LRG1 - leucine rich alpha-2-glycoprotein 1 Gene

Also Known as LRG; HMFT1766

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 116844

About LRG1

Cytogenetic location: 19p13.3 Genomic coordinates (GRCh38): 19:4,536,402-4,540,036 (from NCBI)

This gene has 2 transcripts (splice variants), 289 orthologues and 22 paralogues. Biased expression in liver (RPKM 150.7), esophagus (RPKM 16.6) and 4 other tissues.

Summary

The leucine-rich repeat (LRR) family of proteins, including LRG1, have been shown to be involved in protein-protein interaction, signal transduction, and cell adhesion and development. LRG1 is expressed during granulocyte differentiation (O'Donnell et al., 2002 [PubMed 12223515]).[supplied by OMIM, Mar 2008]

LRG1 Products (1)

mRNA Protein Name
NM_052972.3 NP_443204.1 leucine-rich alpha-2-glycoprotein precursor
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
23868260 GOA
enables type I transforming growth factor beta receptor binding IPI
IPI: Inferred from physical interaction
23868260 GOA
enables type II transforming growth factor beta receptor binding IPI
IPI: Inferred from physical interaction
23868260 GOA
Cellular Component GO Annotation Evidence References Source
located in extracellular space IDA
IDA: Inferred from direct assay
20363744 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

LRG1 Protein Structure

LRR_1

LRR_1: Leucine Rich Repeat (93 - 111)

LRR_8

LRR_8: Leucine rich repeat (116 - 176)

LRR_1

LRR_1: Leucine Rich Repeat (190 - 208)

LRR_8

LRR_8: Leucine rich repeat (213 - 272)

  • 0
  • 100
  • 200
  • 300
  • 347 a.a.
Protein Preferred Names Protein Names

leucine-rich alpha-2-glycoprotein

  • 1300008B03Rik

LRG1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
LRG1 P02750 ENG Homo sapiens P17813-1 23868260
Intra
LRG1 P02750 ENG Homo sapiens P17813-1
SPR
23868260
Intra
LRG1 P02750 TGFBR2 Homo sapiens P37173-2 23868260
Intra
LRG1 P02750 TGFBR1 Homo sapiens P36897-1 23868260
Intra
LRG1 P02750 CYCS Homo sapiens P99999 33961781
Intra
LRG1 P02750 CYCS Homo sapiens P99999 28514442
Intra
LRG1 P02750 ACVRL1 Homo sapiens P37023 23868260
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant LRG1 Proteins

Cat. No. Product Name Accession Purity
HY-P70166 LRG1 Protein, Human (HEK293, His) AAH34389.1 (V36-Q347) ≥ 95%, as determined by reducing SDS-PAGE.
HY-P70175 LRG1 Protein, Human (HEK293, Fc-His) P02750/AAH70198.1 (V36-Q347) ≥ 95%, as determined by reducing SDS-PAGE.

LRG1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P82042 LRG1 Antibody (YA1787) WB, IHC-P, IP Human

Related Diseases

Diseases Alias
Appendicitis
  • Acute Appendicitis

  • Acute Appendicitis With Generalized Peritonitis

  • Acute Appendicitis Nos

  • Acute Appendicitis With Peritoneal Abscess

  • Appendiceal Inflammation

  • Appendicitis, Unqualified

  • Acute Appendix Inflammation

  • Acute Appendicitis With Diffuse Peritonitis Following Rupture Or Perforation

  • Acute Appendicitis With Free Peritonitis

  • Acute Appendicitis With Free Perforation To The Abdominal Cavity

  • Perforated Appendix With Generalised Peritonitis

  • Appendicitis With Perforation And Free Pus In The Peritoneal Cavity

  • Perforated Appendix With Localised Peritonitis

  • Acute Appendicitis With Contained Perforation To A Localised Abscess

  • Acute Appendicitis With Localised Peritonitis With Rupture Or Perforation

  • Acute Appendicitis With Localised Peritonitis Without Rupture Or Perforation

  • Acute Appendicitis With Perforation And Contained Peritonitis Into An Abscess

  • Appendicitis With Abscess

  • Appendicitis With Peritoneal Abscess

  • Ruptured Appendix Nos

  • Acute Appendicitis With No Perforation Or Abscess And No Visible Pus

  • Acute Appendicitis With No Specification If Perforated Or Not

  • Acute Appendicitis With Phlegmone

Cecal Disease
  • Cecal Diseases

  • Disorder Of Cecum

Communicating Hydrocephalus
  • Acquired Communicating Hydrocephalus

Hydrocephalus
  • Hydrocephalus, Nonsyndromic, Autosomal Recessive

  • Hydrocephalus, X-Linked

  • Hydrocephalus Adverse Event

  • Hydrocephaly Nos

Normal Pressure Hydrocephalus
  • Low Pressure Hydrocephalus

  • Hydrocephalus Normal Pressure

  • Hydrocephalus, Normal Pressure

  • Normal Pressure Hydrocephalus Nos

  • Nph - [Normal Pressure Hydrocephalus]

  • Normal Pressure Hydrocephaly

Cardiomyopathy, Dilated, 1e
  • Left Ventricular Noncompaction 9

  • Left Ventricular Noncompaction 5

  • Dilated Cardiomyopathy 1e

  • Dilated Cardiomyopathy 1s

  • CMD1E

  • Cdcd2

  • Cardiomyopathy, Dilated, 1y

  • CMD1Y

  • Cardiomyopathy, Dilated, 1s

  • CMD1S

  • Dilated Cardiomyopathy 1y

  • Dilated Cardiomyopathy With Conduction Defect 2

  • Dilated Cardiomyopathy With Conduction Disorder And Arrhythmia

  • Cardiomyopathy, Dilated, With Conduction Disorder And Arrhythmia

  • Cardiomyopathy, Dilated, With Conduction Defect 2

  • Cardiomyopathy Dilated With Conduction Defect Type 2

  • Cardiomyopathy, Dilated 1e

  • Cardiomyopathy, Dilated 1s

  • Cardiomyopathy, Dilated 1y

  • Left Ventricular Non-Compaction 5

  • LVNC5

  • Left Ventricular Non-Compaction 9

  • LVNC9

  • Cardiomyopathy, Dilated, Type 1e

  • Cardiomyopathy, Dilated, Type 1s

  • Cardiomyopathy, Dilated, Type 1y

Cardiomyopathy, Familial Hypertrophic, 1
  • Asymmetric Septal Hypertrophy

  • Familial Hypertrophic Cardiomyopathy

  • Hypertrophic Cardiomyopathy 1

  • CMH1

  • Hypertrophic Cardiomyopathy 19

  • CMH

  • Ventricular Hypertrophy, Hereditary

  • Ash

  • Hypertrophic Subaortic Stenosis, Idiopathic

  • Cardiomyopathy, Familial Hypertrophic

  • Cardiomyopathy, Hypertrophic, 1, Digenic

  • Cardiomyopathy, Familial Hypertrophic 1

  • Hcm

  • Hereditary Ventricular Hypertrophy

  • Idiopathic Hypertrophic Subaortic Stenosis

  • Hypertrophic Cardiomyopathy

  • Cardiomyopathy, Hypertrophic, Familial

  • Cardiomyopathy, Hypertrophic, 1

  • Familial Asymmetric Septal Hypertrophy

  • Heritable Hypertrophic Cardiomyopathy

  • Fhc

  • Cardiomyopathy, Hypertrophic, Familial, Type 1

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
Rattus norvegicus LRG1 RGD RGD:1359464
Macaca mulatta LRG1 VGNC VGNC:74394
Bos taurus LRG1 VGNC VGNC:30980
Felis catus LRG1 VGNC VGNC:102630
Canis familiaris LRG1 VGNC VGNC:42765
Mus musculus LRG1 MGD MGI:1924155
Others LRG1 NCBI