|
Symbol Name ID |
Smc3
structural maintenance of chromosomes 3 MGI:1339795 |
| Darker colors indicate more annotations |
| Human Phenotypes | Frontal bossing |
Brachycephaly |
Plagiocephaly |
Micrognathia |
Primary microcephaly |
Secondary microcephaly |
Delayed closure of the anterior fontanelle |
Short neck |
Short 5th finger |
Clinodactyly of the 5th finger |
Proximal placement of thumb |
Toe syndactyly |
Brachydactyly |
Short foot |
Small hand |
Limited elbow movement |
| Disease(s) Associated with SMC3 | ||||||||||||||||
| Cornelia de Lange syndrome 3 |
| Mouse Phenotypes | small cranium |
decreased bone mineral content |
|
| Availability | Mouse Genotype | ||
| Smc3tm1a(EUCOMM)Wtsi/Smc3+ | |||
| Smc3tm1.1Toshi/Smc3tm1.1Toshi 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 04/23/2024 MGI 6.23 |
|
|
|
||
Analysis Tools