- About
- Home
- Introduction
- Statistics
- Programs
- Dignet
- Gene
- GenePair
- BioSummarAI
- Help & Docs
- Documents
- Help
- FAQs
- Links
- Acknowledge
- Disclaimer
- Contact Us
Gene Information
Gene symbol: CTNS
Gene name: cystinosin, lysosomal cystine transporter
HGNC ID: 2518
Synonyms: CTNS-LSB, PQLC4
Related Genes
| # | Gene Symbol | Number of hits |
| 1 | AMMECR1 | 1 hits |
| 2 | APOB | 1 hits |
| 3 | AVP | 1 hits |
| 4 | CAST | 1 hits |
| 5 | CFH | 1 hits |
| 6 | CLCNKB | 1 hits |
| 7 | GHR | 1 hits |
| 8 | GYS1 | 1 hits |
| 9 | IKBKAP | 1 hits |
| 10 | INS | 1 hits |
| 11 | KCNJ11 | 1 hits |
| 12 | LIPC | 1 hits |
| 13 | LPL | 1 hits |
| 14 | P2RY2 | 1 hits |
| 15 | PON2 | 1 hits |
| 16 | SLC4A1 | 1 hits |
| 17 | TRH | 1 hits |
| 18 | VWF | 1 hits |
Related Sentences
| # | PMID | Sentence |
| 1 | 804049 | The diseases causing end-stage kidney failure in recipients were Alport syndrome, amyloidosis, cystinosis, diabetes mellitus, Fabry disease, familial nephritis, gout, medullary cystic disease, oxalosis, and systemic lupus erythematosus. |
| 2 | 3389874 | Nephrogenic diabetes insipidus, cystinosis, and vitamin D. |
| 3 | 3389874 | We describe a patient with early diagnosed cystinosis who presented with nephrogenic diabetes insipidus in addition to proximal tubular dysfunction. |
| 4 | 3389874 | Nephrogenic diabetes insipidus, cystinosis, and vitamin D. |
| 5 | 3389874 | We describe a patient with early diagnosed cystinosis who presented with nephrogenic diabetes insipidus in addition to proximal tubular dysfunction. |
| 6 | 3816859 | Infantile cystinosis and insulin-dependent diabetes mellitus. |
| 7 | 8061694 | We describe two patients with infantile nephropathic cystinosis who presented nephrogenic diabetes insipidus in addition to Fanconi syndrome. |
| 8 | 17137217 | Analyses of covariance adjusting for age, body mass index, hyperlipidemia, diabetes, smoking, drinking, and antihypertensive medication revealed that 17 polymorphisms in 16 genes (APOB, CAST, CLCNKB, CTNS, GHR, GYS1, HF1, IKBKAP, KCNJ11, LIPC, LPL, P2RY2, PON2, SLC4A1, TRH, VWF) were significantly associated with blood pressure variations. |
| 9 | 17137217 | Multivariate logistic regression analysis with adjustment for the same factors revealed that 11 polymorphisms in 11 genes (CAST, CTLA4, F5, GC, GHR, LIPC, PLA2G7, SLC4A1, SLCI8A1, TRH, VWF) showed significant associations with hypertension. |
| 10 | 17137217 | Five polymorphisms in five genes, CAST(calpastatin), LIPC (hepatic lipase), SLC4A1 (band 3 anion transporter), TRH (thyrotropin-releasing hormone), and VWF (von Willebrand factor), were significantly associated with both blood pressure variation and hypertension. |