Symbol Name ID |
Dpcd
deleted in primary ciliary dyskinesia MGI:1924407 |
Age | E10.5 | E11.5 | E12.5 | E15.5 | P |
In situ RNA (whole mount) | 1 | 1 | |||
RT-PCR | 2 | 1 | 1 | 1 |
Dpcd deleted in primary ciliary dyskinesia (Synonyms: 5330431N19Rik, Gm17018, Ndac) | |
Results | Reference |
1 | J:334109 Cova G, Glaser J, Schopflin R, Prada-Medina CA, Ali S, Franke M, Falcone R, Federer M, Ponzi E, Ficarella R, Novara F, Wittler L, Timmermann B, Gentile M, Zuffardi O, Spielmann M, Mundlos S, Combinatorial effects on gene expression at the Lbx1/Fgf8 locus resolve split-hand/foot malformation type 3. Nat Commun. 2023 Mar 17;14(1):1475 |
2 | J:196292 Marinic M, Aktas T, Ruf S, Spitz F, An integrated holo-enhancer unit defines tissue and gene specificity of the Fgf8 regulatory landscape. Dev Cell. 2013 Mar 11;24(5):530-42 |
4 | J:350459 McCallum-Loudeac J, Moody E, Williams J, Johnstone G, Sircombe KJ, Clarkson AN, Wilson MJ, Deletion of a conserved genomic region associated with adolescent idiopathic scoliosis leads to vertebral rotation in mice. Hum Mol Genet. 2024 Apr 18;33(9):787-801 |
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 12/10/2024 MGI 6.24 |
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