Gene
lmnb1
- ID
- ZDB-GENE-020424-2
- Name
- lamin B1
- Symbol
- lmnb1 Nomenclature History
- Previous Names
-
- fc06g01
- wu:fc06g01 (1)
- Type
- protein_coding_gene
- Location
- Chr: 10 Mapping Details/Browsers
- Description
- Predicted to be a structural constituent of cytoskeleton. Predicted to be involved in several processes, including heterochromatin formation; nucleus organization; and protein localization to nuclear envelope. Predicted to be located in intermediate filament. Predicted to be active in nuclear envelope and nuclear lamina. Human ortholog(s) of this gene implicated in atypical autosomal dominant adult-onset demyelinating leukodystrophy; autosomal dominant primary microcephaly 26; and typical adult-onset autosomal dominant demyelinating leukodystrophy. Orthologous to human LMNB1 (lamin B1).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 2 figures from 2 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:55459 (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 |
---|---|---|---|
atypical autosomal dominant adult-onset demyelinating leukodystrophy | Alliance | Leukodystrophy, demyelinating, adult-onset, autosomal dominant, atypical | 621061 |
typical adult-onset autosomal dominant demyelinating leukodystrophy | Alliance | Leukodystrophy, demyelinating, adult-onset, autosomal dominant, typical | 169500 |
Microcephaly 26, primary, autosomal dominant | 619179 |
Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Length | Intermediate filament protein, conserved site | Intermediate filament, rod domain | Lamin tail domain | Lamin tail domain superfamily |
---|---|---|---|---|---|
UniProtKB:Q803N8
|
588 | ||||
UniProtKB:F1QHC4
|
588 |
Interactions and Pathways
No data available
Plasmids
No data available