|
Symbol Name ID |
Kat6b
K(lysine) acetyltransferase 6B MGI:1858746 |
| Darker colors indicate more annotations |
| Human Phenotypes | Prominent occiput |
Micrognathia |
Retrognathia |
Microcephaly |
Abnormal cheek morphology |
Sloping forehead |
Thin upper lip vermilion |
Submucous cleft hard palate |
Bifid uvula |
Cleft palate |
Microdontia |
Neoplasm of the tongue |
Bulbous nose |
Depressed nasal bridge |
Long nose |
Prominent nose |
Blepharophimosis |
Short palpebral fissure |
Epicanthus inversus |
Abnormal nasolacrimal system morphology |
| 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 |
shortened head |
abnormal ear position |
|
| 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