Details for: ATP6AP2
Associated with
Other Information
Genular Protein ID: 2179136597
Symbol: RENR_HUMAN
Name: ATPase H(+)-transporting lysosomal accessory protein 2
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 12045255
Title: Pivotal role of the renin/prorenin receptor in angiotensin II production and cellular responses to renin.
PubMed ID: 12045255
DOI: 10.1172/jci14276
PubMed ID: 10931946
Title: Gene expression profiling in the human hypothalamus-pituitary-adrenal axis and full-length cDNA cloning.
PubMed ID: 10931946
PubMed ID: 14702039
Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.
PubMed ID: 14702039
DOI: 10.1038/ng1285
PubMed ID: 16303743
Title: Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries.
PubMed ID: 16303743
PubMed ID: 15772651
PubMed ID: 15489334
Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
PubMed ID: 15489334
DOI: 10.1101/gr.2596504
PubMed ID: 17974005
Title: The full-ORF clone resource of the German cDNA consortium.
PubMed ID: 17974005
PubMed ID: 9556572
Title: Identification and characterization of a novel 9.2-kDa membrane sector-associated protein of vacuolar proton-ATPase from chromaffin granules.
PubMed ID: 9556572
PubMed ID: 15746149
Title: A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor.
PubMed ID: 15746149
DOI: 10.1093/hmg/ddi094
PubMed ID: 21269460
Title: Initial characterization of the human central proteome.
PubMed ID: 21269460
PubMed ID: 23595882
Title: Altered splicing of ATP6AP2 causes X-linked parkinsonism with spasticity (XPDS).
PubMed ID: 23595882
DOI: 10.1093/hmg/ddt180
PubMed ID: 25944712
Title: N-terminome analysis of the human mitochondrial proteome.
PubMed ID: 25944712
PubMed ID: 29127204
Title: Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defects.
PubMed ID: 29127204
DOI: 10.1084/jem.20170453
PubMed ID: 30374053
Title: TMEM9 promotes intestinal tumorigenesis through vacuolar-ATPase-activated Wnt/beta-catenin signalling.
PubMed ID: 30374053
PubMed ID: 30985297
Title: ATP6AP2 variant impairs CNS development and neuronal survival to cause fulminant neurodegeneration.
PubMed ID: 30985297
DOI: 10.1172/jci79990
PubMed ID: 32276428
Title: Interaction between PHB2 and Enterovirus A71 VP1 Induces Autophagy and Affects EV-A71 Infection.
PubMed ID: 32276428
DOI: 10.3390/v12040414
PubMed ID: 21420935
Title: Structural analysis of the intracellular domain of (pro)renin receptor fused to maltose-binding protein.
PubMed ID: 21420935
PubMed ID: 33065002
Title: Structures of a Complete Human V-ATPase Reveal Mechanisms of Its Assembly.
PubMed ID: 33065002
Sequence Information:
- Length: 350
- Mass: 39008
- Checksum: 84084A4ACE9C5DE8
- Sequence:
MAVFVVLLAL VAGVLGNEFS ILKSPGSVVF RNGNWPIPGE RIPDVAALSM GFSVKEDLSW PGLAVGNLFH RPRATVMVMV KGVNKLALPP GSVISYPLEN AVPFSLDSVA NSIHSLFSEE TPVVLQLAPS EERVYMVGKA NSVFEDLSVT LRQLRNRLFQ ENSVLSSLPL NSLSRNNEVD LLFLSELQVL HDISSLLSRH KHLAKDHSPD LYSLELAGLD EIGKRYGEDS EQFRDASKIL VDALQKFADD MYSLYGGNAV VELVTVKSFD TSLIRKTRTI LEAKQAKNPA SPYNLAYKYN FEYSVVFNMV LWIMIALALA VIITSYNIWN MDPGYDSIIY RMTNQKIRMD
Database document:
This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.