ADAMTS-like protein 4 isoform X9 [Homo sapiens]

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Biallelic ADAMTSL4 variants in a Chinese cohort of congenital ectopia lentis: Implications for genotype-phenotype relationships. [Hum Mutat. 2022]
Biallelic ADAMTSL4 variants in a Chinese cohort of congenital ectopia lentis: Implications for genotype-phenotype relationships.
Chen ZX, Jia WN, Sun Y, Chen TH, Zhao ZN, Lan LN, Liu Y, Song LH, Jiang YX. Hum Mutat. 2022 Dec; 43(12):2141-2152. Epub 2022 Oct 17.
ADAMTSL4 assessment in ectopia lentis reveals a recurrent founder mutation in Polynesians. [Ophthalmic Genet. 2017]
ADAMTSL4 assessment in ectopia lentis reveals a recurrent founder mutation in Polynesians.
van Bysterveldt KA, Al Taie R, Ikink W, Oliver VF, Vincent AL. Ophthalmic Genet. 2017 Dec; 38(6):537-543. Epub 2017 Apr 10.
A founder mutation in ADAMTSL4 causes early-onset bilateral ectopia lentis among Jews of Bukharian origin. [Mol Genet Metab. 2016]
A founder mutation in ADAMTSL4 causes early-onset bilateral ectopia lentis among Jews of Bukharian origin.
Reinstein E, Smirin-Yosef P, Lagovsky I, Davidov B, Peretz Amit G, Neumann D, Orr-Urtreger A, Ben-Shachar S, Basel-Vanagaite L. Mol Genet Metab. 2016 Jan; 117(1):38-41. Epub 2015 Nov 26.

RefSeq genomic sequence
See the genomic reference sequence for the ADAMTSL4 gene (NG_012172.1).
RefSeq mRNA
See reference mRNA sequence for the ADAMTSL4 gene (XM_011509651.3).
RefSeq protein isoforms
See 35 reference sequence protein isoforms for the ADAMTSL4 gene.

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Protein