MRGX4 Polyclonal Antibody, 100ul Site-directed Mutagenesis disease:A chromosomal aberration involving TAL1

disease:A chromosomal aberration involving TAL1 may be a cause of some T-cell acute lymphoblastic leukemias (T-ALL)

The protein is thought to be involved in clathrin-mediated endocytosis

Alternatively spliced transcript variants encoding the different isoforms have been identified

SLC39A1 encodes a member of the zinc-iron permease family

MRGX4 Polyclonal Antibody, 100ul Site-directed Mutagenesis disease:A chromosomal aberration involving TAL1Orphan receptor. Probably involved in the function of nociceptive neurons. May regulate nociceptor function and or development, including the sensation or modulation of pain. Potently activated by enkephalins.