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

FAM13C Gene

protein-coding   GIFtS: 47
GCID: GC10M061005

Family With Sequence Similarity 13, Member C

(Previous names: family with sequence similarity 13, member C1)
(Previous symbol: FAM13C1)
Alzheimer's & Parkinson's Diseases Congress
  See related disease
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 13, Member C1 2
FAM13C11 2 3
Family With Sequence Similarity 13, Member C11 2
Protein FAM13C2

External Ids:    HGNC: 193711   Entrez Gene: 2209652   Ensembl: ENSG000001485417   UniProtKB: Q8NE313   

Export aliases for FAM13C gene to outside databases

Previous GC identifers: GC10M060676 GC10M054996


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

GeneCards Summary for FAM13C Gene: 
FAM13C (family with sequence similarity 13, member C) is a protein-coding gene. Diseases associated with FAM13C include alzheimer's disease. An important paralog of this gene is FAM13B.


(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_000010.10  NT_030059.13  NC_018921.2  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the FAM13C gene promoter:
         FOXI1   HFH-3   AML1a   POU2F1   POU2F1a   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidFAM13C promoter sequence
   Search SABiosciences Chromatin IP Primers for FAM13C

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat FAM13C


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

Entrez Gene cytogenetic band: 10q21.1   Ensembl cytogenetic band:  10q21.1   HGNC cytogenetic band: 10q21

FAM13C Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
FAM13C gene location

GeneLoc information about chromosome 10         GeneLoc Exon Structure

GeneLoc location for GC10M061005:  view genomic region     (about GC identifiers)

Start:
61,005,889 bp from pter      End:
61,122,939 bp from pter
Size:
117,051 bases      Orientation:
minus 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: FA13C_HUMAN, Q8NE31 (See protein sequence)
Recommended Name: Protein FAM13C  
Size: 585 amino acids; 65727 Da
Sequence caution: Sequence=CAI15709.1; Type=Erroneous gene model prediction;
Secondary accessions: B7ZB77 Q5T631 Q6P2M3 Q99787
Alternative splicing: 5 isoforms:  Q8NE31-1   Q8NE31-2   Q8NE31-3   Q8NE31-4   Q8NE31-5   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for FAM13C: NX_Q8NE31

Explore proteomics data for FAM13C at MOPED 

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_Q8NE31

  • FAM13C Protein expression data from MOPED1, PaxDb2 and MAXQB3 :    About this image 

    FAM13C Protein Expression
    REFSEQ proteins (4 alternative transcripts): 
    NP_001001971.1  NP_001137245.1  NP_001160170.1  NP_937858.2  

    ENSEMBL proteins: 
     ENSP00000362975   ENSP00000395661   ENSP00000277705   ENSP00000424249   ENSP00000391993  
     ENSP00000423896   ENSP00000392302   ENSP00000400241   ENSP00000445068   ENSP00000423620  
     ENSP00000425820   ENSP00000424797   ENSP00000362974  

    Human Recombinant Protein Products for FAM13C: 
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    OriGene MassSpec for FAM13C 
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    Novus Biologicals FAM13C Protein
    Novus Biologicals FAM13C Lysates
    Browse Sino Biological Recombinant Proteins
    Browse Sino Biological Cell Lysates 
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    Cloud-Clone Corp. Proteins for FAM13C 


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    LSBio Antibodies in human, mouse, rat for FAM13C 

    Assay Products for FAM13C: 
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    Cloud-Clone Corp. ELISAs for FAM13C 
    Cloud-Clone Corp. CLIAs for FAM13C


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

    ProtoNet protein and cluster: Q8NE31

    UniProtKB/Swiss-Prot: FA13C_HUMAN, Q8NE31
    Similarity: Belongs to the FAM13 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,
    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

    Phenotypes:
         1 GenomeRNAi human phenotype for FAM13C:
     Increased gamma-H2AX phosphory 

    Animal Models:
       inGenious Targeting Laboratory - Custom generated mouse model solutions for FAM13C 
       inGenious Targeting Laboratory - Custom generated inducible mouse model solutions for FAM13C

       genOway customized KO model: permanent, tissue-specific or time-controlled inactivation for FAM13C 
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    miRNA
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    hsa-miR-30c hsa-miR-520d-5p hsa-miR-106a hsa-miR-30d hsa-miR-30a hsa-miR-9 hsa-miR-3658 hsa-miR-93
    SwitchGear 3'UTR luciferase reporter plasmidFAM13C 3' UTR sequence
    Inhib. RNA
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    Browse for Gene Knock-down Tools from EMD Millipore
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    Gene Editing
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    Clone
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    Browse Sino Biological Human cDNA Clones
    DNA2.0 Custom Codon Optimized Gene Synthesis Service for FAM13C
    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat FAM13C
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                         Customized lentivirus expression plasmids for stable overexpression of FAM13C 

    Cell Line
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    Search LifeMap BioReagents cell lines for FAM13C
    In Situ Assay
    Products:
       

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for FAM13C


    (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 FAM13C

    STRING Interaction Network Preview (showing 1 interactants - click image to see more details)

    1 Interacting protein for FAM13C (Q8NE312, 3 ENSP000003919934) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    CCDC85BQ158342, 3, ENSP000003116954MINT-68055 I2D: score=4 STRING: ENSP00000311695
    About this table

    (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 FAM13C (FA13C)

    Search CenterWatch for drugs/clinical trials and news about FAM13C / FA13C

    (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 FAM13C gene (4 alternative transcripts): 
    NM_001001971.2  NM_001143773.1  NM_001166698.1  NM_198215.3  

    Unigene Cluster for FAM13C:

    Family with sequence similarity 13, member C
    Hs.607594  [show with all ESTs]
    Unigene Representative Sequence: NM_001143773
    18/20 Ensembl transcripts including schematic representations, and UCSC links where relevant (see all 20):
    ENST00000373868 ENST00000442566 ENST00000277705 ENST00000513059 ENST00000419214
    ENST00000468840 ENST00000489341 ENST00000435852(uc010qif.1) ENST00000422313(uc001jkp.3)
    ENST00000468696 ENST00000507568 ENST00000513377 ENST00000477101 ENST00000510215
    ENST00000470220 ENST00000507862 ENST00000504410 ENST00000512919

    miRNA
    Products:
         
    QIAGEN Custom miScript Target Protector blocks miRNA-binding site of human, mouse, rat FAM13C
    8/18 QIAGEN miScript miRNA Assays for microRNAs that regulate FAM13C (see all 18):
    hsa-miR-30c hsa-miR-520d-5p hsa-miR-106a hsa-miR-30d hsa-miR-30a hsa-miR-9 hsa-miR-3658 hsa-miR-93
    SwitchGear 3'UTR luciferase reporter plasmidFAM13C 3' UTR sequence
    Inhib. RNA
    Products:
         
    Browse for Gene Knock-down Tools from EMD Millipore
    OriGene RNAi products in human, mouse, rat for FAM13C
    QIAGEN FlexiTube/FlexiPlate siRNA for gene silencing in human, mouse, rat FAM13C
    Clone
    Products:
         
    OriGene clones in human, mouse for FAM13C (see all 22)
    OriGene ORF clones in mouse, rat for FAM13C
    OriGene custom cloning services - gene synthesis, subcloning, mutagenesis, variant library, vector shuttling
    GenScript: all cDNA clones in your preferred vector (see all 4): FAM13C (NM_001001971)
    DNA2.0 Custom Codon Optimized Gene Synthesis Service for FAM13C
    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat FAM13C
    Sirion Biotech Customized lentivirus for stable overexpression of FAM13C 
                         Customized lentivirus expression plasmids for stable overexpression of FAM13C 
    Primer
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    OriGene qSTAR qPCR primer pairs in human, mouse for FAM13C
    SABiosciences RT2 qPCR Primer Assay in human, mouse, rat FAM13C
      QIAGEN QuantiTect SYBR Green Assays in human, mouse, rat FAM13C
      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat FAM13C

    Additional mRNA sequence: 

    AK289796.1 AK294805.1 AK299924.1 AK316542.1 BC036453.1 BC064431.1 U79304.1 

    14 DOTS entries:

    DT.101975907  DT.444580  DT.97818242  DT.95079100  DT.312714  DT.86846383  DT.312713  DT.121213465 
    DT.101955001  DT.121213469  DT.121213630  DT.91715399  DT.99990095  DT.40113993 

    24/64 AceView cDNA sequences (see all 64):

    BU076522 BM702090 CD677123 CA397141 BU076265 CA391990 BM664410 AI362528 
    BM696126 BM725799 AV727971 AL532155 AL046116 CA406959 BQ218467 AI193962 
    AA430296 BF575482 R68272 AW296427 AI580948 BF448024 CB053614 T32807 

    GeneLoc Exon Structure

    5/14 Alternative Splicing Database (ASD) splice patterns (SP) for FAM13C (see all 14)    About this scheme

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

    ExUns: 14 ^ 15a · 15b ^ 16 ^ 17a · 17b · 17c ^ 18a · 18b · 18c ^ 19 ^ 20a · 20b
    SP1:              -                                                               
    SP2:                                                                              
    SP3:                                                                              
    SP4:                                                                              
    SP5:                                                                              


    ECgene alternative splicing isoforms for FAM13C

    (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

    FAM13C expression in normal human tissues (normalized intensities)      FAM13C embryonic expression: see
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: TACACAGTTG
    FAM13C Expression
    About this image


    FAM13C expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database 
     5/7 selected tissues (see all 7) fully expand
     
     Pancreas (Endocrine System)
             Posterior foregut-like cells ( A scalable, suspension protocol for derivation of...
     
     Epidermis (Integumentary System)
             Detroit 551
     
     Nose (Sensory Organs)
             sensory organ/nose/nasal cavity   
     
     Umbilical Cord (Extraembryonic Tissues)
             Umbilical cord blood-derived endothelial progenitor cells
     
     Endothelium (Cardiovascular System)
             Umbilical cord blood-derived endothelial progenitor cells

    See FAM13C Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for FAM13C

    SOURCE GeneReport for Unigene cluster: Hs.607594
        SABiosciences Custom PCR Arrays for FAM13C
    Primer
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    QIAGEN QuantiFast Probe-based Assays in human, mouse, rat FAM13C
    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for FAM13C

    (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 animals.

    Orthologs for FAM13C gene from 6/13 species (see all 13)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Fam13c1 , 5 family with sequence similarity 13, member C1, 5 84.31(n)1
    84.48(a)1
      10 (36.68 cM)5
    717211  NM_024244.41  NP_077206.31 
     704408805 
    chicken
    (Gallus gallus)
    Aves FAM13C1 family with sequence similarity 13, member C 70.07(n)
    64.7(a)
      423602  XM_421488.3  XP_421488.3 
    lizard
    (Anolis carolinensis)
    Reptilia FAM13C6
    family with sequence similarity 13, member C
    62(a)
    1 ↔ 1
    GL343251.1(579657-674487)
    tropical clawed frog
    (Xenopus tropicalis)
    Amphibia Str.135992 Transcribed sequences 89.43(n)    BX732879.1 
    zebrafish
    (Danio rerio)
    Actinopterygii LOC1005370561 uncharacterized LOC100537056 56.96(n)
    51.29(a)
      100537056  XM_003199566.1  XP_003199614.1 
    fruit fly
    (Drosophila melanogaster)
    Insecta CG64246
    --
    10(a)
    1 → many
    2R(13590840-13606832)


    ENSEMBL Gene Tree for FAM13C (if available)
    TreeFam Gene Tree for FAM13C (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for FAM13C gene
    FAM13B2  FAM13A2  
    1 SIMAP similar gene for FAM13C using alignment to 7 protein entries:     FA13C_HUMAN (see all proteins):
    FAM13A

    FAM13C 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

    10/2278 SNPs in FAM13C are shown (see all 2278)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 10 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1157738821,2
    C,F--54996538(+) TCATTC/TAGAAC 4 -- int11Minor allele frequency- T:0.02WA 118
    rs1507590011,2
    --54996581(+) CACTAC/TTTTCA 4 -- int10--------
    rs747949731,2
    C,F--54996591(+) AATGAT/CGAAAT 4 -- int11Minor allele frequency- C:0.07WA 118
    rs1391046461,2
    --54996599(+) AATACC/GCTAAG 4 -- int10--------
    rs763412671,2
    C,F--54996652(+) GTTTTT/CATGTT 4 -- int11Minor allele frequency- C:0.01WA 118
    rs1905346341,2
    --54996757(+) TTAATC/TTACTG 4 -- int10--------
    rs1831351271,2
    --54996761(+) TCTACC/TGAACA 4 -- int10--------
    rs110064151,2
    C,H--54996816(+) CATGAG/ATTAAA 4 -- int16Minor allele frequency- A:0.00NS EA NA 420
    rs1498956781,2
    --54997069(+) CCTCAA/GATAGT 4 -- ut310--------
    rs412837001,2
    F--54997105(+) ATGACC/TTCAAT 4 -- ut310--------

    HapMap Linkage Disequilibrium report for FAM13C (61005889 - 61122939 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 8 variations for FAM13C:    About this table     
    Variant IDTypeSubtypePubMed ID
    esv4266CNV Deletion18987735
    esv2737429CNV Deletion23290073
    esv273164CNV Insertion20981092
    esv269602CNV Insertion20981092
    nsv507558CNV Insertion20534489
    nsv528505CNV Loss19592680
    nsv467289CNV Loss19166990
    nsv831888CNV Gain17160897

    SABiosciences Cancer Mutation PCR Assays
    SeqTarget long-range PCR primers for resequencing FAM13C
    DNA2.0 Custom Variant and Variant Library Synthesis for FAM13C

    (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 FAM13C:    About MalaCards
    alzheimer's disease    


    FAM13C for disorders           About GeneDecksing


    Congresses - knowledge worth sharing:  
    Alzheimer's & Parkinson's Diseases Congress (ADPD) 18 - 22 March 2015
    Genetic Association Database (GAD): FAM13C
    Human Genome Epidemiology (HuGE) Navigator: FAM13C (2 documents)

    Export disorders for FAM13C 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 FAM13C gene, integrated from 9 sources (see all 15):
    (articles sorted by number of sources associating them with FAM13C)
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    1. A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. (PubMed id 16385451)1, 4 Grupe A....Goate A. (2006)
    2. 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)
    3. Large-scale concatenation cDNA sequencing. (PubMed id 9110174)1, 2 Yu W.... Gibbs R.A. (1997)
    4. Genome-wide association study identifies novel loci as sociated with concentrations of four plasma phospholipid fatty acids in the de n ovo lipogenesis pathway: results from the Cohorts for Heart and Aging Research i n Genomic Epidemiology (CHARGE) consortium. (PubMed id 23362303)1 Wu J.H....Mozaffarian D. (2013)
    5. Genome-wide pleiotropy of osteoporosis-related phenot ypes: The Framingham study. (PubMed id 20200953)1 Karasik D....Demissie S. (2010)
    6. A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study. (PubMed id 17903299)4 Kathiresan S....Cupples L.A. (2007)
    7. Genome-wide association with diabetes-related traits in the Framingham Heart Study. (PubMed id 17903298)4 Meigs J.B....Dupuis J. (2007)
    8. Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes. (PubMed id 17903304)4 Larson M.G....Levy D. (2007)
    9. Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. (PubMed id 16344560)1 Kimura K.... Sugano S. (2006)
    10. Towards a proteome-scale map of the human protein-protein interaction network. (PubMed id 16189514)1 Rual J.F....Vidal M. (2005)

    (in PubMed, OMIM, and NCBI Bookshelf)
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    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 220965 HGNC: 19371 AceView: FAM13C1 Ensembl:ENSG00000148541 euGenes: HUgn220965
    ECgene: FAM13C H-InvDB: FAM13C

    (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 FAM13C 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 FAM13C gene:
    Search GeneIP for patents involving FAM13C

    GeneCards and IP:
    Japan Patent Office Licenses GeneCards     European Patent Office Licenses GeneCards     Improving the IP Search



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