Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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10814 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Complexin 2 |
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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CPLX2 |
SynonymsGene synonyms aliases
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921-L, CPX-2, CPX2, Hfb1 |
ChromosomeChromosome number
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5 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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5q35.2 |
SummarySummary of gene provided in NCBI Entrez Gene.
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Proteins encoded by the complexin/synaphin gene family are cytosolic proteins that function in synaptic vesicle exocytosis. These proteins bind syntaxin, part of the SNAP receptor. The protein product of this gene binds to the SNAP receptor complex and di |
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
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UniProt ID |
Q6PUV4 |
Protein name |
Complexin-2 (Complexin II) (CPX II) (Synaphin-1) |
Protein function |
Negatively regulates the formation of synaptic vesicle clustering at active zone to the presynaptic membrane in postmitotic neurons. Positively regulates a late step in exocytosis of various cytoplasmic vesicles, such as synaptic vesicles and ot |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF05835 |
Synaphin |
1 → 133 |
Synaphin protein |
Family |
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Sequence |
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Sequence length |
134 |
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 hyperactivity disorder |
rs120074176, rs786205019 |
23527680 |
Myocardial infarction |
Myocardial Infarction |
rs12316150, rs41303970, rs909253, rs7291467, rs2234693 |
21211798 |
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 |
14708030, 11483314 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Bipolar disorder |
Bipolar Disorder, Depression, Bipolar |
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14708030 |
Manic disorder |
Manic, Manic Disorder |
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14708030 |
Mental depression |
Mental Depression, Depressive disorder |
rs587778876, rs587778877 |
20584925 |
Psychosis |
Psychosis, Brief Reactive, Psychotic Disorders |
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14708030 |
Schizoaffective disorder |
Schizoaffective Disorder |
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14708030 |
Schizophreniform disorders |
Schizophreniform Disorders |
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14708030 |
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