Gene
lrit3b
- ID
- ZDB-GENE-070424-130
- Name
- leucine-rich repeat, immunoglobulin-like and transmembrane domains 3b
- Symbol
- lrit3b Nomenclature History
- Previous Names
-
- lrit3
- si:ch211-146m5.3
- Type
- protein_coding_gene
- Location
- Chr: 13 Mapping Details/Browsers
- Description
- Human ortholog(s) of this gene implicated in congenital stationary night blindness 1F. Orthologous to human LRIT3 (leucine rich repeat, Ig-like and transmembrane domains 3).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Thisse et al., 2008
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- cssl:d0659 (1 image)
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| congenital stationary night blindness 1F | Alliance | Night blindness, congenital stationary (complete), 1F, autosomal recessive | 615058 |
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
No data available
| Type | Name | Annotation Method | Length (nt) | Analysis |
|---|---|---|---|---|
| mRNA |
lrit3b-201
(1)
|
Havana | 1317 nt |
Interactions and Pathways
No data available
Plasmids
No data available