Gene
myt1lb
- ID
- ZDB-GENE-100806-2
- Name
- myelin transcription factor 1-like, b
- Symbol
- myt1lb Nomenclature History
- Previous Names
- None
- Type
- protein_coding_gene
- Location
- Chr: 17 Mapping Details/Browsers
- Description
- Human ortholog(s) of this gene implicated in autosomal dominant non-syndromic intellectual disability 39. Is expressed in nervous system and testis. Orthologous to human MYT1L (myelin transcription factor 1 like).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 4 figures from 2 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 1 Figure from Blanchet et al., 2017
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| autosomal dominant intellectual developmental disorder 39 | Alliance | Intellectual developmental disorder, autosomal dominant 39 | 616521 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Myelin transcription factor 1 | Zinc finger, C2H2C-type | Zinc finger, C2H2C-type superfamily |
|---|---|---|---|---|
|
UniProtKB:A0A8M9PKZ2
|
1136 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available
- Comparative Orthology
- Alliance