Image | |||||
Caption | Craniofacial skeletal abnormalities in Ptch1dl/Ptch1dl mutants. E18.5 control (a, c, e, g, i, k) and mutant skulls (b, d, f, h, j, l) shown in lateral (a, b), dorsal (c, d), and ventral views with mandibles removed (e-h). (g) and (h) show detail of cranial base with hyoid bone removed. [Note that the pila postoptica (Ppso), which forms a component of the orbitosphenoid, was occasionally present in the mutants. It can also be absent in control embryos at this stage]. (i, j) Lateral views of control dentary bone (i) and dentary bones from two separate mutants (j). (k, l) Details of lambdoid suture between parietal and interparietal bones. Midline is to left and lateral to right. Asterisk shows expected junction between bones. Key. (b) Abnormal flexure at skull and nasal juncture is shown by a black arrow. (d) Red arrows demonstrate delayed or abnormal development of the bones of the cranial vault in the midline in mutants. (f) White asterisk highlights the absence of the presphenoid bone and the underdevelopment of the palatal shelves, and red arrow shows the abnormal morphology of the alisphenoid bone in mutants. ap, angular process; Bo, basioccipital; Bs, basisphenoid; cdp, condylar process; crp, coronoid process; Fr, frontal bone; Hy, hyoid; Ip, interparietal bone; Mx, palatine process of the maxilla; N, nasal bone; Pl, palatine; Ppso, pila postoptica; Pr, parietal bone; Ps, presphenoid; Px, premaxilla. | ||||
Copyright | This image is from Feng W, Genesis 2013 Oct;51(10):677-89, and is displayed with the permission of Wiley-Blackwell, who owns the Copyright. J:204468 | ||||
Associated Alleles |
|
||||
Associated Genotypes |
|
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 |
|
|