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| Retinitis pigmentosa v1.0 | KLHL7 | Gene migrated from ENSG00000122550 to ENSG00000122550 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Retinitis pigmentosa v0.188 | Bryony Thompson Copied gene KLHL7 from panel Retinitis pigmentosa_Autosomal Dominant | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Retinitis pigmentosa v0.188 | KLHL7 |
Bryony Thompson gene: KLHL7 was added gene: KLHL7 was added to Retinitis pigmentosa_Autosomal Recessive/X-linked. Sources: Expert Review Green,Royal Melbourne Hospital Mode of inheritance for gene: KLHL7 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: KLHL7 were set to Retinitis pigmentosa 42, 612943 |
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