Annotation inferences using phylogenetic trees

Architecture of the human interactome defines protein communities and disease networks.

Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility.

Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.

In situ structure of the mouse sperm central apparatus reveals mechanistic insights into asthenozoospermia.

Mutations in CFAP47, a previously reported MMAF causative gene, also contribute to the respiratory defects in patients with PCD.

A novel mutation in CFAP47 causes male infertility due to multiple morphological abnormalities of the sperm flagella.

WDR87 interacts with CFAP47 protein in the middle piece of spermatozoa flagella to participate in sperm tail assembly.

CFAP47 is Implicated in X-Linked Polycystic Kidney Disease.