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FAM89B Gene

protein-coding   GIFtS: 41
GCID: GC11P065339

Family With Sequence Similarity 89, Member B
  See related diseases
at
MalaCards
 

Aliases
for FAM89B gene

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


Summaries
for FAM89B gene

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




Genomic Views
for FAM89B 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 75), Regulatory elements and Epigenetics data according to QIAGEN, and/or SwitchGear Genomics)
About This Section

TryGeneCards Plus		 Regulatory elements:
   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 plasmid: FAM89B promoter sequence
   Search Chromatin IP Primers for FAM89B

Epigenetics:
DNA Methylation CpG Assay Predesigned for Pyrosequencing 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

Proteins
for FAM89B gene

(According to 1UniProtKB, HORDE, 2neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, 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., Antibodies by EMD Millipore, R&D Systems, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, and/or Cloud-Clone Corp.)
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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)
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: 

  • Modification sites at neXtProt
  • Modification sites at PhosphoSitePlus

    • See FAM89B Protein Expression from SPIRE MOPED, PaxDB, and MaxQB

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

    ENSEMBL proteins: 
     ENSP00000314829   ENSP00000402439   ENSP00000431459  

    FAM89B Human Recombinant Protein Products:

    Browse Purified and Recombinant Proteins at EMD Millipore
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    OriGene Purified Protein for FAM89B
    OriGene Protein Over-expression Lysate for FAM89B
    OriGene MassSpec 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

    FAM89B Antibody Products:

    Browse EMD Millipore's Extensive Line of Mono- and Polyclonal Antibodies
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    Novus Biologicals FAM89B Antibodies
    Abcam antibodies for FAM89B
    Cloud-Clone Corp. Antibodies for FAM89B
    Search ThermoFisher Antibodies for FAM89B
    Search LSBio for Antibodies for FAM89B

    FAM89B Assay Products:

    Browse Kits and Assays available from EMD Millipore
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    Browse Enzo Life Sciences for kits & assays
    Cloud-Clone Corp. ELISAs for FAM89B
    Cloud-Clone Corp. CLIAs for FAM89B

    Domains /
    Families
    for FAM89B gene

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

    TryGeneCards Plus    		 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


    Function
    for FAM89B gene

    (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,
    transcription factor targeting from QIAGEN and/or HOMER, miRNA Gene Targets from miRTarBase, shRNA from OriGene, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, SwitchGear Genomics, Gene Editing from DNA2.0, Clones from OriGene, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, ESI BIO, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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    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:    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: Let us create your new Knockout/Knockin mouse model for FAM89B
       inGenious Targeting Laboratory: Contact us about creating complex and humanized mouse models 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
    Products:            		miRTarBase miRNAs that target FAM89B:
    hsa-mir-7-5p (MIRT025771), hsa-mir-93-3p (MIRT038867)

    Block miRNA regulation of human, mouse, rat FAM89B using miScript Target Protectors
    3 qRT-PCR Assays for microRNAs that regulate FAM89B:
    hsa-miR-22 hsa-miR-4303 hsa-miR-646
    SwitchGear 3'UTR luciferase reporter plasmid: FAM89B 3' UTR sequence
    Inhib. RNA
    Products:            		OriGene RNAi products in human, mouse, rat for FAM89B
    Predesigned siRNA for gene silencing in human, mouse, rat FAM89B

    Gene Editing
    Products:    		DNA2.0 Custom Protein Engineering Service for FAM89B

    Clone
    Products:             		 OriGene clones in human, mouse for FAM89B (see all 18)
    OriGene ORF clones in mouse, rat for FAM89B
    OriGene custom cloning services - gene synthesis, subcloning, mutagenesis, variant library, vector shuttling
    GenScript: all cDNA clones in your preferred vector (see all 3): FAM89B (NM_152832)
    Browse Sino Biological Human cDNA Clones
    DNA2.0 Custom Codon Optimized Gene Synthesis Service for FAM89B
    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat FAM89B

    Cell Line
    Products:             		GenScript Custom overexpressing Cell Line Services for FAM89B
    Browse ESI BIO Cell Lines and PureStem Progenitors for FAM89B 
    In Situ Assay
    Products:       
         		Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for FAM89B


    Localization
    for FAM89B gene

    (According to UniProtKB, COMPARTMENTS Subcellular localization database, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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    Subcellular locations from UniProtKB/Swiss-Prot
    FA89B_HUMAN, Q8N5H3: Isoform 3: Cytoplasm (By similarity)
    FA89B_HUMAN, Q8N5H3: Isoform 1: Cell surface (By similarity)
    Subcellular locations from COMPARTMENTS: 

    CompartmentConfidence
    cytosol1
    extracellular1
    mitochondrion1
    nucleus1
    peroxisome1

    Gene Ontology (GO): 2 cellular component terms:    About this table

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

    FAM89B for ontologies           About GeneDecksing


    Pathways & Interactions
    for FAM89B gene

    (SuperPaths according to PathCards, Pathways according to 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 QIAGEN, 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 Apr 2014 via Entrez Gene).
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        Custom Pathway & Disease-focused RT2 Profiler PCR Arrays for FAM89B
    Interactions:

        Search GeneGlobe Interaction Network 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:    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



    Drugs & Compounds
    for FAM89B gene

    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience, ApexBio, HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB)
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    Browse Small Molecules at EMD Millipore
       Browse drugs & compounds from Enzo Life Sciences
      Browse compounds at ApexBio 

    Browse Tocris compounds for FAM89B (FA89B)



    Transcripts
    for FAM89B gene

    (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,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN, SwitchGear Genomics,
    Tagged/untagged cDNA clones from OriGene, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, and/or QIAGEN )
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    REFSEQ mRNAs for FAM89B gene (3 alternative transcripts): 
    NM_001098784.1  NM_001098785.1  NM_152832.2  

    3 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000316409(uc001oem.2 uc001oen.2 uc001oel.2) ENST00000449319
    ENST00000530349
    miRNA
    Products:             		 Block miRNA regulation of human, mouse, rat FAM89B using miScript Target Protectors
    3 qRT-PCR Assays for microRNAs that regulate FAM89B:
    hsa-miR-22 hsa-miR-4303 hsa-miR-646
    SwitchGear 3'UTR luciferase reporter plasmid: FAM89B 3' UTR sequence
    Inhib. RNA
    Products:             		OriGene RNAi products in human, mouse, rat for FAM89B
    Predesigned siRNA for gene silencing in human, mouse, rat FAM89B
    Clone
    Products:             		 OriGene clones in human, mouse for FAM89B (see all 18)
    OriGene ORF clones in mouse, rat for FAM89B
    OriGene custom cloning services - gene synthesis, subcloning, mutagenesis, variant library, vector shuttling
    GenScript: all cDNA clones in your preferred vector (see all 3): FAM89B (NM_152832)
    DNA2.0 Custom Codon Optimized Gene Synthesis Service for FAM89B
    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat FAM89B
    Primer
    Products:            		OriGene qPCR primer pairs and template standards for FAM89B
    OriGene qSTAR qPCR primer pairs in human, mouse for FAM89B
    Search Pre-validated RT2 qPCR Primer Assays in human, mouse, rat FAM89B
      QuantiTect SYBR Green Assays in human, mouse, rat FAM89B
      QuantiFast Probe-based Assays in human, mouse, rat FAM89B

    Selected AceView cDNA sequences (see all 429):

    BM127932 CR610230 AI214414 AF052151 AI050809 AI125339 BC014791 BM128003 
    AI189581 AI367075 AI968474 AI271516 BU625777 AA236870 AA313202 AI991293 
    CB148370 AI494494 BG740803 AI123851 CR612503 BX379528 BQ879514 AW275991 

    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

    Expression
    for FAM89B gene

    (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™, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MaxQB, plus additional links to SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from QIAGEN, Primers from OriGene, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
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    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

    FAM89B Protein expression data from MOPED1, PaxDb2 and MaxQB3:     About this image

    FAM89B Protein Expression
        Custom PCR Arrays for FAM89B
    Primer
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    OriGene qSTAR qPCR primer pairs in human, mouse for FAM89B
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    In Situ
    Assay Products:     
         		Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for FAM89B

    Orthologs
    for FAM89B gene

    (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)
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    This gene was present in the common ancestor of chordates.

    Orthologs for FAM89B gene from Selected 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
    for FAM89B gene

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
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    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



    Genomic Variants
    for FAM89B gene

    (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), the Human Cytochrome P450 Allele Nomenclature Database, and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers, Cancer Mutation PCR Arrays and Assays, and Copy Number PCR Arrays from QIAGEN)
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    Selected SNPs for FAM89B (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) Selected 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

    Site Specific Mutation Identification with PCR Assays
    SeqTarget long-range PCR primers for resequencing FAM89B
    DNA2.0 Custom Variant and Variant Library Synthesis for FAM89B

    Disorders / Diseases
    for FAM89B gene

    (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

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    2 diseases for FAM89B:    
    About MalaCards
    sjogren's syndrome    scleroderma


    FAM89B for disorders           About GeneDecksing


    Export disorders for FAM89B gene to outside databases

    Publications
    for FAM89B gene

    (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

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    PubMed articles for FAM89B gene, integrated from 10 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. (Genome Res. 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. (Biochem. Biophys. Res. Commun. 1999)
    3. A novel membrane protein is a mouse mammary tumor virus receptor. (PubMed id 9525630)1, 3 Golovkina T.V....Ross S.R. (J. Virol. 1998)
    4. Identification of human homologues of the mouse mammary tumor virus receptor. (PubMed id 11958456)1, 9 Stewart A.F. (Arch. Virol. 2002)
    5. Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis. (PubMed id 20068231)2 Olsen J.V....Mann M. (Sci. Signal. 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. (Genomics 2007)
    7. Human chromosome 11 DNA sequence and analysis including novel gene identification. (PubMed id 16554811)2 Taylor T.D....Sakaki Y. (Nature 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. (Proc. Natl. Acad. Sci. U.S.A. 2002)
    9. Large-scale concatenation cDNA sequencing. (PubMed id 9110174)1 Yu W.... Gibbs R.A. (Genome Res. 1997)
    10. A "double adaptor" method for improved shotgun library construction. (PubMed id 8619474)1 Andersson B.... Gibbs R.A. (Anal. Biochem. 1996)

    External Searches for FAM89B gene

    (in PubMed, OMIM, and NCBI Bookshelf)
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     ANDOR
    Aliases
    Free Text  
      Query String
    		PubMed
    OMIM
    NCBI Bookshelf
      (Note: In FireFox, select the above section and copy using Ctrl-C)

    Genome Databases showing FAM89B gene

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
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    Entrez Gene: 23625 HGNC: 16708 AceView: SSSCA1andMTVR1 Ensembl:ENSG00000176973 euGenes: HUgn23625
    ECgene: FAM89B H-InvDB: FAM89B

    Other Databases showing FAM89B gene

    (According to HUGE)
    About This Section

    TryGeneCards Plus    		   --

    Specialized Databases showing FAM89B gene

    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL, and/or others, e.g. Wikipedia and GeneReviews, via UniProtKB/Swiss-Prot)
    About This Section

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    NameDescription
    PharmGKB entry for FAM89B Pharmacogenomics, SNPs, Pathways

    Intellectual Property
    for FAM89B gene

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section

    TryGeneCards Plus    		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



    Products
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    About This Section

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