GFRα3: Difference between revisions
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'''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


