1. Gene
  2. SSTR3 - somatostatin receptor 3 Gene

SSTR3 - somatostatin receptor 3 Gene

中文名称:生长抑素受体 3

种属: Homo sapiens

同用名: SS3R; SST3; SS3-R; SS-3-R; SSR-28

基因 ID: 6753 | 基因类型: protein coding

关于 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.

功能概要

该基因编码生长抑素受体蛋白家族的一个成员。生长抑素是调节多种细胞功能 (例如神经传递、细胞增殖和内分泌信号传导) 以及抑制许多激素和其他分泌蛋白的释放的肽类激素。生长抑素有 14 和 28 个氨基酸的两种活性形式。生长抑素的生物学效应由以组织特异性方式表达的 G 蛋白偶联生长抑素受体家族介导。生长抑素受体与超家族的其他成员以及其他 G 蛋白偶联受体和受体酪氨酸激酶形成同二聚体和异二聚体。该蛋白质在功能上与腺苷酸环化酶偶联。交替剪接导致多个转录本变体。[RefSeq 提供,2013 年 7 月]

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 基因产物(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
基因本体论
  • 分子功能
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
19071123 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in cilium IDA
IDA: 通过直接分析推断
28154160 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

SSTR3 蛋白结构

7tm_1

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

  • 0
  • 100
  • 200
  • 300
  • 418 a.a.
蛋白主名 其他名称

somatostatin receptor type 3

SSTR3 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
SSTR3 P32745 SSTR2 Homo sapiens P30874
IF
22651821
种属内
SSTR3 P32745 MPDZ Homo sapiens O75970 19071123
种属内
SSTR3 P32745 MPDZ Homo sapiens O75970
IF
19071123
种属间
SSTR3 P32745 Mpdz Rattus norvegicus O55164 19071123
种属间: 跨种属相互作用 种属内: 同种属相互作用

SSTR3 抗体

目录号 产品名 应用 反应物种
HY-P82287 Somatostatin Receptor 3 Antibody (YA2032) WB Human

关联疾病

疾病名称 别名
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

疾病名称 别名
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

直系同源

种属 基因名 来源 基因 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
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