Disease Info Card

Congenital Failure Of Fusion

Information about Congenital Failure Of Fusion: 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 Congenital Failure Of Fusion

Most recent studies have shown that Congenital Failure Of Fusion shares some biological mechanisms with cleft-lip, cleft-palate, cleft-palate-with-cleft-lip, congenital-abnormality, diastematomyelia, hydrocephalus, lipoma, meningocele, meningomyelocele, neoplasms, neurogenic-urinary-bladder, pain, scoliosis-unspecified, spina-bifida, spina-bifida-occulta, spinal-cord-diseases, spinal-cord-neoplasms, spinal-neoplasms, syringomyelia, tethered-spinal-cord-syndrome.

Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Failure Of Fusion, and have been seen in publications frequently: Brain Development, Cell Migration, Defecation, Dehiscence, Fertilization, Gastrulation, Innervation, Localization, Micturition, Muscle Atrophy, Neural Tube Closure, Ossification, Palate Development, Pathogenesis, Pigmentation, Reflex, Segmentation, Transposition, Tube Closure, Wound Healing

Quite a number of genes have been found to play important roles in Congenital Failure Of Fusion, such as C2, C6, CERS2, CIC, CSF2, HNRNPC, LAMC2, LPA, PES1, PPFIBP1, RANGAP1, RPL3, RPL4, RPL5, SEPSECS, SS18L1, ZACN. 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.

Congenital Failure Of Fusion Related Genes

click to see detail information for each gene

C2 C6 CERS2
CIC CSF2 HNRNPC
LAMC2 LPA PES1
PPFIBP1 RANGAP1 RPL3
RPL4 RPL5 SEPSECS
SS18L1 ZACN