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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
neuronal ceroid lipofuscinosis 6A
Summary
- Synonym
-
- CLN6
- neuronal ceroid lipofuscinosis 6
- neuronal ceroid lipofuscinosis 6 variable age of onset
- Definition
- A neuronal ceroid lipofuscinosis that is characterized by progressive decline of neurologic function, including visual deterioration in most, cognitive impairment, loss of motor function, and seizures and has_material_basis_in homozygous mutation in the CLN6 gene on chromosome 15q21-q23.
- Super Class
- autosomal recessive disease neuronal ceroid lipofuscinosis
External Links
- Disease Ontology
- DOID:0110729
- Mondo Disease Ontology
- ORDO
- OMIM
- GARD
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 47 | ACLY | ATP citrate lyase | |
| 1203 | CLN5 | CLN5 intracellular trafficking protein | |
| 2571 | GAD1 | glutamate decarboxylase 1 | |
| 2572 | GAD2 | glutamate decarboxylase 2 | |
| 3956 | LGALS1 | galectin 1 | |
| 5310 | PKD1 | polycystin 1, transient receptor potential channel interacting | |
| 5538 | PPT1 | palmitoyl-protein thioesterase 1 | |
| 5660 | PSAP | prosaposin | |
| 6609 | SMPD1 | sphingomyelin phosphodiesterase 1 | |
| 7957 | EPM2A | EPM2A glucan phosphatase, laforin |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| O75503 | Bis(monoacylglycero)phosphate synthase CLN5 | |
| P07602 | Prosaposin | |
| P09382 | Galectin-1 | |
| P17405 | Sphingomyelin phosphodiesterase | |
| P50897 | Palmitoyl-protein thioesterase 1 | |
| P53396 | ATP-citrate synthase | |
| P98161 | Polycystin-1 | |
| Q96EG1 | Arylsulfatase G | |
| Q9UMR5 | Lysosomal thioesterase PPT2 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0011209 | EEG with generalized slow activity grade 4 |
| HP:0012379 | Abnormal circulating enzyme concentration or activity |
| HP:0010536 | Central sleep apnea |
| HP:0002071 | Abnormality of extrapyramidal motor function |
| HP:0007256 | Abnormal pyramidal sign |
| HP:0001337 | Tremor |
| HP:0000529 | Progressive visual loss |
| HP:0007360 | Aplasia/Hypoplasia of the cerebellum |
| HP:0001627 | Abnormal heart morphology |
| HP:0100543 | Cognitive impairment |
