Identity
HGNC
LOCATION
19q13.41
LOCUSID
ALIAS
CTRCT19,MP17,MP19
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 3982
MIM: 154045
HGNC: 6610
Ensembl: ENSG00000105370
Variants:
dbSNP: 3982
ClinVar: 3982
TCGA: ENSG00000105370
COSMIC: LIM2
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000105370 | ENST00000221973 | P55344 |
| ENSG00000105370 | ENST00000596399 | P55344 |
Expression (GTEx)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38178039 | 2024 | Novel and known variants in GJA3 and LIM2 in congenital cataract families from North India. | 0 |
| 38178039 | 2024 | Novel and known variants in GJA3 and LIM2 in congenital cataract families from North India. | 0 |
| 35736209 | 2022 | A recurrent variant in LIM2 causes an isolated congenital sutural/lamellar cataract in a Japanese family. | 3 |
| 35736209 | 2022 | A recurrent variant in LIM2 causes an isolated congenital sutural/lamellar cataract in a Japanese family. | 3 |
| 32202185 | 2020 | A novel missense mutation in LIM2 causing isolated autosomal dominant congenital cataract. | 6 |
| 32202185 | 2020 | A novel missense mutation in LIM2 causing isolated autosomal dominant congenital cataract. | 6 |
| 27814360 | 2016 | Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts. | 13 |
| 27814360 | 2016 | Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts. | 13 |
| 21386927 | 2011 | Genetic variations in GJA3, GJA8, LIM2, and age-related cataract in the Chinese population: a mutation screening study. | 18 |
| 22103961 | 2011 | Absence of mutations in four genes encoding for congenital cataract and expressed in the human brain in Tunisian families with cataract and mental retardation. | 3 |
| 21386927 | 2011 | Genetic variations in GJA3, GJA8, LIM2, and age-related cataract in the Chinese population: a mutation screening study. | 18 |
| 22103961 | 2011 | Absence of mutations in four genes encoding for congenital cataract and expressed in the human brain in Tunisian families with cataract and mental retardation. | 3 |
| 18596884 | 2008 | A missense mutation in LIM2 causes autosomal recessive congenital cataract. | 27 |
| 18596884 | 2008 | A missense mutation in LIM2 causes autosomal recessive congenital cataract. | 27 |
| 15968979 | 2004 | Identification of a lens-specific cis-acting element within the basal promoter of the human lens intrinsic membrane protein MP19 gene (LIM2). | 0 |
Citation
Dessen P
LIM2 (lens intrinsic membrane protein 2)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/65268/lim2-(lens-intrinsic-membrane-protein-2)
