p57 Polyclonal Antibody, 100ul[BT-AP06843] Mechanical Pipette Mutations in this gene cause

Mutations in this gene cause syndromic microphthalmia 5 (MCOPS5) and combined pituitary hormone deficiency 6 (CPHD6)

The congenital disorder of glycosylation type Ij is caused by mutation in the gene encoding this enzyme

Multiple alternatively spliced variants encoding different isoforms have been described

AURKB (aurora kinase B) encodes a member of the aurora kinase subfamily of serine/threonine kinases

This gene is a member of an anti-proliferative gene family that regulates cell growth and differentiation

p57 Polyclonal Antibody, 100ul[BT-AP06843] Mechanical Pipette Mutations in this gene causeCDKN1C is imprinted, with preferential expression of the maternal allele. The cyclin dependent kinase inhibitor 1C is a tight binding, strong inhibitor of several G1 cyclin Cdk complexes and a negative regulator of cell proliferation. Mutations in this gene are implicated in sporadic cancers and Beckwith Wiedemann syndorome, suggesting that CDKN1C is a tumor suppressor candidate. Three transcript variants encoding two different isoforms have been