Griscelli Syndrome Type 2

A rare, autosomal recessive genetic syndrome caused by mutations in the RAB27A gene. It is characterized by hypopigmentation of the skin, hair and eyes, recurrent infections, neutropenia, and immune system abnormalities. Patients are prone to develop hemophagocytic lymphohistiocytosis. (NCI Thesaurus)

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Grip

The ability to hold or grasp.

GRIN2B wt Allele

Human GRIN2B wild-type allele is located in the vicinity of 12p12 and is approximately 419 kb in length. This allele, which encodes…

GRIN2B Gene

This gene plays a role in both neurotransmitter binding and ion transport.

GRIN2A wt Allele

Human GRIN2A wild-type allele is located in the vicinity of 16p13.2 and is approximately 429 kb in length. This allele, which encodes…

GRIN2A Gene

This gene is involved in the regulation of ion transport.

Grimontia hollisae

A species of Gram negative, rod shaped bacteria assigned to the phylum Proteobacteria. This species is motile by a single polar flagellum,…