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

ZDHHC9 Gene

protein-coding   GIFtS: 55
GCID: GC0XM128938

Zinc Finger, DHHC-Type Containing 9

(Previous names: zinc finger, DHHC-type containing 10, chromosome X open...)
(Previous symbols: ZDHHC10, CXorf11)
  See related diseases
at  

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, 10fRNAdb, 12H-InvDB, 13NCBI, 14NONCODE, and/or 15RNAdb)
About This Section

Aliases
Zinc Finger, DHHC-Type Containing 91 2     CGI892
CXorf111 2 3     MMSA12
ZDHHC101 2 3     Antigen MMSA-12
DHHC92 3 5     Asp-His-His-Cys Domain Containing Protein 92
Zinc Finger Protein 3792 3     Palmitoyltransferase ZDHHC92
Zinc Finger Protein 3802 3     Zinc Finger, DHHC Domain Containing 102
ZNF3792 3     DHHC-93
ZNF3802 3     EC 2.3.1.-3
MRXSZ2 5     Zinc Finger DHHC Domain-Containing Protein 93
Chromosome X Open Reading Frame 111     EC 2.3.18
Zinc Finger, DHHC-Type Containing 101     EC 2.3.1.128

External Ids:    HGNC: 184751   Entrez Gene: 511142   Ensembl: ENSG000001887067   OMIM: 3006465   UniProtKB: Q9Y3973   

Export aliases for ZDHHC9 gene to outside databases

Previous GC identifers: GC0XM123585 GC0XM125785 GC0XM126883 GC0XM127645 GC0XM128664 GC0XM128766 GC0XM118338


(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 ZDHHC9 Gene:
This gene encodes an integral membrane protein that is a member of the zinc finger DHHC domain-containing protein
family. The encoded protein forms a complex with golgin subfamily A member 7 and functions as a
palmitoyltransferase. This protein specifically palmitoylates HRAS and NRAS. Mutations in this gene are
associated with X-linked mental retardation. Alternate splicing results in multiple transcript variants that
encode the same protein.(provided by RefSeq, May 2010)

GeneCards Summary for ZDHHC9 Gene: 
ZDHHC9 (zinc finger, DHHC-type containing 9) is a protein-coding gene. Diseases associated with ZDHHC9 include mental retardation, x-linked, syndromic, raymond type, and mental retardation, x-linked, zdhhc9-related. GO annotations related to this gene include transferase activity, transferring acyl groups and zinc ion binding. An important paralog of this gene is ZDHHC1.

UniProtKB/Swiss-Prot: ZDHC9_HUMAN, Q9Y397
Function: The ZDHHC9-GOLGA7 complex is a palmitoyltransferase specific for HRAS and NRAS

Gene Wiki entry for ZDHHC9 Gene


(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 73), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000023.10  NC_018934.2  NT_011786.16  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the ZDHHC9 gene promoter:
         PPAR-alpha   Ik-3   Evi-1   Arnt   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidZDHHC9 promoter sequence
   Search SABiosciences Chromatin IP Primers for ZDHHC9

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat ZDHHC9


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

Entrez Gene cytogenetic band: Xq26.1   Ensembl cytogenetic band:  Xq26.1   HGNC cytogenetic band: Xq26.1

ZDHHC9 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
ZDHHC9 gene location

GeneLoc information about chromosome X         GeneLoc Exon Structure

GeneLoc location for GC0XM128938:  view genomic region     (about GC identifiers)

Start:
128,937,264 bp from pter      End:
128,977,910 bp from pter
Size:
40,647 bases      Orientation:
minus strand

(According to UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MAXQB 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 Cloud-Clone Corp.,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Cloud-Clone Corp., Ontologies according to Gene Ontology Consortium 01 Oct 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, and/or Cloud-Clone Corp.)
About This Section

UniProtKB/Swiss-Prot: ZDHC9_HUMAN, Q9Y397 (See protein sequence)
Recommended Name: Palmitoyltransferase ZDHHC9  
Size: 364 amino acids; 40916 Da
Subunit: Interacts with GOLGA7
Subcellular location: Endoplasmic reticulum membrane; Multi-pass membrane protein. Golgi apparatus membrane;
Multi-pass membrane protein
Sequence caution: Sequence=AAD34084.1; Type=Erroneous initiation; Sequence=BAA91683.1; Type=Erroneous initiation;
Sequence=BAD93044.1; Type=Erroneous initiation; Sequence=CAB82308.1; Type=Erroneous initiation;
Secondary accessions: B4F6G2 D3DTF9 Q59EK4 Q5JSW5 Q8WWS7 Q9BPY4 Q9NSP0 Q9NVL0 Q9NVR6

Explore the universe of human proteins at neXtProt for ZDHHC9: NX_Q9Y397

Explore proteomics data for ZDHHC9 at MOPED 

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_Q9Y397

  • 4/9 DME Specific Peptides for ZDHHC9 (Q9Y397) (see all 9)
     IEMEIEA  RPPRASHCS  VLCGPLPPS  RFDHHCPWVG 

    ZDHHC9 Protein expression data from MOPED1, PaxDb2 and MAXQB3 :    About this image 

    ZDHHC9 Protein Expression
    REFSEQ proteins (2 alternative transcripts): 
    NP_001008223.1  NP_057116.2  

    ENSEMBL proteins: 
     ENSP00000349689   ENSP00000360103   ENSP00000406165   ENSP00000383991  

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    Cloud-Clone Corp. Proteins for ZDHHC9 

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000139Golgi membrane IEA--
    GO:0005737cytoplasm IDA--
    GO:0005789endoplasmic reticulum membrane IEA--
    GO:0005794Golgi apparatus IDA--
    GO:0016021integral to membrane IEA--

    ZDHHC9 for ontologies           About GeneDecksing



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    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section
    HGNC Gene Families: 
    ZDHHC: Zinc fingers, DHHC-type

    1 InterPro protein domain:
     IPR001594 Znf_DHHC_palmitoyltrfase

    Graphical View of Domain Structure for InterPro Entry Q9Y397

    ProtoNet protein and cluster: Q9Y397

    1 Blocks protein domain: IPB001594 Zn-finger

    UniProtKB/Swiss-Prot: ZDHC9_HUMAN, Q9Y397
    Domain: The DHHC domain is required for palmitoyltransferase activity
    Similarity: Belongs to the DHHC palmitoyltransferase family. ERF2/ZDHHC9 subfamily
    Similarity: Contains 1 DHHC-type zinc finger


    ZDHHC9 for domains           About GeneDecksing


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

    Molecular Function:

         UniProtKB/Swiss-Prot Summary: ZDHC9_HUMAN, Q9Y397
    Function: The ZDHHC9-GOLGA7 complex is a palmitoyltransferase specific for HRAS and NRAS
    Catalytic activity: Palmitoyl-CoA + protein-cysteine = S-palmitoyl protein + CoA

         Enzyme Numbers (IUBMB): EC 2.3.1.122 EC 2.3.12 EC 2.3.1.-1

         Gene Ontology (GO): 2 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0008270zinc ion binding IEA--
    GO:0016746transferase activity, transferring acyl groups IEA--
         
    ZDHHC9 for ontologies           About GeneDecksing


    Phenotypes:
         1 GenomeRNAi human phenotype for ZDHHC9:
     Decreased melanin production 

         1 MGI phenotypic allele for Zdhhc9 (no phenotypes)

    ZDHHC9 for phenotypes           About GeneDecksing

    Animal Models:
         MGI mouse knock-out Zdhhc9tm1Lex for ZDHHC9

       inGenious Targeting Laboratory - Custom generated mouse model solutions for ZDHHC9 
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    SwitchGear 3'UTR luciferase reporter plasmidZDHHC9 3' UTR sequence
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    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Sino Biological, 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 Oct 2013 via Entrez Gene).
    About This Section



    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for ZDHHC9

    STRING Interaction Network Preview (showing 1 interactants - click image to see more details)

    5/13 Interacting proteins for ZDHHC9 (Q9Y3973 ENSP000003496894) via UniProtKB, MINT, STRING, and/or I2D (see all 13)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    USP14P545783I2D: score=4 
    ACAA1P091103I2D: score=1 
    ACO2Q997983I2D: score=1 
    CBWD1Q9BRT83I2D: score=1 
    CDC40O605083I2D: score=1 
    About this table

    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, 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 ZDHHC9 (ZDHC9)

    Search CenterWatch for drugs/clinical trials and news about ZDHHC9 / ZDHC9

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 236 Homo sapiens; Apr 25 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    Conferences by KenesGroup, 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, Sirion Biotech, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for ZDHHC9 gene (2 alternative transcripts): 
    NM_001008222.2  NM_016032.3  

    Unigene Cluster for ZDHHC9:

    Zinc finger, DHHC-type containing 9
    Hs.193566  [show with all ESTs]
    Unigene Representative Sequence: NM_001008222
    5 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000357166(uc004euv.3 uc004euw.3) ENST00000371064(uc004eux.1 uc004euy.1)
    ENST00000433917 ENST00000406492 ENST00000491039
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    Additional mRNA sequence: 

    AB209807.1 AK001112.1 AK001424.1 AK001524.1 AK096967.1 AL161962.1 AY358558.1 AY952881.8 
    BC000035.2 BC003128.1 BC006200.2 BC012826.2 

    20 DOTS entries:

    DT.454533  DT.100646216  DT.310011  DT.100711787  DT.100646210  DT.97851658  DT.91910108  DT.121322515 
    DT.121322529  DT.100730804  DT.100803359  DT.91824195  DT.91997682  DT.92395896  DT.95151569  DT.95151577 
    DT.40121502  DT.445956  DT.91855535  DT.95269138 

    24/421 AceView cDNA sequences (see all 421):

    BU951890 BQ889732 BU181865 BQ025530 BC006200 BM739157 BF476766 CB156351 
    AA369833 BU729830 AI378902 BG167168 BQ219155 AI620090 BQ721615 BU616841 
    CR596648 AI361596 CR591887 AA293441 CD516743 AI221864 BP336883 BC000035 

    GeneLoc Exon Structure

    5/9 Alternative Splicing Database (ASD) splice patterns (SP) for ZDHHC9 (see all 9)    About this scheme

    ExUns: 1a · 1b · 1c ^ 2a · 2b · 2c ^ 3 ^ 4a · 4b · 4c ^ 5a · 5b · 5c · 5d · 5e ^ 6a · 6b ^ 7 ^ 8a · 8b ^ 9 ^ 10 ^ 11 ^ 12 ^ 13
    SP1:                    -     -                             -                                               -     -                                       
    SP2:                    -     -                 -     -     -     -                                         -     -                                       
    SP3:                                                        -                                               -     -                                       
    SP4:                                                                                                                                                      
    SP5:                    -     -     -     -                 -                                                                                             


    ECgene alternative splicing isoforms for ZDHHC9

    (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

    ZDHHC9 expression in normal human tissues (normalized intensities)      ZDHHC9 embryonic expression: see
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: GCCTCAGCCA
    ZDHHC9 Expression
    About this image


    ZDHHC9 expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database 
     5/1 selected tissues (see all 1) fully expand
     
     Brain (Nervous System)    fully expand to see all 2 entries
             Myelinating Oligodendrocyte Cells Forebrain White Matter
             corpus callosum   

    See ZDHHC9 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for ZDHHC9

    SOURCE GeneReport for Unigene cluster: Hs.193566

    UniProtKB/Swiss-Prot: ZDHC9_HUMAN, Q9Y397
    Tissue specificity: Highly expressed in kidney, skeletal muscle, brain, lung and liver. Absent in thymus, spleen
    and leukocytes

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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 ZDHHC9 gene from 9/17 species (see all 17)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Zdhhc91 , 5 zinc finger, DHHC domain containing 91, 5 93.41(n)1
    98.35(a)1
      X (25.55 cM)5
    2088841  NM_172465.41  NP_766053.11 
     481719695 
    chicken
    (Gallus gallus)
    Aves ZDHHC91 zinc finger, DHHC-type containing 9 78.83(n)
    87.47(a)
      422139  XM_420141.3  XP_420141.1 
    lizard
    (Anolis carolinensis)
    Reptilia ZDHHC96
    zinc finger, DHHC-type containing 9
    81(a)
    1 ↔ 1
    GL343451.1(428100-434999)
    tropical clawed frog
    (Xenopus tropicalis)
    Amphibia Str.120602 Transcribed sequence with weak similarity to protein more 76.97(n)    BX703960.1 
    zebrafish
    (Danio rerio)
    Actinopterygii zgc:1369361 zgc:136936 69.52(n)
    77.21(a)
      560095  NM_001110026.1  NP_001103496.1 
    fruit fly
    (Drosophila melanogaster)
    Insecta app6
    approximated
    23(a)
    1 → many
    3L(12199338-12259941)
    worm
    (Caenorhabditis elegans)
    Secernentea Y47H9C.23   -- 46(a)   I(11852803-11857214)   --
    baker's yeast
    (Saccharomyces cerevisiae)
    Saccharomycetes ERF2(YLR246W)4 Subunit of a palmitoyltransferase, composed of Erf2p more   --   12(627118-628197) 850947  NP_013347.1 
    rice
    (Oryza sativa)
    Liliopsida Os11g05343001 hypothetical protein 52.4(n)
    42.81(a)
      4350651  NM_001074555.2  NP_001068023.2 


    ENSEMBL Gene Tree for ZDHHC9 (if available)
    TreeFam Gene Tree for ZDHHC9 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for ZDHHC9 gene
    ZDHHC12  ZDHHC142  ZDHHC112  ZDHHC52  ZDHHC11B2  ZDHHC42  ZDHHC82  ZDHHC192  
    ZDHHC182  
    4 SIMAP similar genes for ZDHHC9 using alignment to 3 protein entries:     ZDHC9_HUMAN (see all proteins):
    ZDHHC14    ZDHHC18    ZDHHC8    ZDHHC19

    ZDHHC9 for paralogs           About GeneDecksing



    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, 4UniProtKB, 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

    10/522 SNPs in ZDHHC9 are shown (see all 522)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr X posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    VAR_0626744
    Mental retardation, X-linked, syndromic, ZDHHC9-related (MRXSZ)4--see VAR_0626742 R W mis40--------
    VAR_0626754
    Mental retardation, X-linked, syndromic, ZDHHC9-related (MRXSZ)4--see VAR_0626752 P S mis40--------
    rs1844718191,2
    --128893081(+) GGATGA/GTCAGG 2 -- ut310--------
    rs135251,2
    C,F--128893146(+) CTCACT/ACCTGG 2 -- ut31 ese32Minor allele frequency- A:0.01MN WA 186
    rs1880591271,2
    --128893198(+) GGAAGC/GCCTCA 2 -- ut310--------
    rs1924750401,2
    --128893524(+) AAAGAA/GGGCAG 2 -- ut310--------
    rs1846460841,2
    --128893740(+) CCAAGG/TTACCT 2 -- ut310--------
    rs1446945801,2
    C--128893749(+) CTGGGA/GAAACC 2 -- ut310--------
    rs1889628811,2
    --128893768(+) TACAAA/GTTCTC 2 -- ut310--------
    rs1485140021,2
    C--128893923(+) TGTTAA/CAAGGA 2 -- ut310--------

    HapMap Linkage Disequilibrium report for ZDHHC9 (128937264 - 128977910 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 4 variations for ZDHHC9:    About this table     
    Variant IDTypeSubtypePubMed ID
    nsv7087CNV Loss18451855
    nsv528290CNV Gain19592680
    nsv526197CNV Gain19592680
    dgv2475e1CNV Complex17122850


    Human Gene Mutation Database (HGMD): ZDHHC9

    Locus Specific Mutation Databases (LSDB): ZDHHC9
    SABiosciences Cancer Mutation PCR Assays
    SeqTarget long-range PCR primers for resequencing ZDHHC9
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    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Conferences by KenesGroup, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section
    OMIM gene information: 300646   
    OMIM disorders: 300799  
    UniProtKB/Swiss-Prot: ZDHC9_HUMAN, Q9Y397
  • Mental retardation, X-linked, syndromic, ZDHHC9-related (MRXSZ) [MIM:300799]: A disorder characterized by
    significantly below average general intellectual functioning associated with impairments in adaptative behavior
    and manifested during the developmental period. Some MRXSZ patients have marfanoid habitus as an additional
    feature. Note=The disease is caused by mutations affecting the gene represented in this entry

  • 7 diseases for ZDHHC9:    About MalaCards
    mental retardation, x-linked, syndromic, raymond type    mental retardation, x-linked, zdhhc9-related    mental retardation    mental retardation, x-linked
    multiple myeloma    myeloma    colorectal cancer


    ZDHHC9 for disorders           About GeneDecksing


    Export disorders for ZDHHC9 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 ZDHHC9 gene, integrated from 9 sources (see all 21):
    (articles sorted by number of sources associating them with ZDHHC9)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Identification of novel human genes evolutionarily conserved in Caenorhabditis elegans by comparative proteomics. (PubMed id 10810093)1, 2, 3 Lai C.H....Lin W. (2000)
    2. DHHC9 and GCP16 constitute a human protein fatty acyltransferase with specificity for H- and N-Ras. (PubMed id 16000296)1, 2, 9 Swarthout J.T.... Linder M.E. (2005)
    3. Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus. (PubMed id 17436253)1, 2 Raymond F.L.... Futreal P.A. (2007)
    4. Serological identification and bioinformatics analysis of immunogenic antigens in multiple myeloma. (PubMed id 16193335)1, 2 Zhou F.L.... Liu S.H. (2006)
    5. The DNA sequence of the human X chromosome. (PubMed id 15772651)1, 2 Ross M.T.... Bentley D.R. (2005)
    6. 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)
    7. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (2004)
    8. The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment. (PubMed id 12975309)1, 2 Clark H.F.... Gray A.M. (2003)
    9. Differential expression of DHHC9 in microsatellite stable and instable human colorectal cancer subgroups. (PubMed id 17519897)1, 9 Mansilla F....Orntoft T.F. (2007)
    10. [The research on the expression and localization of mu ltiple myeloma associated antigen MMSA-1]. (PubMed id 22230506)1 Meng S....Bai G.G. (2012)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
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    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 51114 HGNC: 18475 AceView: ZDHHC9 Ensembl:ENSG00000188706 euGenes: HUgn51114
    ECgene: ZDHHC9 H-InvDB: ZDHHC9

    (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 ZDHHC9 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 ZDHHC9 gene:
    Search GeneIP for patents involving ZDHHC9

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



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    GeneCards Homepage - Last full update: 23 Oct 2013 - Incrementals: 4 Nov 2013 , 7 Nov 2013 , 23 Jan 2014

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