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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
leucine rich repeat, Ig-like and transmembrane domains 3
Summary
- Gene Symbol
-
- LRIT3
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Cell projection
- Congenital stationary night blindness
- Disease variant
- Disulfide bond
- Endoplasmic reticulum
- Glycoprotein
- Immunoglobulin domain
- Leucine-rich repeat
- Reference proteome
- Repeat
- Signal
- Transmembrane helix
- Vision
- Proteins
| UniProt | Protein Name |
|---|---|
| A0A0A0MR64 |
|
| Q3SXY7 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| visual perception | ||
| response to light stimulus | ||
| synaptic signaling | ||
| regulation of fibroblast growth factor receptor signaling pathway | ||
| synapse assembly involved in innervation |
| GO Term | Evidence Code | PMID |
|---|---|---|
| cell tip | ||
| perikaryon | ||
| endoplasmic reticulum membrane | ||
| dendrite | ||
| synapse |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Leucine-rich repeat
- Functional Category
-
- O: Posttranslational modification, protein turnover, chaperones
- P: Inorganic ion transport and metabolism
- T: Signal transduction mechanisms
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110864 | congenital stationary night blindness 1F |
Ortholog
| Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|---|
| 104682419 | RHIRO26432 | |||
| 105486261 | MACNE03339 | |||
| 105532397 | MANLE36891 | |||
| 105571427 | CERAT08691 | |||
| 105706296 | AOTNA12229 | |||
| 105818965 | PROCO10679 | |||
| 106829797 | EQUAS17580 | |||
| 107602592 | SINGR58582 | |||
| 108541022 | RHIBE22932 | |||
| 108706092 | Xenbase:XB-GENE-17330274 |
