| Health / Medical Topics |
B9D2 wt Allele
Human B9D2 wild-type allele is located in the vicinity of 19q13.2 and is approximately 10 kb in length. This allele, which encodes B9 domain-containing protein 2, is involved in ciliogenesis. Mutation of the gene is associated with Meckel syndrome 10. (NCI Thesaurus)
YOU MAY ALSO LIKE
This gene plays a role in cilia formation.
B9 domain-containing protein 2 (175 aa, ~19 kDa) is encoded by the human B9D2 gene. This protein plays a role in the…
A recombinant form of the monoclonal IgM antibody M12 isolated from a Waldenstrom macroglobulinaemia patient (rHIgM12) with potential immunomodulating activity. B7-DC cross-linking…
A protein found on the surface of some immune system cells, including B cells and monocytes. Cells with B7-1 on their surface…
An allogenic whole tumor cell vaccine with potential antineoplastic activity. B7 transfected melanoma cell vaccine consists of melanoma cells that have…
Derived from a cross between a C57BL/6 female and a C3H male, this hybrid strain is commonly used in the production of…
