Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3416
Gene name Gene Name - the full gene name approved by the HGNC.
Insulin degrading enzyme
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
IDE
Synonyms (NCBI Gene) Gene synonyms aliases
INSULYSIN
Chromosome Chromosome number
10
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10q23.33
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a zinc metallopeptidase that degrades intracellular insulin, and thereby terminates insulins activity, as well as participating in intercellular peptide signalling by degrading diverse peptides such as glucagon, amylin, bradykinin, and k
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT025720 hsa-miR-7-5p Microarray 17612493
MIRT025720 hsa-miR-7-5p Microarray 19073608
MIRT675952 hsa-miR-3529-3p HITS-CLIP 23824327
MIRT623645 hsa-miR-6890-3p HITS-CLIP 23824327
MIRT623644 hsa-miR-6736-3p HITS-CLIP 23824327
Transcription factors
Transcription factor Regulation Reference
NRF1 Activation 22870279
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0001540 Function Amyloid-beta binding IEA
GO:0001618 Function Virus receptor activity IEA
GO:0003824 Function Catalytic activity IEA
GO:0004175 Function Endopeptidase activity IDA 20364150
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
146680 5381 ENSG00000119912
Protein
UniProt ID P14735
Protein name Insulin-degrading enzyme (EC 3.4.24.56) (Abeta-degrading protease) (Insulin protease) (Insulinase) (Insulysin)
Protein function Plays a role in the cellular breakdown of insulin, APP peptides, IAPP peptides, natriuretic peptides, glucagon, bradykinin, kallidin, and other peptides, and thereby plays a role in intercellular peptide signaling (PubMed:10684867, PubMed:170512
PDB 2G47 , 2G48 , 2G49 , 2G54 , 2G56 , 2JBU , 2JG4 , 2WBY , 2WC0 , 2WK3 , 2YPU , 3CWW , 3E4A , 3E4Z , 3E50 , 3H44 , 3HGZ , 3N56 , 3N57 , 3OFI , 3QZ2 , 4DTT , 4DWK , 4GS8 , 4GSC , 4GSF , 4IFH , 4IOF , 4LTE , 4M1C , 4NXO , 4PES , 4PF7 , 4PF9 , 4PFC , 4QIA , 4RAL , 4RE9 , 5CJO , 5UOE , 5WOB , 6B3Q , 6B70 , 6B7Y , 6B7Z , 6BF6 , 6BF7 , 6BF8 , 6BF9 , 6BFC , 6BYZ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00675 Peptidase_M16 74 212 Insulinase (Peptidase family M16) Family
PF05193 Peptidase_M16_C 237 417 Peptidase M16 inactive domain Domain
PF16187 Peptidase_M16_M 422 703 Middle or third domain of peptidase_M16 Family
PF05193 Peptidase_M16_C 706 889 Peptidase M16 inactive domain Domain
Tissue specificity TISSUE SPECIFICITY: Detected in brain and in cerebrospinal fluid (at protein level). {ECO:0000269|PubMed:9830016}.
Sequence
MRYRLAWLLHPALPSTFRSVLGARLPPPERLCGFQKKTYSKMNNPAIKRIGNHITKSPED
KREYRGLELANGIKVLLISDPTTDKSSAALDVHIGSLSDPPNIAGLSHFCEHMLFLGTKK
YPKENEYSQFLSEHAGSSNAFTSGEHTNYYFDVSHEHLEGALDRFAQFFLCPLFDESCKD
REVNAVDSEHEKNVMNDAWRLFQLEKATGNPK
HPFSKFGTGNKYTLETRPNQEGIDVRQE
LLKFHSAYYSSNLMAVCVLGRESLDDLTNLVVKLFSEVENKNVPLPEFPEHPFQEEHLKQ
LYKIVPIKDIRNLYVTFPIPDLQKYYKSNPGHYLGHLIGHEGPGSLLSELKSKGWVNTLV
GGQKEGARGFMFFIINVDLTEEGLLHVEDIILHMFQYIQKLRAEGPQEWVFQECKDL
NAV
AFRFKDKERPRGYTSKIAGILHYYPLEEVLTAEYLLEEFRPDLIEMVLDKLRPENVRVAI
VSKSFEGKTDRTEEWYGTQYKQEAIPDEVIKKWQNADLNGKFKLPTKNEFIPTNFEILPL
EKEATPYPALIKDTAMSKLWFKQDDKFFLPKACLNFEFFSPFAYVDPLHCNMAYLYLELL
KDSLNEYAYAAELAGLSYDLQNTIYGMYLSVKGYNDKQPILLKKIIEKMATFEIDEKRFE
IIKEAYMRSLNNFRAEQPHQHAMYYLRLLMTEVAWTKDELKEA
LDDVTLPRLKAFIPQLL
SRLHIEALLHGNITKQAALGIMQMVEDTLIEHAHTKPLLPSQLVRYREVQLPDRGWFVYQ
QRNEVHNNCGIEIYYQTDMQSTSENMFLELFCQIISEPCFNTLRTKEQLGYIVFSGPRRA
NGIQGLRFIIQSEKPPHYLESRVEAFLITMEKSIEDMTEEAFQKHIQAL
AIRRLDKPKKL
SAECAKYWGEIISQQYNFDRDNTEVAYLKTLTKEDIIKFYKEMLAVDAPRRHKVSVHVLA
REMDSCPVVGEFPCQNDINLSQAPALPQPEVIQNMTEFKRGLPLFPLVKPHINFMAAKL
Sequence length 1019
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Virion - Herpesvirus
Alzheimer disease
  Ub-specific processing proteases
Peroxisomal protein import
<
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
AA amyloidosis Associate 17653279, 18317569, 33865867
Alzheimer Disease Inhibit 12507914
Alzheimer Disease Associate 17244626, 17496198, 17613531, 18813847, 19019493, 19896952, 20098734, 20142614, 20663017, 20724036, 21185309, 21731745, 21992747, 22107728, 23036584
View all (12 more)
Amyloid angiopathy Associate 19019493
Amyotrophic Lateral Sclerosis Associate 27244217
Brain Infarction Associate 23076436
Breast Neoplasms Associate 18813847
Carcinogenesis Associate 25945652
Central Nervous System Neoplasms Stimulate 23188819
Cognition Disorders Associate 24660790, 28050343