|
Symbol Name ID |
Kctd1
potassium channel tetramerisation domain containing 1 MGI:1918269 |
| Darker colors indicate more annotations |
| Human Phenotypes | Cardiac myxoma |
Hypertension |
Supraventricular tachycardia |
Congestive heart failure |
| Disease(s) Associated with KCTD1 | ||||
| scalp-ear-nipple syndrome |
| Mouse Phenotypes | decreased heart weight |
eye hemorrhage |
corneal vascularization |
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| Availability | Mouse Genotype | |||
| Kctd1em1(IMPC)J/Kctd1em1(IMPC)J | ||||
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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