SPZ1 Polyclonal Antibody, 100ul Mechanical Pipette Mutations in this gene can

Mutations in this gene can also cause autosomal dominant deafness 6 (DFNA6)

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It is a member of the C-C subfamily of chemokines which are characterized by having two adjacent cysteine residues

Genetic variation in this gene influences susceptibility to occlusive vascular disease

Mutations in this gene cause distal hereditary motor neuronopathy type VIIB (HMN7B) which is also known as distal spinal and bulbar muscular atrophy (dSBMA)

SPZ1 Polyclonal Antibody, 100ul Mechanical Pipette Mutations in this gene canSPZ1 (spermatogenic leucine zipper 1) encodes a bHLH zip transcription factor which functions in the mitogen activate protein kinase (MAPK) signaling pathway. Because of its role in the upregulation of cell proliferation and tumorigenesis, SPZ1 may serve as a target for Ras induced tumor treatments.