|
Symbol Name ID |
Kat6b
K(lysine) acetyltransferase 6B MGI:1858746 |
| Darker colors indicate more annotations |
| Human Phenotypes | Prominent occiput |
Micrognathia |
Retrognathia |
Microcephaly |
Clinodactyly of the 5th finger |
Camptodactyly of finger |
Long thumb |
Long hallux |
Patellar dislocation |
Joint hypermobility |
| Disease(s) Associated with KAT6B | ||||||||||
| Ohdo syndrome, SBBYS variant |
| Mouse Phenotypes | abnormal coronal suture morphology |
abnormal cranium morphology |
abnormal occipital bone morphology |
abnormal parietal bone morphology |
short mandible |
abnormal limb long bone morphology |
abnormal long bone hypertrophic chondrocyte zone |
abnormal epiphyseal plate morphology |
delayed cranial suture closure |
|
| Availability | Mouse Genotype | |||||||||
| Kat6bGt(pKC199)1Pgr/Kat6bGt(pKC199)1Pgr | ||||||||||
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 04/16/2024 MGI 6.23 |
|
|
|
||
Analysis Tools