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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
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- kinase
- Functional Category
-
- O: Posttranslational modification, protein turnover, chaperones
- P: Inorganic ion transport and metabolism
- T: Signal transduction mechanisms
| InterPro |
|---|
| Leucine-rich repeat domain superfamily |
| Leucine-rich repeat, typical subtype |
| Leucine-rich repeat |
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 | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|---|
| 181983 | WB:WBGene00020693 | |||
| 236690 | MGI:2448607 | MOUSE66532 | ||
| 302516 | RGD:1561300 | RATNO44481 | ||
| 447568 | Xenbase:XB-GENE-949925 | |||
| 473571 | 9598_0:0058b0 | PANTR45808 | ||
| 568821 | ZFIN:ZDB-GENE-061026-3 | DANRE44600 | ||
| 700641 | MACMU48451 | |||
| 100230787 | TAEGU11926 | |||
| 100343596 | RABIT13427 | |||
| 100396889 | CALJA48311 |
