Gene Gene information from NCBI Gene database.
Entrez ID 290
Gene name Alanyl aminopeptidase, membrane
Gene symbol ANPEP
Synonyms (NCBI Gene)
AP-MAP-NAPNCD13GP150LAP1P150PEPNhAPN
Chromosome 15
Chromosome location 15q26.1
Summary Aminopeptidase N is located in the small-intestinal and renal microvillar membrane, and also in other plasma membranes. In the small intestine aminopeptidase N plays a role in the final digestion of peptides generated from hydrolysis of proteins by gastri
miRNA miRNA information provided by mirtarbase database.
143
miRTarBase ID miRNA Experiments Reference
MIRT005211 hsa-miR-30a-5p pSILAC 18668040
MIRT001389 hsa-miR-1-3p pSILAC 18668040
MIRT020955 hsa-miR-155-5p Proteomics 18668040
MIRT022990 hsa-miR-124-3p Proteomics;Microarray 18668037
MIRT001389 hsa-miR-1-3p Proteomics;Other 18668040
Transcription factors Transcription factors information provided by TRRUST V2 database.
3
Transcription factor Regulation Reference
ETS1 Activation 14507917
ETS2 Activation 14507917
MYB Unknown 10477683
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
33
GO ID Ontology Definition Evidence Reference
GO:0001525 Process Angiogenesis IEA
GO:0001618 Function Virus receptor activity IEA
GO:0002003 Process Angiotensin maturation IBA
GO:0002003 Process Angiotensin maturation IEA
GO:0004177 Function Aminopeptidase activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
151530 500 ENSG00000166825
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P15144
Protein name Aminopeptidase N (AP-N) (hAPN) (EC 3.4.11.2) (Alanyl aminopeptidase) (Aminopeptidase M) (AP-M) (Microsomal aminopeptidase) (Myeloid plasma membrane glycoprotein CD13) (gp150) (CD antigen CD13)
Protein function Broad specificity aminopeptidase which plays a role in the final digestion of peptides generated from hydrolysis of proteins by gastric and pancreatic proteases. Also involved in the processing of various peptides including peptide hormones, suc
PDB 4FYQ , 4FYR , 4FYS , 4FYT , 5LHD , 6ATK , 6U7E , 6U7F , 6U7G , 6XWD , 7AEW , 7VPQ , 8WDE
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF17900 Peptidase_M1_N 81 279 Domain
PF01433 Peptidase_M1 316 543 Peptidase family M1 domain Domain
PF11838 ERAP1_C 619 946 ERAP1-like C-terminal domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in epithelial cells of the kidney, intestine, and respiratory tract; granulocytes, monocytes, fibroblasts, endothelial cells, cerebral pericytes at the blood-brain barrier, synaptic membranes of cells in the CNS. Also express
Sequence
MAKGFYISKSLGILGILLGVAAVCTIIALSVVYSQEKNKNANSSPVASTTPSASATTNPA
SATTLDQSKAWNRYRLPNTLKPDSYRVTLRPYLTPNDRGLYVFKGSSTVRFTCKEATDVI
IIHSKKLNYTLSQGHRVVLRGVGGSQPPDIDKTELVEPTEYLVVHLKGSLVKDSQYEMDS
EFEGELADDLAGFYRSEYMEGNVRKVVATTQMQAADARKSFPCFDEPAMKAEFNITLIHP
KDLTALSNMLPKGPSTPLPEDPNWNVTEFHTTPKMSTYL
LAFIVSEFDYVEKQASNGVLI
RIWARPSAIAAGHGDYALNVTGPILNFFAGHYDTPYPLPKSDQIGLPDFNAGAMENWGLV
TYRENSLLFDPLSSSSSNKERVVTVIAHELAHQWFGNLVTIEWWNDLWLNEGFASYVEYL
GADYAEPTWNLKDLMVLNDVYRVMAVDALASSHPLSTPASEINTPAQISELFDAISYSKG
ASVLRMLSSFLSEDVFKQGLASYLHTFAYQNTIYLNLWDHLQEAVNNRSIQLPTTVRDIM
NRW
TLQMGFPVITVDTSTGTLSQEHFLLDPDSNVTRPSEFNYVWIVPITSIRDGRQQQDY
WLIDVRAQNDLFSTSGNEWVLLNLNVTGYYRVNYDEENWRKIQTQLQRDHSAIPVINRAQ
IINDAFNLASAHKVPVTLALNNTLFLIEERQYMPWEAALSSLSYFKLMFDRSEVYGPMKN
YLKKQVTPLFIHFRNNTNNWREIPENLMDQYSEVNAISTACSNGVPECEEMVSGLFKQWM
ENPNNNPIHPNLRSTVYCNAIAQGGEEEWDFAWEQFRNATLVNEADKLRAALACSKELWI
LNRYLSYTLNPDLIRKQDATSTIISITNNVIGQGLVWDFVQSNWKKLFNDYGGGSFSFSN
LIQAVTRRFSTEYELQQLEQFKKDNEETGFGSGTRALEQALEKTKA
NIKWVKENKEVVLQ
WFTENSK
Sequence length 967
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Glutathione metabolism
Metabolic pathways
Renin-angiotensin system
Hematopoietic cell lineage
  Neutrophil degranulation
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
6
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
ANPEP-related disorder Likely benign rs143245843, rs144282919, rs146926671 RCV003919476
RCV003930733
RCV003940613
Cholangiocarcinoma Benign rs17240268 RCV005920446
Colorectal cancer Benign rs17240268 RCV005920445
Ovarian serous cystadenocarcinoma Likely benign rs144282919 RCV005904801
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Acne Vulgaris Associate 16778789
Adenocarcinoma Associate 25879366
Adenomatous Polyposis Coli Inhibit 36748835
Anemia Refractory with Excess of Blasts Stimulate 20662087
Arthritis Associate 7829125
Arthritis Rheumatoid Associate 12355480, 25219368, 8099341
Asthma Associate 34198852
Ataxia Telangiectasia Associate 23687089
Atypical Squamous Cells of the Cervix Associate 35938646
Autoimmune Diseases Associate 16778789