unknown [Homo sapiens]

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Mutations in ADAMTSL4 cause a unique form of autosomal-recessive congenital ectopia lentis. [Exp Eye Res. 2024]
Mutations in ADAMTSL4 cause a unique form of autosomal-recessive congenital ectopia lentis.
Chen T, Liu Y, Zhao Y, Wang M, Song L, Jiang Y. Exp Eye Res. 2024 Nov; 248:110090. Epub 2024 Sep 13.
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.

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

Nucleotide
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Taxonomy
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BioSystems
BioSystems
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MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein