SSTR3 - somatostatin receptor 3 Gene

Also Known as SS3R; SST3; SS3-R; SS-3-R; SSR-28

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 6753

About SSTR3

Cytogenetic location: 22q13.1 Genomic coordinates (GRCh38): 22:37,204,237-37,220,548 (from NCBI)

This gene has 2 transcripts (splice variants), 251 orthologues and 17 paralogues. Biased expression in testis (RPKM 3.5), brain (RPKM 1.1) and 8 other tissues.

Summary

This gene encodes a member of the Somatostatin Receptor protein family. Somatostatins are peptide Hormones that regulate diverse cellular functions such as neurotransmission, cell proliferation, and endocrine signaling as well as inhibiting the release of many Hormones and Other secretory proteins. Somatostatin has two active forms of 14 and 28 Amino acids. The biological effects of somatostatins are mediated by a family of G-protein coupled somatostatin receptors that are expressed in a tissue-specific manner. Somatostatin receptors form homodimers and heterodimers with Other members of the superfamily as well as with Other G-protein coupled receptors and Receptor Tyrosine Kinases. This protein is functionally coupled to adenylyl cyclase. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]

SSTR3 Products (6)

mRNA Protein Name
XM_006724311.4 XP_006724374.1 somatostatin receptor type 3 isoform X1
XM_047441473.1 XP_047297429.1 somatostatin receptor type 3 isoform X1
XM_005261721.5 XP_005261778.1 somatostatin receptor type 3 isoform X1
NM_001051.5 NP_001042.1 somatostatin receptor type 3
XM_017028924.2 XP_016884413.1 somatostatin receptor type 3 isoform X1
NM_001278687.2 NP_001265616.1 somatostatin receptor type 3
Molecular Function GO Annotation Evidence Références Source
enables protein binding IPI
IPI: Inferred from physical interaction
19071123 GOA
Cellular Component GO Annotation Evidence Références Source
located in cilium IDA
IDA: Inferred from direct assay
28154160 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SSTR3 Protein Structure

7tm_1

7tm_1: 7 transmembrane receptor (rhodopsin family) (61 - 313)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 418 a.a.
Protein Preferred Names Protein Names

somatostatin receptor type 3

SSTR3 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Références
Intra
SSTR3 P32745 SSTR2 Homo sapiens P30874
IF
22651821
Intra
SSTR3 P32745 MPDZ Homo sapiens O75970 19071123
Intra
SSTR3 P32745 MPDZ Homo sapiens O75970
IF
19071123
Cross
SSTR3 P32745 Mpdz Rattus norvegicus O55164 19071123
Cross: Cross-species interaction Intra: Intraspecies interaction

SSTR3 Anticorps

Cat. No. Nom du produit Application Reactivity
HY-P82287 Somatostatin Receptor 3 Antibody (YA2032) WB Human
HY-P82287A Somatostatin Receptor 3 Antibody (YA2032)(PBS only) WB Human

Related Diseases

Diseases Alias
Meckel Syndrome, Type 1
  • Meckel Syndrome

  • Meckel-Gruber Syndrome

  • Dysencephalia Splanchnocystica

  • Meckel Syndrome 1

  • MKS1

  • Mks

  • Gruber Syndrome

  • Meckel-Gruber Syndrome, Type 1

  • Mes

  • Dysencephalia Splachnocystica

  • Meckel Gruber Syndrome

  • Meckel Syndrome Type 1

Asphyxiating Thoracic Dystrophy
  • Jeune Thoracic Dystrophy

  • Jeune Syndrome

  • Asphyxiating Thoracic Dysplasia

  • Short-Rib Thoracic Dysplasia With Or Without Polydactyly

  • Thoracic Pelvic Phalangeal Dystrophy

  • Asphyxiating Thoracic Chondrodystrophy

  • Atd

  • Chondroectodermal Dysplasia-Like Syndrome

  • Infantile Thoracic Dystrophy

  • Jeune Thoracic Dysplasia

  • Thoracic Asphyxiant Dystrophy

  • Thoracic-Pelvic-Phalangeal Dystrophy

  • Short-Rib Thoracic Dysplasia Without Polydactyly

  • Asphyxiating Thoracic Dystrophy Of The Newborn

  • Asphyxiating Thorax Dystrophy

Gastrointestinal Neuroendocrine Tumor
  • Gastrointestinal Neuroendocrine Tumour

  • Malignant Gastrointestinal Neuroendocrine Tumor

  • Malignant Gastrointestinal Neuroendocrine Tumour

  • Digestive System Neuroendocrine Neoplasm

  • Digestive System Neuroendocrine Tumor

Cystic Kidney Disease
  • Renal Cyst

  • Simple Renal Cyst

  • Kidney Cysts

  • Kidney Diseases, Cystic

  • Renal Cysts

  • Kidney Cyst

  • Cystic Kidney

  • Congenital Cystic Kidney Disease

  • Cystic Kidney Diseases

  • Bosniak 1 Cyst

Autosomal Dominant Polycystic Kidney Disease
  • Polycystic Kidney Disease, Adult Type

  • Adpkd

  • Polycystic Kidney Diseases

  • Polycystic Kidney, Autosomal Dominant

  • Congenital Biliary Ectasias

  • Polycystic Kidney And Hepatic Disease 1

  • Polycystic Kidney Disease, Autosomal Dominant

  • Kidney, Polycystic, Disease, Autosomal Dominant

  • Adult Polycystic Kidney Disease

  • Polycystic Kidney, Adult Type

  • Apckd - [Autosomal Polycystic Kidney Disease]

Polycystic Kidney Disease
  • Polycystic Kidney Diseases

  • Pkd

  • Polycystic Renal Disease

  • Kidney Disease, Polycystic

  • Polycystic Kidney, Autosomal Dominant

Nephronophthisis
  • Medullary Cystic Disease

  • Medullary Cystic Kidney

  • Nph

  • Nphp

  • Kidney Disease, Cystic, Medullary

Vipoma
  • Wdha Syndrome

  • Pancreatic Cholera

  • Pancreatic Vipoma

  • Verner-Morrison Syndrome

  • Diarrheogenic Islet Cell Tumor

  • Vip-Secreting Tumor

  • Malignant Vasoactive Intestinal Peptide-Secreting Tumor

  • Vasoactive Intestinal Peptide-Secreting Tumor

  • Vip- Secreting Tumor

  • Vipoma, Malignant

  • Vipoma Syndrome

  • Watery Diarrhea Syndrome

  • Watery Diarrhea, Hypokalemia, And Achlorhydria Syndrome

  • Vasoactive Intestinal Peptide Tumor

  • Vasoactive Intestinal Peptide-Producing Tumor

  • Watery Diarrhea-Hypokalemia-Achlorhydria Syndrome

  • Malignant Vipoma

Prolactinoma
  • Prolactin-Producing Pituitary Gland Adenoma

  • Prolactin-Secreting Pituitary Adenoma

  • Forbes-Albright Syndrome

  • Lactotroph Adenoma

  • Prl-Secreting Pituitary Adenoma

  • Prloma

  • Pituitary Lactotrophic Adenoma

  • Familial Prolactinoma

  • Pituitary Adenoma, Prolactin-Secreting

  • Prolactinoma Of Pituitary Gland

  • PSPA

Microcystic Meningioma
Pituitary Adenoma
  • Pituitary Neoplasms

  • Adenoma Of The Pituitary Gland

  • Pituitary Adenomas

  • Adenoma, Pituitary

  • Pituitary Gland Adenoma

Pituitary Gland Disease
  • Pituitary Diseases

  • Pituitary Dysfunction

  • Pituitary Disease

  • Pituitary Deficiency

  • Pituitary Disorders

Retinitis Pigmentosa
  • RP

  • Rod-Cone Dystrophy

  • Autosomal Recessive Retinitis Pigmentosa

  • Non-Syndromic Retinitis Pigmentosa

  • Pericentral Pigmentary Retinopathy

  • Pigmentary Retinopathy

  • Tapetoretinal Degeneration

  • Rcd

  • Retinitis Pigmentosa Autosomal Recessive

  • ARRP

  • Retinitis Pigmentosa, Autosomal Recessive

  • Retinitis Pigmentosa 1

Primary Ciliary Dyskinesia
  • Immotile Cilia Syndrome

  • Kartagener Syndrome

  • Dextrocardia Bronchiectasis And Sinusitis

  • Pcd

  • Ciliary Motility Disorders

  • Ciliary Motility Disorder

  • Immotile Ciliary Syndrome

  • Ciliary Dyskinesia Primary

  • Ics

  • Polynesian Bronchiectasis

  • Dextrocardia-Bronchiectasis-Sinusitis Syndrome

  • Immotile Cilia Syndrome, Kartagener Type

  • Primary Ciliary Dyskinesia And Situs Inversus

  • Primary Ciliary Dyskinesia, Kartagener Type

  • Siewert Syndrome

  • Dyskinesia, Ciliary, Primary

Hormone Producing Pituitary Cancer
  • Growth Hormone Producing Pituitary Tumor

  • Pituitary Tumors, Hormone Producing

  • Somatotropinoma

  • Growth Hormone-Producing Pituitary Gland Neoplasm

Visceral Heterotaxy
  • Situs Ambiguus

  • Heterotaxia

  • Heterotaxy Syndrome

  • Heterotaxy

  • Lateralization Defect

  • Situs Ambiguous

  • Left Isomerism

  • Htx

  • Ivemark Syndrome

  • Right Isomerism

  • Situs Ambiguus Viscerum

  • Incomplete Situs Inversus

  • Partial Situs Inversus

  • Heterotaxy, Visceral

  • Asplenia Syndrome

  • Bilateral Left-Sidedness

  • Polysplenia Syndrome

  • Moller Syndrome

Hydrolethalus Syndrome 1
  • Hydrolethalus Syndrome

  • HLS1

  • Salonen-Herva-Norio Syndrome

  • Hls

  • Hydrolethalus

  • Hydrolethalus Syndrome, Type 1

Joubert Syndrome 1
  • Joubert Syndrome

  • Jbts

  • Cerebellooculorenal Syndrome 1

  • JBTS1

  • Joubert-Boltshauser Syndrome

  • Cerebelloparenchymal Disorder Iv

  • Cpd4

  • Cors1

  • Joubert Syndrome And Related Disorders

  • Jsrd

  • Familial Aplasia Of The Vermis

  • Joubert Syndrome Related Disorders

  • Js

  • Cerebellar Vermis Agenesis

  • Cerebelloparenchymal Disorder 4

  • Agenesis Of Cerebellar Vermis

  • Cerebello-Oculo-Renal Syndrome

  • Cors

  • Joubert-Bolthauser Syndrome

  • Cpd Iv

  • Classic Joubert Syndrome

  • Joubert Syndrome Type A

  • Pure Joubert Syndrome

  • Cerebello-Oculo-Renal Syndrome 1

  • Joubert Syndrome-1

  • Joubert Syndrome, Type 1

  • Joubert'S Syndrome

Functioning Pituitary Adenoma
  • Secretory Adenoma Of The Pituitary Gland

  • Endocrine Active Pituitary Adenoma

  • Secreting Pituitary Adenoma

  • Pituitary Adenoma, Functioning

Hyperpituitarism
Fundus Dystrophy
  • Retinal Dystrophy

  • Retinal Dystrophies

  • Dystrophy, Retinal

Growth Hormone Secreting Pituitary Adenoma
  • Somatotroph Adenoma

  • Growth Hormone-Secreting Pituitary Adenoma

  • Growth Hormone Producing Adenoma Of The Pituitary

  • Growth Hormone Secreting Adenoma Of Pituitary

Bardet-Biedl Syndrome
  • Bbs

  • Biedl-Bardet Syndrome

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus SSTR3 MGD MGI:98329
Canis familiaris SSTR3 VGNC VGNC:46845
Rattus norvegicus SSTR3 RGD RGD:620308
Macaca mulatta SSTR3 VGNC VGNC:77894
Bos taurus SSTR3 VGNC VGNC:35327
Felis catus SSTR3 VGNC VGNC:65712
Others SSTR3 NCBI