SNAT2 Polyclonal Antibody, 20ul Dry Bath Mutations in the gene cause

Mutations in the gene cause X-linked neurological syndromes known as CRASH (corpus callosum hypoplasia

Multiple transcript variants for this gene exist

unlike beta 1 chain

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The protein encoded by CACNG1 (calcium voltage-gated channel auxiliary subunit gamma 1) represents one of these subunits

SNAT2 Polyclonal Antibody, 20ul Dry Bath Mutations in the gene causeSLC38A2 (Solute Carrier Family 38 Member 2) is a Protein Coding gene. Among its related pathways are Circadian entrainment and Protein digestion and absorption. GO annotations related to this gene include symporter activity and amino acid transmembrane transporter activity. An important paralog of this gene is SLC38A1.