Myelin transcription factor 1 like is a protein that in humans is encoded by the MYT1L gene. [5]
Myelin transcription factor 1 like is a protein that in humans is encoded by the MYT1L gene. [5]
This gene encodes a member of the zinc finger superfamily of transcription factors whose expression, thus far, has been found only in neuronal tissues. The encoded protein belongs to a novel class of cystein-cystein-histidine-cystein zinc finger proteins that function in the developing mammalian central nervous system. Forced expression of this gene in combination with the basic helix-loop-helix transcription factor NeuroD1 and the transcription factors POU class 3 homeobox 2 and achaete-scute family basic helix-loop-helix transcription factor 1 can convert fetal and postnatal human fibroblasts into induced neuronal cells, which are able to generate action potentials. Mutations in this gene have been associated with an autosomal dominant form of cognitive disability and with autism spectrum disorder. Alternative splicing results in multiple variants. [provided by RefSeq, Jul 2017].
Forkhead box protein C2 (FOXC2) also known as forkhead-related protein FKHL14 (FKHL14), transcription factor FKH-14, or mesenchyme fork head protein 1 (MFH1) is a protein that in humans is encoded by the FOXC2 gene. FOXC2 is a member of the fork head box (FOX) family of transcription factors.
HNF1 homeobox B, also known as HNF1B or transcription factor 2 (TCF2), is a human gene.
Endothelial PAS domain-containing protein 1 is a protein that is encoded by the EPAS1 gene in mammals. It is a type of hypoxia-inducible factor, a group of transcription factors involved in the physiological response to oxygen concentration. The gene is active under hypoxic conditions. It is also important in the development of the heart, and for maintaining the catecholamine balance required for protection of the heart. Mutation often leads to neuroendocrine tumors.
Myocyte-specific enhancer factor 2A is a protein that in humans is encoded by the MEF2A gene. MEF2A is a transcription factor in the Mef2 family. In humans it is located on chromosome 15q26. Certain mutations in MEF2A cause an autosomal dominant form of coronary artery disease and myocardial infarction.
Transcription factor SOX-10 is a protein that in humans is encoded by the SOX10 gene.
MAX-interacting protein 1 is a protein that in humans is encoded by the MXI1 gene.
Activating transcription factor 5, also known as ATF5, is a protein that, in humans, is encoded by the ATF5 gene.
Forkhead box protein H1 is a protein that in humans is encoded by the FOXH1 gene.
Oligodendrocyte transcription factor 1 is a protein that in humans is encoded by the OLIG1 gene.
Myelin transcription factor 1 is a protein that in humans is encoded by the MYT1 gene.
Musculin is a protein that in humans is encoded by the MSC gene.
Forkhead box protein P4 is a protein that in humans is encoded by the FOXP4 gene.
T-cell acute lymphocytic leukemia 2, also known as TAL2, is a protein which in humans is encoded by the TAL2 gene.
Transcription factor AP-2 beta also known as AP2-beta is a protein that in humans is encoded by the TFAP2B gene.
Early growth response protein 4 (EGR-4), also known as AT133, is a protein that in humans is encoded by the EGR4 gene.
Myelin regulatory factor, also known as myelin gene regulatory factor (MRF), is a protein that in humans is encoded by the MYRF gene.
Additional sex combs like 2, transcriptional regulator is a protein that in humans is encoded by the ASXL2 gene.
Collagen triple helix repeat containing 1 is a protein that in humans is encoded by the CTHRC1 gene.
Coiled-coil-helix-coiled-coil-helix domain containing 2 is a protein that in humans is encoded by the CHCHD2 gene.
Tetraspanin 18 is a protein that in humans is encoded by the TSPAN18 gene.
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This article incorporates text from the United States National Library of Medicine, which is in the public domain.