Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
50632
Gene name Gene Name - the full gene name approved by the HGNC.
Calcyon neuron specific vesicular protein
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CALY
Synonyms (NCBI Gene) Gene synonyms aliases
DRD1IP, NSG3
Chromosome Chromosome number
10
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10q26.3
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a type II single transmembrane protein. It is required for maximal stimulated calcium release after stimulation of purinergic or muscarinic but not beta-adrenergic receptors. The encoded protein interacts with D1 dopami
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT860007 hsa-miR-3135b CLIP-seq
MIRT860008 hsa-miR-3652 CLIP-seq
MIRT860009 hsa-miR-4430 CLIP-seq
MIRT860010 hsa-miR-4492 CLIP-seq
MIRT860011 hsa-miR-4498 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 16595675
GO:0005768 Component Endosome IBA 21873635
GO:0005887 Component Integral component of plasma membrane IDA 14534309
GO:0007212 Process Dopamine receptor signaling pathway IEA
GO:0008089 Process Anterograde axonal transport IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604647 17938 ENSG00000130643
Protein
UniProt ID Q9NYX4
Protein name Neuron-specific vesicular protein calcyon
Protein function Interacts with clathrin light chain A and stimulates clathrin self-assembly and clathrin-mediated endocytosis.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06387 Calcyon 1 181 D1 dopamine receptor-interacting protein (calcyon) Family
Tissue specificity TISSUE SPECIFICITY: Expressed in the pyramidal cells of the prefrontal cortex, in hypothalamus and in caudate nucleus. No expression in spleen. Up-regulated in the prefrontal cortex of schizophrenic patients with nearly twice the levels of non-schizophren
Sequence
Sequence length 217
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  Dopaminergic synapse  
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Attention deficit hyperactivity disorder Attention Deficit Disorder, Attention deficit hyperactivity disorder rs786205019 30753204
Hypertension Essential Hypertension rs13306026 30753204
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
14755439, 15364041
Associations from Text Mining
Disease Name Relationship Type References
Astrocytoma Associate 18670637
Bipolar Disorder Associate 31279243