Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

FAAH2 (fatty acid amide hydrolase 2)

Identity

Alias_namesAMDD
amidase domain containing
Alias_symbol (synonym)RP11-479E16.1
FLJ31204
FAAH-2
Other alias
HGNC (Hugo) FAAH2
LocusID (NCBI) 158584
Atlas_Id 62966
Location Xp11.21  [Link to chromosome band Xp11]
Location_base_pair Starts at 57313110 and ends at 57515629 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
ZNF767P (7q36.1) / FAAH2 (Xp11.21)

Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)FAAH2   26440
Cards
Entrez_Gene (NCBI)FAAH2  158584  fatty acid amide hydrolase 2
AliasesAMDD
GeneCards (Weizmann)FAAH2
Ensembl hg19 (Hinxton)ENSG00000165591 [Gene_View]  chrX:57313110-57515629 [Contig_View]  FAAH2 [Vega]
Ensembl hg38 (Hinxton)ENSG00000165591 [Gene_View]  chrX:57313110-57515629 [Contig_View]  FAAH2 [Vega]
ICGC DataPortalENSG00000165591
TCGA cBioPortalFAAH2
AceView (NCBI)FAAH2
Genatlas (Paris)FAAH2
WikiGenes158584
SOURCE (Princeton)FAAH2
Genetics Home Reference (NIH)FAAH2
Genomic and cartography
GoldenPath hg19 (UCSC)FAAH2  -     chrX:57313110-57515629 +  Xp11.21   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)FAAH2  -     Xp11.21   [Description]    (hg38-Dec_2013)
EnsemblFAAH2 - Xp11.21 [CytoView hg19]  FAAH2 - Xp11.21 [CytoView hg38]
Mapping of homologs : NCBIFAAH2 [Mapview hg19]  FAAH2 [Mapview hg38]
OMIM300654   
Gene and transcription
Genbank (Entrez)AF086253 AK055766 BC048279 BC073922 BX110322
RefSeq transcript (Entrez)NM_174912
RefSeq genomic (Entrez)NC_000023 NC_018934 NG_013232 NT_011630 NW_004929442
Consensus coding sequences : CCDS (NCBI)FAAH2
Cluster EST : UnigeneHs.745495 [ NCBI ]
CGAP (NCI)Hs.745495
Alternative Splicing GalleryENSG00000165591
Gene ExpressionFAAH2 [ NCBI-GEO ]   FAAH2 [ EBI - ARRAY_EXPRESS ]   FAAH2 [ SEEK ]   FAAH2 [ MEM ]
Gene Expression Viewer (FireBrowse)FAAH2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)158584
GTEX Portal (Tissue expression)FAAH2
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ6GMR7   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ6GMR7  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ6GMR7
Splice isoforms : SwissVarQ6GMR7
Catalytic activity : Enzyme3.5.1.99 [ Enzyme-Expasy ]   3.5.1.993.5.1.99 [ IntEnz-EBI ]   3.5.1.99 [ BRENDA ]   3.5.1.99 [ KEGG ]   
PhosPhoSitePlusQ6GMR7
Domaine pattern : Prosite (Expaxy)AMIDASES (PS00571)   
Domains : Interpro (EBI)Amidase    Amidase_CS    Amidase_dom   
Domain families : Pfam (Sanger)Amidase (PF01425)   
Domain families : Pfam (NCBI)pfam01425   
Conserved Domain (NCBI)FAAH2
DMDM Disease mutations158584
Blocks (Seattle)FAAH2
SuperfamilyQ6GMR7
Human Protein AtlasENSG00000165591
Peptide AtlasQ6GMR7
HPRD06551
IPIIPI00043550   
Protein Interaction databases
DIP (DOE-UCLA)Q6GMR7
IntAct (EBI)Q6GMR7
FunCoupENSG00000165591
BioGRIDFAAH2
STRING (EMBL)FAAH2
ZODIACFAAH2
Ontologies - Pathways
QuickGOQ6GMR7
Ontology : AmiGOmetabolic process  integral component of membrane  hydrolase activity  carbon-nitrogen ligase activity, with glutamine as amido-N-donor  
Ontology : EGO-EBImetabolic process  integral component of membrane  hydrolase activity  carbon-nitrogen ligase activity, with glutamine as amido-N-donor  
NDEx NetworkFAAH2
Atlas of Cancer Signalling NetworkFAAH2
Wikipedia pathwaysFAAH2
Orthology - Evolution
OrthoDB158584
GeneTree (enSembl)ENSG00000165591
Phylogenetic Trees/Animal Genes : TreeFamFAAH2
HOVERGENQ6GMR7
HOGENOMQ6GMR7
Homologs : HomoloGeneFAAH2
Homology/Alignments : Family Browser (UCSC)FAAH2
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerFAAH2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)FAAH2
dbVarFAAH2
ClinVarFAAH2
1000_GenomesFAAH2 
Exome Variant ServerFAAH2
ExAC (Exome Aggregation Consortium)FAAH2 (select the gene name)
Genetic variants : HAPMAP158584
Genomic Variants (DGV)FAAH2 [DGVbeta]
DECIPHER (Syndromes)X:57313110-57515629  ENSG00000165591
CONAN: Copy Number AnalysisFAAH2 
Mutations
ICGC Data PortalFAAH2 
TCGA Data PortalFAAH2 
Broad Tumor PortalFAAH2
OASIS PortalFAAH2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICFAAH2  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDFAAH2
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
LOVD (Leiden Open Variation Database)X-chromosome gene database
BioMutasearch FAAH2
DgiDB (Drug Gene Interaction Database)FAAH2
DoCM (Curated mutations)FAAH2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)FAAH2 (select a term)
intoGenFAAH2
Cancer3DFAAH2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM300654   
Orphanet
MedgenFAAH2
Genetic Testing Registry FAAH2
NextProtQ6GMR7 [Medical]
TSGene158584
GENETestsFAAH2
Huge Navigator FAAH2 [HugePedia]
snp3D : Map Gene to Disease158584
BioCentury BCIQFAAH2
ClinGenFAAH2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD158584
Chemical/Pharm GKB GenePA162385543
Clinical trialFAAH2
Miscellaneous
canSAR (ICR)FAAH2 (select the gene name)
Probes
Litterature
PubMed8 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAAH2
EVEXFAAH2
GoPubMedFAAH2
iHOPFAAH2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Mar 14 12:03:19 CET 2017

Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.