Entity Details
Primary name |
SLC34A3 |
Entity type |
gene |
Source |
Source Link |
Details
PrimaryID | 142680 |
RefseqGene | NG_017008 |
Symbol | SLC34A3 |
Name | solute carrier family 34 member 3 |
Chromosome | 9 |
Location | 9q34.3 |
TaxID | 9606 |
Status | live |
SourceGenome | genomic |
SourceOrigin | natural |
CreationDate | 2002-01-19 |
ModificationDate | 2021-06-11 |
Diseases
Show/Hide Table
Disease ID | Source | Name | Description |
241530 | OMIM | Hereditary hypophosphatemic rickets with hypercalciuria (HHRH) | Autosomal recessive form of hypophosphatemia characterized by reduced renal phosphate reabsorption and rickets. Increased serum levels of 1,25-dihydroxyvitamin D lead to increase in urinary calcium excretion. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
5 interactions