Myt1 Gene Search Result

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7 records found for search term Myt1

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RGD ID	Symbol	Name	Description	Chr	Start	Stop	Species	Annotations	Match	Type
1312603	MYT1	myelin transcription factor 1	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]	20	64164452	64242253	Human	112	symbol , COSMIC , Human Proteome Map	gene, protein-coding, REVIEWED [RefSeq]
1603703	PKMYT1	protein kinase, membrane associated tyrosine/threonine 1	This gene encodes a member of the serine/threonine protein kinase family. The encoded protein is a membrane-associated kinase that negatively regulates the G2/M transition of the cell cycle by phosphorylating and inactivating cyclin-dependent kinase 1. The activity of the encoded protein is regulate ... (more) d by polo-like kinase 1. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012]	16	2972808	2980446	Human	162	symbol , old_gene_name , COSMIC , Human Proteome Map , old_gene_symbol	gene, protein-coding, REVIEWED [RefSeq]
731726	MYT1L	myelin transcription factor 1 like	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 cen ... (more) tral 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]	2	1789113	2331275	Human	240	symbol , COSMIC , Human Proteome Map , old_gene_symbol	gene, protein-coding, REVIEWED [RefSeq]
7378214	MYT1L-AS1	MYT1L antisense RNA 1		2	2319232	2327108	Human		symbol , COSMIC , name , Human Proteome Map	gene, ncrna, VALIDATED [RefSeq]
616940485	MYT1L-AS2	MYT1L antisense RNA 2					Human		symbol , GTEx , COSMIC , name , Human Proteome Map	gene, ncrna
16570436	AC093390.2	novel transcript, antisense to MYT1L					Human		name	gene, lncrna
16564241	AC007923.2	myelin transcription factor 1-like (MYT1L) pseudogene					Human		name	gene, processed_pseudogene