Symbol Name ID |
Cad
carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase MGI:1916969 |
Age | E10.5 | E14.5 |
In situ RNA (section) | 1 | 1 |
In situ RNA (whole mount) | 1 |
Cad carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase (Synonyms: 2410008J01Rik) | |
Results | Reference |
2* | J:187427 Rainger J, Bengani H, Campbell L, Anderson E, Sokhi K, Lam W, Riess A, Ansari M, Smithson S, Lees M, Mercer C, McKenzie K, Lengfeld T, Gener Querol B, Branney P, McKay S, Morrison H, Medina B, Robertson M, Kohlhase J, Gordon C, Kirk J, Wieczorek D, Fitzpatrick DR, Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH. Hum Mol Genet. 2012 Sep 15;21(18):3969-83 |
1* | J:122989 Visel A, Thaller C, Eichele G, GenePaint.org: an atlas of gene expression patterns in the mouse embryo. Nucleic Acids Res. 2004 Jan 1;32(Database issue):D552-6 |
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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