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

FAAH Gene

protein-coding   GIFtS: 65
GCID: GC01P046860

fatty acid amide hydrolase

 Explore 42 diseases affiliated with
FAAH via our new
 Human Malady Compendium 
Biological research products
for FAAH
    

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

Aliases
Fatty Acid Amide Hydrolase1 2     EC 3.5.1.993
FAAH-11 2     FAAH13
Anandamide Amidohydrolase 12 3     EC 3.5.18
Oleamide Hydrolase 12 3     EC 3.5.1.N21
Fatty-Acid Amide Hydrolase 12     

External Ids:    HGNC: 35531   Entrez Gene: 21662   Ensembl: ENSG000001174807   OMIM: 6029355   UniProtKB: O005193   

Export aliases for FAAH gene to outside databases

Previous GC identifers: GC01P046501 GC01P045816 GC01P046246 GC01P046229 GC01P046572 GC01P046632 GC01P044975


(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 FAAH:
This gene encodes a protein that is responsible for the hydrolysis of a number of primary and secondary fatty acid
amides, including the neuromodulatory compounds anandamide and oleamide. (provided by RefSeq, Jul 2008)

UniProtKB/Swiss-Prot: FAAH1_HUMAN, O00519
Function: Degrades bioactive fatty acid amides like oleamide, the endogenous cannabinoid, anandamide and myristic amide
to their corresponding acids, thereby serving to terminate the signaling functions of these molecules. Hydrolyzes
polyunsaturated substrate anandamide preferentially as compared to monounsaturated substrates

summary for FAAH:
Fatty acid amide hydrolase, (FAAH, Oleamide hydrolase, Anandamide amidohydrolase), is an integral membrane
protein that hydrolyzes bioactive amides, including anandamide, to free fatty acid and ethanolamine. FAAH
distribution is noticeably different between human and rat. In humans, FAAH is mainly present in the
pancreas, brain, kidney, skeletal muscle, and placenta. In rat, FAAH is mainly detected in the liver, small
intestine, brain, kidney, spleen, testis, and uterus, but is absent from skeletal muscle and heart. A second
FAAH (FAAH2) was identified recently in humans but is absent from rats and mice.




(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_032977.9  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the FAAH gene promoter:
         Pax-5   MEF-2   HTF   Lmo2   Evi-1   MEF-2A   STAT3   aMEF-2   LyF-1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidFAAH promoter sequence
   Search SABiosciences Chromatin IP Primers for FAAH

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


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

Entrez Gene cytogenetic band: 1p35-p34   Ensembl cytogenetic band:  1p33   HGNC cytogenetic band: 1p35-p34

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

GeneLoc information about chromosome 1         GeneLoc Exon Structure

GeneLoc location for GC01P046860:  view genomic region     (about GC identifiers)

Start:
46,859,937 bp from pter      End:
46,879,520 bp from pter
Size:
19,584 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: FAAH1_HUMAN, O00519 (See protein sequence)
Recommended Name: Fatty-acid amide hydrolase 1  
Size: 579 amino acids; 63066 Da
Subunit: Homodimer (By similarity)
Subcellular location: Endomembrane system; Single-pass membrane protein. Cytoplasm, cytoskeleton. Note=Seems to be
attached to intracellular membranes and a portion of the cytoskeletal network
Secondary accessions: D3DQ19 Q52M86 Q5TDF8

Explore the universe of human proteins at neXtProt for FAAH: NX_O00519

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_O00519

  • 3 DME Specific Peptides for FAAH (O00519)
     DIGGSIR  GGSIRFP  ALPGASG 

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

    REFSEQ proteins: NP_001432.2  
    ENSEMBL proteins: 
     ENSP00000243167  

    Human Recombinant Protein Products: 
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    Novus Biologicals FAAH Protein
    Novus Biologicals FAAH Lysate
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    Uscn Proteins for FAAH

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005737cytoplasm IDA--
    GO:0005856cytoskeleton IEA--
    GO:0012505endomembrane system IEA--
    GO:0016021integral to membrane IEA--
    GO:0031090organelle membrane ISS--


    FAAH for ontologies           About GeneDecksing



    FAAH Antibody Products: 
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    Uscn ELISAs and CLIAs for FAAH


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

    FAAH for domains           About GeneDecksing

    4 InterPro domains/families:
     IPR020556 Amidase_CS
     IPR000120 Amidase
     IPR023631 Amidase_dom
     IPR015830 Amidase_fun

    Graphical View of Domain Structure for InterPro Entry O00519

    ProtoNet protein and cluster: O00519

    1 Blocks protein family: IPB000120 Amidase

    UniProtKB/Swiss-Prot: FAAH1_HUMAN, O00519
    Similarity: Belongs to the amidase 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: FAAH1_HUMAN, O00519
    Function: Degrades bioactive fatty acid amides like oleamide, the endogenous cannabinoid, anandamide and myristic amide
    to their corresponding acids, thereby serving to terminate the signaling functions of these molecules. Hydrolyzes
    polyunsaturated substrate anandamide preferentially as compared to monounsaturated substrates
    Catalytic activity: Anandamide + H(2)O = arachidonic acid + ethanolamine
    Catalytic activity: Oleamide + H(2)O = oleic acid + NH(3)
    Enzyme regulation: Inhibited by O-aryl carbamates and alpha-keto heterocytes

         Genatlas biochemistry entry for FAAH:
    fatty acid amide hydroxylase,expressed in liver and brain not in heart and lung,degrading neuromodulatory fatty acids
    such as oleamide and anandamide

    Enzyme Numbers (IUBMB): EC 3.5.1.991 EC 3.5.12 EC 3.5.1.n22

    miRNA
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    hsa-miR-198 hsa-miR-943
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    Inhib. RNA
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for FAAH

    Gene Ontology (GO): 5/8 molecular function terms (GO ID links to tree view) (see all 8):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0004040amidase activity ----
    GO:0005543phospholipid binding ----
    GO:0008289lipid binding ----
    GO:0016788hydrolase activity, acting on ester bonds ----
    GO:0016884carbon-nitrogen ligase activity, with glutamine as amido-N-donor IEA--


    FAAH for ontologies           About GeneDecksing


    3 GenomeRNAi human phenotypes for FAAH:
     Decreased cilium length  Decreased cilium length after   Synthetic lethal with c-Myc af 

    Animal Models:
         Mouse knock-outs for FAAH: Faahtm1Lex Faahtm1Crv
         7 MGI mutant phenotypes (inferred from 2 alleles(MGI details for Faah):
     behavior/neurological  homeostasis/metabolism  integument  mortality/aging  muscle 
     nervous system  normal 

    FAAH for phenotypes           About GeneDecksing


    (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  About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1Acyl chain remodelling of PE
    Anandamide biosynthesis and metabolism0.13
    Anandamide biosynthesis and metabolism0.13
    2anandamide degradation
    anandamide degradation1.00
    3Glucose / Energy Metabolism
    Glucose / Energy Metabolism1.00

    Pathway sources
    See GeneCards unified pathways
    Show all pathways

    1 EMD Millipore Pathway for FAAH
        Anandamide biosynthesis and metabolism


    1 Cell Signaling Technology (CST) Pathway for FAAH
        Glucose / Energy Metabolism

    1 GeneGo (Thomson Reuters) Pathway for FAAH
        Anandamide biosynthesis and metabolism

    1 BioSystems Pathway for FAAH 
        anandamide degradation



    FAAH for pathways           About GeneDecksing

    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for FAAH

    5/16 Interacting proteins for FAAH (O005193) via UniProtKB, MINT, STRING, and/or I2D (see all 16)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    MMEP084733I2D: score=2 
    ACACBO007633I2D: score=1 
    CTU1Q7Z7A33I2D: score=1 
    CYC1P085743I2D: score=1 
    GDAQ9Y2T33I2D: score=1 
    About this table

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0009062fatty acid catabolic process IDA9122178


    FAAH 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

    FAAH for compounds           About GeneDecksing

    EMD Millipore small molecules for FAAH:
    Small Molecule - inhibitor
    Enzo Life Sciences drugs & compounds for FAAH

    Compounds for FAAH available from Tocris Bioscience    About this table
    CompoundAction CAS #
    MAFP Potent, irreversible FAAH inhibitor [188404-10-6]
    Arachidonyl serotoninDual FAAH inhibitor/TRPV1 antagonist[187947-37-1]
    JNJ 1661010 Selective, reversible FAAH inhibitor [681136-29-8]
    PalmitoylisopropylamideInhibitor of FAAH[189939-61-5]
    PF 750Selective FAAH inhibitor[959151-50-9]

    1 HMDB Compound for FAAH    About this table
    CompoundSynonyms CAS #PubMed Ids
    AnandamideAnandamide (20.4, n-6) (see all 13)94421-68-8--

    6 DrugBank Compounds for FAAH    About this table
    CompoundSynonyms CAS #TypeActionsPubMed Ids
    Methoxy arachidonyl fluorophosphonate-- --target--17139284 17016423 10592235
    Propofol2,6-Diisopropylphenol (see all 2)2078-54-8enzymesubstrate19933260 10592235
    ThiopentalPenthiobarbital (see all 10)76-75-5targetinhibitor11752352 12839875
    1-DODECANOL-- --target--10592235
    4-(3-{[5-(trifluoromethyl)pyridin-2-yl]oxy}benzyl)piperidine-1-carboxylic acid-- --target--10592235
    4-(quinolin-3-ylmethyl)piperidine-1-carboxylic acid-- --target--10592235

    10/39 Novoseek chemical compound relationships for FAAH gene (see all 39)    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    anandamide 96.8 337 11353795 (8), 11118429 (6), 17676056 (5), 10431820 (4) (see all 99)
    2-arachidonoylglycerol 94.2 88 11095952 (4), 18566995 (3), 18394720 (3), 15923084 (2) (see all 30)
    oleamide 93.7 48 10805767 (2), 17177441 (2), 11585048 (2), 17279740 (1) (see all 24)
    urb 597 92.8 37 18814866 (3), 17314320 (2), 16834756 (2), 17511970 (2) (see all 20)
    monoacylglycerol 89.6 52 17649977 (2), 18289091 (2), 17621164 (2), 16854070 (1) (see all 33)
    palmitoylethanolamide 89.5 23 11485574 (4), 11585048 (2), 10431820 (1), 10692582 (1) (see all 9)
    glyceryl arachidonate 81.7 1 16181610 (1)
    linoleoyl ethanolamide 79.8 1 9822713 (1)
    mafp 77.3 11 11118429 (3), 15910884 (1), 11353795 (1), 14718261 (1) (see all 5)
    rimonabant 73.9 3 19559363 (1), 19374636 (1), 16129456 (1)

    Search CenterWatch for drugs/clinical trials and news about FAAH / FAAH1 

    (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 FAAH gene: 
    NM_001441.2  

    Unigene Cluster for FAAH:

    Fatty acid amide hydrolase
    Hs.720143  [show with all ESTs]
    Unigene Representative Sequence: NM_001441
    6 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000243167(uc001cpu.2 uc001cpv.2) ENST00000468718 ENST00000493735
    ENST00000484697 ENST00000489366 ENST00000493636

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    Additional cDNA sequence: 

    AL050372.1 BC034478.1 BC093632.1 BC110404.1 BC111941.1 U82535.1 

    11 DOTS entries:

    DT.313625  DT.91741626  DT.121326323  DT.87016642  DT.121326472  DT.95332161  DT.95332175  DT.121326446 
    DT.91685857  DT.121326505  DT.121326373 

    24/336 AceView cDNA sequences (see all 336):

    CR620787 BQ424895 BQ014732 CA502993 AI565253 AL042404 BF726379 AK128066 
    AI686717 AK021577 AI920966 CA395976 AA887288 CF529182 U82535 BU171186 
    AI375665 CB049339 BF913261 NM_199044 AW273419 BI762645 CD722946 AI951464 

    GeneLoc Exon Structure

    5 Alternative Splicing Database (ASD) splice patterns (SP) for FAAH    About this scheme

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


    ECgene alternative splicing isoforms for FAAH

    (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

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

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

    About this image
    See FAAH Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for FAAH

    SOURCE GeneReport for Unigene cluster: Hs.720143

    UniProtKB/Swiss-Prot: FAAH1_HUMAN, O00519
    Tissue specificity: Highly expressed in the brain, small intestine, pancreas, skeletal muscle and testis. Also
    expressed in the kidney, liver, lung, placenta and prostate

        SABiosciences Expression via Pathway-Focused PCR Array including FAAH: 
              Drug Metabolism in human mouse rat

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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for FAAH

    (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 FAAH 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 FAAH1 fatty acid amide hydrolase 63.32(n)
    57.27(a)
      424614  XM_422450.3  XP_422450.1 
    lizard
    (Anolis carolinensis)
    Reptilia FAAH6
    --
    56(a)
    1 ↔ 1
    4(112196096-112226198)
    African clawed frog
    (Xenopus laevis)
    Amphibia Xl.113062 Xenopus laevis transcribed sequence with weak similarity more 71.61(n)    BX851598.1 
    zebrafish
    (Danio rerio)
    Actinopterygii si:zfos-1404b8.26
    si:zfos-1404b8.2
    50(a)
    1 ↔ 1
    6(3324243-3352911)
    worm
    (Caenorhabditis elegans)
    Secernentea C25A1.53 Yeast hypothetical 44.9 KD protein like 45(a)
    (best of 7)
      I(10185243-10186628)   --
    thale cress
    (Arabidopsis thaliana)
    eudicotyledons AT5G073606
    Amidase family protein
    12(a)
    possible ortholog
    5(2326704-2330142)
    rice
    (Oryza sativa)
    Liliopsida --
    amidase, putative, expressed
    11(a)
    possible ortholog
    11(19106088-19110227)


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

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for FAAH gene
    FAAH22  
    1 SIMAP similar gene for FAAH using alignment to 1 protein entry:     FAAH1_HUMAN:
    DKFZp434A091

    FAAH for paralogs           About GeneDecksing


    1 Pseudogenes.org Pseudogene for FAAH
    PGOHUM00000244703


    (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

    UniProtKB/Swiss-Prot: FAAH1_HUMAN, O00519
    Polymorphism: Variant Thr-129 seems to be strongly associated with illegal drug use and dependence. This variant
    displays normal catalytic properties but an enhanced sensitivity to proteolytic degradation


    10/593 NCBI SNPs in FAAH are shown (see all 593    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 1 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs3244201,2
    C,F,O,A,H,other46870761(+) AGGCCC/ACAAGG 2 /T /P mis1 ese341Minor allele frequency- A:0.26EA NA MN NS WA CSA EU 9775
    rs563068491,2
    C,F,--46857947(+) GTGGCA/GCGATC 1 -- us2k13Minor allele frequency- G:0.33WA NA 6
    rs1897595791,2
    --46857967(+) TGCAAC/GCTCCG 1 -- us2k10--------
    rs1829908901,2
    --46858017(+) AGTAGC/TTGGGA 1 -- us2k10--------
    rs617846351,2
    --46858025(+) GGACTA/GCAGGC 1 -- us2k10--------
    rs1501475561,2
    --46858029(+) TACAGA/GCGCCC 1 -- us2k10--------
    rs1879527071,2
    --46858086(+) TTTCAC/TGGTGT 1 -- us2k10--------
    rs120396191,2
    --46858088(+) tcacgA/Gtgtta 1 -- us2k10--------
    rs3244151,2
    C,H,--46858129(-) GCCGGC/TGGATC 1 -- us2k18Minor allele frequency- T:0.00NA WA CSA 16
    rs1916253401,2
    --46858229(+) TCTCTC/GTTTGC 1 -- us2k10--------

    HapMap Linkage Disequilibrium report for FAAH (46859937 - 46879520 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
          Database of Genomic Variants (DGV) variations for FAAH: --
    Human Gene Mutation Database (HGMD): FAAH

    SABiosciences Cancer Mutation PCR Assays
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    DNA2.0 Custom Variant and Variant Library Synthesis for FAAH

    (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

    FAAH for disorders           About GeneDecksing

    OMIM gene information: 602935    OMIM disorders: --

    20/42 diseases for FAAH (see all 42):    About MalaCards
    drug addiction    back pain    cannabis dependence    bulimia nervosa
    somatoform disorder    spontaneous abortion    anorexia nervosa    eating disorder
    inflammatory bowel disease    multiple sclerosis    huntington's disease    insulin resistance
    bipolar disorder    constipation    diabetes mellitus    alzheimer's disease
    rheumatoid arthritis    down syndrome    neurodegenerative disease    obesity, association with

    10/23 Novoseek disease relationships for FAAH gene (see all 23)    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    miscarriage recurrent 36.8 10 18805581 (6), 12744923 (1), 14580383 (1)
    obesity 33.7 46 20044928 (7), 18819056 (3), 20065978 (2), 19958092 (2) (see all 11)
    catalepsy 31.6 1 16834756 (1)
    miscarriage 31.4 7 19419760 (3), 11390466 (1), 15464041 (1), 18805581 (1) (see all 5)
    inflammation 21.5 17 19184452 (2), 17434980 (1), 14561206 (1), 17949010 (1) (see all 10)
    multiple sclerosis 20.9 3 17329437 (1), 16596785 (1)
    motor disorder 19.7 1 12505686 (1)
    hyperalgesia 16.4 1 17279090 (1)
    anxiety depression 15.2 4 17217969 (1), 19850474 (1), 20462810 (1)
    glioma 15.1 2 11118429 (1), 17325653 (1)

    Genetic Association Database (GAD): FAAH
    Human Genome Epidemiology (HuGE) Navigator: FAAH (50 documents)

    Export disorders for FAAH 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 FAAH gene, integrated from 9 sources (see all 329):
    (articles sorted by number of sources associating them with FAAH)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Molecular characterization of human and mouse fatty acid amide hydrolases. (PubMed id 9122178)1, 2, 3, 9 Giang D.K. and Cravatt B.F. (1997)
    2. A missense mutation in human fatty acid amide hydrolase associated with problem drug use. (PubMed id 12060782)1, 2, 4 Sipe J.C.... Cravatt B.F. (2002)
    3. Conserved chromosomal location and genomic structure of human and mouse fatty-acid amide hydrolase genes and evaluation of clasper as a candidate neurological mutation. (PubMed id 9878243)1, 2, 9 Wan M.... Francke U. (1998)
    4. A nonsynonymous polymorphism in the human fatty acid amide hydrolase gene did not associate with either methamphetamine dependence or schizophrenia. (PubMed id 15721218)1, 4, 9 Morita Y....Kuroda S. (2005)
    5. The DNA sequence and biological annotation of human chromosome 1. (PubMed id 16710414)1, 2 Gregory S.G.... Bentley D.R. (2006)
    6. Overweight and obesity associated with a missense polymorphism in fatty acid amide hydrolase (FAAH). (PubMed id 15809662)1, 4 Sipe J.C....Beutler E. (2005)
    7. 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)
    8. Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides. (PubMed id 12665801)1, 2 Gevaert K.... Vandekerckhove J. (2003)
    9. Mutation screen and association studies for the fatty acid amide hydrolase (FAAH) gene and early onset and adult obesity. (PubMed id 20044928)1, 9 MA1ller T.D....Hinney A. (2010)
    10. Expression and function of fatty acid amide hydrolase in prostate cancer. (PubMed id 18566995)1, 9 Endsley M.P....Nithipatikom K. (2008)

    (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: 2166 HGNC: 3553 AceView: FAAHandNSUN4 Ensembl:ENSG00000117480 euGenes: HUgn2166
    ECgene: FAAH H-InvDB: FAAH

    (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 FAAH Pharmacogenomics, SNPs, Pathways
    NIEHS-SNPshttp://egp.gs.washington.edu/data/faah/

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

    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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