| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Pituitary hormone deficiency v1.0 | ARHGAP5 | Gene migrated from ENSG00000100852 to ENSG00000100852 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Pituitary hormone deficiency v0.203 | Chirag Patel Copied gene ARHGAP5 from panel Hypogonadotropic hypogonadism | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Pituitary hormone deficiency v0.203 | ARHGAP5 |
Chirag Patel gene: ARHGAP5 was added gene: ARHGAP5 was added to Pituitary hormone deficiency. Sources: Expert Review Red,Literature Mode of inheritance for gene: ARHGAP5 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: ARHGAP5 were set to 39308770; 36178483 Phenotypes for gene: ARHGAP5 were set to Kallmann syndrome MONDO:0018800 |
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