Disease Info Card

Pili Torti

Information about Pili Torti: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.

Overview of Pili Torti

Most recent studies have shown that Pili Torti shares some biological mechanisms with atrophy, bamboo-hair, brain-diseases-metabolic, cleft-lip, complete-hearing-loss, dermatologic-disorders, dysplasia, ectodermal-dysplasia, exfoliative-dermatitis, hair-diseases, hypotrichosis, ichthyoses, keratosis, menkes-kinky-hair-syndrome, monilethrix, sensorineural-hearing-loss-(disorder), skin-neoplasms.

Among the many pathways, these few ones have gauged particular interests from scientists studying Pili Torti, and have been seen in publications frequently: Anagen, Cell Proliferation, Excretion, Lactation, Myelination, Pathogenesis, Pigmentation, Primary Growth, Secretion, Transport

Quite a number of genes have been found to play important roles in Pili Torti, such as CKAP4, CP, ELN, IGF1, IGFBP5, KRT16, KRT17, MB, USB1, UVRAG. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.

Pili Torti Related Genes

click to see detail information for each gene

CKAP4 CP ELN
IGF1 IGFBP5 KRT16
KRT17 MB USB1
UVRAG

Pathways Related to Pili Torti

This information is being compiled and will come in a future update

Anagen Cell Proliferation Excretion
Lactation Myelination Pathogenesis
Pigmentation Primary Growth Secretion
Transport