Assay
Age
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In situ RNA (section)
12.5 DPC
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Mid1 midline 1 (Synonyms: 61B3-R, DXHXS1141, Fxy, Trim18) | |
Results | Reference |
1* | J:46361 Dal Zotto L, Quaderi NA, Elliott R, Lingerfelter PA, Carrel L , Valsecchi V , Montini E , Yen CH , Chapman V , Kalcheva I , Arrigo G , Zuffardi O , Thomas S , Willard HF , Ballabio A , Disteche CM , Rugarli EI, The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region. Hum Mol Genet. 1998 Mar;7(3):489-99 |
1 | J:157828 Lancioni A, Pizzo M, Fontanella B, Ferrentino R, Napolitano LM, De Leonibus E, Meroni G, Lack of Mid1, the mouse ortholog of the Opitz syndrome gene, causes abnormal development of the anterior cerebellar vermis. J Neurosci. 2010 Feb 24;30(8):2880-7 |
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 04/16/2024 MGI 6.23 |
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