|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any functional anomaly of a CD4-positive, CXCR5-positive, CCR7-negative alpha-beta T cell located in follicles of secondary lymph nodes that expresses high levels of BCL-6, ICOS and PD1 and stimulate follicular B cells to undergo class-switching and antibody production (Mammalian Phenotype Ontology, MP_0010189)|
|Downloads & Tools|
2 gene mutations causing the abnormal t follicular helper cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.