CNTRL/FGFR1 Fusion Gene

A fusion gene that results from a chromosomal translocation t(8;9)(p12;q33) which fuses exon 15 of the CNTRL gene with exon 8 of the FGFR1 gene. This translocation is associated with 8p11 myeloproliferative syndrome. (NCI Thesaurus)

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CNTRL wt Allele

Human CNTRL wild-type allele is located in the vicinity of 9q33.2 and is approximately 103 kb in length. This allele, which encodes…

CNTRL Gene

This gene plays a role in cell cycle progression.

CNTO 328

A chimeric (made from human and mouse proteins) monoclonal antibody being studied in the treatment of advanced kidney cancer and other types…

CNTNAP2 wt Allele

Human CNTNAP2 wild-type allele is located within 7q35-q36 and is approximately 2305 kb in length. This allele, which encodes contactin associated protein-like…

CNTNAP2 Gene

This gene may be involved in axonal structure.

CNTNAP1 wt Allele

Human CNTNAP1 wild-type allele is located within 17q21 and is approximately 17 kb in length. This allele, which encodes contactin-associated protein 1,…