Gene Gene information from NCBI Gene database.
Entrez ID 59342
Gene name Serine carboxypeptidase 1
Gene symbol SCPEP1
Synonyms (NCBI Gene)
HSCP1RISC
Chromosome 17
Chromosome location 17q22
miRNA miRNA information provided by mirtarbase database.
26
miRTarBase ID miRNA Experiments Reference
MIRT1330611 hsa-miR-1184 CLIP-seq
MIRT1330612 hsa-miR-1205 CLIP-seq
MIRT1330613 hsa-miR-298 CLIP-seq
MIRT1330614 hsa-miR-3158-5p CLIP-seq
MIRT1330615 hsa-miR-320e CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
15
GO ID Ontology Definition Evidence Reference
GO:0004180 Function Carboxypeptidase activity IEA
GO:0004185 Function Serine-type carboxypeptidase activity IBA
GO:0004185 Function Serine-type carboxypeptidase activity IEA
GO:0004185 Function Serine-type carboxypeptidase activity ISS
GO:0005576 Component Extracellular region IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
619723 29507 ENSG00000121064
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9HB40
Protein name Retinoid-inducible serine carboxypeptidase (EC 3.4.16.-) (Serine carboxypeptidase 1)
Protein function May be involved in vascular wall and kidney homeostasis.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00450 Peptidase_S10 29 451 Serine carboxypeptidase Domain
Sequence
Sequence length 452
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
Cervical cancer Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
COLORECTAL CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GLAUCOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Uterine corpus endometrial carcinoma Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Breast Carcinoma Breast Carcinoma BEFREE 24806942, 25446899
★☆☆☆☆
Found in Text Mining only
Conventional (Clear Cell) Renal Cell Carcinoma Renal Carcinoma BEFREE 25293974
★☆☆☆☆
Found in Text Mining only
Depressive disorder Mental Depression BEFREE 31654919
★☆☆☆☆
Found in Text Mining only
Diabetes Diabetes BEFREE 27334352
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Diabetes Mellitus BEFREE 27334352
★☆☆☆☆
Found in Text Mining only
Hyperglycemia Hyperglycemia BEFREE 30529353
★☆☆☆☆
Found in Text Mining only
Hypertensive disease Hypertension BEFREE 24586188, 27984413
★☆☆☆☆
Found in Text Mining only
Leukemia, Myelocytic, Acute Leukemia BEFREE 10584877
★☆☆☆☆
Found in Text Mining only
Liver carcinoma Liver carcinoma BEFREE 28428278
★☆☆☆☆
Found in Text Mining only
Lymphoma, T-Cell, Cutaneous Lymphoma BEFREE 11149944, 11807795
★☆☆☆☆
Found in Text Mining only