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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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Guidelines
MIRAGE
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
- Proteomics identification
- Reference proteome
- Repeat
- Signal
- Transmembrane helix
- Vision
- Proteins
| UniProt | Protein Name |
|---|---|
| Q3SXY7 |
|
| A0A0A0MR64 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| visual perception | ||
| protein localization | ||
| response to light stimulus | ||
| gene expression | ||
| regulation of fibroblast growth factor receptor signaling pathway |
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum membrane | ||
| dendrite | ||
| perikaryon | ||
| synapse | ||
| cell tip |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Leucine-rich repeat
- Functional Category
-
- K: Transcription
- O: Posttranslational modification, protein turnover, chaperones
- T: Signal transduction mechanisms
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110864 | congenital stationary night blindness 1F |
