DISEASES

Disease-gene associations mined from literature

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Human genes for hereditary spastic paraplegia 61

Hereditary spastic paraplegia 61 [DOID:0110812]

A hereditary spastic paraplegia that has_material_basis_in mutation in the ARL6IP1 gene on chromosome 16p12.

Synonyms:  hereditary spastic paraplegia 61,  DOID:0110812,  familial spastic paraplegia 61,  SPG61,  autosomal recessive spastic paraplegia 61 ...

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.

Currently maintained by Qingyao Huang at Swiss Institute of Bioinformatics, University of Zurich. Licensed under CC BY 4.0.