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Symbol Name ID |
Ift172
intraflagellar transport 172 MGI:2682064 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Atrial septal defect |
Ventricular septal defect |
Splenomegaly |
Attenuation of retinal blood vessels |
Retinal vascular tortuosity |
| Disease(s) Associated with IFT172 | |||||
| Bardet-Biedl syndrome 20 | |||||
| retinitis pigmentosa 71 | |||||
| short-rib thoracic dysplasia 10 with or without polydactyly |
| Mouse Phenotypes | cardiovascular system phenotype |
abnormal cardiovascular system morphology |
abnormal retina blood vessel morphology |
abnormal cardiac outflow tract development |
abnormal direction of heart looping |
abnormal heart morphology |
increased heart atrium size |
atrioventricular septal defect |
complete atrioventricular septal defect |
decreased heart right ventricle size |
increased heart ventricle size |
abnormal pericardium morphology |
hemorrhage |
|
| Availability | Mouse Genotype | |||||||||||||
| Ift172avc1/Ift172avc1 | * | |||||||||||||
| Ift172tm1Lmgd/Ift172tm1Lmgd | ||||||||||||||
| Ift172tm2b(EUCOMM)Hmgu/Ift172tm2b(EUCOMM)Hmgu | ||||||||||||||
| Ift172wim/Ift172wim | ||||||||||||||
| Ift172avc1/Ift172wim | ||||||||||||||
| Ift172tm2b(EUCOMM)Hmgu/Ift172+ | ||||||||||||||
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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