Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
1506
Gene name Gene Name - the full gene name approved by the HGNC.
Chymotrypsin like
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CTRL
Synonyms (NCBI Gene) Gene synonyms aliases
CTRL1
Chromosome Chromosome number
16
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
16q22.1
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004252 Function Serine-type endopeptidase activity IBA 21873635
GO:0005515 Function Protein binding IPI 32296183
GO:0005615 Component Extracellular space IDA 9065485
GO:0006508 Process Proteolysis IBA 21873635
GO:0008236 Function Serine-type peptidase activity IDA 9065485
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
118888 2524 ENSG00000141086
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
24287731
Associations from Text Mining
Disease Name Relationship Type References
Hematologic Neoplasms Associate 19671918, 25578495
Idiopathic Pulmonary Fibrosis Associate 34524912
Leukemia Lymphocytic Chronic B Cell Stimulate 18224667
Multiple Myeloma Associate 19671918
Prostatic Neoplasms Associate 25578495
Stomach Neoplasms Associate 12616123