- About
- Home
- Introduction
- Statistics
- Programs
- Dignet
- Gene
- GenePair
- Help & Docs
- Documents
- Help
- FAQs
- Links
- Acknowledge
- Disclaimer
- Contact Us
Gene Information
Gene symbol: MCKD1
Gene name: medullary cystic kidney disease 1 (autosomal dominant)
HGNC ID: 6941
Related Genes
| # | Gene Symbol | Number of hits |
| 1 | NPHS1 | 1 hits |
| 2 | PTPRO | 1 hits |
| 3 | SYNPO | 1 hits |
Related Sentences
| # | PMID | Sentence |
| 1 | 11793093 | We therefore analyzed kidney tissue from normal children (n=3), children with congenital nephrotic syndrome of the Finnish type (CNF, n=3), minimal change disease (MCD, n=3), focal segmental glomerulosclerosis (FSGS, n=3), and Galloway-Mowat syndrome (n=4) by immunohistochemistry for expression of synaptopodin, GLEPP1, intracellular domain of nephrin (nephrin-I), and extracellular domain of nephrin (nephrin-E). |
| 2 | 21414970 | Regarding GKD subtypes, patients with focal segmental glomerulosclerosis (FSGS), but not patients with minimal change disease (MCD), had a significantly higher mRNA expression of B7-1 and NPHS1 than healthy subjects (P = 0.012 and P = 0.030, respectively). |