Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
57620
Gene name Gene Name - the full gene name approved by the HGNC.
Stromal interaction molecule 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
STIM2
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4p15.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene is a member of the stromal interaction molecule (STIM) family and likely arose, along with related family member STIM1, from a common ancestral gene. The encoded protein functions to regulate calcium concentrations in the cytosol and endoplasmic
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT036939 hsa-miR-877-3p CLASH 23622248
MIRT439526 hsa-miR-1185-2-3p HITS-CLIP 24374217
MIRT439524 hsa-miR-1185-1-3p HITS-CLIP 24374217
MIRT439526 hsa-miR-1185-2-3p HITS-CLIP 24374217
MIRT439524 hsa-miR-1185-1-3p HITS-CLIP 24374217
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002115 Process Store-operated calcium entry IBA
GO:0005246 Function Calcium channel regulator activity IBA
GO:0005246 Function Calcium channel regulator activity IEA
GO:0005246 Function Calcium channel regulator activity IMP 18160041
GO:0005509 Function Calcium ion binding IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
610841 19205 ENSG00000109689
Protein
UniProt ID Q9P246
Protein name Stromal interaction molecule 2
Protein function Plays a role in mediating store-operated Ca(2+) entry (SOCE), a Ca(2+) influx following depletion of intracellular Ca(2+) stores. Functions as a highly sensitive Ca(2+) sensor in the endoplasmic reticulum which activates both store-operated and
PDB 2L5Y
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07647 SAM_2 133 202 SAM domain (Sterile alpha motif) Domain
PF16533 SOAR 345 445 STIM1 Orai1-activating region Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in all tissues and tumor cell lines examined. {ECO:0000269|PubMed:11463338}.
Sequence
MLVLGLLVAGAADGCELVPRHLRGRRATGSAATAASSPAAAAGDSPALMTDPCMSLSPPC
FTEEDRFSLEALQTIHKQMDDDKDGGIEVEESDEFIREDMKYKDATNKHSHLHREDKHIT
IEDLWKRWKTSEVHNWTLEDTLQWLIEFVELPQYEKNFRDNNVKGTTLPRIAVHEPSFMI
SQLKISDRSHRQKLQLKALDVV
LFGPLTRPPHNWMKDFILTVSIVIGVGGCWFAYTQNKT
SKEHVAKMMKDLESLQTAEQSLMDLQERLEKAQEENRNVAVEKQNLERKMMDEINYAKEE
ACRLRELREGAECELSRRQYAEQELEQVRMALKKAEKEFELRSSWSVPDALQKWLQLTHE
VEVQYYNIKRQNAEMQLAIAKDEAEKIKKKRSTVFGTLHVAHSSSLDEVDHKILEAKKAL
SELTTCLRERLFRWQQIEKICGFQI
AHNSGLPSLTSSLYSDHSWVVMPRVSIPPYPIAGG
VDDLDEDTPPIVSQFPGTMAKPPGSLARSSSLCRSRRSIVPSSPQPQRAQLAPHAPHPSH
PRHPHHPQHTPHSLPSPDPDILSVSSCPALYRNEEEEEAIYFSAEKQWEVPDTASECDSL
NSSIGRKQSPPLSLEIYQTLSPRKISRDEVSLEDSSRGDSPVTVDVSWGSPDCVGLTETK
SMIFSPASKVYNGILEKSCSMNQLSSGIPVPKPRHTSCSSAGNDSKPVQEAPSVARISSI
PHDLCHNGEKSKKPSKIKSLFKKKSK
Sequence length 746
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  Calcium signaling pathway  
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Eosinophilia Eosinophilic esophagitis N/A N/A GWAS
Heart Failure Heart failure N/A N/A GWAS
Hirschsprung Disease Hirschsprung disease N/A N/A GWAS
Hypertension Hypertension N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 20395295
Colonic Neoplasms Associate 25143380
Colorectal Neoplasms Associate 25143380
Cysts Associate 33943042
Diabetes Mellitus Type 1 Associate 30543678
Epilepsy Associate 32315120
Glioblastoma Associate 17002787
Hypoxia Stimulate 29351410
Migraine Disorders Associate 32315120
Neoplasms Associate 17002787, 36057880