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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
nyctalopin
Summary
- Gene Symbol
-
- NYX
- Aliases
-
- CLRP
- CSNB1A
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Congenital stationary night blindness
- Disease variant
- Extracellular matrix
- Leucine-rich repeat
- Proteoglycan
- Reference proteome
- Repeat
- Signal
- Vision
- Proteins
| UniProt | Protein Name |
|---|---|
| Q9GZU5 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| biological_process | ||
| visual perception |
| GO Term | Evidence Code | PMID |
|---|---|---|
| extracellular matrix | ||
| extracellular space |
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| molecular_function |
GO Hierarchy
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:13399 | color blindness | |
| DOID:13909 | red-green color blindness | |
| DOID:13910 | red color blindness | |
| DOID:13911 | achromatopsia | |
| DOID:13912 | acquired color blindness | |
| DOID:331 | central nervous system disease | |
| DOID:3612 | retinitis | |
| DOID:539 | ophthalmoplegia | |
| DOID:540 | strabismus | |
| DOID:5614 | eye disease |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0007984 | Electronegative electroretinogram |
| HP:0011003 | High myopia |
| HP:0011463 | Childhood onset |
| HP:0012047 | Hemeralopia |
| Disease ID | Disease Name |
|---|---|
| OMIM:310500 |
|
| ORPHA:215 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 181983 | WB:WBGene00020693 | ||
| 102353311 | LATCH06602 | ||
| 568821 | ZFIN:ZDB-GENE-061026-3 | DANRE44600 | |
| 108266365 | ICTPU31103 | ||
| 113574351 | ELEEL13930 | ||
| 106586793 | SALSA90989 | ||
| 101167659 | ORYLA09615 | ||
| 100711308 | ORENI21340 | ||
| 115587612 | SPAAU27406 | ||
| 447568 | Xenbase:XB-GENE-949925 |
