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Details of CISD2 gene in Homo sapiens
IDs |
|---|
| Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
|
| CISD2 | CDGSH2 | ERIS | ZCD2 | Q8N5K1
| Q7Z3D5
| 3FNV
3FNV | sensorineural deafn |
Disease |
|---|
| Disease |
OMIM id |
| Wolfram syndrome 2 (WFS2) [MIM:604928]: A rare disorder characterized by juvenile-onset insulin-dependent diabetes mellitus with optic atrophy. Other manifestations include diabetes insipidus |
dementia |
Orthologs in other species |
|---|
| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
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