Gene
myt1la
- ID
- ZDB-GENE-041001-172
- Name
- myelin transcription factor 1-like, a
- Symbol
- myt1la Nomenclature History
- Previous Names
-
- si:dkey-260n20.1
- Type
- protein_coding_gene
- Location
- Chr: 20 Mapping Details/Browsers
- Description
- Predicted to have RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to localize to nucleus. Human ortholog(s) of this gene implicated in autosomal dominant non-syndromic intellectual disability 39. Is expressed in central nervous system and retina. Orthologous to human MYT1L (myelin transcription factor 1 like).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 7 figures from 5 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:Q5TZG3
|
1257 | |||
|
UniProtKB:A0A8M3ALM3
|
1229 | |||
|
UniProtKB:A0A8M9P2M7
|
632 | |||
|
UniProtKB:A0A8M2B7M3
|
1236 |
| Type | Name | Annotation Method | Length (nt) | Analysis |
|---|---|---|---|---|
| mRNA |
myt1la-201
(1)
|
Havana | 4144 nt |
Interactions and Pathways
No data available
Plasmids
No data available