MYT1 Chromosome 20
Myelin transcription factor 1
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What This Gene Does
The protein encoded by this gene is a member of a family of neural specific, zinc finger-containing DNA-binding proteins. The protein binds to the promoter regions of proteolipid proteins of the central nervous system and plays a role in the developing nervous system. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Zinc fingers C2H2C-type
Locus Type
gene with protein product
Location
20q13.33
Ensembl
ENSG00000196132
Associated Conditions (3)
Autism spectrum disorder
Intellectual disability
Hereditary spastic paraplegia
Key Variants
All Variants (3)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS1983951845 | Health Risk | association | Autism spectrum disorder, Autism spectrum disorder |
| RS1983540456 | Health Risk | Likely pathogenic | Intellectual disability, Intellectual disability |
| RS1983951301 | Trait | Affects | Hereditary spastic paraplegia, Hereditary spastic paraplegia |