Lens intrinsic membrane protein 2, 19kDa [Homo sapiens]

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A recurrent variant in LIM2 causes an isolated congenital sutural/lamellar cataract in a Japanese family. [Ophthalmic Genet. 2022]
A recurrent variant in LIM2 causes an isolated congenital sutural/lamellar cataract in a Japanese family.
Berry V, Fujinami K, Mochizuki K, Iwata T, Pontikos N, Quinlan RA, Michaelides M. Ophthalmic Genet. 2022 Oct; 43(5):622-626. Epub 2022 Jun 23.
Molecular and Genetic Mechanism of Non-Syndromic Congenital Cataracts. Mutation Screening in Spanish Families. [Genes (Basel). 2021]
Molecular and Genetic Mechanism of Non-Syndromic Congenital Cataracts. Mutation Screening in Spanish Families.
Fernández-Alcalde C, Nieves-Moreno M, Noval S, Peralta JM, Montaño VEF, Del Pozo Á, Santos-Simarro F, Vallespín E. Genes (Basel). 2021 Apr 16; 12(4). Epub 2021 Apr 16.
Elongated axial length and myopia-related fundus changes associated with the Arg130Cys mutation in the LIM2 gene in four Chinese families with congenital cataracts. [Ann Transl Med. 2021]
Elongated axial length and myopia-related fundus changes associated with the Arg130Cys mutation in the LIM2 gene in four Chinese families with congenital cataracts.
Wang X, Qin Y, Abudoukeremuahong A, Dongye M, Zhang X, Wang D, Li J, Lin Z, Yang Y, Ding L, et al. Ann Transl Med. 2021 Feb; 9(3):235.

RefSeq genomic sequence
See the genomic reference sequence for the LIM2 gene (NG_012924.1).
RefSeq protein isoforms
See 2 reference sequence protein isoforms for the LIM2 gene.

Nucleotide
Nucleotide sequence from coding region
PubMed
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Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

lens intrinsic membrane protein 2, partial [Homo sapiens]
lens intrinsic membrane protein 2, partial [Homo sapiens]
gi|1057500947|gb|AOE45495.1|

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Protein