Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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50632 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Calcyon neuron specific vesicular protein |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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CALY |
SynonymsGene synonyms aliases
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DRD1IP, NSG3 |
ChromosomeChromosome number
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10 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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10q26.3 |
SummarySummary of gene provided in NCBI Entrez Gene.
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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 |
miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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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 |
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Sequence |
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Sequence length |
217 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Attention deficit hyperactivity disorder |
Attention Deficit Disorder, Attention deficit hyperactivity disorder |
rs120074176, rs786205019 |
30753204 |
Hypertension |
Essential Hypertension |
rs13306026, rs13333226 |
30753204 |
Schizophrenia |
Schizophrenia |
rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 |
14755439, 15364041 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Memory disorders |
Memory Disorders |
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30753204 |
Age-related memory disorders |
Age-Related Memory Disorders |
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30753204 |
Minimal brain dysfunction |
Minimal Brain Dysfunction |
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30753204 |
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