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

MYO19 Gene

protein-coding   GIFtS: 45
GCID: GC17M034851

myosin XIX

(Previous name: myosin head domain containing 1 )
(Previous symbol: MYOHD1)
 Explore 1 disease affiliated with
MYO19 via our new
 Human Malady Compendium 
Biological research products
for MYO19
    

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

Aliases
Myosin XIX1 2     FLJ228651
MYOHD11 2 3     Myosin-XIX1
Myosin Head Domain Containing 11 2     Unconventional Myosin-XIX2
Myosin Head Domain-Containing Protein 12 3     

External Ids:    HGNC: 262341   Entrez Gene: 801792   Ensembl: ENSG000001411407   UniProtKB: Q96H553   

Export aliases for MYO19 gene to outside databases

Previous GC identifers: GC17M031926 GC17M030788


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

UniProtKB/Swiss-Prot: MYO19_HUMAN, Q96H55
Function: Myosins are actin-based motor molecules with ATPase activity. Unconventional myosins serve in intracellular
movements. Their highly divergent tails are presumed to bind to membranous compartments, which would be moved relative
to actin filaments. MYO19 is involved in mitochondrial motility




(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_010783.15  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the MYO19 gene promoter:
         NF-AT4   NF-AT2   NF-AT3   Nkx2-5   NF-AT1   NF-AT   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidMYO19 promoter sequence
   Search SABiosciences Chromatin IP Primers for MYO19

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat MYO19


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

Entrez Gene cytogenetic band: 17q12   Ensembl cytogenetic band:  17q12   HGNC cytogenetic band: 17q21.1

MYO19 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
MYO19 gene location

GeneLoc information about chromosome 17         GeneLoc Exon Structure

GeneLoc location for GC17M034851:  view genomic region     (about GC identifiers)

Start:
34,851,477 bp from pter      End:
34,899,284 bp from pter
Size:
47,808 bases      Orientation:
minus strand

1 alternative location:
Chr17-,PATCHES 34,837,360-34,877,060     

(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: MYO19_HUMAN, Q96H55 (See protein sequence)
Recommended Name: Unconventional myosin-XIX  
Size: 970 amino acids; 109135 Da
Subcellular location: Cytoplasm, cytoskeleton. Mitochondrion outer membrane. Note=Probably associated with the outer
membrane via its N-terminal mitochondrial targeting region
Sequence caution: Sequence=BAD92272.1; Type=Erroneous initiation;
Secondary accessions: Q59GS4 Q9H5X2
Alternative splicing: 4 isoforms:  Q96H55-1   Q96H55-2   Q96H55-3   Q96H55-4   

Explore the universe of human proteins at neXtProt for MYO19: NX_Q96H55

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q96H55

  • MYO19 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins (3 alternative transcripts): 
    NP_001028752.1  NP_001157207.1  NP_079385.2  

    ENSEMBL proteins: 
     ENSP00000409936   ENSP00000468792   ENSP00000468488   ENSP00000268852   ENSP00000467845  
     ENSP00000468228   ENSP00000466786   ENSP00000438365   ENSP00000465350   ENSP00000467285  
     ENSP00000466713   ENSP00000467683  

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    Browse ProSpec Recombinant Proteins
    Uscn Proteins for MYO19

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005737cytoplasm IDA--
    GO:0005741mitochondrial outer membrane IEA--
    GO:0016459myosin complex IEA--


    MYO19 for ontologies           About GeneDecksing



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    Uscn ELISAs and CLIAs for MYO19


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

    MYO19 for domains           About GeneDecksing

    2 InterPro domains/families:
     IPR000048 IQ_motif_EF-hand-BS
     IPR001609 Myosin_head_motor_dom

    Graphical View of Domain Structure for InterPro Entry Q96H55

    ProtoNet protein and cluster: Q96H55

    1 Blocks protein family: IPB000048 IQ calmodulin-binding region

    UniProtKB/Swiss-Prot: MYO19_HUMAN, Q96H55
    Similarity: Contains 2 IQ domains
    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,
    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: MYO19_HUMAN, Q96H55
    Function: Myosins are actin-based motor molecules with ATPase activity. Unconventional myosins serve in intracellular
    movements. Their highly divergent tails are presumed to bind to membranous compartments, which would be moved relative
    to actin filaments. MYO19 is involved in mitochondrial motility

    miRNA
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    hsa-miR-31 hsa-miR-328 hsa-miR-1271 hsa-miR-1291 hsa-miR-511 hsa-miR-124 hsa-miR-182 hsa-miR-9
    SwitchGear 3'UTR luciferase reporter plasmidMYO19 3' UTR sequence
    Inhib. RNA
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for MYO19

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003774motor activity IEA--
    GO:0003779actin binding IEA--
    GO:0005524ATP binding IEA--


    MYO19 for ontologies           About GeneDecksing


    2 GenomeRNAi human phenotypes for MYO19:
     Decreased cilium length after   Increased HPV18 LCR reporter a 


    (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 MYO19

    (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 MYO19
    Search CenterWatch for drugs/clinical trials and news about MYO19 

    (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 MYO19 gene (4 alternative transcripts): 
    NM_001033579.1  NM_001033580.2  NM_001163735.1  NM_025109.5  

    Unigene Cluster for MYO19:

    Myosin XIX
    Hs.302051  [show with all ESTs]
    Unigene Representative Sequence: NM_001163735
    18/27 Ensembl transcripts including schematic representations, and UCSC links where relevant (see all 27):
    ENST00000431794(uc010cuu.3 uc010wcy.2 uc010wcz.1) ENST00000586908
    ENST00000591794 ENST00000588377 ENST00000268852(uc002hmw.3 uc010wda.1 uc002hmx.2)
    ENST00000593275 ENST00000592110 ENST00000590233 ENST00000586328 ENST00000593222
    ENST00000591477 ENST00000592735 ENST00000588727 ENST00000588471 ENST00000591017
    ENST00000587389 ENST00000590585 ENST00000586007

    miRNA
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    8/12 QIAGEN miScript miRNA Assays for microRNAs that regulate MYO19 (see all 12):
    hsa-miR-31 hsa-miR-328 hsa-miR-1271 hsa-miR-1291 hsa-miR-511 hsa-miR-124 hsa-miR-182 hsa-miR-9
    SwitchGear 3'UTR luciferase reporter plasmidMYO19 3' UTR sequence
    Inhib. RNA
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    Additional cDNA sequence: 

    AK026518.1 AK293903.1 AK299802.1 AK304073.1 AL049275.1 AL133017.1 AY545559.1 BC008900.2 
    BC036325.1 BC041980.1 

    24/30 DOTS entries (see all 30):

    DT.423511  DT.95373367  DT.95373374  DT.99976135  DT.91941231  DT.95373356  DT.100826435  DT.121643737 
    DT.92426495  DT.40298847  DT.91729248  DT.121002667  DT.92426497  DT.100020445  DT.121002684  DT.91938169 
    DT.446418  DT.100031461  DT.419655  DT.91755398  DT.91910903  DT.92038196  DT.100837437  DT.408274 

    24/162 AceView cDNA sequences (see all 162):

    BU196917 BQ650642 BQ050997 AL525887 BP358072 AI867088 BU543266 BQ181670 
    AA703821 BM982398 CN482232 AW005609 BX280258 CB159365 BU509222 BF968765 
    AI168838 BM666622 BX457543 AI378368 BQ063197 AA398414 BI837872 AW005600 

    GeneLoc Exon Structure

    5/32 Alternative Splicing Database (ASD) splice patterns (SP) for MYO19 (see all 32)    About this scheme

    ExUns: 1a · 1b · 1c · 1d · 1e · 1f · 1g · 1h ^ 2a · 2b · 2c · 2d ^ 3a · 3b · 3c ^ 4a · 4b ^ 5 ^ 6a · 6b ^ 7a · 7b · 7c ^ 8 ^ 9a · 9b ·
    SP1:                                      -     -     -     -                 -     -     -                 -                 -                                 
    SP2:                                                                                                                                                            
    SP3:                                                                                                                                                            
    SP4:                                                  -     -                 -     -     -                 -                 -                                 
    SP5:                                                                                                                                                            

    ExUns: 9c ^ 10 ^ 11a · 11b ^ 12a · 12b ^ 13a · 13b · 13c ^ 14 ^ 15a · 15b ^ 16a · 16b · 16c ^ 17a · 17b · 17c ^ 18a · 18b ^ 19a · 19b · 19c ^ 20a · 20b · 20c ·
    SP1:                                                                                                                                                            
    SP2:                                                                                      -                             -                       -               
    SP3:                                                  -     -     -     -                 -                                                                     
    SP4:                                                                                                                                                            
    SP5:                                                                                                                                                            

    ExUns: 20d · 20e ^ 21a · 21b ^ 22a · 22b · 22c ^ 23a · 23b ^ 24a · 24b · 24c ^ 25a · 25b · 25c ^ 26a · 26b · 26c ^ 27a · 27b ^ 28a · 28b ^ 29 ^ 30a · 30b
    SP1:                                                                                                                                                      
    SP2:                                                                                                                                                      
    SP3:                                                                                                                                                      
    SP4:                                                                                                                                                      
    SP5:                                                        -     -                       -     -                             -                           


    ECgene alternative splicing isoforms for MYO19

    (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

    MYO19 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: --

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

    About this image

    MYO19 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 CellCategory (developmental path)
    BoneThoracic RibBone
    CartilageMeckel's CartilageCartilage
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization

    See MYO19 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for MYO19

    SOURCE GeneReport for Unigene cluster: Hs.302051

    UniProtKB/Swiss-Prot: MYO19_HUMAN, Q96H55
    Tissue specificity: Widely expressed in multiple tissues and cell lines

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    In Situ
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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 MYO19 gene from 5/17 species (see all 17)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves MYO191 myosin XIX 62.99(n)
    61.2(a)
      417649  XM_415895.3  XP_415895.3 
    lizard
    (Anolis carolinensis)
    Reptilia MYO196
    --
    55(a)
    1 ↔ 1
    GL344386.1(1971-26489)
    zebrafish
    (Danio rerio)
    Actinopterygii LOC5622791 myosin-XIX-like 57.67(n)
    52.64(a)
      562279  XM_001920048.3  XP_001920083.3 
    thale cress
    (Arabidopsis thaliana)
    eudicotyledons VIIIB6
    VIIIA6
    (see all 4)
    myosin heavy chain-like protein
    P-loop containing nucleoside triphosphate hydrolas...
    (see all 4)
    22(a)
    22(a)
    (see all 4)
    many ↔ many
    many ↔ many
    (see all 4)
    4(13694881-13700780)
    1(18649747-18657376)
    rice
    (Oryza sativa)
    Liliopsida --
    --
    myosin-Vb, putative, expressed
    26(a)
    20(a)
    many ↔ many
    many ↔ many
    10(18459629-18468400)
    7(22487833-22496731)


    ENSEMBL Gene Tree for MYO19 (if available)
    TreeFam Gene Tree for MYO19 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for MYO19 gene
    MYO1F2  MYO1G2  MYO1E2  MYO1B2  MYO1D2  MYO1H2  MYO1A2  MYO1C2  
    18/19 SIMAP similar genes for MYO19 using alignment to 11 protein entries:     MYO19_HUMAN (see all proteins) (see all similar genes):
    MYH7B    MYO3B    MYO1H    MYO1A    MYO1C    MYO1B
    MYO1E    MYH2    MYO6    MYO5C    MYO1G    MYH14
    MYO5B    MYO10    MYO7A    MYO9A    MYO1D    MYO7B

    MYO19 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

    10/248 NCBI SNPs in MYO19 are shown (see all 248    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 17 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1162760691,2
    C,F,--30789148(+) TAAAAA/GTGCAA 2 -- int11Minor allele frequency- G:0.04WA 118
    rs1112546181,2
    --30789158(+) AGAAGG/ATATGG 2 -- int11Minor allele frequency- A:0.50CSA 2
    rs347051141,2
    C,F--30789832(+) AATAC-/AAAAAA 2 -- int12Minor allele frequency- A:0.50NA CSA 4
    rs793591931,2
    --30790145(+) GGACTA/GATTAG 2 -- int11Minor allele frequency- G:0.01WA 118
    rs583888511,2
    C,--30790508(+) AAAGTG/ACTGGG 2 -- int11Minor allele frequency- A:0.50WA 2
    rs732767521,2
    C,F,--30791591(+) ATACAT/CGAGGA 2 -- int13Minor allele frequency- C:0.05WA 122
    rs711596081,2
    C--30792516(+) TTTTTT/-GAGAC 2 -- int11Minor allele frequency- -:0.00NA 2
    rs580112901,2
    C,F,--30793261(+) CACTTC/GTTACA 2 -- int13Minor allele frequency- G:0.05WA 122
    rs780830581,2
    C,--30793805(+) GGCTGC/GTGCCT 4 P A mis10--------
    rs126038511,2
    C,F,H--30794564(+) CAAAGG/TAGACA 2 -- int18Minor allele frequency- T:0.01NS EA NA 608

    HapMap Linkage Disequilibrium report for MYO19 (34851477 - 34899284 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 9 variations for MYO19
         8 CNVs: 2223 0800 3142 49849 4031 8841 2222 8843
         1 Inversion: 37189

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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

    MYO19 for disorders           About GeneDecksing

    1 disease for MYO19:    About MalaCards
    malaria


    Export disorders for MYO19 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 MYO19 gene integrated from 9 sources:
    (articles sorted by number of sources associating them with MYO19)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Human Myo19 is a novel myosin that associates with mi tochondria. (PubMed id 19932026)1, 2, 3 Quintero O.A....Cheney R.E. (2009)
    2. Drawing the tree of eukaryotic life based on the analysis of 2,269 manually annotated myosins from 328 species. (PubMed id 17877792)1, 3 Odronitz F. and Kollmar M. (2007)
    3. The proteomic analysis of endogenous FAT10 substrates identifies p62/SQSTM1 as a substrate of FAT10ylation. (PubMed id 22797925)1 Aichem A....Groettrup M. (2012)
    4. Systematic and quantitative assessment of the ubiquiti n-modified proteome. (PubMed id 21906983)1 Kim W....Gygi S.P. (2011)
    5. Toward a confocal subcellular atlas of the human proteome. (PubMed id 18029348)1 Barbe L....Andersson-Svahn H. (2008)
    6. DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage. (PubMed id 16625196)2 Zody M.C.... Nusbaum C. (2006)
    7. 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)
    8. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)2 Ota T.... Sugano S. (2004)
    9. 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)
    10. Normalization and subtraction: two approaches to facilitate gene discovery. (PubMed id 8889548)1 Bonaldo M.F.... Soares M.B. (1996)

    (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: 80179 HGNC: 26234 AceView: MYOHD1 Ensembl:ENSG00000141140 euGenes: HUgn80179
    ECgene: MYO19 H-InvDB: MYO19

    (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 MYO19 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 MYO19 gene:
    Search GeneIP for patents involving MYO19

    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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    GeneCards Homepage - Last full update: 18 Mar 2013 - Incrementals: 21 Mar 2013 , 15 Apr 2013 , 26 Apr 2013

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