Homo sapiens collagen type IV alpha 5 chain (COL4A5), transcript varia - Nucleotide

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Four novel mutations identified in the COL4A3, COL4A4 and COL4A5 genes in 10 families with Alport syndrome. [BMC Med Genomics. 2024]
Four novel mutations identified in the COL4A3, COL4A4 and COL4A5 genes in 10 families with Alport syndrome.
Wang D, Pan M, Li H, Li M, Li P, Xiong F, Xiao H. BMC Med Genomics. 2024 Jul 8; 17(1):181. Epub 2024 Jul 8.
A novel COL4A5 splicing mutation causes alport syndrome in a Chinese family. [BMC Med Genomics. 2024]
A novel COL4A5 splicing mutation causes alport syndrome in a Chinese family.
Chen S, Xu G, Zhao Z, Du J, Shen B, Li C. BMC Med Genomics. 2024 Apr 26; 17(1):108. Epub 2024 Apr 26.
Genetic diagnosis of Alport syndrome in 16 Chinese families. [Mol Genet Genomic Med. 2024]
Genetic diagnosis of Alport syndrome in 16 Chinese families.
Xiao T, Zhang J, Liu L, Zhang B. Mol Genet Genomic Med. 2024 Mar; 12(3):e2406.

RefSeq protein product
See the reference protein sequence for collagen alpha-5(IV) chain isoform 1 precursor (NP_000486.1).

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Protein sequence from Nucleotide coding region
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Nucleotide