Entity Details
| Primary name |
LMIP_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | P55344 |
| EntryName | LMIP_HUMAN |
| FullName | Lens fiber membrane intrinsic protein |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 173 |
| SequenceStatus | complete |
| DateCreated | 1997-11-01 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Membrane |
Domains
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| Domain | Name | Category | Type |
| IPR003935 | Lens fibre membrane intrinsic protein | Family | Family |
| IPR004031 | PMP-22/EMP/MP20/Claudin superfamily | Family | Family |
| IPR004032 | PMP-22/EMP/MP20 | Family | Family |
Diseases
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| Disease ID | Source | Name | Description |
| 615277 | OMIM | Cataract, multiple types 19 (CTRCT19) | An opacification of the crystalline lens of the eye that frequently results in visual impairment or blindness. Opacities vary in morphology, are often confined to a portion of the lens, and may be static or progressive. In general, the more posteriorly located and dense an opacity, the greater the impact on visual function. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
1 interaction