Gene
lins1
- ID
- ZDB-GENE-101019-1
- Name
- lines homolog 1
- Symbol
- lins1 Nomenclature History
- Previous Names
-
- lins
- Type
- protein_coding_gene
- Location
- Chr: 7 Mapping Details/Browsers
- Description
- Human ortholog(s) of this gene implicated in autosomal recessive non-syndromic intellectual disability. Orthologous to human LINS1 (lines homolog 1).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- No data available
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
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 |
|---|---|---|---|
| autosomal recessive intellectual developmental disorder 27 | Alliance | Intellectual developmental disorder, autosomal recessive 27 | 614340 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Protein Lines | Protein Lines, C-terminal | Protein Lines, N-terminal |
|---|---|---|---|---|
|
UniProtKB:A0A8M9QHG2
|
603 | |||
|
UniProtKB:A0A8M9QCF7
|
351 | |||
|
UniProtKB:F1QRU0
|
604 | |||
|
UniProtKB:A0A8M9PPE3
|
309 |
Interactions and Pathways
No data available
Plasmids
No data available
- Comparative Orthology
- Alliance