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| Structural eye disease v0.76 | GRM6 | Nicola Ragge reviewed gene: GRM6: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Night blindness, congenital stationary (complete), 1B, autosomal recessive, 257270; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | GRM6 | Ivone Leong reviewed gene: GRM6: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Night blindness, congenital stationary (complete), 1B, autosomal recessive, 257270; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | GRM6 |
Ivone Leong Source NHS GMS was added to GRM6. Mode of inheritance for gene GRM6 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Night blindness, congenital stationary (complete), 1B, autosomal recessive, 257270 for gene: GRM6 |
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| Structural eye disease v0.2 | GRM6 |
Ellen McDonagh gene: GRM6 was added gene: GRM6 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: GRM6 was set to Phenotypes for gene: GRM6 were set to Eye Disorders |
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