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

FAM89B Gene

protein-coding   GIFtS: 43
GCID: GC11P065339

Family With Sequence Similarity 89, Member B

  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
Family With Sequence Similarity 89, Member B1 2
MTVR12
Mammary Tumor Virus Receptor Homolog 12
Protein FAM89B2

External Ids:    HGNC: 167081   Entrez Gene: 236252   Ensembl: ENSG000001769737   UniProtKB: Q8N5H33   

Export aliases for FAM89B gene to outside databases

Previous GC identifers: GC11P065097 GC11P061667


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

GeneCards Summary for FAM89B Gene: 
FAM89B (family with sequence similarity 89, member B) is a protein-coding gene. Diseases associated with FAM89B include sjogren's syndrome, and scleroderma. GO annotations related to this gene include transcription corepressor binding. An important paralog of this gene is FAM89A.

UniProtKB/Swiss-Prot: FA89B_HUMAN, Q8N5H3
Function: Negatively regulates TGF-beta-induced signaling; in cooperation with SKI prevents the translocation of
SMAD2 from the nucleus to the cytoplasm in response to TGF-beta (By similarity)




(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_000011.9  NC_018922.2  NT_167190.1  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the FAM89B gene promoter:
         Spz1   E2F-1   E2F   p53   NRSF form 1   FOXO3   Nkx2-5   NRSF form 2   C/EBPalpha   GATA-2   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidFAM89B promoter sequence
   Search SABiosciences Chromatin IP Primers for FAM89B

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat FAM89B


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

Entrez Gene cytogenetic band: 11q13   Ensembl cytogenetic band:  11q13.1   HGNC cytogenetic band: 11q23

FAM89B Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
FAM89B gene location

GeneLoc information about chromosome 11         GeneLoc Exon Structure

GeneLoc location for GC11P065339:  view genomic region     (about GC identifiers)

Start:
65,339,820 bp from pter      End:
65,341,669 bp from pter
Size:
1,850 bases      Orientation:
plus 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: FA89B_HUMAN, Q8N5H3 (See protein sequence)
Recommended Name: Protein FAM89B  
Size: 189 amino acids; 20147 Da
Subunit: Interacts with SKI (By similarity)
Subcellular location: Isoform 3: Cytoplasm (By similarity)
Subcellular location: Isoform 1: Cell surface (By similarity)
Secondary accessions: E9PB01 E9PL72 Q6PJ27
Alternative splicing: 4 isoforms:  Q8N5H3-3   Q8N5H3-1   Q8N5H3-2   Q8N5H3-4   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for FAM89B: NX_Q8N5H3

Explore proteomics data for FAM89B at MOPED 

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_Q8N5H3

  • FAM89B Protein expression data from MOPED1, PaxDb2 and MAXQB3 :    About this image 

    FAM89B Protein Expression
    REFSEQ proteins (3 alternative transcripts): 
    NP_001092254.1  NP_001092255.1  NP_690045.1  

    ENSEMBL proteins: 
     ENSP00000314829   ENSP00000402439   ENSP00000431459  

    Human Recombinant Protein Products for FAM89B: 
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    GenScript Custom Purified and Recombinant Proteins Services for FAM89B
    Novus Biologicals FAM89B Protein
    Novus Biologicals FAM89B Lysates
    Browse Sino Biological Recombinant Proteins
    Browse Sino Biological Cell Lysates 
    Browse ProSpec Recombinant Proteins
    Cloud-Clone Corp. Proteins for FAM89B 

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005737cytoplasm ISS--
    GO:0009986cell surface IEA--

    FAM89B for ontologies           About GeneDecksing



    FAM89B Antibody Products: 
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    Cloud-Clone Corp. ELISAs for FAM89B 
    Cloud-Clone Corp. CLIAs for FAM89B


    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section
    1 InterPro protein domain:
     IPR026654 FAM89

    Graphical View of Domain Structure for InterPro Entry Q8N5H3

    ProtoNet protein and cluster: Q8N5H3

    UniProtKB/Swiss-Prot: FA89B_HUMAN, Q8N5H3
    Similarity: Belongs to the FAM89 family


    FAM89B 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: FA89B_HUMAN, Q8N5H3
    Function: Negatively regulates TGF-beta-induced signaling; in cooperation with SKI prevents the translocation of
    SMAD2 from the nucleus to the cytoplasm in response to TGF-beta (By similarity)

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0001222transcription corepressor binding ISS--
    GO:0005515protein binding ----
         
    FAM89B for ontologies           About GeneDecksing


    Phenotypes:
         1 GenomeRNAi human phenotype for FAM89B:
     Decreased melanin production 

    Animal Models:
       inGenious Targeting Laboratory - Custom generated mouse model solutions for FAM89B 
       inGenious Targeting Laboratory - Custom generated inducible mouse model solutions for FAM89B

       genOway customized KO model: permanent, tissue-specific or time-controlled inactivation for FAM89B 
       genOway customized Knockin model: humanization, point mutation, expression monitoring, etc. for FAM89B 

    miRNA
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    3 QIAGEN miScript miRNA Assays for microRNAs that regulate FAM89B:
    hsa-miR-22 hsa-miR-4303 hsa-miR-646
    SwitchGear 3'UTR luciferase reporter plasmidFAM89B 3' UTR sequence
    Inhib. RNA
    Products:
        
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    GenScript: all cDNA clones in your preferred vector (see all 3): FAM89B (NM_152832)
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                         Customized lentivirus expression plasmids for stable overexpression of FAM89B 

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    In Situ Assay
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for FAM89B


    (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 FAM89B

    1 Interacting protein for FAM89B (Q8N5H33) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    SEPT8Q925993I2D: score=1 
    About this table

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0030512negative regulation of transforming growth factor beta receptor signaling pathway ISS--
    GO:0060392negative regulation of SMAD protein import into nucleus ISS--

    FAM89B for ontologies           About GeneDecksing



    (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 FAM89B (FA89B)

    Search CenterWatch for drugs/clinical trials and news about FAM89B / FA89B

    (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 FAM89B gene (3 alternative transcripts): 
    NM_001098784.1  NM_001098785.1  NM_152832.2  

    Unigene Cluster for FAM89B:

    Family with sequence similarity 89, member B
    Hs.731854  [show with all ESTs]
    Unigene Representative Sequence: BC023991
    3 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000316409(uc001oem.2 uc001oen.2 uc001oel.2) ENST00000449319
    ENST00000530349
    miRNA
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    QIAGEN Custom miScript Target Protector blocks miRNA-binding site of human, mouse, rat FAM89B
    3 QIAGEN miScript miRNA Assays for microRNAs that regulate FAM89B:
    hsa-miR-22 hsa-miR-4303 hsa-miR-646
    SwitchGear 3'UTR luciferase reporter plasmidFAM89B 3' UTR sequence
    Inhib. RNA
    Products:
         
    Browse for Gene Knock-down Tools from EMD Millipore
    OriGene RNAi products in human, mouse, rat for FAM89B
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    DNA2.0 Custom Codon Optimized Gene Synthesis Service for FAM89B
    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat FAM89B
    Sirion Biotech Customized lentivirus for stable overexpression of FAM89B 
                         Customized lentivirus expression plasmids for stable overexpression of FAM89B 
    Primer
    Products:
        
    OriGene qPCR primer pairs and template standards for FAM89B
    OriGene qSTAR qPCR primer pairs in human, mouse for FAM89B
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      QIAGEN QuantiTect SYBR Green Assays in human, mouse, rat FAM89B
      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat FAM89B

    Additional mRNA sequence: 

    AF052151.1 BC023991.2 BC032373.1 

    4 DOTS entries:

    DT.100038097  DT.447144  DT.120737182  DT.100773817 

    24/429 AceView cDNA sequences (see all 429):

    BM468381 BM127932 CR610230 AI214414 AF052151 BQ672827 CR615607 H68581 
    CB121478 AJ712654 AI669222 CB138486 AI083960 CB137711 CB135184 AI872507 
    F20427 BF928812 BM788839 AI277698 T34020 BM128255 CA426777 CB130083 

    GeneLoc Exon Structure

    3 Alternative Splicing Database (ASD) splice patterns (SP) for FAM89B    About this scheme

    ExUns: 1 ^ 2a · 2b · 2c · 2d · 2e
    SP1:                                    
    SP2:        -                           
    SP3:        -     -                     


    ECgene alternative splicing isoforms for FAM89B

    (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

    FAM89B expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: TGTGCACCCC
    FAM89B Expression
    About this image


    See FAM89B Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for FAM89B

    SOURCE GeneReport for Unigene cluster: Hs.731854
        SABiosciences Custom PCR Arrays for FAM89B
    Primer
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    OriGene qPCR primer pairs and template standards for FAM89B
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for FAM89B

    (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 chordates.

    Orthologs for FAM89B gene from 3/9 species (see all 9)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Fam89b1 , 5 family with sequence similarity 89, member B1, 5 88.36(n)1
    96.3(a)1
      19 (4.34 cM)5
    178261  NM_181452.21  NP_852117.21 
     57280875 
    African clawed frog
    (Xenopus laevis)
    Amphibia MGC534072 similar to Sjogren's syndrome/scleroderma autoantigen more 69.38(n)    BC043979.1 
    zebrafish
    (Danio rerio)
    Actinopterygii Dr.188832 Transcribed sequence with weak similarity to protein more 79.14(n)    CK356398.1 


    ENSEMBL Gene Tree for FAM89B (if available)
    TreeFam Gene Tree for FAM89B (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for FAM89B gene
    FAM89A2  
    1 SIMAP similar gene for FAM89B using alignment to 1 protein entry:     FA89B_HUMAN:
    FAM89A

    FAM89B 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

    10/27 SNPs in FAM89B are shown (see all 27)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 11 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1812263031,2
    --65339890(+) TGAGTA/GGATGT 3 -- ut510--------
    rs108960171,2
    C,F--65340135(+) CGGCCC/TCGGCC 3 -- ut51 ese31Minor allele frequency- T:0.12EA 120
    rs1867440491,2
    --65340754(+) TGGGCG/TGGGGC 3 -- int10--------
    rs1416940061,2
    C--65341056(+) TGCCCC/GAGACG 5 Q E mis1 ut311Minor allele frequency- G:0.00NA 4538
    rs1906860761,2
    C--65341192(+) GGAGCC/TTGCGC 3 -- ut310--------
    rs1119253081,2
    C--65341198(+) TGCGCA/C/GTTCCC 6 -- ut311CSA 1
    rs1829767401,2
    --65341252(+) AGAGGC/TGAAAC 3 -- ut310--------
    rs802830681,2
    C,F--65341273(+) TTTCTC/TCTGTC 3 -- ut311Minor allele frequency- T:0.04NA 120
    rs1876378451,2
    --65341439(+) GATTGA/GGATGA 3 -- ut310--------
    rs2015028241,2
    ----65341025(+) AGCCTG/ACCTCC 5 /L syn1 ut311Minor allele frequency- A:0.00EU 1311

    HapMap Linkage Disequilibrium report for FAM89B (65339820 - 65341669 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 10/12 variations for FAM89B (see all 12):    About this table     
    Variant IDTypeSubtypePubMed ID
    nsv897723CNV Loss21882294
    dgv1175n71CNV Loss21882294
    nsv897739CNV Loss21882294
    dgv1180n71CNV Loss21882294
    nsv897736CNV Loss21882294
    nsv897730CNV Loss21882294
    dgv1176n71CNV Loss21882294
    dgv1181n71CNV Loss21882294
    dgv1179n71CNV Loss21882294
    nsv897718CNV Loss21882294

    SABiosciences Cancer Mutation PCR Assays
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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
    2 diseases for FAM89B:    About MalaCards
    sjogren's syndrome    scleroderma


    FAM89B for disorders           About GeneDecksing


    Export disorders for FAM89B 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 FAM89B gene, integrated from 9 sources (see all 11):
    (articles sorted by number of sources associating them with FAM89B)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. 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)
    2. Novel related cDNAs (C184L, C184M, and C184S) from developing mouse brain encoding two apparently unrelated proteins. (PubMed id 10512749)1, 3 Sakuma-Takagi M....Kurihara T. (1999)
    3. A novel membrane protein is a mouse mammary tumor virus receptor. (PubMed id 9525630)1, 3 Golovkina T.V....Ross S.R. (1998)
    4. Identification of human homologues of the mouse mammary tumor virus receptor. (PubMed id 11958456)1, 9 Stewart A.F. (2002)
    5. Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis. (PubMed id 20068231)2 Olsen J.V....Mann M. (2010)
    6. hORFeome v3.1: a resource of human open reading frames representing over 10,000 human genes. (PubMed id 17207965)1 Lamesch P.... Vidal M. (2007)
    7. Human chromosome 11 DNA sequence and analysis including novel gene identification. (PubMed id 16554811)2 Taylor T.D....Sakaki Y. (2006)
    8. 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)
    9. Hepatitis C virus core protein interacts with 14-3-3 protein and activates the kinase Raf-1. (PubMed id )2 Aoki H.... Hino O. (2000)
    10. Large-scale concatenation cDNA sequencing. (PubMed id 9110174)1 Yu W.... Gibbs R.A. (1997)

    (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: 23625 HGNC: 16708 AceView: SSSCA1andMTVR1 Ensembl:ENSG00000176973 euGenes: HUgn23625
    ECgene: FAM89B H-InvDB: FAM89B

    (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 FAM89B 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 FAM89B gene:
    Search GeneIP for patents involving FAM89B

    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, Cloud-Clone Corp., Thermo Fisher Scientific, LSBio, Gene Editing from DNA2.0 and Sirion Biotech, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Sirion Biotech, 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, In Situ Hybridization Assays from
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     Proteins for FAM89B
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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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