Gene
LIM2
lens intrinsic membrane protein 2
- HGNC 6610↗(opens in a new tab)
- Ensembl gene ENSG00000105370↗(opens in a new tab)
- NCBI Gene 3982↗(opens in a new tab)
Summary
- Cytogenetic location
- 19q13.41
- Coordinates
- Chromosome 19: 51,379,909–51,387,974 (GRCh38)
- Exons
- 5 exons across 8.1 kb
- Protein
- 173 amino acids
- Also known as
- MP19, MP17
- MANE Select transcript
- ENST00000596399.2NM_001161748.2
- Locus type
- gene with protein product
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Hereditary Congenital & Juvenile Cataract
- Early-Onset Non-Syndromic Cataract
Cataract that appears at birth or early in life without other features, caused by changes in lens genes such as the crystallins (CRYAA, CRYBB2, CRYGD and others), GJA3, GJA8 and MIP.
- 3 GenCC submitters rate it definitive or strong
What knowing changes
Early detection and surgery in children help prevent permanent vision loss from amblyopia, and family members can be offered eye checks.
How LIM2 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 0.9 kb of the gene's 8.1 kb; 522 of those bases code for the protein.
How a genome test reads LIM2
1
position in LIM2 where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 8.1 kb of LIM2, introns included, not only the 0.9 kb of exons.
Genes linked to the same conditions
- BFSP1beaded filament structural protein 1Shares 1 condition
- CHMP4Bcharged multivesicular body protein 4BShares 1 condition
- CRYABcrystallin alpha BShares 1 condition
- CRYBA1crystallin beta A1Shares 1 condition
- CRYBA2crystallin beta A2Shares 1 condition
- CRYBA4crystallin beta A4Shares 1 condition
- CRYBB1crystallin beta B1Shares 1 condition
- CRYBB3crystallin beta B3Shares 1 condition
- CRYGScrystallin gamma SShares 1 condition
- EPHA2EPH receptor A2Shares 1 condition
- GCNT2glucosaminyl (N-acetyl) transferase 2 (I blood group)Shares 1 condition
- GJA3gap junction protein alpha 3Shares 1 condition
Traits linked to LIM2
The Human Phenotype Ontology lists these as features of the rare conditions LIM2 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the eye
- Abnormal optic disc morphology
- Blurred vision
- Clouding of the lens of the eye
- Cortical pulverulent cataract
- Decreased clarity of vision
- Glaucoma
- Lazy eye
- Outward facing eye ball
Show 12 more traits
- Visual fixation instability
- Alternating cross eyes
- Increased front to back length of eyeball
- Involuntary, rapid, rhythmic eye movements
- Lamellar cataract
- Membranous cataract
- Posterior polar cataract
- Chorioretinal atrophy
- Inward turning cross eyed
- Phthisis bulbi
- Pulverulent cataract
- Yellowish cloudy center of lens
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). LIM2 gene: lens intrinsic membrane protein 2. Retrieved 16 October 2026, from https://dantelabs.com/genes/lim2
Dante Labs. LIM2 gene: lens intrinsic membrane protein 2 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/lim2
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