ICAM5 Polyclonal Antibody, 50ul Lentiviral Packaging MIM 600432) and a C-terminal

MIM 600432) and a C-terminal C1q signature domain (see MIM 120550) that mediates trimeric assembly of atypical collagen complexes

Certain mutations in this gene have been associated with idiopathic generalized epilepsy (IGE)

This gene encodes a member of the RecQ subfamily and the DEAH (Asp-Glu-Ala-His) subfamily of DNA and RNA helicases

disease:A chromosomal aberration involving BCL6 may be a cause of a form of B-cell leukemia

Mutations in CEP41 have been associated with Joubert Syndrome 15

ICAM5 Polyclonal Antibody, 50ul Lentiviral Packaging MIM 600432) and a C-terminalThe protein encoded by this gene is a member of the intercellular adhesion molecule (ICAM) family. All ICAM proteins are type I transmembrane glycoproteins contain 2 9 immunoglobulin like C2 type domains and bind to the leukocyte adhesion LFA 1 protein. This protein is expressed on the surface of telencephalic neurons and displays two types of adhesion activity homophilic binding between neurons and heterophilic binding between neurons and leukocytes.