|
Symbol Name ID |
Nobox
NOBOX oogenesis homeobox MGI:108011 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hypoplasia of the ovary |
Streak ovary |
Reduced antral follicle count |
Premature ovarian insufficiency |
Primary amenorrhea |
Secondary amenorrhea |
| Disease(s) Associated with NOBOX | ||||||
| primary ovarian insufficiency 5 |
| Mouse Phenotypes | abnormal oocyte morphology |
decreased oocyte number |
absent oocytes |
oocyte degeneration |
abnormal seminal vesicle morphology |
abnormal ovarian follicle number |
absent secondary ovarian follicles |
impaired ovarian folliculogenesis |
ovary atrophy |
ovary cyst |
female infertility |
|
| Availability | Mouse Genotype | |||||||||||
| Noboxtm1.1(KOMP)Vlcg/Noboxtm1.1(KOMP)Vlcg | ||||||||||||
| Noboxtm1Rajk/Noboxtm1Rajk | ||||||||||||
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