GFRα3: Difference between revisions

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#REDIRECT [[GFRA3]]
'''GFRα3''' is a protein that in humans is encoded by the GFRA3 gene. It is a member of the GDNF receptor family. It is a glycosylphosphatidylinositol (GPI)-linked cell surface receptor for both GDNF and NTN, and mediates activation of the RET tyrosine kinase receptor.
 
== Function ==
GFRα3 is a receptor for [[neurturin]] (NTN). Together with the [[Glial cell line-derived neurotrophic factor|GDNF]], NTN forms complexes with and mediates the activity of the [[RET]] proto-oncogene. GFRα3 is a member of the GDNF receptor family. It is a glycosylphosphatidylinositol (GPI)-linked cell surface receptor for both GDNF and NTN, and mediates activation of the RET tyrosine kinase receptor.
 
== Clinical significance ==
Alterations in the GFRA3 gene have been associated with [[Hirschsprung's disease]], a genetic disorder that results in an absence of nerve cells in the colon, leading to severe constipation and intestinal obstruction.
 
== See also ==
* [[GDNF family receptor alpha]]
* [[RET proto-oncogene]]
 
== References ==
<references />
 
== External links ==
* [https://www.ncbi.nlm.nih.gov/gene/26706 GFRA3] at the National Center for Biotechnology Information
 
[[Category:Human proteins]]
[[Category:Genes on human chromosome 15]]
{{stub}}

Latest revision as of 20:41, 12 March 2025

GFRα3 is a protein that in humans is encoded by the GFRA3 gene. It is a member of the GDNF receptor family. It is a glycosylphosphatidylinositol (GPI)-linked cell surface receptor for both GDNF and NTN, and mediates activation of the RET tyrosine kinase receptor.

Function[edit]

GFRα3 is a receptor for neurturin (NTN). Together with the GDNF, NTN forms complexes with and mediates the activity of the RET proto-oncogene. GFRα3 is a member of the GDNF receptor family. It is a glycosylphosphatidylinositol (GPI)-linked cell surface receptor for both GDNF and NTN, and mediates activation of the RET tyrosine kinase receptor.

Clinical significance[edit]

Alterations in the GFRA3 gene have been associated with Hirschsprung's disease, a genetic disorder that results in an absence of nerve cells in the colon, leading to severe constipation and intestinal obstruction.

See also[edit]

References[edit]

<references />

External links[edit]

  • GFRA3 at the National Center for Biotechnology Information
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