HKR1 Polyclonal Antibody, 20ul Protein Expression Several transcript variants encoding different

Several transcript variants encoding different isoforms have been found for ENTPD1

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Defects in this gene are a cause of xeroderma pigmentosum complementation group F (XP-F)

but is actually an apelin receptor that inhibits adenylate cyclase activity and plays a counter-regulatory role against the pressure action of angiotensin II by exerting hypertensive effect

Homopolymers of desmin form a stable intracytoplasmic filamentous network connecting myofibrils to each other and to the plasma membrane

HKR1 Polyclonal Antibody, 20ul Protein Expression Several transcript variants encoding differentHKR1 is a Protein Coding gene. Krueppel related zinc finger protein 1 may be involved in transcriptional regulation. Among its related pathways are Gene Expression. Gene Ontology (GO) annotations related to this gene include nucleic acid binding. An important paralog of this gene is ZNF169.