
In situ reporter (knock in) | 1 | 2 | 1 | |||||||||||||
Northern blot | 1 | 1 | 1 | 1 | 1 | |||||||||||
RT-PCR | 1 | 1 | 1 | 1 | 1 | 1 | 1 | |||||||||
cDNA clones | 1 | 1 |
Evc2 EvC ciliary complex subunit 2 (Synonyms: 1110017L09Rik, Ellis van Creveld syndrome 2, Lbn, limbin) | |
Results | Reference |
6 | J:316640 Badri MK, Zhang H, Ohyama Y, Venkitapathi S, Alamoudi A, Kamiya N, Takeda H, Ray M, Scott G, Tsuji T, Kunieda T, Mishina Y, Mochida Y, Expression of Evc2 in craniofacial tissues and craniofacial bone defects in Evc2 knockout mouse. Arch Oral Biol. 2016 Aug;68:142-52 |
1* | J:237132 Burnicka-Turek O, Steimle JD, Huang W, Felker L, Kamp A, Kweon J, Peterson M, Reeves RH, Maslen CL, Gruber PJ, Yang XH, Shendure J, Moskowitz IP, Cilia gene mutations cause atrioventricular septal defects by multiple mechanisms. Hum Mol Genet. 2016 Jul 15;25(14):3011-3028 |
4* | J:301228 Laugel-Haushalter V, Langer A, Marrie J, Fraulob V, Schuhbaur B, Koch-Phillips M, Dolle P, Bloch-Zupan A, From the transcription of genes involved in ectodermal dysplasias to the understanding of associated dental anomalies. Mol Syndromol. 2012 Oct;3(4):158-68 |
2 | J:196977 Nakatomi M, Hovorakova M, Gritli-Linde A, Blair HJ, MacArthur K, Peterka M, Lesot H, Peterkova R, Ruiz-Perez VL, Goodship JA, Peters H, Evc regulates a symmetrical response to Shh signaling in molar development. J Dent Res. 2013 Mar;92(3):222-8 |
12* | J:147578 Sund KL, Roelker S, Ramachandran V, Durbin L, Benson DW, Analysis of Ellis van Creveld syndrome gene products: implications for cardiovascular development and disease. Hum Mol Genet. 2009 May 15;18(10):1813-24 |
10* | J:78363 Takeda H, Takami M, Oguni T, Tsuji T, Yoneda K, Sato H, Ihara N, Itoh T, Kata SR, Mishina Y, Womack JE, Moritomo Y, Sugimoto Y, Kunieda T, Positional cloning of the gene LIMBIN responsible for bovine chondrodysplastic dwarfism. Proc Natl Acad Sci U S A. 2002 Aug 6;99(16):10549-54 |
1 | J:238710 Zhang H, Kamiya N, Tsuji T, Takeda H, Scott G, Rajderkar S, Ray MK, Mochida Y, Allen B, Lefebvre V, Hung IH, Ornitz DM, Kunieda T, Mishina Y, Elevated Fibroblast Growth Factor Signaling Is Critical for the Pathogenesis of the Dwarfism in Evc2/Limbin Mutant Mice. PLoS Genet. 2016 Dec;12(12):e1006510 |
2 | J:274043 Zhang H, Takeda H, Tsuji T, Kamiya N, Kunieda T, Mochida Y, Mishina Y, Loss of Function of Evc2 in Dental Mesenchyme Leads to Hypomorphic Enamel. J Dent Res. 2017 Apr;96(4):421-429 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 11/12/2024 MGI 6.24 |
|
|