DISEASES

Disease-gene associations mined from literature

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Literature associating FAM101B and frontometaphyseal dysplasia

FAM101B [ENSP00000331915]

Family with sequence similarity 101, member B; Involved in the regulation of the perinuclear actin network and nuclear shape through interaction with filamins. Plays an essential role in the formation of cartilaginous skeletal elements.

Synonyms:  FAM101B,  FAM101Bp,  hFAM101B,  Q8N5W9,  RFLNB ...

Linkouts:  STRING  Pharos  UniProt

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.