LPIN2 Polyclonal Antibody, 100ul Supplements Deletions that remove the entire

Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities

Multiple transcript variants encoding distinct isoforms have been identified for RGS12

Diseases associated with CEBPB includeShort-Rib Thoracic Dysplasia 1 With Or Without PolydactylyandShort-Rib Thoracic Dysplasia 2 With Or Without Polydactyly

This gene encodes an enzyme which catalyzes the sulfation of chondroitin

LPIN2 Polyclonal Antibody, 100ul Supplements Deletions that remove the entireMouse studies suggest that this gene functions during normal adipose tissue development and may play a role in human triglyceride metabolism. This gene represents a candidate gene for human lipodystrophy, characterized by loss of body fat, fatty liver, hypertriglyceridemia, and insulin resistance.