Gene Gene information from NCBI Gene database.
Entrez ID 79634
Gene name Secernin 3
Gene symbol SCRN3
Synonyms (NCBI Gene)
SES3
Chromosome 2
Chromosome location 2q31.1
miRNA miRNA information provided by mirtarbase database.
149
miRTarBase ID miRNA Experiments Reference
MIRT024716 hsa-miR-215-5p Microarray 19074876
MIRT026160 hsa-miR-192-5p Microarray 19074876
MIRT732863 hsa-let-7b-5p MicroarrayqRT-PCR 33946378
MIRT1330835 hsa-miR-1293 CLIP-seq
MIRT1330836 hsa-miR-186 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
5
GO ID Ontology Definition Evidence Reference
GO:0006508 Process Proteolysis IEA
GO:0016805 Function Dipeptidase activity IEA
GO:0050965 Process Detection of temperature stimulus involved in sensory perception of pain IEA
GO:0050965 Process Detection of temperature stimulus involved in sensory perception of pain ISS
GO:0070004 Function Cysteine-type exopeptidase activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
614967 30382 ENSG00000144306
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q0VDG4
Protein name Secernin-3
Protein function Plays a role in thermal nociception.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03577 Peptidase_C69 77 271 Peptidase family C69 Family
Sequence
MEPFSCDTFVALPPATVDNRIIFGKNSDRLYDEVQEVVYFPAVVHDNLGERLKCTYIEID
QVPETYAVVLSRPAWLWGAEMGANEHGVCIGNEAVWGREEVCDEEALLGMDLVRLGLERA
DTAEKALNVIVDLLEKYGQGGNCTEGRMVFSYHNSFLIADRNEAWILETAGKYWAAEKVQ
EGVRNISNQLSITTKIAREHPDMRNYAKRKGWWDGKKEFDFAAAYSYLDTAKMMTSSGRY
CEGYKLLNKHKGNITFETMMEILRDKPSGIN
MEGEFLTTASMVSILPQDSSLPCIHFFTG
TPDPERSVFKPFIFVPHISQLLDTSSPTFELEDLVKKKSHFKPDRRHPLYQKHQQALEVV
NNNEEKAKIMLDNMRKLEKELFREMESILQNKHLDVEKIVNLFPQCTKDEIQIYQSNLSV
KVSS
Sequence length 424
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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
METABOLIC SYNDROME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SCOLIOSIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
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
Alzheimer Disease Alzheimer disease Pubtator 37149819 Associate
★☆☆☆☆
Found in Text Mining only