dysferlin
| UniProt | Protein Name |
|---|---|
| A0A0N4SUN3 |
|
| A0A0N4SV63 |
|
| A0A0N4SWH3 |
|
| E9QL12 |
|
| A0A0N4SUJ2 |
|
| E9PXU9 |
|
| E9Q423 |
|
| Q9ESD7 |
|
| A0A0N4SVX9 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| lipid storage | ||
| protein catabolic process | ||
| T-tubule organization | ||
| T-tubule organization | ||
| T-tubule organization |
| GO Term | Evidence Code | PMID |
|---|---|---|
| calcium ion binding | ||
| calcium ion binding | ||
| protein binding | ||
| phospholipid binding | ||
| phospholipid binding |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110276 | autosomal recessive limb-girdle muscular dystrophy type 2B | |
| DOID:11720 | distal myopathy |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
GlyCosmos Portal v4.5.0
Last updated: April 6, 2026