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| Renal Tubulopathies and related disorders v2.0 | FXYD2 | Gene migrated from ENSG00000137731 to ENSG00000137731 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Renal Tubulopathies and related disorders v1.26 | Sangavi Sivagnanasundram Added reviews for gene FXYD2 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Renal Tubulopathies and related disorders v0.4 | FXYD2 |
Zornitza Stark gene: FXYD2 was added gene: FXYD2 was added to Renal Tubulopathies and related disorders. Sources: KidGen_Magnesium v38.1.0,Expert Review Amber Mode of inheritance for gene: FXYD2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: FXYD2 were set to 17980699; 18448590; 12763862; 25765846; 27014088; 11062458 Phenotypes for gene: FXYD2 were set to Renal hypomagnesemia 2 MONDO:0007937 |
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