Gene Gene information from NCBI Gene database.
Entrez ID 1506
Gene name Chymotrypsin like
Gene symbol CTRL
Synonyms (NCBI Gene)
CTRL1
Chromosome 16
Chromosome location 16q22.1
Summary This gene encodes a serine-type endopeptidase with chymotrypsin- and elastase-2-like activities. The gene encoding this zymogen is expressed specifically in the pancreas and likely functions as a digestive enzyme. [provided by RefSeq, Sep 2016]
miRNA miRNA information provided by mirtarbase database.
19
miRTarBase ID miRNA Experiments Reference
MIRT1971489 hsa-miR-1321 CLIP-seq
MIRT1971490 hsa-miR-2861 CLIP-seq
MIRT1971491 hsa-miR-3925-3p CLIP-seq
MIRT1971492 hsa-miR-4270 CLIP-seq
MIRT1971493 hsa-miR-4441 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
GO ID Ontology Definition Evidence Reference
GO:0004252 Function Serine-type endopeptidase activity IBA
GO:0004252 Function Serine-type endopeptidase activity IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005615 Component Extracellular space IDA 9065485
GO:0006508 Process Proteolysis IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
118888 2524 ENSG00000141086
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P40313
Protein name Chymotrypsin-like protease CTRL-1 (EC 3.4.21.-)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00089 Trypsin 34 257 Trypsin Domain
Sequence
Sequence length 264
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Pancreatic secretion
Protein digestion and absorption
 
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
Long QT syndrome Likely benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SCHIZOPHRENIA Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Hematologic Neoplasms Associate 19671918, 25578495
★☆☆☆☆
Found in Text Mining only
Idiopathic Pulmonary Fibrosis Associate 34524912
★☆☆☆☆
Found in Text Mining only
Leukemia Lymphocytic Chronic B Cell Stimulate 18224667
★☆☆☆☆
Found in Text Mining only
Multiple Myeloma Associate 19671918
★☆☆☆☆
Found in Text Mining only
Prostatic Neoplasms Associate 25578495
★☆☆☆☆
Found in Text Mining only
Stomach Neoplasms Associate 12616123
★☆☆☆☆
Found in Text Mining only