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Category Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21

GIFtS
-

MYT1L Gene

protein-coding GIFtS: 53
GCID: GC02M001763

myelin transcription factor 1-like

Explore 7 diseases affiliated with
MYT1L via

MalaCards

our new
Human Malady Compendium

(According to ¹HGNC, ²Entrez Gene,
³UniProtKB/Swiss-Prot, ⁴UniProtKB/TrEMBL, ⁵OMIM, ⁶GeneLoc, ⁷Ensembl, ⁸DME, ⁹miRBase, and/or ¹⁰fRNAdb)
About This Section

Aliases
Myelin Transcription Factor 1-Like¹ ²		Myelin Transcription Factor 1-Like Protein²
KIAA1106¹ ³ ⁵		Neural Zinc Finger Transcription Factor 1²
NZF1¹ ²		MyT1-L³
ZC2HC4B¹ ²		MyT1L³
MyT1-L³

External Ids:	HGNC: 7623¹	Entrez Gene: 23040²	Ensembl: ENSG00000186487⁷	OMIM: 613084⁵	UniProtKB: Q9UL68³

Export aliases for MYT1L gene to outside databases

Previous GC identifers: GC02P002305 GC02P002420 GC02P002327

(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

UniProtKB/Swiss-Prot: MYT1L_HUMAN, Q9UL68

Function: May function as a panneural transcription factor associated with neuronal differentiation. May play a role in

the development of neurons and oligodendrogalia in the CNS (By similarity)

(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section

RefSeq DNA sequence:

NC_000002.11 NC_018913.1 NT_022221.13

Regulatory elements:

SABiosciences Regulatory transcription factor binding sites in the MYT1L gene promoter:
Pax-6 Tal-1beta E4BP4 E47 GATA-1 MEF-2A POU2F1 POU2F1a TFIID aMEF-2
Other transcription factors

SwitchGear Promoter luciferase reporter plasmid: MYT1L promoter sequence

Search SABiosciences Chromatin IP Primers for MYT1L

Epigenetics:

QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat MYT1L

Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: 2p25.3 Ensembl cytogenetic band: 2p25.3 HGNC cytogenetic band: 2p25.3

MYT1L Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
MYT1L gene location

GeneLoc information about chromosome 2 GeneLoc Exon Structure

GeneLoc location for GC02M001763: view genomic region (about GC identifiers)

Start:	1,792,885 bp from pter	End:	2,335,045 bp from pter
Size:	542,161 bases	Orientation:	minus strand

(According to ¹UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to ²PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section

UniProtKB/Swiss-Prot: MYT1L_HUMAN, Q9UL68 (See protein sequence)

Recommended Name: Myelin transcription factor 1-like protein

Size: 1186 amino acids; 133043 Da

Subcellular location: Nucleus (By similarity)

Sequence caution: Sequence=AAF14051.1; Type=Frameshift; Positions=1185; Sequence=BAA83058.2; Type=Erroneous initiation;

Note=Translation N-terminally shortened;

Secondary accessions: A7E2C7 B2RP54 Q6IQ17 Q9UPP6

Alternative splicing: 4 isoforms: Q9UL68-1 Q9UL68-2 Q9UL68-3 Q9UL68-4 (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for MYT1L: NX_Q9UL68

Post-translational modifications:

View modification sites using PhosphoSitePlus²

View neXtProt modification sites for NX_Q9UL68

MYT1L Protein expression data from MOPED and PaxDb: About this image

REFSEQ proteins: NP_055840.2

ENSEMBL proteins:

ENSP00000382114 ENSP00000384219 ENSP00000382111 ENSP00000396103

Human Recombinant Protein Products:

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	Uscn Proteins for MYT1L

Gene Ontology (GO): 1 cellular component term (GO ID links to tree view): About this table

GO ID	Qualified GO term	Evidence	PubMed IDs
GO:0005634	nucleus	ISS	--

MYT1L for ontologies About GeneDecksing

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Assay Products for MYT1L:

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	Uscn ELISAs and CLIAs for MYT1L

(According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
About This Section

MYT1L for domains About GeneDecksing

2 InterPro domains/families:

IPR002515 Znf_C2HC

IPR013681 Myelin_TF

Graphical View of Domain Structure for InterPro Entry Q9UL68

ProtoNet protein and cluster: Q9UL68

1 Blocks protein family: IPB013681 Myelin transcription factor 1

UniProtKB/Swiss-Prot: MYT1L_HUMAN, Q9UL68

Similarity: Contains 6 C2HC-type zinc fingers

(According to ¹UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or ²DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013,
bound targets from SABiosciences, miRNA Gene Targets from miRTarBase shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
About This Section

Function Summary:

UniProtKB/Swiss-Prot: MYT1L_HUMAN, Q9UL68

Function: May function as a panneural transcription factor associated with neuronal differentiation. May play a role in

the development of neurons and oligodendrogalia in the CNS (By similarity)

miRNA Products:		OriGene 3'-UTR Clone: MYT1L Browse MicroRNA Expression Plasmids
		QIAGEN Custom miScript Target Protector blocks miRNA-binding site of human, mouse, rat MYT1L
		8/188 QIAGEN miScript miRNA Assays for microRNAs that regulate MYT1L (see all 188):
		hsa-miR-576-3p hsa-miR-100* hsa-miR-361-5p hsa-miR-106a hsa-miR-605 hsa-miR-519a hsa-miR-877* hsa-miR-1273d

		SwitchGear 3'UTR luciferase reporter plasmid: MYT1L 3' UTR sequence

Inhib. RNA Products:		Browse for Gene Knock-down Tools from EMD Millipore
		OriGene 29mer shRNA kits in GFP-retroviral vector in human, mouse, rat for MYT1L (see all 7) OriGene shRNA RFP: MYT1L OriGene siRNA: MYT1L
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Gene Editing
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DNA2.0 Custom Protein Engineering Service for MYT1L

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		Search LifeMap BioReagents cell lines for MYT1L

In Situ Assay
Products:

Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for MYT1L

Gene Ontology (GO): 5 molecular function terms (GO ID links to tree view): About this table

GO ID	Qualified GO term	Evidence	PubMed IDs
GO:0003677	DNA binding	IEA	--
GO:0003700	sequence-specific DNA binding transcription factor activity	IEA	--
GO:0005515	protein binding	--	--
GO:0008270	zinc ion binding	IEA	--
GO:0016563	transcription activator activity	--	--

MYT1L for ontologies About GeneDecksing

1 GenomeRNAi human phenotype for MYT1L:

Decreased influenza A/WSN/33 r

(Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to ¹UniProtKB, ²MINT, ³I2D, and/or ⁴STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene).
About This Section

Interactions:

Search SABiosciences Gene Network Central^TM Interacting Genes and Proteins Networks for MYT1L

STRING Interaction Network Preview (showing 5 interactants - click image to see more details)

5/7 Interacting proteins for MYT1L (Q9UL68³ ENSP00000396103⁴) via UniProtKB, MINT, STRING, and/or I2D (see all 7)

Interactant		Interaction Details
GeneCard	External ID(s)	Interaction Details
DISC1	Q9NRI5³, ENSP00000355596⁴	I2D: score=2 STRING: ENSP00000355596
CDC5L	Q99459³, ENSP00000360532⁴	I2D: score=2 STRING: ENSP00000360532
TNIK	Q9UKE5³, ENSP00000399511⁴	I2D: score=1 STRING: ENSP00000399511
NR4A1	P22736³	I2D: score=1
PCBD1	P61457³	I2D: score=1

About this table

Gene Ontology (GO): 3 biological process terms (GO ID links to tree view): About this table

GO ID	Qualified GO term	Evidence	PubMed IDs
GO:0006351	transcription, DNA-dependent	IEA	--
GO:0007399	nervous system development	IEA	--
GO:0030154	cell differentiation	IEA	--

MYT1L for ontologies About GeneDecksing

(Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
About This Section

Browse Small Molecules at EMD Millipore

Browse drugs & compounds from Enzo Life Sciences

Browse Tocris compounds for MYT1L
Search CenterWatch for drugs/clinical trials and news about MYT1L

(Secondary structures according to fRNAdb,
GenBank/EMBL/DDBJ Accessions according to
Unigene (Build 235 Homo sapiens; Mar 10 2013) or GenBank,
RefSeq according to Entrez Gene,
DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
RNAi Products from EMD Millipore,
siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, SABiosciences, and/or QIAGEN )
About This Section

REFSEQ mRNAs for MYT1L gene:

NM_015025.2

Unigene Clusters for MYT1L:

Myelin transcription factor 1-like

Hs.434418 [show with all ESTs], Hs.669852 [show with all ESTs]

Unigene Representative Sequences: NM_015025, BC043230

12 Ensembl transcripts including schematic representations, and UCSC links where relevant:

ENST00000399161(uc010ewl.2 uc002qxd.3 uc002qxe.3) ENST00000407844(uc010ewk.3)

ENST00000399157 ENST00000428368(uc002qxf.1) ENST00000471668 ENST00000470954

ENST00000490585 ENST00000485547 ENST00000485348 ENST00000479156 ENST00000476547

ENST00000460585

miRNA Products:		OriGene 3'-UTR Clone: MYT1L Browse OriGene MicroRNA Expression Plasmids
		QIAGEN Custom miScript Target Protector blocks miRNA-binding site of human, mouse, rat MYT1L
		8/188 QIAGEN miScript miRNA Assays for microRNAs that regulate MYT1L (see all 188):
		hsa-miR-576-3p hsa-miR-100* hsa-miR-361-5p hsa-miR-106a hsa-miR-605 hsa-miR-519a hsa-miR-877* hsa-miR-1273d

		SwitchGear 3'UTR luciferase reporter plasmid: MYT1L 3' UTR sequence

Inhib. RNA Products:		Browse for Gene Knock-down Tools from EMD Millipore
		OriGene 29mer shRNA kits in GFP-retroviral vector in human, mouse, rat for MYT1L (see all 7) OriGene shRNA RFP: MYT1L OriGene siRNA: MYT1L
		QIAGEN FlexiTube/FlexiPlate siRNA for gene silencing in human, mouse, rat MYT1L

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		GenScript: all cDNA clones in your preferred vector: MYT1L (NM_015025)
		DNA2.0 Custom Codon Optimized Gene Synthesis Service for MYT1L
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Additional cDNA sequence: BC043230.1

11 DOTS entries:

DT.95263373 DT.100669960 DT.113247 DT.75140045 DT.120938384 DT.120938427 DT.423323 DT.95085604

DT.65286674 DT.97814501 DT.409114

24/88 AceView cDNA sequences (see all 88):

AW207596 AA935924 BC031690 AI696518 BX645114 BM662061 Z41381 BE217813

AW419345 BF223003 F08380 BM312185 BF110887 AB029029 AW450432 BM701291

BM678566 BE218864 F04633 Z45757 CK825025 AW510843 AW952686 AI280086

GeneLoc Exon Structure

5/7 Alternative Splicing Database (ASD) splice patterns (SP) for MYT1L (see all 7) About this scheme

ExUns:	1a	·	1b	^	2	^	3	^	4	^	5	^	6	^	7	^	8a	·	8b	^	9	^	10a	·	10b	^	11	^	12a	·	12b	·	12c	^	13	^	14	^	15	^	16	^	17	^	18	^	19	^	20a	·	20b	^
SP1:																																	-										-				-
SP2:																															-		-
SP3:
SP4:					-		-
SP5:

ExUns:	21	^	22	^	23a	·	23b	^	24	^	25a	·	25b
SP1:
SP2:
SP3:
SP4:
SP5:

ECgene alternative splicing isoforms for MYT1L

(RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
About This Section

MYT1L expression in normal human tissues (normalized intensities)
See probesets specificity/sensitivity at GeneAnnot
About this imageBioGPS
CGAP TAG: CTGGATGTTA

About this image

MYT1L expression in embryonic tissues and stem cells

Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine About this table

2 LifeMap In Vivo Development Anatomical Compartments/Cells

Tissue

Anatomical Compartment

Cell

Category (developmental path)

Brain

Blood Brain Barrier

Endothelial Cells

Blood Brain Barrier, Endothelium

Eye

Inner Nuclear Layer

nGnG Amacrine Cells

Amacrine, Retina

Expression:

Positive

Negative

Selective marker

Experimental details:

Curated

Microarrays

In-situ hybridization

See MYT1L Protein Expression from SPIRE MOPED and PaxDB
Genevestigator expression for MYT1L

SOURCE GeneReport for Unigene clusters: Hs.434418 Hs.669852

SABiosciences Custom PCR Arrays for MYT1L

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In Situ
Assay Products:

Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for MYT1L

(Orthologs according to ^1,2HomoloGene (²older version, for species not in ¹newer version), ³euGenes, ⁴SGD , ⁵MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or ⁶Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
About This Section

This gene was present in the common ancestor of eukaryotes.

Orthologs for MYT1L gene from 6/19 species (see all 19) About this table

Organism	Taxonomic classification	Gene	Description	Human Similarity	Orthology Type	Details
chicken (Gallus gallus)	Aves	MYT1L¹	myelin transcription factor 1-like	84.4(n) 94.08(a)		421915 XM_419932.3 XP_419932.3
lizard (Anolis carolinensis)	Reptilia	MYT1L⁶	--	89(a)	1 ↔ 1	1(161470128-161640843)
zebrafish (Danio rerio)	Actinopterygii	myt1la¹	myelin transcription factor 1-like, a	71.24(n) 73.26(a)		559505 NM_001044899.2 NP_001038364.1
fruit fly (Drosophila melanogaster)	Insecta	CG43689⁶	--	12(a)	1 → many	X(3970107-3986186)
worm (Caenorhabditis elegans)	Secernentea	ztf-11⁶	Zinc finger Transcription Factor family member (zt...	23(a)	1 → many	I(9904294-9910536)
wheat (Triticum aestivum)	Liliopsida	Ta.6362²	Triticum aestivum transcribed sequence with weak similarity more	72.07(n)		CD903123.1

ENSEMBL Gene Tree for MYT1L (if available)
TreeFam Gene Tree for MYT1L (if available)

(Paralogs according to ¹HomoloGene,
²Ensembl, and ³SIMAP, Pseudogenes according to ⁴Pseudogene.org Build 68)
About This Section

Paralogs for MYT1L gene

ST18² MYT1²

3 SIMAP similar genes for MYT1L using alignment to 3 protein entries: MYT1L_HUMAN (see all proteins):

MYT1 L3MBTL1 ST18

MYT1L for paralogs About GeneDecksing

1 Pseudogenes.org Pseudogene for MYT1L
PGOHUM00000237356

(SNPs/Variants according to the ¹NCBI SNP Database, ²Ensembl, ³PupaSUITE, UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
About This Section

SNP ID	Valid	Clinical significance	Chr 2 pos	Sequence	#	AA Chg	Type	More	#	Allele freq	Pop	Total sample	More
Genomic Data					Transcription Related Data				Allele Frequencies
				--	--	--		--	--
rs189905096^1,2	C,	unknown	2304433(+)	`CCATGC/G/TGCATT`	1	--	int¹		0	--	--	--	--
rs141704507^1,2		--	1792390(+)	`GTCTGC/TTCAGT`	1	--	int¹		0	--	--	--	--
rs10175467^1,2	C,A,	--	1792451(-)	`GGCGCG/ACTGCT`	1	--	int¹		4		NA CSA	125
rs111858086^1,2		--	1792492(+)	`ACAAAG/AGACGT`	1	--	int¹		1		CSA	2
rs10209349^1,2	C,A,	--	1792612(-)	`CTCCCG/AGCACA`	1	--	int¹		3		NA CSA	5
rs75240715^1,2		--	1792631(+)	`TCCTCC/TGTCCA`	1	--	int¹		1		WA	118
rs75566399^1,2	F,	--	1792632(+)	`CCTCCG/ATCCAG`	1	--	int¹		1		WA	118
rs149633997^1,2		--	1792755(+)	`TTCTAC/TATGCC`	1	--	int¹		0	--	--	--	--
rs2161970^1,2	H	--	1792950(-)	`TGCTGG/CATGTT`	1	--	ut3¹		4		NS EA	420
rs79054023^1,2		--	1793211(+)	`ATCCAC/TATGAA`	1	--	ut3¹		0	--	--	--	--

HapMap Linkage Disequilibrium report for MYT1L (1792885 - 2042885 bp, first 250kb of MYT1L)
Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
Database of Genomic Variants (DGV): 25 variations for MYT1L
15/16 CNVs (see all 16): 89411 72299 7247 89408 78367 78369 66850 97741 97740 3342 78370 78365 89410 72290 72300
9 Indels: 78368 45927 26536 89413 33329 78366 89412 89409 26535
Human Gene Mutation Database (HGMD): MYT1L

SABiosciences Cancer Mutation PCR Assays

QIAGEN SeqTarget long-range PCR primers in human, mouse, rat for resequencing MYT1L

DNA2.0 Custom Variant and Variant Library Synthesis for MYT1L

(in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
About This Section

MYT1L for disorders           About GeneDecksing

OMIM gene information: 613084    OMIM disorders: --

7 diseases for MYT1L:    About MalaCards

major depressive disorder intellectual disability diffuse astrocytoma adhd

astrocytoma schizophrenia neuronitis

1 disease from the University of Copenhagen DISEASES database for MYT1L:

Schizophrenia

Human Genome Epidemiology (HuGE) Navigator: MYT1L (4 documents)

Export disorders for MYT1L gene to outside databases

(in PubMed. Associations of this gene to articles via ¹Entrez Gene, ²UniProtKB/Swiss-Prot, ³HGNC, ⁴GAD, ⁵PharmGKB, ⁶HMDB, ⁷DrugBank, ⁸UniProtKB/TrEMBL, ⁹ Novoseek, and/or ¹⁰fRNAdb)
About This Section

PubMed articles for MYT1L gene, integrated from 9 sources (see all 18):
(articles sorted by number of sources associating them with MYT1L)

Utopia: connect your pdf to the dynamic
world of online information

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)^{1, 2} Gerhard D.S....Malek J. (2004)
Construction of expression-ready cDNA clones for KIAA genes: manual curation of 330 KIAA cDNA clones. (PubMed id 12168954)^{1, 2} Nakajima D.... Nagase T. (2002)
Prediction of the coding sequences of unidentified human genes. XIV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. (PubMed id 10470851)^{1, 2} Kikuno R....Ohara O. (1999)
Myelin transcription factor 1 (Myt1) of the oligodendrocyte lineage, along with a closely related CCHC zinc finger, is expressed in developing neurons in the mammalian central nervous system. (PubMed id 9373037)^{1, 3} Kim J.G....Hudson L.D. (1997)
Germline mosaic transmission of a novel duplication of PXDN and MYT1L to two male half-siblings with autism. (PubMed id 22157634)¹ Meyer K.J....Wassink T.H. (2012)
Association study of myelin transcription factor 1-lik e polymorphisms with schizophrenia in Han Chinese population. (PubMed id 21923761)¹ Li W....Lv L.X. (2012)
Microduplications disrupting the MYT1L gene (2p25.3) a re associated with schizophrenia. (PubMed id 22547139)¹ Lee Y....Addington A.M. (2012)
MYT1L is a candidate gene for intellectual disability in patients with 2p25.3 (2pter) deletions. (PubMed id 21990140)¹ Stevens S.J....Engelen J.J. (2011)
Genome-wide meta-analysis for severe diabetic retinop athy. (PubMed id 21441570)¹ Grassi M.A....Nicolae D.L. (2011)
Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. (PubMed id 20379614)¹ Rose J.E....Uhl G.R. (2010)

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(According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
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Entrez Gene: 23040	HGNC: 7623	AceView: MYT1L	Ensembl:ENSG00000186487	euGenes: HUgn23040
ECgene: MYT1L	H-InvDB: MYT1L

(According to HUGE)
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HUGE: KIAA1106

(According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
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Name	Description
PharmGKB entry for MYT1L	Pharmacogenomics, SNPs, Pathways

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myelin transcription factor 1-like

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myelin transcription factor 1-like

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