Symbol Name ID |
Ofd1
OFD1, centriole and centriolar satellite protein MGI:1350328 |
Darker colors indicate more annotations |
Human Phenotypes | Inguinal hernia |
Short stature |
Obesity |
Growth delay |
Disease(s) Associated with OFD1 | ||||
Joubert syndrome 10 | ||||
orofaciodigital syndrome I | ||||
retinitis pigmentosa | ||||
Simpson-Golabi-Behmel syndrome type 2 |
Mouse Phenotypes | cleft palate |
decreased embryo size |
renal glomerulus cyst |
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Availability | Mouse Genotype | |||
Ofd1tm2.1Bfra/Ofd1+ Tg(CAG-cre)1Nagy/0 (conditional) |
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Ofd1tm2.1Bfra/Y Tg(CAG-cre)1Nagy/0 (conditional) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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