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Index > Protein center > WNT7A(Gene name) > Human
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  • WNT7A (Gene name),
  • Protein Wnt-7a (Protein name ),  WNT7A_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:
    WNT7A;
    Protein name:
    Protein Wnt-7a;
    Alternative:

    Organism:
    Human (Homo sapiens). 
    General Annotation
    Sub Unit:
    Interacts with PORCN.
    Function:
    Ligand for members of the frizzled family of seven transmembrane receptors. Probable developmental protein. Signaling by Wnt-7a allows sexually dimorphic development of the mullerian ducts.
    Subcellular Location:
    Secreted extracellular space extracellular matrix
    Protein Attributes:
    Sequence length:
    349
    Sequence:
    50:
    MNRKARRCLG | HLFLSLGMVY | LRIGGFSSVV | ALGASIICNK | IPGLAPRQRA | 
    100:
    ICQSRPDAII | VIGEGSQMGL | DECQFQFRNG | RWNCSALGER | TVFGKELKVG | 
    150:
    SREAAFTYAI | IAAGVAHAIT | AACTQGNLSD | CGCDKEKQGQ | YHRDEGWKWG | 
    200:
    GCSADIRYGI | GFAKVFVDAR | EIKQNARTLM | NLHNNEAGRK | ILEENMKLEC | 
    250:
    KCHGVSGSCT | TKTCWTTLPQ | FRELGYVLKD | KYNEAVHVEP | VRASRNKRPT | 
    300:
    FLKIKKPLSY | RKPMDTDLVY | IEKSPNYCEE | DPVTGSVGTQ | GRACNKTAPQ | 
    349:
    ASGCDLMCCG | RGYNTHQYAR | VWQCNCKFHW | CCYVKCNTCS | ERTEMYTCK
    3D Structure:
    N/A
    Predicted Eptitope:
    Please Sign in.
    EIAab Sequence  Vaild Sequence:
    Please Sign in.
    Related Databases
    KEGG:
    UniGene:
    Pfam:
    MIM:
    String:
    SMR:
    Uniprot:
     
    FOR
    ELISA Kit for Human Protein Wnt-7a
    Cat.:
    E5407h
    Price:
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    MSDS:
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    Packing:
    96T
    Range:
    Please sign in first.
    ELISA Kit for Human Protein Wnt-7a
    Cat.:
    E5407m
    Price:
    Please sign in first.
    MSDS:
    Please sign in first.
    Packing:
    96T
    Range:
    Please sign in first.
    CLIA Kit for Human Protein Wnt-7a
    Cat.:
    U5407m
    Price:
    Please sign in first.
    MSDS:
    Please sign in first.
    Packing:
    96T
    CLIA Kit for Human Protein Wnt-7a
    Cat.:
    U5407h
    Price:
    Please sign in first.
    MSDS:
    Please sign in first.
    Packing:
    96T
    Polyclonal Antibody for Human Protein Wnt-7a
    Cat.:
    P5407Rb-m
    Price:
    Please sign in first.
    Packing:
    40ug/0.2ml
    Polyclonal Antibody for Human Protein Wnt-7a
    Cat.:
    P5407Rb-h
    Price:
    Please sign in first.
    Packing:
    40ug/0.2ml
    Monoclonal Antibody for Human Protein Wnt-7a
    Monoclonal Antibody for Human Protein Wnt-7a
    Protein for Human Protein Wnt-7a
    Protein for Human Protein Wnt-7a

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    Precision
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    Recovery
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    Linearity
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    References
    1. 1.
      "Isolation of a full-length human WNT7A gene implicated in limb development and cell transformation, and mapping to chromosome 3p25."
      Bui T.D. , Lako M. , Lejeune S. , Curtis A.R.J. , Strachan T. , Lindsay S. , Harris A.L.
      Gene189:25-29(1997) [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: Fetal brain.
    2. 2.
      "Isolation, characterization and chromosomal assignment of the human WNT7A gene."
      Ikegawa S. , Kumano Y. , Okui K. , Fujiwara T. , Takahashi E. , Nakamura Y.
      Cytogenet. Cell Genet.74:149-152(1996) [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]
    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: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]
    4. 4.
      "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
      The MGC Project Team
      Genome Res.14:2121-2127(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 [LARGE SCALE MRNA]
      tissue: Ovary.
    5. 5.
      "Differential expression of human Wnt genes 2, 3, 4, and 7B in human breast cell lines and normal and disease states of human breast tissue."
      Huguet E.L. , McMahon J.A. , McMahon A.P. , Bicknell R. , Harris A.L.
      Cancer Res.54:2615-2621(1994) [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] OF 204-327
      tissue: Mammary gland.
    6. 6.
      "Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome."
      Woods C.G. , Stricker S. , Seemann P. , Stern R. , Cox J. , Sherridan E. , Roberts E. , Springell K. , Scott S. , Karbani G. , Sharif S.M. , Toomes C. , Bond J. , Kumar D. , Al-Gazali L. , Mundlos S.
      Am. J. Hum. Genet.79:402-408(2006) [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 FUHRS THR-109;VARIANT LPHAS CYS-292;CHARACTERIZATION OF VARIANT FUHRS THR-109;CHARACTERIZATION OF VARIANT LPHAS CYS-292
    7. 7.
      "Al-Awadi/Raas-Rothschild syndrome: two new cases and review."
      Lonardo F. , Sabba G. , Luquetti D.V. , Monica M.D. , Scarano G.
      Am. J. Med. Genet. A143:3169-3174(2007) [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 LPHAS CYS-292
    8. 8.
      "A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome."
      Kantaputra P.N. , Mundlos S. , Sripathomsawat W.
      Am. J. Med. Genet. A152:2832-2837(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 LPHAS TRP-222
    9. 9.
      "Al-Awadi-Raas-Rothschild (limb/pelvis/uterus-hypoplasia/aplasia) syndrome and WNT7A mutations: genetic homogeneity and nosological delineation."
      Garavelli L. , Wischmeijer A. , Rosato S. , Gelmini C. , Reverberi S. , Sassi S. , Ferrari A. , Mari F. , Zabel B. , Lausch E. , Unger S. , Superti-Furga A.
      Am. J. Med. Genet. A155:332-336(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: VARIANT LPHAS LYS-72
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