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Protein-coding gene in the species Homo sapiens
transcription factor 1 like is a protein that in humans is encoded by the MYT1L gene. This gene encodes a member of the zinc finger superfamily of transcription
MYT1L
Abnormally strong sensation of hunger or desire to eat
conditions: Chromosome 22q13 duplication syndrome Chromosome 2p25.3 deletion (MYT1L syndrome) Chromosome Xq26.3 duplication syndrome Congenital generalized
Polyphagia
Chronic multi-symptomatic pain disorder
fibromyalgia. These include a coding variation in Huntingtin, SLC6A4, TRPV2, MYT1L, NRXN3, and the 5-HT2A receptor 102T/C polymorphism. The heritability of
Fibromyalgia
Protein-coding gene in the species Homo sapiens
expression in the mouse brain: interaction of its intracellular domain with Myt1l". Developmental Neurobiology. 68 (4): 521–541. doi:10.1002/dneu.20607. PMID 18186492
LINGO1
specific TF according to literature or domain structure – No motif [569] MYT1L ENSG00000186487 C2H2 ZF Inferred motif from similar protein – High-throughput
List of human transcription factors
List_of_human_transcription_factors
Q8NFW9 10172 MYSM1 HGNC:29401; Q5VVJ2 10173 MYT1 HGNC:7622; Q01538 10174 MYT1L HGNC:7623; Q9UL68 10175 MYZAP HGNC:43444; P0CAP1 10176 MZB1 HGNC:30125;
List of human protein-coding genes 5
List_of_human_protein-coding_genes_5
Process in developmental biology
cells. Pang et al. found that while transcription factors Ascl1, Brn2 and Myt1l turned mouse cells into mature neurons, the same set of factors only turned
Transdifferentiation
Overview of the events of 2023 in science
in human neurons and in mice tested in-use lamotrigine for recovering MYT1L-caused autism (14 Feb), phase 3 trial results (~94% efficacy against severe
January–March_2023_in_science
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