Gene Gene information from NCBI Gene database.
Entrez ID 132203
Gene name Sentan, cilia apical structure protein
Gene symbol SNTN
Synonyms (NCBI Gene)
S100A1LS100ALsentan
Chromosome 3
Chromosome location 3p14.2
miRNA miRNA information provided by mirtarbase database.
458
miRTarBase ID miRNA Experiments Reference
MIRT017854 hsa-miR-335-5p Microarray 18185580
MIRT634315 hsa-miR-3677-5p HITS-CLIP 23824327
MIRT634314 hsa-miR-1228-3p HITS-CLIP 23824327
MIRT634313 hsa-miR-383-3p HITS-CLIP 23824327
MIRT634312 hsa-miR-342-3p HITS-CLIP 23824327
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:0005509 Function Calcium ion binding IBA
GO:0005929 Component Cilium IEA
GO:0042995 Component Cell projection IEA
GO:0046914 Function Transition metal ion binding IEA
GO:0048306 Function Calcium-dependent protein binding IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617832 33706 ENSG00000188817
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
A6NMZ2
Protein name Sentan (Protein S100-A1-like) (S100 calcium-binding protein A1-like)
Protein function May be a component of the linker structure that bridges the ciliary membrane and peripheral singlet microtubules.
Family and domains
Sequence
MGGCMHSTQDKSLHLEGDPNPSAAPTSTCAPRKMPKRISISKQLASVKALRKCSDLEKAI
ATTALIFRNSSDSDGKLEKAIAKDLLQTQFRNFAEGQETKPKYREILSELDEHTENKLDF
EDFMILLLSITVMSDLLQNIRNVKIMK
Sequence length 147
Interactions View interactions
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
ATYPICAL FEMORAL FRACTURE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MAJOR DEPRESSIVE DISORDER 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
ovarian neoplasm Ovarian neoplasm BEFREE 26512784
★☆☆☆☆
Found in Text Mining only