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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 |
|---|---|---|
| protein localization | ||
| gene expression |
| 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 |
|---|---|---|---|---|
| 100144406 | ZFIN:ZDB-GENE-070424-130 | |||
| 100221593 | TAEGU24392 | |||
| 100391417 | CALJA28470 | |||
| 100454657 | 9601_0:001477 | PONAB27826 | ||
| 100476351 | AILME02352 | |||
| 100494489 | Xenbase:XB-GENE-6076513 | |||
| 100516451 | PIGXX34277 | |||
| 100543614 | MELGA10028 | |||
| 100589747 | NOMLE15282 | |||
| 100696521 | ORENI48388 |
