Entity Details
Primary name |
CLDN16 |
Entity type |
gene |
Source |
Source Link |
Details
PrimaryID | 10686 |
RefseqGene | NG_008149 |
Symbol | CLDN16 |
Name | claudin 16 |
Chromosome | 3 |
Location | 3q28 |
TaxID | 9606 |
Status | live |
SourceGenome | genomic |
SourceOrigin | natural |
CreationDate | 2000-01-07 |
ModificationDate | 2021-06-11 |
Diseases
Show/Hide Table
Disease ID | Source | Name | Description |
248250 | OMIM | Hypomagnesemia 3 (HOMG3) | A progressive renal disease characterized by primary renal magnesium wasting with hypomagnesemia, hypercalciuria and nephrocalcinosis. Recurrent urinary tract infections and kidney stones are often observed. In spite of hypercalciuria, patients do not show hypocalcemia. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
3 interactions