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Monogenic Diabetes v0.84 DMXL2 Zornitza Stark Marked gene: DMXL2 as ready
Monogenic Diabetes v0.84 DMXL2 Zornitza Stark Gene: dmxl2 has been classified as Red List (Low Evidence).
Monogenic Diabetes v0.84 DMXL2 Zornitza Stark Phenotypes for gene: DMXL2 were changed from Sensorineural Hearing Loss; OMIM:612186; ORPHA90636 to Polyendocrine-polyneuropathy syndrome , MIM# 616113
Monogenic Diabetes v0.83 DMXL2 Zornitza Stark Publications for gene: DMXL2 were set to 22875945; 27657680; 25248098
Monogenic Diabetes v0.82 DMXL2 Zornitza Stark Classified gene: DMXL2 as Red List (low evidence)
Monogenic Diabetes v0.82 DMXL2 Zornitza Stark Gene: dmxl2 has been classified as Red List (Low Evidence).
Monogenic Diabetes v0.74 DMXL2 Hali Van Niel reviewed gene: DMXL2: Rating: RED; Mode of pathogenicity: None; Publications: 30237576, 31688942, 27657680, 25248098; Phenotypes: ; Mode of inheritance: Unknown
Monogenic Diabetes v0.0 DMXL2 Zornitza Stark gene: DMXL2 was added
gene: DMXL2 was added to Monogenic diabetes. Sources: Expert Review Amber,Other
Mode of inheritance for gene: DMXL2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: DMXL2 were set to 22875945; 27657680; 25248098
Phenotypes for gene: DMXL2 were set to Sensorineural Hearing Loss; OMIM:612186; ORPHA90636