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Index > Protein center > ANO5(Gene name) > Human
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  • ANO5 (Gene name),
  • Anoctamin-5 (Protein name ),  ANO5_HUMAN from NCBI database.
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  • General Annotation
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  • Antigen Annotation
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  • 3D
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  • Predicted Eptitope
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  • Vaild Sequence
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  • Gene name:
    ANO5(GDD1;TMEM16E);
    Protein name:
    Anoctamin-5;
    Alternative:
    Transmembrane protein 16E;Gnathodiaphyseal dysplasia 1 protein;
    Organism:
    Human (Homo sapiens). 
    General Annotation
    Sub Unit:
    N/A
    Function:
    May act as a calcium-activated chloride channel.
    Subcellular Location:
    Endoplasmic reticulum membrane Multi-pass membrane protein Co-localized with CALR/calreticulin.
    Protein Attributes:
    Sequence length:
    913
    Sequence:
    50:
    MGDPDLLEVL | AEEGEKVNKH | IDYSFQMSEQ | SLSSRETSFL | INEETMPAKR | 
    100:
    FNLFLRRRLM | FQKNQQSKDS | IFFRDGIRQI | DFVLSYVDDV | KKDAELKAER | 
    150:
    RKEFETNLRK | TGLELEIEDK | RDSEDGRTYF | VKIHAPWEVL | VTYAEVLGIK | 
    200:
    MPIKESDIPR | PKHTPISYVL | GPVRLPLSVK | YPHPEYFTAQ | FSRHRQELFL | 
    250:
    IEDQATFFPS | SSRNRIVYYI | LSRCPFGIED | GKKRFGIERL | LNSNTYSSAY | 
    300:
    PLHDGQYWKP | SEPPNPTNER | YTLHQNWARF | SYFYKEQPLD | LIKNYYGEKI | 
    350:
    GIYFVFLGFY | TEMLFFAAVV | GLACFIYGLL | SMEHNTSSTE | ICDPEIGGQM | 
    400:
    IMCPLCDQVC | DYWRLNSTCL | ASKFSHLFDN | ESTVFFAIFM | GIWVTLFLEF | 
    450:
    WKQRQARLEY | EWDLVDFEEE | QQQLQLRPEF | EAMCKHRKLN | AVTKEMEPYM | 
    500:
    PLYTRIPWYF | LSGATVTLWM | SLVVTSMVAV | IVYRLSVFAT | FASFMESDAS | 
    550:
    LKQVKSFLTP | QITTSLTGSC | LNFIVILILN | FFYEKISAWI | TKMEIPRTYQ | 
    600:
    EYESSLTLKM | FLFQFVNFYS | SCFYVAFFKG | KFVGYPGKYT | YLFNEWRSEE | 
    650:
    CDPGGCLIEL | TTQLTIIMTG | KQIFGNIKEA | IYPLALNWWR | RRKARTNSEK | 
    700:
    LYSRWEQDHD | LESFGPLGLF | YEYLETVTQF | GFVTLFVASF | PLAPLLALIN | 
    750:
    NIVEIRVDAW | KLTTQYRRTV | ASKAHSIGVW | QDILYGMAVL | SVATNAFIVA | 
    800:
    FTSDIIPRLV | YYYAYSTNAT | QPMTGYVNNS | LSVFLIADFP | NHTAPSEKRD | 
    850:
    FITCRYRDYR | YPPDDENKYF | HNMQFWHVLA | AKMTFIIVME | HVVFLVKFLL | 
    900:
    AWMIPDVPKD | VVERIKREKL | MTIKILHDFE | LNKLKENLGI | NSNEFAKHVM | 
    913:
    IEENKAQLAK | STL
    3D Structure:
    N/A
    Predicted Eptitope:
    Please Sign in.
    EIAab Sequence  Vaild Sequence:
    Please Sign in.
    Related Databases
    Pfam:
    MIM:
    UniGene:
    String:
    Uniprot:
     
    FOR
    ELISA Kit for Human Anoctamin-5
    ELISA Kit for Human Anoctamin-5
    CLIA Kit for Human Anoctamin-5
    CLIA Kit for Human Anoctamin-5
    Polyclonal Antibody for Human Anoctamin-5
    Polyclonal Antibody for Human Anoctamin-5
    Monoclonal Antibody for Human Anoctamin-5
    Monoclonal Antibody for Human Anoctamin-5
    Protein for Human Anoctamin-5
    Protein for Human Anoctamin-5

    R&D Technical Data
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    Precision
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    Recovery
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    Linearity
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    For more information, please refer to the manual,Or contact our technical support: tech@eiaab.com.
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    For more information, please refer to the manual,Or contact our technical support: tech@eiaab.com.
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    References
    1. 1.
      "The novel gene encoding a putative transmembrane protein is mutated in gnathodiaphyseal dysplasia (GDD)."
      Tsutsumi S. , Kamata N. , Vokes T.J. , Maruoka Y. , Nakakuki K. , Enomoto S. , Omura K. , Amagasa T. , Nagayama M. , Saito-Ohara F. , Inazawa J. , Moritani M. , Yamaoka T. , Inoue H. , Itakura M.
      Am. J. Hum. Genet.74:1255-1261(2004) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [MRNA];TISSUE SPECIFICITY;SUBCELLULAR LOCATION;VARIANTS GDD GLY-356 AND ARG-356;CHARACTERIZATION OF VARIANTS GDD GLY-356 AND ARG-356
      tissue: Skeletal muscle.
    2. 2.
      "Identification and characterization of TMEM16E and TMEM16F genes in silico."
      Katoh M. , Katoh M.
      Int. J. Oncol.24:1345-1349(2004) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: TISSUE SPECIFICITY
    3. 3.
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: ABSENCE OF CALCIUM-ACTIVATED CHLORIDE CHANNEL ACTIVITY;SUBCELLULAR LOCATION
    4. 4.
      "Physiological roles and diseases of Tmem16/Anoctamin proteins: are they all chloride channels?"
      Duran C. , Hartzell H.C.
      Acta Pharmacol. Sin.32:685-692(2011) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: REVIEW
    5. 5.
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: REVIEW
    6. 6.
      "ANOs 3-7 in the anoctamin/Tmem16 Cl- channel family are intracellular proteins."
      Duran C. , Qu Z. , Osunkoya A.O. , Cui Y. , Hartzell H.C.
      Am. J. Physiol.302:C482-C493(2012) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: ABSENCE OF CALCIUM-ACTIVATED CHLORIDE CHANNEL ACTIVITY;SUBCELLULAR LOCATION
    7. 7.
      "The anoctamin (TMEM16) gene family: calcium-activated chloride channels come of age."
      Winpenny J.P. , Gray M.A.
      Exp. Physiol.97:175-176(2012) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: REVIEW
    8. 8.
      "Anoctamins are a family of Ca2+ activated Cl- channels."
      Tian Y. , Schreiber R. , Kunzelmann K.
      J. Cell Sci.125:4991-4998(2012) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: SUBCELLULAR LOCATION
    9. 9.
      "Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies."
      Bolduc V. , Marlow G. , Boycott K.M. , Saleki K. , Inoue H. , Kroon J. , Itakura M. , Robitaille Y. , Parent L. , Baas F. , Mizuta K. , Kamata N. , Richard I. , Linssen W.H. , Mahjneh I. , de Visser M. , Bashir R. , Brais B.
      Am. J. Hum. Genet.86:213-221(2010) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT LGMD2L VAL-231;VARIANT MMD3 CYS-758
    10. 10.
      "Novel ANO5 mutations causing hyper-CK-emia, limb girdle muscular weakness and Miyoshi type of muscular dystrophy."
      Schessl J. , Kress W. , Schoser B.
      Muscle Nerve45:740-742(2012) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT TRP-58;VARIANT MMD3 CYS-655
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