Cat Eye Syndrome

Overview of Cat Eye Syndrome

Most recent studies have shown that Cat Eye Syndrome shares some biological mechanisms with aneuploidy, anus-imperforate, atresia, chromosomal-translocation, chromosome-markers, congenital-abnormality, congenital-coloboma-of-iris, congenital-heart-defects, congenital-ocular-coloboma-(disorder), craniofacial-abnormalities, cytogenetic-abnormality, digeorge-syndrome, embryonic-mosaic, extra-unidentified-structurally-abnormal-chromosome-(disorder), eye-abnormalities, orbital-separation-excessive, partial-trisomy, tetrasomy, trisomy.

Among the many pathways, these few ones have gauged particular interests from scientists studying Cat Eye Syndrome, and have been seen in publications frequently: Cell Proliferation, Chromatin Remodeling, Development Of Secondary Sexual Characteristics, Dna Amplification, Interphase, Localization, Metaphase, Organ Development, Pathogenesis, Reverse Transcription

Quite a number of genes have been found to play important roles in Cat Eye Syndrome, such as A4GALT, ADA, ATP6V1E1, B3GALNT1, BID, CAT, CECR2, CRAT, GLYAT, INVS, LMLN, NUCKS1, PIK3CA, PMEL, PRF1, PRM1, RPLP1, TBX1. 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.

Cat Eye Syndrome Related Genes

click to see detail information for each gene

Pathways Related to Cat Eye Syndrome

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

Related Diseases