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FAM168A Gene

protein-coding   GIFtS: 44
GCID: GC11M073111

Family With Sequence Similarity 168, Member A

(Previous name: KIAA0280)
(Previous symbol: KIAA0280)
  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)
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Aliases
Family With Sequence Similarity 168, Member A1 2
KIAA02801 2 3
Tongue Cancer Chemotherapy Resistance-Associated Protein 11 2 3
TCRP12 3
Protein FAM168A2

External Ids:    HGNC: 289991   Entrez Gene: 232012   Ensembl: ENSG000000549657   UniProtKB: Q925673   

Export aliases for FAM168A gene to outside databases

Previous GC identifers: GC11U901028 GC11M072795 GC11M073117 GC11M069412


(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 FAM168A Gene:
FAM168A (family with sequence similarity 168, member A) is a protein-coding gene. Diseases associated with FAM168A include tongue cancer, and oral squamous cell carcinoma. An important paralog of this gene is FAM168B.


(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)
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RefSeq DNA sequence:
NC_000011.10  NT_167190.2  NC_018922.2  
Regulatory elements:
   Regulatory transcription factor binding sites in the FAM168A gene promoter:
         AhR   E2F-3a   E2F-4   E2F-5   E2F-2   NF-kappaB   E2F-1   E2F   FOXC1   NF-kappaB1   
         Other transcription factors

Browse SwitchGear Promoter luciferase reporter plasmids
   Search Chromatin IP Primers for FAM168A

Epigenetics:
DNA Methylation CpG Assay Predesigned for Pyrosequencing in human, mouse, rat FAM168A


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

Entrez Gene cytogenetic band: 11q13.4   Ensembl cytogenetic band:  11q13.4   HGNC cytogenetic band: 11q13.4

FAM168A Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
FAM168A gene location

GeneLoc information about chromosome 11         GeneLoc Exon Structure

GeneLoc location for GC11M073111:  view genomic region     (about GC identifiers)

Start:
73,111,532 bp from pter      End:
73,309,234 bp from pter
Size:
197,703 bases      Orientation:
minus strand

(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, Cloud-Clone Corp, and/or others.)
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UniProtKB/Swiss-Prot: F168A_HUMAN, Q92567 (See protein sequence)
Recommended Name: Protein FAM168A  
Size: 244 amino acids; 26184 Da
Subunit: May interact with FAM168B
Sequence caution: Sequence=BAA13408.1; Type=Erroneous initiation;
Secondary accessions: A2ICY2 A2ID81 Q86UG2
Alternative splicing: 3 isoforms:  Q92567-1   Q92567-2   Q92567-3   

Explore the universe of human proteins at neXtProt for FAM168A: NX_Q92567

Explore proteomics data for FAM168A at MOPED

Post-translational modifications: 

  • Modification sites at neXtProt
  • Modification sites at PhosphoSitePlus

  • See FAM168A Protein Expression from SPIRE MOPED, PaxDB, and MaxQB

    REFSEQ proteins (3 alternative transcripts): 
    NP_001272979.1  NP_001272980.1  NP_055974.1  

    ENSEMBL proteins: 
     ENSP00000064778   ENSP00000390501   ENSP00000348852  

    FAM168A Human Recombinant Protein Products:

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    OriGene Protein Over-expression Lysate for FAM168A
    OriGene Custom MassSpec
    OriGene Custom Protein Services for FAM168A
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    Novus Biologicals FAM168A Lysate
    Browse Sino Biological Recombinant Proteins
    Browse Sino Biological Cell Lysates
    Browse ProSpec Recombinant Proteins
    Browse Proteins at Cloud-Clone Corp.

    FAM168A Antibody Products:

    Browse EMD Millipore's Extensive Line of Mono- and Polyclonal Antibodies
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    Novus Biologicals FAM168A Antibodies
    Search for Antibodies for FAM168A at Abcam
    Browse Antibodies at Cloud-Clone Corp.
    ThermoFisher Antibodies for FAM168A
    Search LSBio for Antibodies for FAM168A

    FAM168A Assay Products:

    Browse Kits and Assays available from EMD Millipore
    OriGene Custom Assay Services for FAM168A
    Browse R&D Systems for biochemical assays
    GenScript Custom Assay Services for FAM168A
    Browse Enzo Life Sciences for kits & assays
    Browse ELISAs at Cloud-Clone Corp.
    Browse CLIAs at Cloud-Clone Corp.


    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
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    ProtoNet protein and cluster: Q92567

    UniProtKB/Swiss-Prot: F168A_HUMAN, Q92567
    Similarity: Belongs to the FAM168 family


    (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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    Phenotypes:
         3 GenomeRNAi human phenotypes for FAM168A:
     Decreased cell number  Decreased viability of wild-ty  Increased cell size 

    Animal Models:
       inGenious Targeting Laboratory: Let us create your new Knockout/Knockin mouse model for FAM168A
       inGenious Targeting Laboratory: Contact us about creating complex and humanized mouse models for FAM168A

       genOway customized KO model: permanent, tissue-specific or time-controlled inactivation for FAM168A
       genOway customized Knockin model: humanization, point mutation, expression monitoring, etc. for FAM168A

    miRNA
    Products:
        
    miRTarBase miRNAs that target FAM168A:
    hsa-mir-16-5p (MIRT032061), hsa-mir-10a-5p (MIRT047685)

    Block miRNA regulation of human, mouse, rat FAM168A using miScript Target Protectors
    Selected qRT-PCR Assays for microRNAs that regulate FAM168A (see all 28):
    hsa-miR-579 hsa-miR-142-5p hsa-miR-448 hsa-miR-520d-5p hsa-miR-106a hsa-miR-1244 hsa-miR-499-5p hsa-miR-93
    Browse SwitchGear 3'UTR luciferase reporter plasmids
    Inhib. RNA
    Products:
        
    OriGene RNAi products in human, mouse, rat for FAM168A
    Predesigned siRNA for gene silencing in human, mouse, rat FAM168A

    Gene Editing
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    DNA2.0 Custom Protein Engineering Service for FAM168A

    Clone
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    OriGene clones in human, mouse for FAM168A (see all 6)
    OriGene ORF clones in mouse, rat for FAM168A
    OriGene custom cloning services - gene synthesis, subcloning, mutagenesis, variant library, vector shuttling
    GenScript: all cDNA clones in your preferred vector: FAM168A (NM_015159)
    Browse Sino Biological Human cDNA Clones
    DNA2.0 Custom Codon Optimized Gene Synthesis Service for FAM168A
    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat FAM168A

    Cell Line
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    GenScript Custom overexpressing Cell Line Services for FAM168A
    Browse ESI BIO Cell Lines and PureStem Progenitors for FAM168A 
    In Situ Assay
    Products:
       

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for FAM168A


    (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 COMPARTMENTS: 

    CompartmentConfidence
    cytosol2
    nucleus2
    extracellular1
    peroxisome1

    (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 FAM168A
    Interactions:

        Search GeneGlobe Interaction Network for FAM168A

    3 Interacting proteins for FAM168A (Q925672, 3) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    FBXW5Q969U63I2D: score=1 
    SS18L1O751773I2D: score=1 
    --D4AEP32MINT-8383573
    About this table

    (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 FAM168A (F168A)



    (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,
    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 FAM168A gene (3 alternative transcripts): 
    NM_001286050.1  NM_001286051.1  NM_015159.2  

    Unigene Cluster for FAM168A:

    Family with sequence similarity 168, member A
    Hs.475334  [show with all ESTs]
    Unigene Representative Sequence: D87470
    4 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000064778(uc001otz.1) ENST00000450446 ENST00000356467(uc001oty.1 uc009ytp.1)
    ENST00000432223
    miRNA
    Products:
         
    Block miRNA regulation of human, mouse, rat FAM168A using miScript Target Protectors
    Selected qRT-PCR Assays for microRNAs that regulate FAM168A (see all 28):
    hsa-miR-579 hsa-miR-142-5p hsa-miR-448 hsa-miR-520d-5p hsa-miR-106a hsa-miR-1244 hsa-miR-499-5p hsa-miR-93
    Browse SwitchGear 3'UTR luciferase reporter plasmids
    Inhib. RNA
    Products:
         
    OriGene RNAi products in human, mouse, rat for FAM168A
    Predesigned siRNA for gene silencing in human, mouse, rat FAM168A
    Clone
    Products:
         
    OriGene clones in human, mouse for FAM168A (see all 6)
    OriGene ORF clones in mouse, rat for FAM168A
    OriGene custom cloning services - gene synthesis, subcloning, mutagenesis, variant library, vector shuttling
    GenScript: all cDNA clones in your preferred vector: FAM168A (NM_015159)
    DNA2.0 Custom Codon Optimized Gene Synthesis Service for FAM168A
    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat FAM168A
    Primer
    Products:
        
    OriGene qSTAR qPCR primer pairs in human, mouse for FAM168A
    Pre-validated RT2 qPCR Primer Assay in human, mouse, rat FAM168A
      QuantiTect SYBR Green Assays in human, mouse, rat FAM168A
      QuantiFast Probe-based Assays in human, mouse, rat FAM168A

    Additional mRNA sequence: 

    AK292054.1 BC014932.1 BC052341.1 D87470.1 EF197985.1 EF363480.1 

    9 DOTS entries:

    DT.452639  DT.95165154  DT.100779225  DT.95153821  DT.95165156  DT.91655226  DT.91754879  DT.91898471 
    DT.91989642 

    Selected AceView cDNA sequences (see all 254):

    AA402756 AI423371 BG820745 BE858044 BE220833 BF112244 AL135208 BM683205 
    BM825679 BM541787 BM699047 AA151263 BG260569 AA255701 BC014932 AW073772 
    AA348118 F07352 AW128965 R79936 AI375120 Z44643 BQ425692 AI141898 

    GeneLoc Exon Structure

    3 Alternative Splicing Database (ASD) splice patterns (SP) for FAM168A    About this scheme

    ExUns: 1a · 1b ^ 2 ^ 3a · 3b ^ 4 ^ 5 ^ 6 ^ 7 ^ 8 ^ 9
    SP1:                          -                                       
    SP2:                          -     -                                 
    SP3:                                                                  


    ECgene alternative splicing isoforms for FAM168A

    (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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    FAM168A expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: GCCTTGCCTG
    FAM168A Expression
    About this image


    FAM168A expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database
     
     Brain (Nervous System)
             Cerebral Cortex
    FAM168A Protein expression data from MOPED1, PaxDb2 and MaxQB3    About this image

    FAM168A Protein Expression

    SOURCE GeneReport for Unigene cluster: Hs.475334
        Custom PCR Arrays for FAM168A
    Primer
    Products:
    OriGene qSTAR qPCR primer pairs in human, mouse for FAM168A
    Pre-validated RT2 qPCR Primer Assay in human, mouse, rat FAM168A
    QuantiTect SYBR Green Assays in human, mouse, rat FAM168A
    QuantiFast Probe-based Assays in human, mouse, rat FAM168A
    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for FAM168A

    (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 FAM168A gene from Selected species (see all 12)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Fam168a1 , 5 family with sequence similarity 168, member A1, 5 94.89(n)1
    100(a)1
      7 (54.39 cM)5
    3196041  NM_178764.31  NP_848879.11 
     1007067025 
    chicken
    (Gallus gallus)
    Aves FAM168A1 family with sequence similarity 168, member A 81.28(n)
    94.89(a)
      419066  XM_004939005.1  XP_004939062.1 
    lizard
    (Anolis carolinensis)
    Reptilia FAM168A6
    family with sequence similarity 168, member A
    93(a)
    1 ↔ 1
    GL343489.1(46081-228441)
    African clawed frog
    (Xenopus laevis)
    Amphibia Xl.131762 Xenopus laevis transcribed sequences 81.69(n)    BX846189.1 
    zebrafish
    (Danio rerio)
    Actinopterygii wufc28c052 Transcribed sequences 74.52(n)    57048198 


    ENSEMBL Gene Tree for FAM168A (if available)
    TreeFam Gene Tree for FAM168A (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
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    Paralogs for FAM168A gene
    FAM168B2  
    1 SIMAP similar gene for FAM168A using alignment to 1 protein entry:     F168A_HUMAN:
    FAM168B

    FAM168A 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), 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 FAM168A (see all 3643)    About this table    
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 11 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1857013851,2
    --73116543(+) TTACTC/GTAAGG 1 -- int10--------
    rs122774101,2
    F,H--73116547(+) tgtaaG/Cgtcta 1 -- int1 ese35Minor allele frequency- C:0.07NS EA WA 536
    rs1905598701,2
    --73116554(+) TCTAGA/GGAAGT 1 -- int10--------
    rs1176874301,2
    C,F--73116610(+) GAAATG/TGATGA 1 -- int11Minor allele frequency- T:0.03NA 120
    rs1399486891,2
    --73116657(+) TGAAAC/TGTTTA 1 -- int10--------
    rs1925099401,2
    --73116692(+) CCTCAC/GCTTCA 1 -- int10--------
    rs1498269901,2
    --73116726(+) TGTGGA/TTCCTT 1 -- int10--------
    rs1129553201,2
    C--73117115(+) AGCACC/TGCTCC 1 -- ut310--------
    rs1835933661,2
    --73117134(+) TCCCTC/TTCCTT 1 -- ut310--------
    rs1468477321,2
    --73117221(+) TTAAGC/TTGCTA 1 -- ut310--------

    HapMap Linkage Disequilibrium report for FAM168A (73111532 - 73309234 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 7 variations for FAM168A:    About this table    
    Variant IDTypeSubtypePubMed ID
    esv2677115CNV Deletion23128226
    nsv389CNV Insertion18451855
    esv271125CNV Insertion20981092
    nsv38888CNV Insertion16902084
    esv22737CNV Loss19812545
    nsv508641CNV Loss20534489
    nsv520130CNV Gain19592680

    Site Specific Mutation Identification with PCR Assays
    SeqTarget long-range PCR primers for resequencing FAM168A
    DNA2.0 Custom Variant and Variant Library Synthesis for FAM168A

    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
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    4 diseases for FAM168A:    
    About MalaCards
    tongue cancer    oral squamous cell carcinoma    pulmonary function    squamous cell carcinoma

    1 disease from the University of Copenhagen DISEASES database for FAM168A:
    Tongue cancer

    FAM168A for disorders           About GeneDecksing


    Export disorders for FAM168A 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)
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    PubMed articles for FAM168A gene, integrated from 10 sources (see all 16):
    (articles sorted by number of sources associating them with FAM168A)
        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. Prediction of the coding sequences of unidentified human genes. VI. The coding sequences of 80 new genes (KIAA0201-KIAA0280) deduced by analysis of cDNA clones from cell line KG-1 and brain. (PubMed id 9039502)1, 2 Nagase T.... Nomura N. (DNA Res. 1996)
    3. Bcl2-associated athanogene 3 interactome analysis reveals a new role in modulating proteasome activity. (PubMed id 23824909)1 Chen Y....Ge F. (amp 2013)
    4. Microarray-assisted pathway analysis identifies MT1X &amp; NFI_B as mediators of TCRP1-associated resistance to cisplatin in oral squamous cell carcinoma. (PubMed id 23251525)1 Peng B....He Z. (PLoS ONE 2012)
    5. Purification and biochemical characterization of a novel protein-tongue cancer chemotherapy resistance-associated protein1 (TCRP1). (PubMed id 22365988)1 Peng B....He Z. (Protein Expr. Purif. 2012)
    6. Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function. (PubMed id 23284291)1 Hancock D.B....London S.J. (PLoS Genet. 2012)
    7. Characterizing the neurite outgrowth inhibitory effect of Mani. (PubMed id 22771904)2 Mishra M.... Heese K. (FEBS Lett. 2012)
    8. Cloning and functional characterization of TCRP1, a novel gene mediating resistance to cisplatin in an oral squamous cell carcinoma cell line. (PubMed id 21334329)1 Gu Y....He Z. (FEBS Lett. 2011)
    9. TCRP1 promotes radioresistance of oral squamous cell carcinoma cells via Akt signal pathway. (PubMed id 21603883)1 Gu Y....He Z. (Mol. Cell. Biochem. 2011)
    10. Mass spectrometric analysis of lysine ubiquitylation reveals promiscuity at site level. (PubMed id 21139048)1 Danielsen J.M....Nielsen M.L. (amp 2011)

    (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)

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
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    Entrez Gene: 23201 HGNC: 28999 AceView: KIAA0280 Ensembl:ENSG00000054965 euGenes: HUgn23201
    ECgene: FAM168A H-InvDB: FAM168A

    (According to HUGE)
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    HUGE: KIAA0280

    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL, and/or others, e.g. Wikipedia and GeneReviews, via UniProtKB/Swiss-Prot)
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    NameDescription
    PharmGKB entry for FAM168A Pharmacogenomics, SNPs, Pathways

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
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    Patent Information for FAM168A gene:
    Search GeneIP for patents involving FAM168A

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    Advanced Cell Diagnostics, Animal models from inGenious Targeting Laboratory, genOway)
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     Block miRNA regulation of human, mouse, rat FAM168A using miScript Target Protectors SeqTarget long-range PCR primers for resequencing FAM168A
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     Browse ESI BIO Cell Lines and PureStem Progenitors for FAM168A
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