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Guanylate cyclase 1 soluble subunit beta 2 (GUCY1B2) is annotated as a *pseudogene* in humans and therefore does not encode a functional protein product. While predictions exist about possible guanylate cyclase activity and involvement in cGMP-mediated signaling, there is no evidence that GUCY1B2 expresses an active protein or participates in established human physiological pathways. GUCY1B2 is structurally related to the family of soluble guanylate cyclase enzymes, which are important mediators of nitric oxide signaling via cGMP production, but, unlike other functional guanylate cyclase subunits such as GUCY1B1 or GUCY1A1, GUCY1B2 lacks demonstrated enzymatic or receptor activity in humans[6][7]. Therefore, it is not considered a therapeutic target.
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