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Gene Gene information from NCBI Gene database.
Entrez ID 51032
Gene name Chymotrypsin like elastase 2B
Gene symbol CELA2B
Synonyms (NCBI Gene)
ELA2B
Chromosome 1
Chromosome location 1p36.21
Summary Elastases form a subfamily of serine proteases that hydrolyze many proteins in addition to elastin. Humans have six elastase genes which encode the structurally similar proteins elastase 1, 2, 2A, 2B, 3A, and 3B. Like most of the human elastases, elastase
miRNA miRNA information provided by mirtarbase database.
14 Show/Hide all (14)
miRTarBase ID miRNA Experiments Reference
MIRT883633 hsa-miR-132 CLIP-seq
MIRT883634 hsa-miR-153 CLIP-seq
MIRT883635 hsa-miR-1915 CLIP-seq
MIRT883636 hsa-miR-212 CLIP-seq
MIRT883637 hsa-miR-3691-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12 Show/Hide all (12)
GO ID Ontology Definition Evidence Reference
GO:0004252 Function Serine-type endopeptidase activity IBA
GO:0004252 Function Serine-type endopeptidase activity IEA
GO:0004252 Function Serine-type endopeptidase activity TAS 3427074
GO:0005515 Function Protein binding IPI 32296183
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
609444 29995 ENSG00000215704
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P08218
Protein name Chymotrypsin-like elastase family member 2B (EC 3.4.21.71) (Elastase-2B)
Protein function Acts upon elastin.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00089 Trypsin 29 → 262 Trypsin Domain
Tissue specificity TISSUE SPECIFICITY: Pancreas.
Sequence
Sequence length 269
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
KEGG Pathway
Pancreatic secretion
Protein digestion and absorption
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 Reference Evidence Score
ERECTILE DYSFUNCTION — GWAS catalog 20932654
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GOUT — GWAS catalog 33462484
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PROSTATE CARCINOMA — GWAS catalog 20932654
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TREATMENT-RESISTANT HYPERTENSION — GWAS catalog 30237584
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations