Symbol Name ID |
Dph1
diphthamide biosynthesis 1 MGI:2151233 |
Darker colors indicate more annotations |
Human Phenotypes | Sagittal craniosynostosis |
Scaphocephaly |
Trigonocephaly |
Micrognathia |
Dandy-Walker malformation |
Disease(s) Associated with DPH1 | |||||
diphthamide deficiency syndrome 1 |
Mouse Phenotypes | abnormal craniofacial bone morphology |
short Meckel's cartilage |
decreased cranium length |
small cranium |
mandible hypoplasia |
short mandible |
micrognathia |
short nasal bone |
absent palatine bone |
abnormal skeleton development |
|
Availability | Mouse Genotype | ||||||||||
Dph1tm1Bhr/Dph1tm1Bhr | |||||||||||
Dph1tm2Bhr/Dph1tm2Bhr | |||||||||||
Dph1tm1.1Cmch/Dph1tm1.1Cmch Edil3Tg(Sox2-cre)1Amc/Edil3+ (conditional) |
|||||||||||
Dph1tm1.1Cmch/Dph1tm1.1Cmch H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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 05/14/2024 MGI 6.23 |
|
|