Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
1889
Gene name Gene Name - the full gene name approved by the HGNC.
Endothelin converting enzyme 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ECE1
Synonyms (NCBI Gene) Gene synonyms aliases
ECE
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p36.12
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is involved in proteolytic processing of endothelin precursors to biologically active peptides. Mutations in this gene are associated with Hirschsprung disease, cardiac defects and autonomic dysfunction. Alternatively spli
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs3026906 G>A Pathogenic Coding sequence variant, missense variant
rs200894751 G>A Likely-pathogenic Missense variant, coding sequence variant
rs765763704 A>C Likely-pathogenic Coding sequence variant, missense variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT016794 hsa-miR-335-5p Microarray 18185580
MIRT022165 hsa-miR-124-3p Microarray 18668037
MIRT042082 hsa-miR-484 CLASH 23622248
MIRT042082 hsa-miR-484 CLASH 23622248
MIRT444784 hsa-miR-4422 PAR-CLIP 22100165
Transcription factors
Transcription factor Regulation Reference
ETS1 Activation 11723240;9595399
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001921 Process Positive regulation of receptor recycling IMP 18039931
GO:0003100 Process Regulation of systemic arterial blood pressure by endothelin IC 7805846
GO:0004175 Function Endopeptidase activity IDA 7805846, 18039931
GO:0004222 Function Metalloendopeptidase activity IBA 21873635
GO:0004222 Function Metalloendopeptidase activity ISS 8062389
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600423 3146 ENSG00000117298
Protein
UniProt ID P42892
Protein name Endothelin-converting enzyme 1 (ECE-1) (EC 3.4.24.71)
Protein function Converts big endothelin-1 to endothelin-1.
PDB 3DWB
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05649 Peptidase_M13_N 121 507 Peptidase family M13 Family
PF01431 Peptidase_M13 566 769 Peptidase family M13 Family
Tissue specificity TISSUE SPECIFICITY: All isoforms are expressed in umbilical vein endothelial cells, polynuclear neutrophils, fibroblasts, atrium cardiomyocytes and ventricles. Isoforms A, B and C are also expressed in placenta, lung, heart, adrenal gland and phaeochromoc
Sequence
Sequence length 770
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Peptide ligand-binding receptors
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Atrial septal defect Atrial Septal Defects rs137852951, rs137852953, rs137852955, rs267607106, rs104893900, rs104893901, rs104893903, rs606231358, rs606231359, rs137852683, rs606231360, rs104893907, rs104894073, rs1585703301, rs104894074
View all (25 more)
Congenital heart defects Congenital Heart Defects rs267607101, rs121434422, rs387906498, rs397509416, rs587777371, rs587777372, rs587777374, rs367537998, rs797044882, rs886041730, rs768027510, rs1064793873, rs1555447012, rs1554263268, rs1554263321
View all (13 more)
9915973, 9449665
Diabetes mellitus Diabetes Mellitus, Non-Insulin-Dependent rs587776515, rs61730328, rs606231121, rs606231122, rs79020217, rs77625743, rs78378398, rs606231123, rs1362648752, rs104893649, rs80356624, rs80356616, rs80356625, rs80356611, rs104894237
View all (293 more)
16387788
Dysautonomia Dysautonomia rs111033171, rs137853022, rs28939712, rs754348901, rs749052963, rs1057517169, rs1057516865, rs763445509, rs767527819, rs781333644, rs1239081703, rs1554696574, rs539544212, rs1201626345, rs774890086
View all (27 more)
Unknown
Disease term Disease name Evidence References Source
Neuroticism Neuroticism GWAS
Breast Cancer Breast Cancer Importantly, breast cancer patients bearing PRC2 LOF mutations displayed significantly worse prognosis compared with PRC2 wild-type patients GWAS, CBGDA
Prostate cancer Prostate cancer Together, these results show that PRRX2 is an oncogene and might play a role in the aggressiveness of PC within the DNPC population. GWAS, CBGDA
Oligodendroglioma Oligodendroglioma GWAS
Associations from Text Mining
Disease Name Relationship Type References
Acute Kidney Injury Associate 31777301
Alzheimer Disease Associate 18334739, 20037208, 20663017, 27249223
Atherosclerosis Associate 31777301, 9786493
Candidiasis Vulvovaginal Stimulate 29259175
Carcinoma Hepatocellular Associate 30168613, 38062093
Cardiovascular Abnormalities Associate 24454898
Cardiovascular Diseases Associate 9607404
Coronary Artery Disease Associate 18334739, 9786493
Dementia Associate 20663017
Ductus Arteriosus Patent Associate 33837257