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

FAM168B Gene

protein-coding   GIFtS: 44
GCID: GC02M131805

family with sequence similarity 168, member B

 Explore 2 diseases affiliated with
FAM168B via our new
 Human Malady Compendium 
Biological research products
for FAM168B
    

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section

Aliases
Family With Sequence Similarity 168, Member B1 2     Myelin-Associated Neurite-Outgrowth Inhibitor2
KIAA0280L1 3     Protein FAM168B2
MANI2 3     Mani3
P201     

External Ids:    HGNC: 270161   Entrez Gene: 1300742   Ensembl: ENSG000001521027   UniProtKB: A1KXE43   

Export aliases for FAM168B gene to outside databases

Previous GC identifers: GC02M131524 GC02M123873


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

UniProtKB/Swiss-Prot: F168B_HUMAN, A1KXE4
Function: Modulates neuronal axonal outgrowth by acting as a negative regulator of CDC42 and STAT3 and a positive
regulator of STMN2. Positive regulator of CDC27 (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 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000002.11  NC_018913.1  NT_022135.16  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the FAM168B gene promoter:
         AhR   E4BP4   Arnt   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidFAM168B promoter sequence
   Search SABiosciences Chromatin IP Primers for FAM168B

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat FAM168B


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

Entrez Gene cytogenetic band: 2q21.1   Ensembl cytogenetic band:  2q21.1   HGNC cytogenetic band: 2q21.1

FAM168B Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
FAM168B gene location

GeneLoc information about chromosome 2         GeneLoc Exon Structure

GeneLoc location for GC02M131805:  view genomic region     (about GC identifiers)

Start:
131,805,449 bp from pter      End:
131,851,033 bp from pter
Size:
45,585 bases      Orientation:
minus strand

(According to 1UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to 2PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, 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 Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section

UniProtKB/Swiss-Prot: F168B_HUMAN, A1KXE4 (See protein sequence)
Recommended Name: Myelin-associated neurite-outgrowth inhibitor  
Size: 195 amino acids; 20324 Da
Subunit: May form homodimers. May interact with DAZAP2, FAM168A, PRDX6, RBM6, TMTC1 and YPEL2. Interacts with CDC27
Subcellular location: Cytoplasm, perinuclear region (By similarity). Cell membrane; Multi-pass membrane protein (By
similarity). Cell projection, axon (By similarity). Note=Expressed in neuronal cell bodies and axonal fibers (By
similarity)
Secondary accessions: Q2TAZ6 Q6NZ40
Alternative splicing: 2 isoforms:  A1KXE4-1   A1KXE4-2   

Explore the universe of human proteins at neXtProt for FAM168B: NX_A1KXE4

Post-translational modifications:

  • N-glycosylated (By similarity)1
  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_A1KXE4

  • FAM168B Protein expression data from MOPED and PaxDb:    About this image 
    FAM168B Protein Expression
    REFSEQ proteins: NP_001009993.2  
    ENSEMBL proteins: 
     ENSP00000387051   ENSP00000374565  

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    Gene Ontology (GO): 4 cellular component terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005886plasma membrane IEA--
    GO:0016021integral to membrane IEA--
    GO:0030424axon IEA--
    GO:0048471perinuclear region of cytoplasm IEA--

    FAM168B for ontologies           About GeneDecksing



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

    ProtoNet protein and cluster: A1KXE4

    UniProtKB/Swiss-Prot: F168B_HUMAN, A1KXE4
    Similarity: Belongs to the FAM168 protein 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,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase, shRNA from OriGene, Sirion Biotech, 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, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, Sirion Biotech, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section

    Molecular Function:

         UniProtKB/Swiss-Prot Summary: F168B_HUMAN, A1KXE4
    Function: Modulates neuronal axonal outgrowth by acting as a negative regulator of CDC42 and STAT3 and a positive
    regulator of STMN2. Positive regulator of CDC27 (By similarity)

    Animal Models:

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    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, 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 Mar 2013 via Entrez Gene).
    About This Section



    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for FAM168B

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

    2 Interacting proteins for FAM168B (A1KXE42, 3 ENSP000003745654) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    PARP2Q9UGN52, 3, ENSP000002504164MINT-8202046 I2D: score=1 STRING: ENSP00000250416
    --P031882MINT-6770231
    About this table

    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, 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
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    Browse Tocris compounds for FAM168B
    Search CenterWatch for drugs/clinical trials and news about FAM168B / F168B 

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 235 Homo sapiens; Mar 10 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
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    Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for FAM168B gene: 
    NM_001009993.2  

    Unigene Cluster for FAM168B:

    Family with sequence similarity 168, member B
    Hs.534679  [show with all ESTs]
    Unigene Representative Sequence: NM_001009993
    2 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000409185(uc002tsd.3) ENST00000389915

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    hsa-miR-640 hsa-miR-1245 hsa-miR-134 hsa-miR-3653 hsa-miR-519a hsa-miR-149 hsa-miR-208b hsa-miR-200b
    Browse SwitchGear 3'UTR luciferase reporter plasmids
    Inhib. RNA
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    OriGene shRNA RFP: FAM168B
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    Additional cDNA sequence: 

    AK022529.1 AK023868.1 AL137406.1 AL137413.1 AL833819.1 AY253283.1 BC035115.1 BC066347.1 
    BC110642.1 BC127804.1 BX647486.1 

    23 DOTS entries:

    DT.92053523  DT.101955989  DT.95155687  DT.99969272  DT.120980780  DT.95207827  DT.100667079  DT.120981186 
    DT.101969909  DT.120981368  DT.91846690  DT.120981245  DT.120981392  DT.92034728  DT.100667080  DT.91760223 
    DT.91842552  DT.100667076  DT.102837983  DT.120980723  DT.120981333  DT.91783289  DT.91808163 

    GeneLoc Exon Structure


    (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

    FAM168B expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: CCAAGGAATG
    FAM168B Expression
    About this image
    See FAM168B Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for FAM168B

    SOURCE GeneReport for Unigene cluster: Hs.534679

    UniProtKB/Swiss-Prot: F168B_HUMAN, A1KXE4
    Tissue specificity: Expressed in the brain, within neuronal axonal fibers and associated with myelin sheets (at protein
    level). Expression tends to be lower in the brain of Alzheimer disease patients compared to healthy individuals (at
    protein level)

        SABiosciences Custom PCR Arrays for FAM168B
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for FAM168B

    (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 FAM168B gene from 4/10 species (see all 10)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Fam168b1 , 5 family with sequence similarity 168, member B1, 5 92.1(n)1
    98.97(a)1
      1 (13.34 cM)5
    2144691  NM_001160236.11  NP_001153708.11 
     348132215 
    chicken
    (Gallus gallus)
    Aves FAM168B1 family with sequence similarity 168, member B 84.44(n)
    97.95(a)
      424759  XM_422581.3  XP_422581.1 
    lizard
    (Anolis carolinensis)
    Reptilia FAM168B6
    --
    96(a)
    1 ↔ 1
    3(37505011-37510503)
    zebrafish
    (Danio rerio)
    Actinopterygii zgc:1539801 zgc:153980 76.98(n)
    86.6(a)
      561051  NM_001076569.1  NP_001070037.1 


    ENSEMBL Gene Tree for FAM168B (if available)
    TreeFam Gene Tree for FAM168B (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for FAM168B gene
    FAM168A2  
    1 SIMAP similar gene for FAM168B using alignment to 1 protein entry:     F168B_HUMAN:
    FAM168A

    FAM168B for paralogs           About GeneDecksing



    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, UniProtKB, 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

    10/746 NCBI SNPs in FAM168B are shown (see all 746    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 2 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1143671081,2
    F--131805399(+) GGCCAT/CGCTAC 1 -- int11Minor allele frequency- C:0.03WA 118
    rs788674231,2
    C,F--131805402(+) CATGCT/CACCTC 1 -- int11Minor allele frequency- C:0.03WA 118
    rs1819029421,2
    --131805577(+) AATAGC/TATCAA 1 -- ut310--------
    rs1387705351,2
    --131805602(+) AACTGA/GCTCAG 1 -- ut310--------
    rs1489576111,2
    --131805625(+) ATTCCA/TTGGCA 1 -- ut310--------
    rs1861282061,2
    --131805815(+) TCTCCA/GTGTGG 1 -- ut310--------
    rs102060851,2
    C,F,H--131805898(+) TGCACA/GGGGAC 1 -- ut31 ese35Minor allele frequency- G:0.01NS EA CSA 394
    rs1905014611,2
    --131805982(+) CCCGGG/TGGGGG 1 -- ut310--------
    rs115412201,2
    C,F--131805984(+) CGGGGC/G/TGGGGT 2 -- ut317MN WA NA CSA EA 547
    rs1813430011,2
    --131806091(+) TTCTTC/GAAATA 1 -- ut310--------

    HapMap Linkage Disequilibrium report for FAM168B (131805449 - 131851033 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 6 variations for FAM168B
         1 CNV: 3393
         5 Indels: 97977 12095 45856 42179 33704

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    (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.)
    About This Section

    FAM168B for disorders           About GeneDecksing

    2 diseases for FAM168B:    About MalaCards
    alzheimer's disease    neuronitis


    Export disorders for FAM168B 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 FAM168B gene integrated from 9 sources:
    (articles sorted by number of sources associating them with FAM168B)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. The novel protein MANI modulates neurogenesis and neu rite-cone growth. (PubMed id 20716133)1, 2 Mishra M....Heese K. (2011)
    2. Characterizing the neurite outgrowth inhibitory effect of Mani. (PubMed id 22771904)2 Mishra M.... Heese K. (2012)
    3. Mass spectrometric analysis of lysine ubiquitylation r eveals promiscuity at site level. (PubMed id 21139048)1 Danielsen J.M....Nielsen M.L. (2011)
    4. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)2 Gerhard D.S....Malek J. (2004)
    5. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1 Ota T.... Sugano S. (2004)
    6. 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)

    (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: 130074 HGNC: 27016 Ensembl:ENSG00000152102 euGenes: HUgn130074 ECgene: FAM168B
    H-InvDB: FAM168B

    (According to HUGE)
    About This Section
    HUGE: KIAA0280L

    (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 FAM168B 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 FAM168B gene:
    Search GeneIP for patents involving FAM168B

    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, Uscn, Thermo Fisher Scientific, Gene Editing from DNA2.0 and Sirion Biotech, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript, LifeMap BioReagents, and Sirion Biotech, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or Enzo Life Sciences, In Situ Hybridization Assays from
    Advanced Cell Diagnostics, Animal models from inGenious Targeting Laboratory)
    About This Section

     
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    GeneCards Homepage - Last full update: 18 Mar 2013 - Incrementals: 21 Mar 2013 , 15 Apr 2013 , 27 Apr 2013 , 14 May 2013

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    VWF
    (GIFTS: 73)
    von Willebrand factor
    GIFtS Group
    The GeneCards human gene database gene index: 1 3 5 6 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 


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