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

MYH10 Gene

protein-coding   GIFtS: 65
GCID: GC17M008318

myosin, heavy chain 10, non-muscle

(Previous names: myosin, heavy polypeptide 10, non-muscle )
 Explore 15 diseases affiliated with
MYH10 via our new
 Human Malady Compendium 
Biological research products
for MYH10
    

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

Aliases
Myosin, Heavy Chain 10, Non-Muscle1 2     Nonmuscle Myosin II Heavy Chain-B2
NMMHCB1 2     NMMHC-B3
Myosin, Heavy Polypeptide 10, Non-Muscle1 2     Myosin Heavy Chain 103
Cellular Myosin Heavy Chain, Type B2 3     Myosin Heavy Chain, Non-Muscle IIb3
NMMHC-IIB2 3     NMMHC II-B3
Myosin Heavy Chain, Nonmuscle Type B2     Non-Muscle Myosin Heavy Chain B3
Myosin-101     Non-Muscle Myosin Heavy Chain IIb3
Nonmuscle Myosin Heavy Chain IIB2     

External Ids:    HGNC: 75681   Entrez Gene: 46282   Ensembl: ENSG000001330267   OMIM: 1607765   UniProtKB: P355803   

Export aliases for MYH10 gene to outside databases

Previous GC identifers: GC17M008754 GC17M009471 GC17M008320 GC17M008579 GC17M008580


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

Entrez Gene summary for MYH10:
This gene encodes a member of the myosin superfamily. The protein represents a conventional non-muscle myosin; it
should not be confused with the unconventional myosin-10 (MYO10). Myosins are actin-dependent motor proteins with
diverse functions including regulation of cytokinesis, cell motility, and cell polarity. Mutations in this gene have
been associated with May-Hegglin anomaly and developmental defects in brain and heart. Multiple transcript variants
encoding different isoforms have been found for this gene. (provided by RefSeq, Dec 2011)

UniProtKB/Swiss-Prot: MYH10_HUMAN, P35580
Function: Cellular myosin that appears to play a role in cytokinesis, cell shape, and specialized functions such as
secretion and capping. Involved with LARP6 in the stabilization of type I collagen mRNAs for CO1A1 and CO1A2

summary for MYH10:
Myosins are a large family of motor proteins that share the common features of ATP hydrolysis, actin binding
and potential for kinetic energy transduction. Originally isolated from muscle cells (hence the name),
almost all eukaryotic cells are now known to contain myosins. Structurally, mysoins contain a head domain
that binds to actin filaments (microfilaments) and is the site of ATP hydrolysis. The tail domain interacts
with cargo molecules, and the neck acts as a linker between the head and tail and is the site of regulatory
myosin light chain binding. There are 17 myosin families and the most well characterized is myosin II.
Myosin II is found predominantly in myocytes and mediates plus-ended movement along microfilaments. It is
involved in muscle contraction through cyclic interactions with actin-rich thin filaments, creating a
contractile force. It is regulated by phosphorylation via myosin light chain kinase (MLCK) and by
intracellular Ca2+ concentrations.

Gene Wiki entry for MYH10


(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_000017.10  NC_018928.1  NT_010718.16  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the MYH10 gene promoter:
         STAT5B   PPAR-alpha   Spz1   MyoD   FOXJ2   IRF-1   Pax-4a   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidMYH10 promoter sequence
   Search SABiosciences Chromatin IP Primers for MYH10

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat MYH10


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

Entrez Gene cytogenetic band: 17p13   Ensembl cytogenetic band:  17p13.1   HGNC cytogenetic band: 17p13

MYH10 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
MYH10 gene location

GeneLoc information about chromosome 17         GeneLoc Exon Structure

GeneLoc location for GC17M008318:  view genomic region     (about GC identifiers)

Start:
8,377,523 bp from pter      End:
8,534,079 bp from pter
Size:
156,557 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: MYH10_HUMAN, P35580 (See protein sequence)
Recommended Name: Myosin-10  
Size: 1976 amino acids; 228999 Da
Subunit: Myosin is a hexameric protein that consists of 2 heavy chain subunits (MHC), 2 alkali light chain subunits
(MLC) and 2 regulatory light chain subunits (MLC-2). Interacts with PLEKHG6. Interacts with ECM29. Interacts with
KIF26B (By similarity). Interacts with LARP6
Caution: Represents a conventional non-muscle myosin. This protein should not be confused with the unconventional
myosin-10 (MYO10)
Sequence caution: Sequence=BAE06108.1; Type=Erroneous initiation; Note=Translation N-terminally shortened;
Secondary accessions: F8VTL3 Q12989 Q149N3 Q149N4 Q16087 Q4LE45 Q6PK16
Alternative splicing: 4 isoforms:  P35580-1   P35580-2   P35580-3   P35580-4   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for MYH10: NX_P35580

Post-translational modifications:

  • Phosphorylated by ABL2 (By similarity)1
  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_P35580

  • MYH10 Protein expression data from MOPED and PaxDb:    About this image 
    MYH10 Protein Expression
    REFSEQ proteins (3 alternative transcripts): 
    NP_001242941.1  NP_001243024.1  NP_005955.3  

    ENSEMBL proteins: 
     ENSP00000353590   ENSP00000269243   ENSP00000408220   ENSP00000379539   ENSP00000369315  
    Reactome Protein details: P35580
    Human Recombinant Protein Products for MYH10: 
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    Uscn Proteins for MYH10

    Gene Ontology (GO): 5/15 cellular component terms (GO ID links to tree view) (see all 15):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0001725stress fiber IDA15774463
    GO:0005737cytoplasm IDA7699007
    GO:0005819spindle IEA--
    GO:0005886plasma membrane IEA--
    GO:0005938cell cortex IDA7699007

    MYH10 for ontologies           About GeneDecksing



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

    MYH10 for domains           About GeneDecksing

    5 InterPro domains/families:
     IPR004009 Myosin_N
     IPR000048 IQ_motif_EF-hand-BS
     IPR002928 Myosin_tail
     IPR001609 Myosin_head_motor_dom
     IPR008989 Myosin_S1_N

    Graphical View of Domain Structure for InterPro Entry P35580

    ProtoNet protein and cluster: P35580

    4 Blocks protein families:
    IPB000048 IQ calmodulin-binding region
    IPB002017 Spectrin repeat
    IPB002928 Myosin tail
    IPB004009 Myosin N-terminal SH3-like domain


    UniProtKB/Swiss-Prot: MYH10_HUMAN, P35580
    Domain: The rodlike tail sequence is highly repetitive, showing cycles of a 28-residue repeat pattern composed of 4
    heptapeptides, characteristic for alpha-helical coiled coils
    Similarity: Contains 1 IQ domain
    Similarity: Contains 1 myosin head-like domain


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

    Molecular Function:

         UniProtKB/Swiss-Prot Summary: MYH10_HUMAN, P35580
    Function: Cellular myosin that appears to play a role in cytokinesis, cell shape, and specialized functions such as
    secretion and capping. Involved with LARP6 in the stabilization of type I collagen mRNAs for CO1A1 and CO1A2

         Genatlas biochemistry entry for MYH10:
    myosin,motor contractile protein moving towards the "plus" end of actin track,heavy polypeptide 10,non muscle

         Gene Ontology (GO): 5/9 molecular function terms (GO ID links to tree view) (see all 9):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000146microfilament motor activity IDA15845534
    GO:0003774motor activity ----
    GO:0003779actin binding NAS7782316
    GO:0005515protein binding IPI7542763
    GO:0005516calmodulin binding IEA--
         
    MYH10 for ontologies           About GeneDecksing


    Phenotypes:
         1 GenomeRNAi human phenotype for MYH10:
     Decreased cilium length after  

         13 MGI mutant phenotypes (inferred from 8 alleles(MGI details for Myh10):
     behavior/neurological  cardiovascular system  cellular  craniofacial  growth/size 
     homeostasis/metabolism  immune system  liver/biliary system  mortality/aging  muscle 
     nervous system  skeleton  vision/eye 

    MYH10 for phenotypes           About GeneDecksing

    Animal Models:
         Mouse knock-outs for MYH10: Myh10tm1Rsad Myh10tm4Rsad Myh10tm2Rsad Myh10tm5Rsad
       inGenious Targeting Laboratory - Customizable classic, inducible, and humanized mouse model solutions for MYH10 

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    SwitchGear 3'UTR luciferase reporter plasmidMYH10 3' UTR sequence
    Inhib. RNA
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    (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

    Unified GeneCards pathways - 5/17 super-pathways (see all 17About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1Cell adhesion_Integrin-mediated cell adhesion and migration
    Cell adhesion_Integrin-mediated cell adhesion and migration1.00
    Cytoskeleton remodeling Regulation of actin cytoskeleton by Rho GTPases0.49
    Cell adhesion Integrin-mediated cell adhesion and migration1.00
    Cytoskeleton remodeling_Regulation of actin cytoskeleton by Rho GTPases0.49
    2Immune response _CCR3 signaling in eosinophils
    Immune response _CCR3 signaling in eosinophils1.00
    Inhibitory action of Lipoxins on neutrophil migration0.51
    Immune response CCR3 signaling in eosinophils1.00
    3PAK Pathway
    PAK Pathway1.00
    Epithelial Adherens Junctions0.36
    Antioxidant Action of Vitamin-C0.56
    4Sema4D in semaphorin signaling
    Sema4D in semaphorin signaling1.00
    Semaphorin interactions0.44
    Sema4D induced cell migration and growth-cone collapse0.83
    5Axon guidance
    Axon guidance1.00
    Developmental Biology0.69

    Pathway sources
    See GeneCards unified pathways
    Show all pathways

    5 EMD Millipore Pathways for MYH10
        Cell adhesion Integrin-mediated cell adhesion and migration
    Cell adhesion Tight junctions
    Cytoskeleton remodeling Regulation of actin cytoskeleton by Rho GTPases
    Immune response CCR3 signaling in eosinophils
    Development MAG-dependent inhibition of neurite outgrowth

    5/11 Downloadable PowerPoint Slides of QIAGEN Pathway Central Maps for MYH10 (see all 11)
        RhoA Pathway
    Antioxidant Action of Vitamin-C
    Transendothelial Migration of Leukocytes
    Actin Nucleation by ARP-WASP Complex
    Epithelial Adherens Junctions

    1 Cell Signaling Technology (CST) Pathway for MYH10
        Cytoskeletal Signaling

    5/6 GeneGo (Thomson Reuters) Pathways for MYH10 (see all 6)
        Cell adhesion Integrin-mediated cell adhesion and migration
    Cytoskeleton remodeling Regulation of actin cytoskeleton by Rho GTPases
    Inhibitory action of Lipoxins on neutrophil migration
    Immune response CCR3 signaling in eosinophils
    Cell adhesion Tight junctions

    1 BioSystems Pathway for MYH10 
        Regulation of Actin Cytoskeleton

    5        Reactome Pathways for MYH10
        Developmental Biology
    Sema4D induced cell migration and growth-cone collapse
    Semaphorin interactions
    Sema4D in semaphorin signaling
    Axon guidance


    3         Kegg Pathways  (Kegg details for MYH10):
        Tight junction
    Regulation of actin cytoskeleton
    Viral myocarditis


    MYH10 for pathways           About GeneDecksing

    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for MYH10

    STRING Interaction Network Preview (showing 5 interactants - click image to see 25)

    5/93 Interacting proteins for MYH10 (P355802, 3 ENSP000002692434) via UniProtKB, MINT, STRING, and/or I2D (see all 93)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    TRPM6Q9BX842, 3, ENSP000003540064MINT-6699529 I2D: score=1 STRING: ENSP00000354006
    IKBKEQ141642, 3MINT-48102 I2D: score=4 
    IKBKGQ9Y6K92, 3MINT-48167 I2D: score=2 
    MAP3K1Q132332, 3MINT-48299 I2D: score=2 
    MAP3K3Q997592, 3MINT-48425 I2D: score=2 
    About this table

    Gene Ontology (GO): 5/25 biological process terms (GO ID links to tree view) (see all 25):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000281cytokinesis after mitosis IDA15774463
    GO:0001701in utero embryonic development IEA--
    GO:0001764neuron migration IEA--
    GO:0001778plasma membrane repair IEA--
    GO:0006887exocytosis IEA--

    MYH10 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

    MYH10 for compounds           About GeneDecksing

    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Compounds for MYH10 available from Tocris Bioscience    About this table
    CompoundAction CAS #
    (R)-(+)-BlebbistatinSelective inhibitor of myosin II. Inactive enantiomer of (±)-blebbistatin (Cat. No. 1760)--
    (S)-(-)-BlebbistatinSelective inhibitor of myosin II. Active enantiomer of (±)-blebbistatin (Cat. No. 1760)[856925-71-8]
    (±)-BlebbistatinSelective inhibitor of myosin II[674289-55-5]
    3 Novoseek chemical compound relationships for MYH10 gene    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    actomyosin 68.6 3 16901965 (1), 12605685 (1), 17023528 (1)
    estrogen 25.8 4 16901965 (2), 17023528 (2)
    atp 0.0441 1 8663598 (1)

    Search CenterWatch for drugs/clinical trials and news about MYH10 

    (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, Sirion Biotech, 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 MYH10 gene (3 alternative transcripts): 
    NM_001256012.1  NM_001256095.1  NM_005964.3  

    Unigene Cluster for MYH10:

    Myosin, heavy chain 10, non-muscle
    Hs.16355  [show with all ESTs]
    Unigene Representative Sequence: NM_001256012
    12 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000360416(uc002glm.3) ENST00000269243(uc002gll.3) ENST00000476737
    ENST00000488329 ENST00000465458 ENST00000469865 ENST00000584124 ENST00000459986
    ENST00000472728 ENST00000411957 ENST00000396239 ENST00000379980(uc010cnx.3 uc010cny.1)


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    hsa-miR-3678-3p hsa-miR-300 hsa-miR-200a hsa-miR-128 hsa-miR-30d hsa-miR-550a* hsa-miR-890 hsa-miR-30a
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    Additional cDNA sequence: 

    AB210026.1 AB621820.1 AF086505.1 AK026977.1 BC000280.1 BC008968.2 BC117690.1 BC117691.1 
    BC144668.1 BC150634.1 DQ925667.1 M69181.1 S67247.1 U15618.1 U34304.1 

    20 DOTS entries:

    DT.219373  DT.100821046  DT.91719949  DT.91817109  DT.102837546  DT.219370  DT.120920828  DT.435880 
    DT.92434433  DT.99994616  DT.100821044  DT.92434421  DT.95235074  DT.95309574  DT.95343009  DT.97818271 
    DT.100821042  DT.40211646  DT.75158458  DT.91955343 

    24/395 AceView cDNA sequences (see all 395):

    CA435874 CB154893 AI277797 AA505470 BU166935 F04914 BC000280 U34304 
    BE383159 AA476595 BU173337 AI825348 W74368 AI678861 BQ425468 AA490700 
    N75446 BM729029 BQ575843 U15618 AI582253 T96820 CR602815 CB243057 

    GeneLoc Exon Structure

    5/13 Alternative Splicing Database (ASD) splice patterns (SP) for MYH10 (see all 13)    About this scheme

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

    ExUns: 20 ^ 21a · 21b · 21c ^ 22a · 22b ^ 23a · 23b ^ 24 ^ 25a · 25b ^ 26 ^ 27
    SP1:                                                                              
    SP2:                                                                              
    SP3:                                                                              
    SP4:                                                                              
    SP5:                                                                              


    ECgene alternative splicing isoforms for MYH10

    (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

    MYH10 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: TACCTCTCTA
    MYH10 Expression
    About this image
    See MYH10 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for MYH10

    SOURCE GeneReport for Unigene cluster: Hs.16355

    UniProtKB/Swiss-Prot: MYH10_HUMAN, P35580
    Tissue specificity: Isoform 1 is expressed in cerebellum and spinal chord. Isoform 2 is expressed in cerebrum and
    retina. Isoform 3 is expressed in the cerebrum and to a much lower extent in cerebellum

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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 animals.

    Orthologs for MYH10 gene from 6/23 species (see all 23)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves MYH101 myosin, heavy chain 10, non-muscle 83.01(n)
    95.95(a)
      396465  NM_205474.1  NP_990805.1 
    lizard
    (Anolis carolinensis)
    Reptilia MYH106
    --
    93(a)
    1 ↔ 1
    2(104959907-105037471)
    African clawed frog
    (Xenopus laevis)
    Amphibia Xl.8332 Xenopus laevis nonmuscle myosin heavy chain mRNA, complete more 79.66(n)    L09740.1 
    zebrafish
    (Danio rerio)
    Actinopterygii myh101 myosin, heavy polypeptide 10, non-muscle 78.58(n)
    90.22(a)
      555454  XM_677954.5  XP_683046.5 
    fruit fly
    (Drosophila melanogaster)
    Insecta zip1 , 3 NOT muscle attachment myosin ATPase3
    zipper1
    61(a)
    (best of 2)3
    61.57(n)1
    63.49(a)1
      380011  NM_079136.31  NP_523860.21 
    worm
    (Caenorhabditis elegans)
    Secernentea hcp-13
    nmy-11
    Expression: 2-cell embryo3
    Protein NMY-11
    20(a)
    (best of 2)3
    57(n)1
    52.52(a)1
      V(6596826-6601602)3
    1805811  NM_076103.31  NP_508504.21 


    ENSEMBL Gene Tree for MYH10 (if available)
    TreeFam Gene Tree for MYH10 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for MYH10 gene
    MYH82  MYH12  MYH22  MYH112  MYH142  MYH92  MYH132  MYH7B2  
    MYH42  MYH32  MYH152  MYH62  MYH72  
    18/37 SIMAP similar genes for MYH10 using alignment to 8 protein entries:     MYH10_HUMAN (see all proteins) (see all similar genes):
    DKFZp686D10126    MYH9    MYH11    FLJ00279    MYH14    MYH2
    MYO18A    MYO9A    MYO1C    MYO5C    MYH4    MYH8
    MYH7    MYH1    MYO3B    MYH6    MYO10    MYH3

    MYH10 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

    10/2697 NCBI SNPs in MYH10 are shown (see all 2697    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 17 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs784904761,2
    F--8377056(+) GAAATC/TGGCAT 3 -- ds50011Minor allele frequency- T:0.04NA 120
    rs1892932211,2
    --8377143(+) CATCAC/TTGAAT 3 -- ds50010--------
    rs768270491,2
    C--8377162(+) AGCATC/TTTCAA 3 -- ds50012Minor allele frequency- T:0.18NA EA 122
    rs116501371,2
    C,F,A,H--8377201(+) AATGTA/CCTGGA 3 -- ds500126Minor allele frequency- N:0.00EA NA NS WA 2566
    rs1815775881,2
    --8377237(+) GTGAGC/TTTCAT 3 -- ds50010--------
    rs1414540151,2
    --8377366(+) AGTTGA/GAGCCA 3 -- ds50010--------
    rs1867821711,2
    --8377377(+) GGACTA/GGCCTG 3 -- ds50010--------
    rs1131629571,2
    --8377396(+) TCTGTC/TGTCTG 3 -- ds50012Minor allele frequency- T:0.02CSA WA 120
    rs1470024591,2
    --8377606(+) GCAGGC/TGCAAA 3 -- ut310--------
    rs1381369611,2
    --8377820(+) AGCACA/GTTGCA 3 -- ut310--------

    HapMap Linkage Disequilibrium report for MYH10 (8377523 - 8534079 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 1 variation for MYH10
         1 Indel: 45618

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

    MYH10 for disorders           About GeneDecksing

    OMIM gene information: 160776    OMIM disorders: --

    15 diseases for MYH10:    About MalaCards
    may-hegglin anomaly    ventricular septal defect    gitelman syndrome    muscular dystrophy
    kaposi's sarcoma    lymphangioleiomyomatosis    hydrocephalus    vaginitis
    sarcoma    lung cancer    atherosclerosis    cervicitis
    melanoma    prostatitis    neuronitis

    1 Novoseek disease relationship for MYH10 gene    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    tumors 0 2 12874274 (1), 11244504 (1)

    Human Genome Epidemiology (HuGE) Navigator: MYH10 (2 documents)

    Export disorders for MYH10 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 MYH10 gene, integrated from 9 sources (see all 102):
    (articles sorted by number of sources associating them with MYH10)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Human nonmuscle myosin heavy chains are encoded by two genes located on different chromosomes. (PubMed id 1860190)1, 2, 3 Simons M.... Weir L. (1991)
    2. Neuronal cell expression of inserted isoforms of vertebrate nonmuscle myosin heavy chain II-B. (PubMed id 7782316)1, 2, 9 Itoh K. and Adelstein R.S. (1995)
    3. Cloning of the cDNA encoding human nonmuscle myosin heavy chain-B and analysis of human tissues with isoform-specific antibodies. (PubMed id 7499478)1, 2, 9 Phillips C.L.... Adelstein R.S. (1995)
    4. A protein interaction network for Ecm29 links the 26 S proteasome to molecular motors and endosomal components. (PubMed id 20682791)1, 2 Gorbea C.... Rechsteiner M. (2010)
    5. Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. (PubMed id 17081983)1, 2 Olsen J.V....Mann M. (2006)
    6. Human smooth muscle myosin heavy chain isoforms as molecular markers for vascular development and atherosclerosis. (PubMed id 7916668)1, 2 Aikawa M.... Periasamy M. (1993)
    7. Estrogen modulation of MgATPase activity of nonmuscle myosin-II-B filaments. (PubMed id 17023528)1, 9 Gorodeski G.I. (2007)
    8. Characterization of the nonmuscle myosin heavy chain IIB promoter: regulation by E2F. (PubMed id 8931991)1, 9 Weir L. and Chen D. (1996)
    9. Disease-associated mutations and alternative splicing alter the enzymatic and motile activity of nonmuscle myosins II-B and II-C. (PubMed id 15845534)1, 9 Kim K.Y....Adelstein R.S. (2005)
    10. Protein kinase Cgamma regulates myosin IIB phosphorylation, cellular localization, and filament assembly. (PubMed id 16394101)1, 9 Rosenberg M. and Ravid S. (2006)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    Disorders
    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: 4628 HGNC: 7568 AceView: MYH10 Ensembl:ENSG00000133026 euGenes: HUgn4628
    ECgene: MYH10 Kegg: 4628 H-InvDB: MYH10

    (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 MYH10 Pharmacogenomics, SNPs, Pathways
    ATLAS Chromosomes in Cancer entry for MYH10 Genetics and Cytogenetics in Oncology and Haematology

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for MYH10 gene:
    Search GeneIP for patents involving MYH10

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



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    About This Section

     
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