Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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6809 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Syntaxin 3 |
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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STX3 |
SynonymsGene synonyms aliases
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DIAR12, MVID2, RDMVID, STX3A |
ChromosomeChromosome number
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11 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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11q12.1 |
SummarySummary of gene provided in NCBI Entrez Gene.
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The gene is a member of the syntaxin family. The encoded protein is targeted to the apical membrane of epithelial cells where it forms clusters and is important in establishing and maintaining polarity necessary for protein trafficking involving vesicle f |
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 |
Q13277 |
Protein name |
Syntaxin-3 |
Protein function |
Potentially involved in docking of synaptic vesicles at presynaptic active zones. Apical receptor involved in membrane fusion of apical vesicles. ; [Isoform B]: Essential for survival of retinal photorecee |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00804 |
Syntaxin |
32 → 226 |
Syntaxin |
Domain |
PF05739 |
SNARE |
227 → 279 |
SNARE domain |
Family |
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Sequence |
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Sequence length |
289 |
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 |
Developmental delay |
Global developmental delay |
rs28941770, rs199469464, rs281865469, rs143747297, rs398123009, rs587777428, rs786205133, rs606231459, rs797044854, rs797045027, rs864309504, rs878853160, rs886039902, rs886042046, rs886041291, rs886041382, rs1057518991, rs1057518699, rs753254213, rs748294403, rs762552974, rs1135401795, rs1553121073, rs1553122926, rs1364690005, rs1554086554, rs1554210415, rs1554168326, rs1554776342, rs1553873247, rs1567860112, rs779009256, rs1557447255, rs1564568350, rs780011005, rs1597464953, rs1200336864, rs1569513017, rs1587459606, rs1570332505, rs748888652, rs1575155995, rs2087029320, rs1589669105, rs1601769604, rs1184981709, rs749201074 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Microvillus inclusion disease |
Microvillus inclusion disease |
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29282386, 24726755 |
Nephrocalcinosis |
Nephrocalcinosis |
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