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Gene Symbol |
WNT3 |
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Aliases |
INT4, TETAMS |
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Entrez Gene ID |
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Gene Name |
Wnt family member 3 |
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Chromosomal Location |
17q21.31-q21.32 |
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HGNC ID |
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Summary |
The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It encodes a protein which shows 98% amino acid identity to mouse Wnt3 protein, and 84% to human WNT3A protein, another WNT gene product. The mouse studies show the requirement of Wnt3 in primary axis formation in the mouse. Studies of the gene expression suggest that this gene may play a key role in some cases of human breast, rectal, lung, and gastric cancer through activation of the WNT-beta-catenin-TCF signaling pathway. This gene is clustered with WNT15, another family member, in the chromosome 17q21 region. [provided by RefSeq, Jul 2008]
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RefSeq DNA |
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RefSeq mRNA |
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e!Ensembl
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Protein Information |
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Protein Name |
Proto-oncogene Wnt-3, WNT-3 proto-oncogene protein, proto-oncogene Int-4 homolog, wingless-type MMTV integration site family, member 3 |
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Function |
Ligand for members of the frizzled family of seven transmembrane receptors (Probable). Functions in the canonical Wnt signaling pathway that results in activation of transcription factors of the TCF/LEF family (PubMed:26902720). Required for normal gastrulation, formation of the primitive streak, and for the formation of the mesoderm during early embryogenesis. Required for normal formation of the apical ectodermal ridge (By similarity). Required for normal embryonic development, and especially for limb development (PubMed:14872406). |
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UniProt |
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Associated Diseases
Disease group | Disease Name | References |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
Tetraamelia Syndrome |
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Digestive System Diseases |
Biliary Cirrhosis |
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Endocrine System Diseases |
PCOS |
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Neoplasms |
Breast Cancer |
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Lung Cancer |
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Lymphoma |
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Nervous System Diseases |
Parkinson Disease |
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Hydrocephalus |
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Respiratory Tract Diseases |
Lung Diseases |
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References |
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PubMed ID |
Associated gene/s |
Associated condition |
Genetic Mutation |
Diagnostic Criteria |
Association with PCOS |
Ethnicity |
Conclusion |
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Endrometrial proliferation and development |
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Rotterdam Criteria |
Direct
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17 PCOS patients and 8 control |
The considerable decrease in the expression of Wnt3, Wnt7a, and Wnt8b may be associated not only with lower endometrial thickness but also with sub-optimal endometrial development which likely is responsible for the poor pregnancy outcome due to the disturbance in estrogen signaling. |
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