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Symbol Name ID |
Kctd1
potassium channel tetramerisation domain containing 1 MGI:1918269 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormality of the kidney |
Duplication of renal pelvis |
Unilateral renal agenesis |
Renal hypoplasia |
Pyelonephritis |
Renal insufficiency |
Ureteral duplication |
Recurrent urinary tract infections |
| Disease(s) Associated with KCTD1 | ||||||||
| scalp-ear-nipple syndrome |
| Mouse Phenotypes | increased urine calcium level |
increased urine magnesium level |
decreased urine osmolality |
decreased urine pH |
decreased urine albumin level |
decreased urine uric acid level |
abnormal kidney physiology |
polyuria |
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| Availability | Mouse Genotype | ||||||||
| Kctd1Mhdahst014/Kctd1+ | |||||||||
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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