|
Symbol Name ID |
Inpp5e
inositol polyphosphate-5-phosphatase E MGI:1927753 |
| Darker colors indicate more annotations |
| Human Phenotypes | Biparietal narrowing |
Plagiocephaly |
Microcephaly |
Macrocephaly |
Encephalocele |
Postaxial hand polydactyly |
Hand polydactyly |
Postaxial foot polydactyly |
Foot polydactyly |
Clinodactyly |
Scoliosis |
Abnormal form of the vertebral bodies |
| Disease(s) Associated with INPP5E | ||||||||||||
| Joubert syndrome | ||||||||||||
| Joubert syndrome 1 |
| Mouse Phenotypes | abnormal phalanx morphology |
abnormal metacarpal bone morphology |
split sternum |
delayed endochondral bone ossification |
|
| Availability | Mouse Genotype | ||||
| Inpp5etm1.2Ssch/Inpp5etm1.2Ssch | |||||
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 05/21/2024 MGI 6.23 |
|
|
|
||
Analysis Tools