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

FEM1C Gene

protein-coding   GIFtS: 52
GCID: GC05M114884

fem-1 homolog c (C. elegans)

 Explore 1 disease affiliated with
FEM1C via our new
 Human Malady Compendium 
Biological research products
for FEM1C
    

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

Aliases
Fem-1 Homolog C (C. Elegans)1 2     KIAA17851 3
EUROIMAGE6866081 2     FEM1-Gamma1
EUROIMAGE7836471 2     Protein Fem-1 Homolog C2
FEM1A1 2     FEM1c3

External Ids:    HGNC: 169331   Entrez Gene: 569292   Ensembl: ENSG000001457807   OMIM: 6087675   UniProtKB: Q96JP03   

Export aliases for FEM1C gene to outside databases

Previous GC identifers: GC05M114624 GC05M115264 GC05M114887 GC05M114932 GC05M110038


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

UniProtKB/Swiss-Prot: FEM1C_HUMAN, Q96JP0
Function: Probable component of an E3 ubiquitin-protein ligase complex, in which it may act as a substrate recognition
subunit (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_000005.9  NC_018916.1  NT_034772.6  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the FEM1C gene promoter:
         FOXO3   CUTL1   Cdc5   HNF-3beta   YY1   Evi-1   FOXO3b   FOXJ2 (long isoform)   FOXO3a   FOXJ2   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidFEM1C promoter sequence
   Search SABiosciences Chromatin IP Primers for FEM1C

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat FEM1C


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

Entrez Gene cytogenetic band: 5q22   Ensembl cytogenetic band:  5q22.3   HGNC cytogenetic band: 5q22

FEM1C Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
FEM1C gene location

GeneLoc information about chromosome 5         GeneLoc Exon Structure

GeneLoc location for GC05M114884:  view genomic region     (about GC identifiers)

Start:
114,856,608 bp from pter      End:
114,880,591 bp from pter
Size:
23,984 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: FEM1C_HUMAN, Q96JP0 (See protein sequence)
Recommended Name: Protein fem-1 homolog C  
Size: 617 amino acids; 68673 Da
Subunit: Component of some E3 ubiquitin-protein ligase complex (By similarity)
Subcellular location: Cytoplasm (By similarity)
Caution: Was initially thought to be the ortholog of mouse FEM1A (PubMed:11733146)
Sequence caution: Sequence=BAB15096.1; Type=Erroneous initiation;
Secondary accessions: B2RE47 Q8N3V8 Q9H704 Q9NPL6 Q9NPL9

Explore the universe of human proteins at neXtProt for FEM1C: NX_Q96JP0

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q96JP0

  • FEM1C Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins: NP_064562.1  
    ENSEMBL proteins: 
     ENSP00000274457  

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    Uscn Proteins for FEM1C

    Gene Ontology (GO): 1 cellular component term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005737cytoplasm IEA--


    FEM1C 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

    FEM1C for domains           About GeneDecksing

    2 InterPro domains/families:
     IPR002110 Ankyrin_rpt
     IPR020683 Ankyrin_rpt-contain_dom

    Graphical View of Domain Structure for InterPro Entry Q96JP0

    ProtoNet protein and cluster: Q96JP0

    1 Blocks protein family: IPB002110 Ankyrin repeat signature

    UniProtKB/Swiss-Prot: FEM1C_HUMAN, Q96JP0
    Similarity: Belongs to the fem-1 family
    Similarity: Contains 9 ANK repeats
    Similarity: Contains 2 TPR repeats


    (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: FEM1C_HUMAN, Q96JP0
    Function: Probable component of an E3 ubiquitin-protein ligase complex, in which it may act as a substrate recognition
    subunit (By similarity)

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    1 GenomeRNAi human phenotype for FEM1C:
     Increased gamma-H2AX phosphory 

    Animal Models:
         2 MGI mutant phenotypes (inferred from 1 allele(MGI details for Fem1c):
     nervous system  reproductive system 

    FEM1C 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



    UniProtKB/Swiss-Prot: FEM1C_HUMAN, Q96JP0
    Pathway: Protein modification; protein ubiquitination

    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for FEM1C

    STRING Interaction Network Preview (showing 4 interactants - click image to see more details)

    5/8 Interacting proteins for FEM1C (Q96JP03 ENSP000002744574) via UniProtKB, MINT, STRING, and/or I2D (see all 8)

    InteractantInteraction Details
    GeneCardExternal ID(s)
    TCEAL1Q151703, ENSP000003617074I2D: score=2 STRING: ENSP00000361707
    CUL2Q136173I2D: score=1 
    FBXW7Q969H03I2D: score=1 
    PPM1FP495933I2D: score=1 
    TCEB1Q153693I2D: score=1 
    About this table

    Gene Ontology (GO): 1 biological process term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0016567protein ubiquitination IEA--


    FEM1C 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 FEM1C
    Search CenterWatch for drugs/clinical trials and news about FEM1C 

    (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 FEM1C gene: 
    NM_020177.2  

    Unigene Cluster for FEM1C:

    Fem-1 homolog c (C. elegans)
    Hs.47367  [show with all ESTs]
    Unigene Representative Sequence: NM_020177
    1 Ensembl transcript including schematic representation, and UCSC links where relevant:
    ENST00000274457(uc003krb.1)

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    hsa-miR-520e hsa-miR-106a hsa-miR-208b hsa-miR-93 hsa-miR-520b hsa-miR-20a hsa-miR-186* hsa-miR-224*
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    Additional cDNA sequence: 

    AB058688.1 AF391093.1 AK025265.1 AK315803.1 AL050087.1 AL110246.1 AL365409.1 AL365415.1 
    AL831817.1 AY249188.1 BC028369.2 BC098385.1 

    4 DOTS entries:

    DT.209778  DT.100022681  DT.100736405  DT.120813046 

    24/93 AceView cDNA sequences (see all 93):

    BQ422068 AI753510 CA941636 CA774558 F07742 BP335508 AY249188 AL831817 
    AL365415 BQ025839 AL050087 Z44988 CB154094 AL110246 AW576227 BG057303 
    AF391093 AK025265 BF445605 BQ573804 AA446691 AB058688 AA814586 NM_020177 

    GeneLoc Exon Structure

    3 Alternative Splicing Database (ASD) splice patterns (SP) for FEM1C    About this scheme

    ExUns: 1a · 1b ^ 2 ^ 3a · 3b · 3c ^ 4
    SP1:              -                           
    SP2:              -                           
    SP3:                                          


    ECgene alternative splicing isoforms for FEM1C

    (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

    FEM1C expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: AAAGGTTGCA

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

    About this image
    See FEM1C Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for FEM1C

    SOURCE GeneReport for Unigene cluster: Hs.47367

    UniProtKB/Swiss-Prot: FEM1C_HUMAN, Q96JP0
    Tissue specificity: Widely expressed. Highly expressed in kidney, cardiac tissue, skeletal muscle and testis. Expressed
    at lower levels in other tissues, including cartilage

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    In Situ
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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 FEM1C gene from 7/24 species (see all 24)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Fem1c1 , 5 fem-1 homolog c (C.elegans)1, 5 92.38(n)1
    99.51(a)1
      18 (24.62 cM)5
    2402631  NM_173423.41  NP_775599.11 
     465017465 
    chicken
    (Gallus gallus)
    Aves FEM1C1 fem-1 homolog c (C. elegans) 82.39(n)
    90.6(a)
      431262  XM_428816.3  XP_428816.3 
    lizard
    (Anolis carolinensis)
    Reptilia FEM1C6
    --
    94(a)
    1 ↔ 1
    GL343193.1(8272090-8282058)
    tropical clawed frog
    (Xenopus tropicalis)
    Amphibia Str.150022 Transcribed sequence with moderate similarity to protein more 79.06(n)    BX715992.1 
    zebrafish
    (Danio rerio)
    Actinopterygii fem1c1 fem-1 homolog c (C.elegans) 66.34(n)
    79.06(a)
      378965  NM_198145.2  NP_937788.2 
    fruit fly
    (Drosophila melanogaster)
    Insecta CG69661 CG6966 53.82(n)
    55.02(a)
      41816  NM_001104326.1  NP_001097796.1 
    worm
    (Caenorhabditis elegans)
    Secernentea fem-11 Protein FEM-1 49.6(n)
    39.59(a)
      177335  NM_068423.4  NP_500824.1 


    ENSEMBL Gene Tree for FEM1C (if available)
    TreeFam Gene Tree for FEM1C (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for FEM1C gene
    ANKRD292  FEM1B2  FEM1A2  KIDINS2202  
    2 SIMAP similar genes for FEM1C using alignment to 1 protein entry:     FEM1C_HUMAN:
    FEM1A    FEM1B

    FEM1C 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

    10/410 NCBI SNPs in FEM1C are shown (see all 410    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 5 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1171740941,2
    C,F,--114856293(+) TCATAA/GTAATA 1 -- ds50011Minor allele frequency- G:0.04EA 120
    rs2020305851,2
    C--114856298(+) ATAATA/GTATTT 1 -- ds50010--------
    rs77120261,2
    C,F,A,H,--114856307(+) TTATGA/GTATAC 1 -- ds500117Minor allele frequency- G:0.13NS EA NA WA CSA 2216
    rs751673041,2
    F,--114856325(+) CACAGC/TAAACC 1 -- ds50011Minor allele frequency- T:0.03NA 120
    rs1828457611,2
    --114856326(+) ACAGCA/TAACCA 1 -- ds50010--------
    rs1414358381,2
    --114856393(+) TCCCCA/GTATCT 1 -- ds50010--------
    rs1878761531,2
    --114856434(+) ATTTAG/TAATAA 1 -- ds50010--------
    rs759006211,2
    C,--114856475(+) ATTAAC/TAATAA 1 -- ds50013Minor allele frequency- T:0.06CSA WA NA 240
    rs1923960821,2
    --114856539(+) AACAGC/GAGTTT 1 -- ds50010--------
    rs1836750511,2
    --114856666(+) TCCATC/TGTGTG 1 -- ut310--------

    HapMap Linkage Disequilibrium report for FEM1C (114856608 - 114880591 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
          Database of Genomic Variants (DGV) variations for FEM1C: --

    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

    FEM1C for disorders           About GeneDecksing

    OMIM gene information: 608767    OMIM disorders: --

    1 disease for FEM1C:    About MalaCards
    polycystic ovary syndrome

    Human Genome Epidemiology (HuGE) Navigator: FEM1C (1 document)

    Export disorders for FEM1C 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 FEM1C gene, integrated from 9 sources (see all 15):
    (articles sorted by number of sources associating them with FEM1C)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. The Fem1c genes: conserved members of the Fem1 gene family in vertebrates. (PubMed id 14527725)1, 2, 3, 9 Ventura-Holman T.... Maher J.F. (2003)
    2. Identification of human FEM1A, the ortholog of a C. elegans sex- differentiation gene. (PubMed id 11733146)1, 2, 3, 9 Krakow D.... Cohn D.H. (2001)
    3. Prediction of the coding sequences of unidentified human genes. XX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. (PubMed id 11347906)1, 2 Nagase T.... Ohara O. (2001)
    4. FEM1A and FEM1B: novel candidate genes for polycystic ovary syndrome. (PubMed id 18757445)1, 9 Goodarzi M.O....Azziz R. (2008)
    5. Systematic and quantitative assessment of the ubiquiti n-modified proteome. (PubMed id 21906983)1 Kim W....Gygi S.P. (2011)
    6. Mass spectrometric analysis of lysine ubiquitylation r eveals promiscuity at site level. (PubMed id 21139048)1 Danielsen J.M....Nielsen M.L. (2011)
    7. A proteome-wide, quantitative survey of in vivo ubiqui tylation sites reveals widespread regulatory roles. (PubMed id 21890473)1 Wagner S.A....Choudhary C. (2011)
    8. Dynamics of cullin-RING ubiquitin ligase network revea led by systematic quantitative proteomics. (PubMed id 21145461)1 Bennett E.J....Harper J.W. (2010)
    9. Defining the human deubiquitinating enzyme interactio n landscape. (PubMed id 19615732)1 Sowa M.E....Harper J.W. (2009)
    10. Ubiquitin-mediated proteolysis of HuR by heat shock. (PubMed id 19322201)1 Abdelmohsen K....Gorospe M. (2009)

    (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: 56929 HGNC: 16933 AceView: FEM1C Ensembl:ENSG00000145780 euGenes: HUgn56929
    ECgene: FEM1C H-InvDB: FEM1C

    (According to HUGE)
    About This Section
    HUGE: KIAA1785

    (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 FEM1C 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 FEM1C gene:
    Search GeneIP for patents involving FEM1C

    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, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript and LifeMap BioReagents, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or Enzo Life Sciences),
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