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

KDM2B Gene

protein-coding   GIFtS: 55
GCID: GC12M121866

lysine (K)-specific demethylase 2B

(Previous name: F-box and leucine-rich repeat protein 10 )
(Previous symbol: FBXL10)
 Explore 2 diseases affiliated with
KDM2B via our new
 Human Malady Compendium 
Biological research products
for KDM2B
    

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

Aliases
Lysine (K)-Specific Demethylase 2B1 2     [Histone-H3]-Lysine-36 Demethylase 1B2 3
CXXC21 2 3     CXXC-Type Zinc Finger Protein 22 3
FBXL101 2 3     F-Box Protein FBL102 3
JHDM1B1 2 3     F-Box/LRR-Repeat Protein 102 3
PCCX21 2 3     EC 1.14.11.273 8
F-Box And Leucine-Rich Repeat Protein 101 2 3     JEMMA (Jumonji Domain, EMSY-Interactor, Methyltransferase Motif) Protein2
Fbl101 2     Jumonji C Domain-Containing Histone Demethylase 1B2
JmjC Domain-Containing Histone Demethylation Protein 1B2 3     Lysine-Specific Demethylase 2B2
Jumonji Domain-Containing EMSY-Interactor Methyltransferase Motif Protein2 3     FBL103
Protein-Containing CXXC Domain 22 3     Protein JEMMA3

External Ids:    HGNC: 136101   Entrez Gene: 846782   Ensembl: ENSG000000890947   OMIM: 6090785   UniProtKB: Q8NHM53   

Export aliases for KDM2B gene to outside databases

Previous GC identifers: GC12M120351 GC12M118876


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

Entrez Gene summary for KDM2B:
This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif,
the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs
(SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3
classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different
protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbls
class. Multiple alternatively spliced transcript variants have been found for this gene, but the full-length nature of
some variants has not been determined. (provided by RefSeq, Jul 2008)

UniProtKB/Swiss-Prot: KDM2B_HUMAN, Q8NHM5
Function: Histone demethylase that demethylates 'Lys-4' and 'Lys-36' of histone H3, thereby playing a central role in
histone code. Preferentially demethylates trimethylated H3 'Lys-4' and dimethylated H3 'Lys-36' residue while it has
weak or no activity for mono- and tri-methylated H3 'Lys-36'. Preferentially binds the transcribed region of ribosomal
RNA and represses the transcription of ribosomal RNA genes which inhibits cell growth and proliferation. May also
serve as a substrate-recognition component of the SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complex




(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_000012.11  NC_018923.1  NT_009775.17  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the KDM2B gene promoter:
         AP-1   ATF-2   c-Jun   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmids (see all 2): KDM2B promoter sequence
   Search SABiosciences Chromatin IP Primers for KDM2B

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat KDM2B


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

Entrez Gene cytogenetic band: 12q24.31   Ensembl cytogenetic band:  12q24.31   HGNC cytogenetic band: 12q24.31

KDM2B Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
KDM2B gene location

GeneLoc information about chromosome 12         GeneLoc Exon Structure

GeneLoc location for GC12M121866:  view genomic region     (about GC identifiers)

Start:
121,866,899 bp from pter      End:
122,018,920 bp from pter
Size:
152,022 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: KDM2B_HUMAN, Q8NHM5 (See protein sequence)
Recommended Name: Lysine-specific demethylase 2B  
Size: 1336 amino acids; 152615 Da
Cofactor: Binds 1 Fe(2+) ion per subunit (By similarity)
Subunit: Directly interacts with SKP1 and CUL1 (By similarity)
Subcellular location: Nucleus, nucleolus
Sequence caution: Sequence=AAH08735.2; Type=Erroneous initiation; Sequence=BAB55112.1; Type=Erroneous initiation;
Sequence=BAB55301.1; Type=Erroneous initiation; Sequence=BAC11159.1; Type=Erroneous initiation;
Secondary accessions: A8MRS1 Q8NCI2 Q96HC7 Q96SL0 Q96T03 Q9NS96 Q9UF75
Alternative splicing: 4 isoforms:  Q8NHM5-1   Q8NHM5-2   Q8NHM5-3   Q8NHM5-4   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for KDM2B: NX_Q8NHM5

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q8NHM5

  • 4/11 DME Specific Peptides for KDM2B (Q8NHM5) (see all 11)
     IHAVYTP  TDFHIDF  GLGIKMP  GTSVWYH 

    KDM2B Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins (2 alternative transcripts): 
    NP_001005366.1  NP_115979.3  

    ENSEMBL proteins: 
     ENSP00000437821   ENSP00000366269   ENSP00000366271   ENSP00000438138   ENSP00000398279  
     ENSP00000444846   ENSP00000445102   ENSP00000437497   ENSP00000443052   ENSP00000440942  
     ENSP00000442293   ENSP00000440373   ENSP00000445741   ENSP00000445196  

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    Browse ProSpec Recombinant Proteins
    Uscn Proteins for KDM2B

    Gene Ontology (GO): 3 cellular component terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005634nucleus NAS10799292
    GO:0005730nucleolus IEA--
    GO:0031519colocalizes with PcG protein complex IDA16943429


    KDM2B for ontologies           About GeneDecksing



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    Uscn ELISAs and CLIAs for KDM2B


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

    KDM2B for domains           About GeneDecksing

    5/6 InterPro domains/families (see all 6):
     IPR001965 Znf_PHD
     IPR002857 Znf_CXXC
     IPR001810 F-box_dom_cyclin-like
     IPR003347 JmjC_dom
     IPR011011 Znf_FYVE_PHD

    Graphical View of Domain Structure for InterPro Entry Q8NHM5

    ProtoNet protein and cluster: Q8NHM5

    2 Blocks protein families:
    IPB002857 Zn-finger
    IPB003347 Transcription factor jumonji


    UniProtKB/Swiss-Prot: KDM2B_HUMAN, Q8NHM5
    Domain: The JmjC domain mediates demethylation activity (By similarity). It is also required for repression of
    ribosomal RNA genes
    Similarity: Belongs to the JHDM1 histone demethylase family
    Similarity: Contains 1 CXXC-type zinc finger
    Similarity: Contains 1 F-box domain
    Similarity: Contains 1 JmjC domain
    Similarity: Contains 7 LRR (leucine-rich) repeats
    Similarity: Contains 1 PHD-type zinc finger


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013,
    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, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section

    Function Summary:

         UniProtKB/Swiss-Prot: KDM2B_HUMAN, Q8NHM5
    Function: Histone demethylase that demethylates 'Lys-4' and 'Lys-36' of histone H3, thereby playing a central role in
    histone code. Preferentially demethylates trimethylated H3 'Lys-4' and dimethylated H3 'Lys-36' residue while it has
    weak or no activity for mono- and tri-methylated H3 'Lys-36'. Preferentially binds the transcribed region of ribosomal
    RNA and represses the transcription of ribosomal RNA genes which inhibits cell growth and proliferation. May also
    serve as a substrate-recognition component of the SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complex
    Catalytic activity: Protein N(6),N(6)-dimethyl-L-lysine + 2-oxoglutarate + O(2) = protein N(6)-methyl-L-lysine +
    succinate + formaldehyde + CO(2)
    Catalytic activity: Protein N(6)-methyl-L-lysine + 2-oxoglutarate + O(2) = protein L-lysine + succinate + formaldehyde
    + CO(2)

    Enzyme Number (IUBMB): EC 1.14.11.271 2

    miRNA
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    hsa-miR-411* hsa-miR-148b* hsa-miR-379* hsa-miR-146a hsa-miR-586 hsa-miR-3065-5p hsa-miR-183 hsa-miR-200a
    SwitchGear 3'UTR luciferase reporter plasmidKDM2B 3' UTR sequence
    Inhib. RNA
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    Gene Ontology (GO): 5/7 molecular function terms (GO ID links to tree view) (see all 7):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003677DNA binding NAS10799292
    GO:0005515protein binding IPI16943429
    GO:0008270zinc ion binding NAS--
    GO:0016702oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen IEA--
    GO:0019843rRNA binding IEA--


    KDM2B for ontologies           About GeneDecksing


    4 GenomeRNAi human phenotypes for KDM2B:
     Decreased nuclei size in G2M  Increased cell death HMECs cel  Synthetic lethal with Ras  Upregulation of Wnt/beta-caten 

    Animal Models:
         9 MGI mutant phenotypes (inferred from 1 allele(MGI details for Kdm2b):
     cardiovascular system  cellular  embryogenesis  growth/size  limbs/digits/tail 
     mortality/aging  nervous system  reproductive system  vision/eye 

    KDM2B for phenotypes           About GeneDecksing


    (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 KDM2B

    STRING Interaction Network Preview (showing 5 interactants - click image to see 18)

    5/27 Interacting proteins for KDM2B (Q8NHM51, 3 ENSP000003662714) via UniProtKB, MINT, STRING, and/or I2D (see all 27)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    BCORQ6W2J91, 3, ENSP000003677054EBI-3955564,EBI-950027 I2D: score=3 STRING: ENSP00000367705
    RNF2Q994963, ENSP000003564804I2D: score=2 STRING: ENSP00000356480
    EZH2Q159103, ENSP000003201474I2D: score=1 STRING: ENSP00000320147
    SKP1P632083, ENSP000002314874I2D: score=3 STRING: ENSP00000231487
    PCGF1Q9BSM13, ENSP000002336304I2D: score=2 STRING: ENSP00000233630
    About this table

    Gene Ontology (GO): 5/16 biological process terms (GO ID links to tree view) (see all 16):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000122negative regulation of transcription from RNA polymerase II promoter ISS--
    GO:0006351transcription, DNA-dependent IEA--
    GO:0007283spermatogenesis ISS--
    GO:0016577histone demethylation TAS--
    GO:0021555midbrain-hindbrain boundary morphogenesis ISS--


    KDM2B for ontologies           About GeneDecksing



    (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
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for KDM2B

    2 HMDB Compounds for KDM2B    About this table
    CompoundSynonyms CAS #PubMed Ids
    FormaldehydeAldeide formica (see all 16)50-00-0--
    L-Lysine(+)-S-Lysine (see all 25)56-87-1--
    Search CenterWatch for drugs/clinical trials and news about KDM2B 

    (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,
    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, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for KDM2B gene (2 alternative transcripts): 
    NM_001005366.1  NM_032590.4  

    Unigene Cluster for KDM2B:

    Lysine (K)-specific demethylase 2B
    Hs.524800  [show with all ESTs]
    Unigene Representative Sequence: NM_032590
    18/21 Ensembl transcripts including schematic representations, and UCSC links where relevant (see all 21):
    ENST00000542973(uc001uap.3 uc001uaq.3) ENST00000538503(uc001uao.3 uc010szx.2 uc010szy.2 uc001uar.3)
    ENST00000377069(uc001uas.3 uc021rfd.1) ENST00000377071(uc001uat.3 uc001uau.3 uc021rfe.1)
    ENST00000543025 ENST00000536036 ENST00000545994 ENST00000538243 ENST00000538046(uc001uav.4)
    ENST00000446152 ENST00000542030 ENST00000538379 ENST00000545022 ENST00000541318
    ENST00000543852 ENST00000541511 ENST00000539394 ENST00000539371

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    8/16 QIAGEN miScript miRNA Assays for microRNAs that regulate KDM2B (see all 16):
    hsa-miR-411* hsa-miR-148b* hsa-miR-379* hsa-miR-146a hsa-miR-586 hsa-miR-3065-5p hsa-miR-183 hsa-miR-200a
    SwitchGear 3'UTR luciferase reporter plasmidKDM2B 3' UTR sequence
    Inhib. RNA
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    Additional cDNA sequence: 

    AB031230.1 AJ459424.1 AK027440.1 AK027692.1 AK055282.1 AK074718.1 AK127328.1 AK299827.1 
    AK316470.1 BC008735.2 BC028612.1 BC115379.1 BC115380.1 BX648928.1 

    24 DOTS entries:

    DT.100779771  DT.95167649  DT.100779773  DT.100731611  DT.100779774  DT.75150484  DT.99954855  DT.100779777 
    DT.101983427  DT.95241592  DT.402976  DT.100655267  DT.100689945  DT.121128640  DT.121128658  DT.121128677 
    DT.95208361  DT.97836402  DT.100697037  DT.121128657  DT.121128720  DT.95262506  DT.86840697  DT.95249316 

    24/205 AceView cDNA sequences (see all 205):

    AI343298 AA648887 BM783125 BG538934 BM757786 AB031230 BX108493 AI088992 
    AI472214 AI870035 AI288446 BG283856 BI819191 AA336363 AK127328 BQ898120 
    BE328676 AA361882 AW196603 BM740439 AA907525 BM759660 AA070843 AW514897 

    GeneLoc Exon Structure

    5/15 Alternative Splicing Database (ASD) splice patterns (SP) for KDM2B (see all 15)    About this scheme

    ExUns: 1 ^ 2a · 2b ^ 3 ^ 4a · 4b ^ 5 ^ 6a · 6b ^ 7 ^ 8a · 8b · 8c ^ 9 ^ 10 ^ 11a · 11b ^ 12a · 12b ^ 13a · 13b · 13c ^ 14 ^ 15 ^ 16 ^ 17a ·
    SP1:                                                                                                                                                            
    SP2:                                                                                                                                                            
    SP3:                                                                                                                                                            
    SP4:                                                                                                                                                            
    SP5:                    -                 -           -                             -     -                                                                     

    ExUns: 17b ^ 18 ^ 19 ^ 20 ^ 21a · 21b ^ 22 ^ 23a · 23b · 23c ^ 24 ^ 25 ^ 26 ^ 27a · 27b ^ 28 ^ 29 ^ 30 ^ 31a · 31b ^ 32a · 32b · 32c · 32d
    SP1:              -                                                                                                     -                           
    SP2:              -                             -                                                           -                                       
    SP3:                                            -                                                           -                                       
    SP4:                                                                                                        -                                       
    SP5:                                                                                                                                                


    ECgene alternative splicing isoforms for KDM2B

    (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

    KDM2B expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: GCTATTTCCT

    Microarray
    RNAseq (Illumina Body Map)
    (100×FPKM)½
    SAGE (Serial Analysis of Gene Expression)

    About this image

    KDM2B expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    2 LifeMap In Vivo Development Anatomical Compartments/Cells 
    Tissue Anatomical Compartment CellCategory (developmental path)
    PancreasIslets of LangerhansMature Beta CellsPancreas
    KidneyMetanephrosKidney
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization

    See KDM2B Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for KDM2B

    SOURCE GeneReport for Unigene cluster: Hs.524800
        SABiosciences Expression via Pathway-Focused PCR Arrays including KDM2B: 
              Polycomb & Trithorax Complexes in human mouse rat
              Ubiquitin Ligases in human mouse rat

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    (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 KDM2B gene from 6/20 species (see all 20)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Kdm2b1 , 5 lysine (K)-specific demethylase 2B1, 5 89.39(n)1
    94.9(a)1
      5 (62.63 cM)5
    308411  NM_001003953.11  NP_001003953.11 
     1228706685 
    chicken
    (Gallus gallus)
    Aves KDM2B1 lysine (K)-specific demethylase 2B 78.77(n)
    87.9(a)
      416844  XM_415137.3  XP_415137.3 
    lizard
    (Anolis carolinensis)
    Reptilia KDM2B6
    --
    78(a)
    1 ↔ 1
    GL343550.1(44269-117133)
    African clawed frog
    (Xenopus laevis)
    Amphibia Xl.70692 Xenopus laevis transcribed sequence with moderate similarity more 76.61(n)    BX852634.1 
    zebrafish
    (Danio rerio)
    Actinopterygii kdm2a1 lysine (K)-specific demethylase 2A 54.49(n)
    50.72(a)
      799441  XM_001339761.3  XP_001339797.2 
    fruit fly
    (Drosophila melanogaster)
    Insecta Kdm26
    Lysine (K)-specific demethylase 2
    30(a)
    1 → many
    3R(4878240-4888967)


    ENSEMBL Gene Tree for KDM2B (if available)
    TreeFam Gene Tree for KDM2B (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for KDM2B gene
    PHF22  PHF82  KDM2A2  JHDM1D2  FBXL192  
    5 SIMAP similar genes for KDM2B using alignment to 11 protein entries:     KDM2B_HUMAN (see all proteins):
    FBXL10    KDM2A    PHF8    FBXL19    kdm2a

    KDM2B 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

    10/2457 NCBI SNPs in KDM2B are shown (see all 2457    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 12 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs795639861,2
    C,F,--121866736(+) GAGCAG/ACTCTT 2 -- ds50015Minor allele frequency- A:0.13NA CSA WA 244
    rs1471723091,2
    C,--121866761(+) GTGTC-/TTAATT 2 -- ds50010--------
    rs1424115721,2
    --121866768(+) TAATTC/TCTACG 2 -- ds50010--------
    rs1839806251,2
    --121866774(+) CTACGC/TGTGGC 2 -- ds50010--------
    rs1512924551,2
    --121866846(+) CTGAAA/GAAAGA 2 -- ds50010--------
    rs1406106781,2
    --121866861(+) TGACGC/TACCAC 2 -- ds50010--------
    rs1176825491,2
    --121866905(+) TTGGAC/TTTCAA 2 -- ut311Minor allele frequency- T:0.01NA 120
    rs1442475301,2
    --121866948(+) TAGTCC/TACTCC 2 -- ut310--------
    rs1465600421,2
    --121866985(+) AGTGGG/TTTTTT 2 -- ut310--------
    rs110655701,2
    C,F,H--121867221(+) AATTAG/AATCTA 2 -- ut3110Minor allele frequency- A:0.01NS EA NA 1134

    HapMap Linkage Disequilibrium report for KDM2B (121866899 - 122018920 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 3 variations for KDM2B
         3 Indels: 76167 86592 76166

    SABiosciences Cancer Mutation PCR Assays
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    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section

    KDM2B for disorders           About GeneDecksing

    OMIM gene information: 609078    OMIM disorders: --

    2 diseases for KDM2B:    About MalaCards
    coloboma    neuronitis

    Human Genome Epidemiology (HuGE) Navigator: KDM2B (1 document)

    Export disorders for KDM2B 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 KDM2B gene, integrated from 9 sources (see all 31):
    (articles sorted by number of sources associating them with KDM2B)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. JHDM1B/FBXL10 is a nucleolar protein that represses transcription of ribosomal RNA genes. (PubMed id 17994099)1, 2, 9 Frescas D....Pagano M. (2007)
    2. Histone demethylation by a family of JmjC domain-containing proteins. (PubMed id 16362057)1, 2 Tsukada Y.... Zhang Y. (2006)
    3. 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)
    4. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (2004)
    5. PCCX1, a novel DNA-binding protein with PHD finger and CXXC domain, is regulated by proteolysis. (PubMed id 10799292)1, 3 Fujino T.... Takano T. (2000)
    6. The F-box protein Fbl10 is a novel transcriptional repressor of c-Jun. (PubMed id 17704768)1, 9 Koyama-Nasu R....Tanese N. (2007)
    7. Polycomb group and SCF ubiquitin ligases are found in a novel BCOR complex that is recruited to BCL6 targets. (PubMed id 16943429)1, 9 Gearhart M.D.... Bardwell V.J. (2006)
    8. JmjC-domain containing histone demethylase 1B-mediated p15(Ink4b) suppression promotes the proliferation of leukemic progenitor cells through modulation of cell cycle progression in acute myeloid leukemia. (PubMed id 22086844)1 Nakamura S....Ohnishi K. (2013)
    9. The H3K4me3 histone demethylase Fbxl10 is a regulator of chemokine expression, cellular morphology, and the metabolome of fibroblasts. (PubMed id 22825849)1 Janzer A....Kirfel J. (2012)
    10. A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resi stance. (PubMed id 22581228)1 Manning A.K....Langenberg C. (2012)

    (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: 84678 HGNC: 13610 AceView: FBXL10 Ensembl:ENSG00000089094 euGenes: HUgn84678
    ECgene: KDM2B H-InvDB: KDM2B

    (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 KDM2B 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 KDM2B gene:
    Search GeneIP for patents involving KDM2B

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



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