DISEASES

Disease-gene associations mined from literature

Literature associating SPG21 and Charcot-Marie-Tooth disease axonal type 2T

SPG21 [ENSP00000204566]

Spastic paraplegia 21 autosomal recessive Mast syndrome protein; May play a role as a negative regulatory factor in CD4- dependent T-cell activation.

Synonyms:  SPG21,  SPG21p,  hSPG21,  A0A024R5Y1,  H0YKB0 ...

Linkouts:  STRING  Pharos  UniProt  OMIM