Activity
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| Amyotrophic lateral sclerosis/motor neuron disease v1.69 | ANXA11 | David Collier reviewed gene: ANXA11: Rating: AMBER; Mode of pathogenicity: None; Publications: PMID: 28469040, PMID: 30337194, PubMed: 34048612; Phenotypes: ALS, amyotrophic lateral sclerosis, ALS 23, motor neuron disease, Inclusion body myopathy and brain white matter abnormalities (IBMWMA, MULTISYSTEM PROTEINOPATHY 6, MSP6); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Amyotrophic lateral sclerosis/motor neuron disease v1.29 | ANXA11 |
Agnese Zarina gene: ANXA11 was added gene: ANXA11 was added to Amyotrophic lateral sclerosis/motor neuron disease. Sources: Literature Mode of inheritance for gene: ANXA11 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: ANXA11 were set to DOI: 10.1126/scitranslmed.aad9157 Phenotypes for gene: ANXA11 were set to Amyotrophic lateral sclerosis 23 Penetrance for gene: ANXA11 were set to Complete Review for gene: ANXA11 was set to AMBER Added comment: gene is added to "Neurodegenerative disorders - adult onset" panel, but one of the phenotype is also ALS Sources: Literature |
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