Mar 30, 2025 · ATP6AP2 (ATPase H+ Transporting Accessory Protein 2) is a Protein Coding gene. Diseases associated with ATP6AP2 include Parkinsonism With Spasticity, X-Linked and Congenital Disorder Of Glycosylation, Type Iir .

Mar 30, 2025 · ATP6AP1 (ATPase H+ Transporting Accessory Protein 1) is a Protein Coding gene. Diseases associated with ATP6AP1 include Immunodeficiency 47 and Congenital Disorder Of Glycosylation, Type In.Among its related pathways are Signaling by Rho GTPases and Insulin receptor recycling.Gene Ontology (GO) annotations related to this gene include transporter activity and proton-transporting ATPase ...

Showing 25 of 4,382 results for ATP6AP2 Search Time: 0 ms in Aliases & Descriptions Drugs & Compounds Disorders Text-Mined Disorders Domains Expression in Human Tissues Function Genomics Localization Orthologs Paralogs Pathways Phenotypes Proteins Publications Summaries Transcripts Variants in category Protein Coding RNA Gene Functional Element ...

Mar 30, 2025 · Interacts with ATP6AP2 (PubMed:29127204). Three dimensional structures from AlphaFold (predicted) for VMA21 Gene Click for interactive 3D structure and sequence

Mar 30, 2025 · By bringing the v-ATPase accessory protein ATP6AP2 and the v-ATPase subunit ATP6V0D1 together, allows v-ATPase complex formation and activation (PubMed:30374053). TMEM9-controlled vesicular acidification induces hyperactivation of Wnt/beta-catenin signaling, involved in development, tissue homeostasis and tissue regeneration, through lysosomal ...

Mar 30, 2025 · Interaction with ATP6AP2 results in a 5-fold increased efficiency in angiotensinogen processing. RENI_HUMAN,P00797 Molecular function for REN Gene according to GENATLAS

Mar 30, 2025 · The proton translocation complex V0 consists of the proton transport subunit a, a ring of proteolipid subunits c9c'', rotary subunit d, subunits e and f, and the accessory subunits ATP6AP1/Ac45 and ATP6AP2/PRR (PubMed:33065002).

Complete information for lnc-ATP6AP2-11 gene (RNA Gene), , including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

Mar 30, 2025 · ATP6V0A2 (ATPase H+ Transporting V0 Subunit A2) is a Protein Coding gene. Diseases associated with ATP6V0A2 include Wrinkly Skin Syndrome and Cutis Laxa, Autosomal Recessive, Type Iia.Among its related pathways are Insulin receptor recycling and Innate Immune System.Gene Ontology (GO) annotations related to this gene include ATPase binding and proton-transporting ATPase activity, rotational ...

PathCards integrated disease information for Peptide hormone metabolism