lamin A/C
| UniProt | Protein Name |
|---|---|
| H0YAB0 |
|
| P02545 |
|
| A0A384MQX1 |
|
| Q5TCI8 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| nuclear pore localization | ||
| ventricular cardiac muscle cell development | ||
| cellular response to hypoxia | ||
| negative regulation of mesenchymal cell proliferation | ||
| negative regulation of release of cytochrome c from mitochondria |
| Gene Ontology |
|---|
| nuclear envelope organization |
| protein localization to nuclear envelope |
| structural constituent of cytoskeleton |
| InterPro |
|---|
| Intermediate filament protein, conserved site |
| Intermediate filament, rod domain |
| Lamin tail domain superfamily |
| Lamin tail domain |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110640 | congenital muscular dystrophy due to LMNA mutation | |
| DOID:0111584 | dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome | |
| DOID:11712 | lipoatrophic diabetes mellitus | |
| DOID:11726 | Emery-Dreifuss muscular dystrophy | |
| DOID:12930 | dilated cardiomyopathy | |
| DOID:3911 | progeria | |
| DOID:5688 | Werner syndrome | |
| DOID:6713 | cerebrovascular disease | |
| DOID:811 | lipodystrophy | |
| DOID:9352 | type 2 diabetes mellitus |
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 4000 | Xenbase:XB-GENE-920722 | ||
| 4001 | FB:FBgn0002525 | ||
| 16905 | Xenbase:XB-GENE-920722 | MOUSE37950 | |
| 16906 | FB:FBgn0010397 | ||
| 16907 | FB:FBgn0002525 | ||
| 60374 | RATNO23658 | ||
| 84823 | FB:FBgn0002525 | ||
| 116685 | FB:FBgn0010397 | ||
| 404144 | BOVIN25762 | ||
| 457385 | PANTR22556 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: December 8, 2025