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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

METTL11B Gene

protein-coding   GIFtS: 35
GCID: GC01P170115

methyltransferase like 11B

(Previous name: chromosome 1 open reading frame 184 )
(Previous symbol: C1orf184)
 Explore 2 diseases affiliated with
METTL11B via our new
 Human Malady Compendium 
Biological research products
for METTL11B
    

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

Aliases
Methyltransferase Like 11B1 2     X-Pro-Lys N-Terminal Protein Methyltransferase 1B2 3
C1orf1841 2 3     Chromosome 1 Open Reading Frame 1841
HOMT1B1 2     Alpha N-Terminal Protein Methyltransferase 1B2
Methyltransferase-Like Protein 11B2 3     EC 2.1.1.2443
NTM1B2 3     

External Ids:    HGNC: 319321   Entrez Gene: 1492812   Ensembl: ENSG000002037407   UniProtKB: Q5VVY13   

Export aliases for METTL11B gene to outside databases

Previous GC identifers: GC01P168382 GC01P141338


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

UniProtKB/Swiss-Prot: NTM1B_HUMAN, Q5VVY1
Function: Alpha-N-methyltransferase that methylates the N-terminus of target proteins containing the N-terminal motif
[Ala/Pro/Ser]-Pro-Lys when the initiator Met is cleaved. Specifically catalyzes mono-, di- or tri-methylation of
exposed alpha-amino group of Ala or Ser residue in the [Ala/Ser]-Pro-Lys motif and mono- or di-methylation of Pro in
the Pro-Pro-Lys motif (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_000001.10  NC_018912.1  NT_004487.19  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the METTL11B gene promoter:
         GCNF   Pax-2   Pax-2a   HNF-1A   Gfi-1   MEF-2A   GCNF-1   HNF-1   aMEF-2   Pax-4a   
         Other transcription factors

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Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat METTL11B


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

Entrez Gene cytogenetic band: 1q24.2   Ensembl cytogenetic band:  1q24.2   HGNC cytogenetic band: 1q24.2

METTL11B Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
METTL11B gene location

GeneLoc information about chromosome 1         GeneLoc Exon Structure

GeneLoc location for GC01P170115:  view genomic region     (about GC identifiers)

Start:
170,115,142 bp from pter      End:
170,136,931 bp from pter
Size:
21,790 bases      Orientation:
plus 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: NTM1B_HUMAN, Q5VVY1 (See protein sequence)
Recommended Name: Alpha N-terminal protein methyltransferase 1B  
Size: 283 amino acids; 32400 Da
Sequence caution: Sequence=CAH72139.1; Type=Erroneous gene model prediction;
Secondary accessions: B2RXI0

Explore the universe of human proteins at neXtProt for METTL11B: NX_Q5VVY1

METTL11B Protein expression data from MOPED and PaxDb:    About this image 

Estimated protein expression log10 (pmol).

REFSEQ proteins: NP_001129579.1  
ENSEMBL proteins: 
 ENSP00000408058  

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

METTL11B for domains           About GeneDecksing

1 InterPro domain/family:
 IPR008576 DUF858_MeTrfase_lik

Graphical View of Domain Structure for InterPro Entry Q5VVY1

ProtoNet protein and cluster: Q5VVY1

UniProtKB/Swiss-Prot: NTM1B_HUMAN, Q5VVY1
Similarity: Belongs to the methyltransferase superfamily. NTM1 family


(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: NTM1B_HUMAN, Q5VVY1
Function: Alpha-N-methyltransferase that methylates the N-terminus of target proteins containing the N-terminal motif
[Ala/Pro/Ser]-Pro-Lys when the initiator Met is cleaved. Specifically catalyzes mono-, di- or tri-methylation of
exposed alpha-amino group of Ala or Ser residue in the [Ala/Ser]-Pro-Lys motif and mono- or di-methylation of Pro in
the Pro-Pro-Lys motif (By similarity)
Catalytic activity: 3 S-adenosyl-L-methionine + N-terminal-(A,S)PK-[protein] = 3 S-adenosyl-L-homocysteine +
N-terminal-N,N,N-trimethyl-N-(A,S)PK-[protein]
Catalytic activity: 2 S-adenosyl-L-methionine + N-terminal-PPK-[protein] = 2 S-adenosyl-L-homocysteine +
N-terminal-N,N-dimethyl-N-PPK-[protein]

Enzyme Number (IUBMB): EC 2.1.1.2441

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

GO IDQualified GO termEvidencePubMed IDs
GO:0008168methyltransferase activity IEA--


METTL11B for ontologies           About GeneDecksing


1 GenomeRNAi human phenotype for METTL11B:
 Increased circadian period len 


(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 CentralTM Interacting Genes and Proteins Networks for METTL11B

(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 METTL11B
Search CenterWatch for drugs/clinical trials and news about METTL11B / NTM1B 

(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,
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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 METTL11B gene: 
NM_001136107.1  

Unigene Cluster for METTL11B:

Methyltransferase like 11B
Hs.553612
Unigene Representative Sequence: BC171858
2 Ensembl transcripts including schematic representations, and UCSC links where relevant:
ENST00000439373(uc009wvv.1) ENST00000367764

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Additional cDNA sequence: 

BC157860.1 BC171858.1 

GeneLoc Exon Structure


(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

METTL11B expression in normal human tissues (normalized intensities)
See probesets specificity/sensitivity at GeneAnnot
About this imageBioGPS
CGAP TAG: GACATCCTCC

Microarray
RNAseq (Illumina Body Map)
(100×FPKM)½
SAGE (Serial Analysis of Gene Expression)

About this image

METTL11B expression in embryonic tissues and stem cells
Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
1 LifeMap In Vivo Development Anatomical Compartment/Cell 
Tissue Anatomical Compartment CellCategory (developmental path)
BoneMaxillary ProcessBone
Expression: Positive    Negative     Selective marker
Experimental details: Curated     Microarrays     In-situ hybridization

See METTL11B Protein Expression from SPIRE MOPED and PaxDB
SOURCE GeneReport for Unigene cluster: Hs.553612
    SABiosciences Custom PCR Arrays for METTL11B
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In Situ
Assay Products:
 

 
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(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 METTL11B gene from 7/23 species (see all 23)    About this table
Organism Taxonomic
classification
Gene Description Human
Similarity
Orthology
Type
Details
chicken
(Gallus gallus)
Aves METTL11B1 methyltransferase like 11B 76.05(n)
76.53(a)
  429066  XM_426622.3  XP_426622.3 
lizard
(Anolis carolinensis)
Reptilia METTL11B6
--
75(a)
1 ↔ 1
GL343300.1(1489838-1503641)
zebrafish
(Danio rerio)
Actinopterygii mettl11b1 methyltransferase like 11B 63.77(n)
61.96(a)
  568419  NM_001202453.1  NP_001189382.1 
fruit fly
(Drosophila melanogaster)
Insecta Ntmt6
N-terminal methyltransferase
32(a)
1 → many
2R(5753137-5754189)
worm
(Caenorhabditis elegans)
Secernentea Y74C9A.36
Alpha N-terminal protein methyltransferase 1
38(a)
1 → many
I(4119-10232)
thale cress
(Arabidopsis thaliana)
eudicotyledons AT5G444506
methyltransferase
24(a)
1 → many
5(17914023-17916019)
rice
(Oryza sativa)
Liliopsida --
ad-003, putative, expressed
23(a)
1 → many
3(32372797-32376692)


ENSEMBL Gene Tree for METTL11B (if available)
TreeFam Gene Tree for METTL11B (if available) 

(Paralogs according to 1HomoloGene,
2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
About This Section
Paralogs for METTL11B gene
NTMT12  
1 SIMAP similar gene for METTL11B using alignment to 1 protein entry:     NTM1B_HUMAN:
NTMT1

METTL11B for paralogs           About GeneDecksing



(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

10/364 NCBI SNPs in METTL11B are shown (see all 364    About this table
Genomic DataTranscription Related DataAllele Frequencies
SNP IDValidClinical
significance
Chr 1 posSequence#AA
Chg
TypeMore#Allele
freq
PopTotal
sample
More
----------
rs1471354321,2
--170113191(+) TCACTG/TACACT 1 -- us2k10--------
rs784690491,2
C,--170113205(+) GTTAGT/AGGATT 1 -- us2k12Minor allele frequency- A:0.05NA 122
rs1850622651,2
--170113324(+) AGTGAC/GAGAAA 1 -- us2k10--------
rs1386892281,2
--170113409(+) TTCAGC/TGGTGA 1 -- us2k10--------
rs1440903611,2
--170113634(+) GGGGAC/TAAGTG 1 -- us2k10--------
rs1893382761,2
--170113736(+) CCCTCA/CCTAGA 1 -- us2k10--------
rs800363201,2
C,--170113740(+) CACTAG/AACATG 1 -- us2k13Minor allele frequency- A:0.05WA NA 240
rs1443921721,2
--170113754(+) TCTGCA/CAGCAC 1 -- us2k10--------
rs1487618411,2
--170113994(+) TTTTCA/CTGTTA 1 -- us2k10--------
rs1508863601,2
--170114030(+) GTCATG/TGTCCC 1 -- us2k10--------

HapMap Linkage Disequilibrium report for METTL11B (170115142 - 170136931 bp)
Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
      Database of Genomic Variants (DGV) variations for METTL11B: --

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(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

METTL11B for disorders           About GeneDecksing

2 diseases for METTL11B:    About MalaCards
homocysteine    neuronitis


Export disorders for METTL11B 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 METTL11B gene integrated from 9 sources:
(articles sorted by number of sources associating them with METTL11B)
    Utopia: connect your pdf to the dynamic
world of online information

  1. The DNA sequence and biological annotation of human chromosome 1. (PubMed id 16710414)1, 2 Gregory S.G.... Bentley D.R. (2006)
  2. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)2 Gerhard D.S....Malek J. (2004)
  3. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. (PubMed id 12477932)1 Strausberg R.L....Marra M.A. (2002)

(in PubMed, OMIM, and NCBI Bookshelf)
About This Section
 ANDOR
Aliases
Free Text  

  Query String
PubMed
OMIM
NCBI Bookshelf
  (Note: In FireFox, select the above section and copy using Ctrl-C)

(According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
About This Section
Entrez Gene: 149281 HGNC: 31932 Ensembl:ENSG00000203740 euGenes: HUgn149281 ECgene: METTL11B
H-InvDB: METTL11B

(According to HUGE)
About This Section
  --

(According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
About This Section
NameDescription
PharmGKB entry for METTL11B Pharmacogenomics, SNPs, Pathways

(Patent information from GeneIP,
Licensable technologies from WIS Yeda, Salk, Tufts,
IP news from LifeMap Sciences, Inc.)
About This Section
Patent Information for METTL11B gene:
Search GeneIP for patents involving METTL11B

GeneCards and IP:
Japan Patent Office Licenses GeneCards     European Patent Office Licenses GeneCards     Improving the IP Search



(Antibodies, recombinant proteins, and assays from EMD Millipore, R&D Systems, OriGene, QIAGEN, GenScript, Cell Signaling Technology, SABiosciences, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Uscn, Thermo Fisher Scientific, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript and LifeMap BioReagents, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or Enzo Life Sciences),
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About This Section

 
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GeneCards Homepage - Last full update: 19 Mar 2013 - Incrementals: 21 Mar 2013 , 15 Apr 2013 , 26 Apr 2013

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VWF
(GIFTS: 73)
von Willebrand factor
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