COL4A3 Gene

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1		Vicky Zhou	+ 472 word(s)	472	2020-12-15 07:48:25

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Zhou, V. COL4A3 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5214 (accessed on 22 September 2026).

Zhou V. COL4A3 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5214. Accessed September 22, 2026.

Zhou, Vicky. "COL4A3 Gene" Encyclopedia, https://encyclopedia.pub/entry/5214 (accessed September 22, 2026).

Zhou, V. (2020, December 24). COL4A3 Gene. In Encyclopedia. https://encyclopedia.pub/entry/5214

Zhou, Vicky. "COL4A3 Gene." Encyclopedia. Web. 24 December, 2020.

COL4A3 Gene

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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/col4a3

collagen type IV alpha 3 chain

genes

References

Frascà GM, Onetti-Muda A, Mari F, Longo I, Scala E, Pescucci C, Roccatello D, Alpa M, Coppo R, Li Volti G, Feriozzi S, Bergesio F, Schena FP, Renieri A;Italian Renal Immunopathology Group. Thin glomerular basement membrane disease:clinical significance of a morphological diagnosis--a collaborative study of the Italian Renal Immunopathology Group. Nephrol Dial Transplant. 2005Mar;20(3):545-51.
Gregory MC. The clinical features of thin basement membrane nephropathy. SeminNephrol. 2005 May;25(3):140-5. Review.
Kashtan CE. Alport Syndrome. 2001 Aug 28 [updated 2019 Feb 21]. In: Adam MP,Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors.GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle;1993-2020. Available from http://www.ncbi.nlm.nih.gov/books/NBK1207/
Kashtan CE. Alport syndrome. An inherited disorder of renal, ocular, andcochlear basement membranes. Medicine (Baltimore). 1999 Sep;78(5):338-60. Review.
Pescucci C, Mari F, Longo I, Vogiatzi P, Caselli R, Scala E, Abaterusso C,Gusmano R, Seri M, Miglietti N, Bresin E, Renieri A. Autosomal-dominant Alportsyndrome: natural history of a disease due to COL4A3 or COL4A4 gene. Kidney Int. 2004 May;65(5):1598-603.
Rana K, Wang YY, Buzza M, Tonna S, Zhang KW, Lin T, Sin L, Padavarat S, SavigeJ. The genetics of thin basement membrane nephropathy. Semin Nephrol. 2005May;25(3):163-70. Review.
Slajpah M, Gorinsek B, Berginc G, Vizjak A, Ferluga D, Hvala A, Meglic A,Jaksa I, Furlan P, Gregoric A, Kaplan-Pavlovcic S, Ravnik-Glavac M, Glavac D.Sixteen novel mutations identified in COL4A3, COL4A4, and COL4A5 genes inSlovenian families with Alport syndrome and benign familial hematuria. KidneyInt. 2007 Jun;71(12):1287-95.
Tazón Vega B, Badenas C, Ars E, Lens X, Milà M, Darnell A, Torra R. Autosomal recessive Alport's syndrome and benign familial hematuria are collagen type IVdiseases. Am J Kidney Dis. 2003 Nov;42(5):952-9.
Wang YY, Rana K, Tonna S, Lin T, Sin L, Savige J. COL4A3 mutations and theirclinical consequences in thin basement membrane nephropathy (TBMN). Kidney Int.2004 Mar;65(3):786-90.

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Subjects: Genetics & Heredity

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Update Date: 24 Dec 2020

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