Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
290
Gene name Gene Name - the full gene name approved by the HGNC.
Alanyl aminopeptidase, membrane
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ANPEP
Synonyms (NCBI Gene) Gene synonyms aliases
AP-M, AP-N, APN, CD13, GP150, LAP1, P150, PEPN, hAPN
Chromosome Chromosome number
15
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
15q26.1
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 factor Regulation Reference
ETS1 Activation 14507917
ETS2 Activation 14507917
MYB Unknown 10477683
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
151530 500 ENSG00000166825
Protein
UniProt ID 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
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Diabetes Type 2 diabetes N/A N/A GWAS
Associations from Text Mining Disease 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