MYT1: Myelin Transcription Factor 1

A zinc finger transcription factor involved in neurogenesis and oligodendrocyte differentiation

Gene Information Card

Symbol MYT1
Full Name Myelin Transcription Factor 1
Gene Type Protein coding
Chromosomal Location 20q13.33
NCBI Gene ID 4661 ncbi.nlm.nih.gov/gene/4661
Ensembl ID ENSG00000101247
UniProt ID Q01538
OMIM ID 600379
HGNC ID 7622
Aliases MTF1, ZC2H2C1, NZF1, ST18

Description

MYT1 (myelin transcription factor 1) encodes a zinc finger protein that acts as a transcriptional repressor. It is essential for central nervous system development, particularly in the differentiation of oligodendrocytes and the formation of myelin sheaths. MYT1 is also expressed in testis and certain neural progenitor cells. Mutations and altered expression have been implicated in neurodevelopmental disorders and cancers.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Neurodevelopmental disorder with or without seizures Loss-of-function mutations impair oligodendrocyte differentiation and neuronal migration ClinVar
Glioblastoma Overexpression of MYT1 promotes tumor cell proliferation and invasion COSMIC
Testicular germ cell tumors MYT1 expression is upregulated and associated with poor prognosis COSMIC

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 12.5 Medium
Testis 8.3 Low
Spinal cord 6.1 Low
Cerebellum 10.2 Medium
Cerebral cortex 14.7 Medium
Cell Line Expression
Cell Line nTPM Notes
SH-SY5Y (neuroblastoma) 18.4 High expression in neuronal-like cells
U87MG (glioblastoma) 22.1 Overexpressed compared to normal astrocytes
HEK293 (embryonic kidney) 3.2 Low endogenous expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1123C>T (p.Arg375Ter) Nonsense Rare Loss of function; truncation of zinc finger domain
c.1456G>A (p.Gly486Ser) Missense Unknown Likely damaging; alters DNA-binding affinity
c.1789_1791del (p.Phe597del) In-frame deletion Rare Disrupts protein stability and repressor activity
Mutation functional classification

Loss of Function (LOF)

Nonsense and frameshift mutations leading to truncated protein lacking functional zinc finger domains; associated with neurodevelopmental disorders.

Gain of Function (GOF)

Not well documented; overexpression in glioblastoma may confer oncogenic properties.

Dominant Negative (DN)

Not reported for MYT1.

Pathways

Oligodendrocyte specification and differentiation (REACT:R-HSA-9617324)
Transcriptional regulation by MYT1 (REACT:R-HSA-212436)

Protein Summary

MYT1 is a 1,123-amino acid zinc finger transcription factor containing multiple C2HC-type zinc fingers. It localizes to the nucleus and functions primarily as a transcriptional repressor. MYT1 is critical for the maturation of oligodendrocyte progenitor cells into myelinating oligodendrocytes. It also plays roles in neuronal survival and testicular development. The protein interacts with other transcription factors such as SOX10 and OLIG2 to coordinate myelin gene expression.

Related Products

Product name Cat.No. Species Gene ID
MYT1 Knockout HEK293 Cell Line EDJ-KQ2740 Human 4661 Details Get a Quote
MYT1L Knockout HEK293 Cell Line EDJ-KQ7787 Human 23040 Details Get a Quote
MYT1 Knockout A-549 Cell Line EDJ-KQ23615 Human 4661 Details Get a Quote
MYT1 Knockout HCT 116 Cell Line EDJ-KQ23616 Human 4661 Details Get a Quote
MYT1 Knockout HeLa Cell Line EDJ-KQ53957 Human 4661 Details Get a Quote
MYT1L Knockout HeLa Cell Line EDJ-KQ55679 Human 23040 Details Get a Quote
MYT1L Knockout A-549 Cell Line EDJ-KQ64178 Human 23040 Details Get a Quote
MYT1L Knockout HCT 116 Cell Line EDJ-KQ72620 Human 23040 Details Get a Quote
Displaying Records 1 To 8 Of 8 Records
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