Gene Gene information from NCBI Gene database.
Entrez ID 8618
Gene name Calcium dependent secretion activator
Gene symbol CADPS
Synonyms (NCBI Gene)
CADPS1CAPSCAPS1UNC-31
Chromosome 3
Chromosome location 3p14.2
Summary This gene encodes a novel neural/endocrine-specific cytosolic and peripheral membrane protein required for the Ca2+-regulated exocytosis of secretory vesicles. The protein acts at a stage in exocytosis that follows ATP-dependent priming, which involves th
miRNA miRNA information provided by mirtarbase database.
128
miRTarBase ID miRNA Experiments Reference
MIRT608231 hsa-miR-8485 HITS-CLIP 23824327
MIRT608230 hsa-miR-4643 HITS-CLIP 23824327
MIRT609474 hsa-miR-8064 HITS-CLIP 23824327
MIRT608229 hsa-miR-377-3p HITS-CLIP 23824327
MIRT608228 hsa-miR-5096 HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
18
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 17984325, 25416956
GO:0005829 Component Cytosol TAS 1516133
GO:0006887 Process Exocytosis IBA
GO:0006887 Process Exocytosis IEA
GO:0006887 Process Exocytosis TAS 1516133
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604667 1426 ENSG00000163618
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9ULU8
Protein name Calcium-dependent secretion activator 1 (Calcium-dependent activator protein for secretion 1) (CAPS-1)
Protein function Calcium-binding protein involved in exocytosis of vesicles filled with neurotransmitters and neuropeptides. Probably acts upstream of fusion in the biogenesis or maintenance of mature secretory vesicles. Regulates catecholamine loading of DCVs.
PDB 1WI1
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00169 PH 522 624 PH domain Domain
PF06292 DUF1041 836 940 Domain of Unknown Function (DUF1041) Domain
Tissue specificity TISSUE SPECIFICITY: Specifically expressed in neural and endocrine secretory tissues. Expressed in brain and pancreas and at low level in heart. Also expressed in fetal heart, cerebellum, cerebral cortex, medulla, occipital pole, frontal and temporal lobe
Sequence
MLDPSSSEEESDEIVEEESGKEVLGSAPSGARLSPSRTSEGSAGSAGLGGGGAGAGAGVG
AGGGGGSGASSGGGAGGLQPSSRAGGGRPSSPSPSVVSEKEKEELERLQKEEEERKKRLQ
LYVFVMRCIAYPFNAKQPTDMARRQQKISKQQLQTVKDRFQAFLNGETQIMADEAFMNAV
QSYYEVFLKSDRVARMVQSGGCSANDSREVFKKHIEKRVRSLPEIDGLSKETVLSSWMAK
FDAIYRGEEDPRKQQARMTASAASELILSKEQLYEMFQNILGIKKFEHQLLYNACQLDNP
DEQAAQIRRELDGRLQMADQIARERKFPKFVSKEMENMYIEELKSSVNLLMANLESMPVS
KGGEFKLQKLKRSHNASIIDMGEESENQLSKSDVVLSFSLEVVIMEVQGLKSLAPNRIVY
CTMEVEGGEKLQTDQAEASKPTWGTQGDFSTTHALPAVKVKLFTESTGVLALEDKELGRV
ILHPTPNSPKQSEWHKMTVSKNCPDQDLKIKLAVRMDKPQNMKHSGYLWAIGKNVWKRWK
KRFFVLVQVSQYTFAMCSYREKKAEPQELLQLDGYTVDYTDPQPGLEGGRAFFNAVKEGD
TVIFASDDEQDRILWVQAMYRATG
QSHKPVPPTQVQKLNAKGGNVPQLDAPISQFYADRA
QKHGMDEFISSNPCNFDHASLFEMVQRLTLDHRLNDSYSCLGWFSPGQVFVLDEYCARNG
VRGCHRHLCYLRDLLERAENGAMIDPTLLHYSFAFCASHVHGNRPDGIGTVTVEEKERFE
EIKERLRVLLENQITHFRYCFPFGRPEGALKATLSLLERVLMKDIVTPVPQEEVKTVIRK
CLEQAALVNYSRLSEYAKIEENQKDAENVGRLITPAKKLEDTIRLAELVIEVLQQNEEHH
AEPHVDKGEAFAWWSDLMVEHAETFLSLFAVDMDAALEVQ
PPDTWDSFPLFQLLNDFLRT
DYNLCNGKFHKHLQDLFAPLVVRYVDLMESSIAQSIHRGFERESWEPVKSLTSNLPNVNL
PNVNLPKVPNLPVNIPLGIPQMPTFSAPSWMAAIYDADNGSGTSEDLFWKLDALQTFIRD
LHWPEEEFGKHLEQRLKLMASDMIESCVKRTRIAFEVKLQKTSRSTDFRVPQSICTMFNV
MVDAKAQSTKLCSMEMGQEHQYHSKIDELIEETVKEMITLLVAKFVTILEGVLAKLSRYD
EGTLFSSFLSFTVKAASKYVDVPKPGMDVADAYVTFVRHSQDVLRDKVNEEMYIERLFDQ
WYNSSMNVICTWLTDRMDLQLHIYQLKTLIRMVKKTYRDFRLQGVLDSTLNSKTYETIRN
RLTVEEATASVSEGGGLQGISMKDSDEEDEEDD
Sequence length 1353
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
34
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
CADPS-related disorder Uncertain significance; Likely benign; Benign rs771045473, rs1707040888, rs1158576022, rs898296147, rs2529893116, rs745876740, rs779869722, rs372017906, rs765741289, rs140977565, rs185882358, rs199626657, rs139420058, rs150724919, rs79260062
View all (16 more)
RCV003966289
RCV003394491
RCV003408477
RCV003402706
RCV003402942
RCV003898943
RCV003897069
RCV003906986
RCV003909418
RCV003909455
RCV003904538
RCV003984763
RCV003909811
RCV003939827
RCV003942108
RCV003964084
RCV003927204
RCV003924555
RCV003951627
RCV003951633
RCV003936994
RCV003924260
RCV003926839
RCV003949226
RCV003944625
RCV003957288
RCV003947273
RCV003959392
RCV003972166
RCV003978048
RCV003978047
Prostate cancer Uncertain significance rs193921128 RCV000149385
Thymoma Benign rs74991517 RCV005933481
Uterine corpus endometrial carcinoma Benign rs145339043 RCV005903109
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Autoimmune Hypophysitis Associate 22193973
Carcinoma Hepatocellular Associate 21659380
Cardiomyopathy Hypertrophic Familial Associate 31638236
Cerebral Infarction Associate 36916413
Colorectal Neoplasms Associate 31638236
Diabetes Mellitus Type 2 Associate 31932636
Infarction Middle Cerebral Artery Stimulate 36916413
Memory Disorders Inhibit 36916413
Neoplasm Metastasis Stimulate 31638236
Neoplasms Associate 34135559, 37284741