wolframin ER transmembrane glycoprotein
| UniProt | Protein Name |
|---|---|
| O76024 |
|
| A0A0S2Z4V6 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| negative regulation of transcription by RNA polymerase II | ||
| kidney development | ||
| renal water homeostasis | ||
| ER overload response | ||
| ER overload response |
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum | ||
| endoplasmic reticulum | ||
| endoplasmic reticulum lumen | ||
| endoplasmic reticulum membrane | ||
| endoplasmic reticulum membrane |
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| calmodulin binding | ||
| ubiquitin protein ligase binding | ||
| calcium-dependent protein binding | ||
| ATPase binding |
| Gene Ontology |
|---|
| calcium ion homeostasis |
| endoplasmic reticulum unfolded protein response |
| InterPro |
|---|
| Wolframin family |
| Wolframin, EF-hand domain |
| Wolframin, OB-fold domain |
| Wolframin, Sel1-like repeat |
| Wolframin, cysteine-rich domain |
| Wolframin |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0080584 | autosomal dominant Wolfram syndrome | |
| DOID:0110241 | cataract 41 | |
| DOID:0110584 | autosomal dominant nonsyndromic deafness 6 | |
| DOID:0110629 | Wolfram syndrome 1 | |
| DOID:0111441 | optic atrophy 1 | |
| DOID:10003 | sensorineural hearing loss | |
| DOID:10632 | Wolfram syndrome | |
| DOID:5723 | optic atrophy | |
| DOID:8947 | diabetic retinopathy | |
| DOID:9351 | diabetes mellitus |
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 7466 | Xenbase:XB-GENE-978820 | ||
| 22393 | Xenbase:XB-GENE-978820 | MOUSE44779 | |
| 42679 | Xenbase:XB-GENE-978820 | ||
| 83725 | RATNO07794 | ||
| 461100 | PANTR33258 | ||
| 482113 | CANLF03348 | ||
| 556580 | DANRE06550 | ||
| 710948 | MACMU37001 | ||
| 100018961 | MONDO27616 | ||
| 100070117 | HORSE31495 |
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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