CSF3R wt Allele

Human CSF3R wild-type allele is located within 1p35-p34.3 and is approximately 17 kb in length. This allele, which encodes granulocyte colony-stimulating factor receptor protein, plays a role in the production, differentiation, and function of granulocytes. Mutations in this gene generate variant alleles that are a cause of Kostmann syndrome, or severe congenital neutropenia. (NCI Thesaurus)

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CSF3R Gene

This gene plays an inhibitory role in cell survival and proliferation.

CSF3 wt Allele

Human CSF3 wild-type allele is located within 17q11.2-q12 and is approximately 2 kb in length. This allele, which encodes granulocyte colony-stimulating factor…

CSF3 Gene

The gene is involved in the regulation of the progenitor cells for granulocytes.

CSF2RB wt Allele

Human CSF2RB wild-type allele is located in the vicinity of 22q13.1 and is approximately 17 kb in length. This allele, which encodes…

CSF2RB Gene

This gene plays a role in receptor-mediated signal transduction.

CSF2RA wt Allele

Human CSF2RA wild-type allele is located in the vicinity of Yp22.33 and is approximately 41 kb in length. This allele, which encodes…