Gene
|
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
6343 |
Gene nameGene Name - the full gene name approved by the HGNC.
|
Secretin |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
|
SCT |
SynonymsGene synonyms aliases
|
- |
ChromosomeChromosome number
|
11 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
11p15.5 |
SummarySummary of gene provided in NCBI Entrez Gene.
|
This gene encodes a member of the glucagon family of peptides. The encoded preproprotein is secreted by endocrine S cells in the proximal small intestinal mucosa as a prohormone, then proteolytically processed to generate the mature peptide hormone. The r |
miRNAmiRNA information provided by mirtarbase database.
|
|
Transcription factors
|
Transcription factor |
Regulation |
Reference |
SP1 |
Unknown |
15118068 |
SP3 |
Unknown |
15118068 |
|
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
|
|
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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|
Protein
|
UniProt ID |
P09683 |
Protein name |
Secretin |
Protein function |
Hormone involved in different processes, such as regulation of the pH of the duodenal content, food intake and water homeostasis (PubMed:25332973). Exerts its biological effects by binding to secretin receptor (SCTR), a G-protein coupled recepto |
PDB |
6WI9
,
6WZG
,
7D3S
|
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00123 |
Hormone_2 |
28 → 55 |
Peptide hormone |
Family |
|
Sequence |
|
Sequence length |
121 |
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
|
Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Autism |
Autistic Disorder |
rs121964908, rs121912597, rs2710102, rs7794745, rs142990298, rs62643608, rs181327458, rs797046134, rs869312704, rs1555013332, rs876657679, rs1057518999, rs1057518658, rs771827120, rs1555187899, rs773080572, rs753871454, rs1684130791, rs1684180699, rs1553510219, rs1684182454, rs1559060428, rs1553510677, rs1576352885, rs1574152522, rs1574152672, rs1696658542, rs1751123722, rs1750373491, rs1751075634 |
12732234, 15272612, 16168596, 15206007 |
|
Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Choledochal cyst |
Choledochal Cyst, Choledochal Cyst, Type I, Choledochal Cyst, Type II, Choledochal Cyst, Type III, Choledochal Cyst, Type IV, Choledochal Cyst, Type V |
|
18988797 |
Sclerocystic ovaries |
Sclerocystic Ovaries |
|
21411543 |
Polycystic ovary syndrome |
Polycystic Ovary Syndrome |
|
21411543 |
|