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| Ataxia v2.0 | GFAP | Gene migrated from ENSG00000131095 to ENSG00000131095 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ataxia v1.92 | Bryony Thompson Copied gene GFAP from panel Ataxia - adult onset | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ataxia v1.92 | GFAP |
Bryony Thompson gene: GFAP was added gene: GFAP was added to Ataxia. Sources: Royal Melbourne Hospital,Expert Review Green Mode of inheritance for gene: GFAP was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: GFAP were set to Alexander disease, 203450; Autosomal Dominant Ataxia; Alexander disease |
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