1. Gene
  2. LGR5 - leucine rich repeat containing G protein-coupled receptor 5 Gene

LGR5 - leucine rich repeat containing G protein-coupled receptor 5 Gene

中文名称:含富含亮氨酸重复序列的 G 蛋白偶联受体 5

种属: Homo sapiens

同用名: FEX; HG38; GPR49; GPR67; GRP49

基因 ID: 8549 | 基因类型: protein coding

关于 LGR5

Cytogenetic location: 12q21.1 Genomic coordinates (GRCh38): 12:71,439,129-71,586,310 (from NCBI)

This gene has 6 transcripts (splice variants), 199 orthologues and 22 paralogues. Biased expression in placenta (RPKM 11.9), small intestine (RPKM 3.2) and 8 other tissues.

功能概要

由该基因编码的蛋白质是富含亮氨酸的重复序列受体 (LGR) ,是 G 蛋白偶联的 7 跨膜受体 (GPCR) 超家族的成员。编码的蛋白质是 R-spondins 的受体,并参与典型的 Wnt 信号通路。这种蛋白质在胚胎后发育过程中在成体肠道干细胞的形成和维持中发挥作用。已发现该基因编码不同亚型的几种转录变体。[RefSeq 提供,2015 年 9 月]

The protein encoded by this gene is a leucine-rich repeat-containing receptor (LGR) and member of the G protein-coupled, 7-transmembrane receptor (GPCR) superfamily. The encoded protein is a receptor for R-spondins and is involved in the canonical Wnt signaling pathway. This protein plays a role in the formation and maintenance of adult intestinal stem cells during postembryonic development. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2015]

LGR5 基因产物(3)

mRNA Protein Name
NM_001277226.2 NP_001264155.1 leucine-rich repeat-containing G-protein coupled receptor 5 isoform 2 precursor
NM_001277227.2 NP_001264156.1 leucine-rich repeat-containing G-protein coupled receptor 5 isoform 3 precursor
NM_003667.4 NP_003658.1 leucine-rich repeat-containing G-protein coupled receptor 5 isoform 1 precursor
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
NOT enables G protein-coupled receptor activity IDA
IDA: 通过直接分析推断
21693646 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
21693646 GOA
enables transmembrane signaling receptor activity IDA
IDA: 通过直接分析推断
21693646 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in positive regulation of canonical Wnt signaling pathway IDA
IDA: 通过直接分析推断
21693646 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in plasma membrane IDA
IDA: 通过直接分析推断
21693646 GOA
located in trans-Golgi network membrane IDA
IDA: 通过直接分析推断
23439653 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

LGR5 蛋白结构

LRRNT

LRRNT: Leucine rich repeat N-terminal domain (33 - 64)

LRR_8

LRR_8: Leucine rich repeat (92 - 150)

LRR_5

LRR_5: Leucine rich repeats (6 copies) (175 - 304)

LRR_1

LRR_1: Leucine Rich Repeat (353 - 372)

LRR_8

LRR_8: Leucine rich repeat (375 - 434)

7tm_1

7tm_1: 7 transmembrane receptor (rhodopsin family) (575 - 820)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 907 a.a.
蛋白主名 其他名称

leucine-rich repeat-containing G-protein coupled receptor 5

G-protein coupled receptor 49

LGR5 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
LGR5 O75473 RSPO1 Homo sapiens Q2MKA7
GMS
23809763
种属内
LGR5 O75473 RSPO1 Homo sapiens Q2MKA7 23809763
种属内
LGR5 O75473 RSPO1 Homo sapiens Q2MKA7 23809763
种属间: 跨种属相互作用 种属内: 同种属相互作用

重组 LGR5 蛋白

目录号 产品名 蛋白编号 纯度
HY-P79308 Lgr5/GPR49 Protein, Human (CHO, hFc) O75473 (G22-I560) ≥95%
HY-P700891 Lgr5/GPR49 Protein, Human (HEK293, hFc) O75473-1 (G22-P543) ≥95%

LGR5 抗体

目录号 产品名 应用 反应物种
HY-P82097 LGR5 Antibody (YA1842) WB, IP, FC Human, Mouse, Rat

关联疾病

疾病名称 别名
Ankyloglossia With Or Without Tooth Anomalies

Ankyloglossia

ANKG

'Tongue-Tie'

Tongue-Tie

Tongue Tie

Aberrant Insertion Of Labial Frenulum

Aberrant Insertion Of Frenum Of Tongue

Short Frenulum Linguae

Short Frenulum Of Tongue

Mucositis

Inflammatory Disease Of Mucous Membrane

Gastrointestinal Mucositis

Mesenteric Vascular Occlusion
Colon Adenoma

Adenomatous Polyp Of Colon

Colonic Benign Neoplasm

Colon Neoplasm

Colonic Mass

Colonic Tumor

Neoplasm Of Colon

Neoplasm Of The Colon

Colonic Neoplasms

Colon Cancer

Colon Carcinoma Nos

Colonic Cancer

Metastatic Colon Cancer Nos

Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1

Eec Syndrome

Rudiger Syndrome 1

Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip-Palate Syndrome 1

EEC1

Eec Syndrome 1

Eec Syndrome-1

Walker-Clodius Syndrome

Ectrodactyly-Ectodermal Dysplasia-Cleft Lip/Palate Syndrome

Eec

Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip-Palate Syndrome

Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome

Ectrodactyly-Cleft Lip/Palate Syndrome

Ectrodactyly-Ectodermal Dysplasia-Cleft Lip/Cleft Palate

Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome

Ectrodactyly, Ectodermal Dysplasia, Clefting Syndrome

Ectrodactyly-Cleft Lip-Palate Syndrome

Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome

Intestinal Benign Neoplasm

Intestinal Neoplasms

Intestinal Tumors

Intestine Growth

Neoplasm Of Intestinal Tract

Hepatocellular Carcinoma

Liver Cancer

Primary Liver Cancer

HCC

Hepatoma

Malignant Neoplasm Of Liver

Liver Neoplasms

Cancer, Hepatocellular

Liver Cell Carcinoma

Lcc

Hepatoblastoma, Somatic

Hepatic Cancer

Primary Malignant Neoplasm Of Liver

Rare Tumor Of Liver And Intrahepatic Biliary Tract

Hepatocellular Carcinoma, Somatic

Hepatocellular Carcinoma, Childhood Type, Somatic

Hepatocellular Cancer, Somatic

Ca Liver - Primary

Hepatic Neoplasm

Malignant Hepato-Biliary Neoplasm

Malignant Neoplasm Of Liver, Not Specified As Primary Or Secondary

Malignant Neoplasm Of Liver, Primary

Malignant Tumor Of Liver

Neoplasm Of Liver

Non-Resectable Primary Hepatic Malignant Neoplasm

Resectable Malignant Neoplasm Of Liver

Resectable Malignant Neoplasm Of The Liver

Primary Liver Carcinoma

Primary Malignant Liver Neoplasm

Primary Cancer Of Liver

Primary Tumor Of The Liver

Rare Tumor Of Liver And Ibt

Hepatocellular Cancer

Neoplasm Of The Liver

Carcinoma, Hepatocellular

Hepatomas

Liver Neoplasm

Liver Carcinoma

Liver And Intrahepatic Biliary Tract Carcinoma

Malignant Hepatobiliary Neoplasm

Adult Primary Hepatocellular Carcinoma

Hepatoblastoma

Carcinoma Of Liver

Malignant Liver Tumour

Malignant Hepatic Tumour

Non-Syndromic X-Linked Intellectual Disability 107

Mrx107

X-Linked Mental Retardation 107

Chemical Colitis
Lymphangioma

Lymphatic Malformation

Lymphatic Malformations

Benign Lymphangioma

Congenital Lymphangioma

Lymphangiomas

Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome

ACOGS

Gastrointestinal System Benign Neoplasm
Perinatal Necrotizing Enterocolitis

Necrotizing Enterocolitis

Enterocolitis Necrotizing

Enterocolitis, Necrotizing

Necrotizing Enterocolitis In Fetus Or Newborn

Perinatal Necrotising Enterocolitis

Pseudomembranous Enterocolitis In Newborn

Nec

Corneal Dystrophy, Posterior Polymorphous, 4

PPCD4

Posterior Polymorphous Corneal Dystrophy 4

Colorectal Cancer

Colon Cancer

Colorectal Carcinoma

Colon Carcinoma

Colorectal Cancer, Susceptibility To

Carcinoma Of Colon

CRC

Colorectal Cancer With Chromosomal Instability, Somatic

Colon Cancer, Somatic

Colon Cancer, Susceptibility To

Colonic Neoplasms

Colorectal Neoplasms

Colorectal Cancer, Somatic

Colon Cancer, Advanced, Somatic

Colonic Carcinoma

Colorectal Carcinomas

Colon Cancers

Colorectal Cancers

Cancer, Colorectal, Somatic

Cancer, Colon

Cancer, Colorectal, Susceptibility To

Colorectal Neoplasm

Colonic Neoplasm

Malignant Tumor Of Colon

Immunodeficiency 58

IMD58

Severe Combined Immunodeficiency Due To Carmil2 Deficiency

Combined Immunodeficiency Due To Carmil2 Deficiency

Combined Immunodeficiency Due To Rltpr Deficiency

Ectodermal Dysplasia 14, Hair/Tooth Type With Or Without Hypohidrosis

ECTD14

Ectodermal Dysplasia 14

Ectn14

Deafness, Autosomal Recessive 98

DFNB98

Autosomal Recessive Nonsyndromic Deafness 98

Autosomal Recessive Deafness 98

Deafness, Autosomal Recessive, 98

Deafness, Autosomal Recessive, Type 98

Retinitis Pigmentosa 11

RP11

Retinitis Pigmentosa-11

Retinitis Pigmentosa, Type 11

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

Congenital Nervous System Abnormality

Congenital Neurologic Anomaly

Congenital Nervous System Disorder

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 LGR5 MGD MGI:1341817
Macaca mulatta LGR5 VGNC VGNC:74181
Felis catus LGR5 VGNC VGNC:67431
Bos taurus LGR5 VGNC VGNC:30862
Rattus norvegicus LGR5 RGD RGD:1307733
Others LGR5 NCBI