LECT2 - leukocyte cell derived chemotaxin 2 Gene

Also Known as chm2; chm-II

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 3950

About LECT2

Cytogenetic location: 5q31.1 Genomic coordinates (GRCh38): 5:135,946,904-135,954,983 (from NCBI)

This gene has 5 transcripts (splice variants) and 213 orthologues. Restricted expression toward liver (RPKM 110.6).

Summary

This gene encodes a secreted, 16 kDa protein that acts as a chemotactic factor to neutrophils and stimulates the growth of chondrocytes and osteoblasts. This protein has high sequence similarity to the chondromodulin repeat regions of the chicken myb-induced myeloid 1 protein. A polymorphism in this gene may be associated with rheumatoid arthritis. [provided by RefSeq, Jul 2008]

LECT2 Products (1)

mRNA Protein Name
NM_002302.3 NP_002293.2 leukocyte cell-derived chemotaxin-2 precursor
Molecular Function GO Annotation Evidence References Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
23352894 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
27334921 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

LECT2 Protein Structure

Peptidase_M23

Peptidase_M23: Peptidase family M23 (51 - 140)

  • 0
  • 100
  • 151 a.a.
Protein Preferred Names Protein Names

leukocyte cell-derived chemotaxin-2

  • chondromodulin-II

LECT2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
LECT2 O14960 WDR26 Homo sapiens Q9H7D7 33961781
Intra
LECT2 O14960 ITIH2 Homo sapiens P19823 33961781
Intra
LECT2 O14960 LRP2 Homo sapiens P98164 33961781
Intra
LECT2 O14960 GID4 Homo sapiens Q8IVV7 33961781
Intra
LECT2 O14960 LECT2 Homo sapiens O14960 23352894
Intra
LECT2 O14960 RNF123 Homo sapiens Q5XPI4 33961781
Intra
LECT2 O14960 GID8 Homo sapiens Q9NWU2 33961781
Intra
LECT2 O14960 THUMPD3 Homo sapiens Q9BV44 33961781
Intra
LECT2 O14960 UBAC1 Homo sapiens Q9BSL1 33961781
Intra
LECT2 O14960 RANBP10 Homo sapiens Q6VN20 33961781
Intra
LECT2 O14960 ARMC8 Homo sapiens Q8IUR7 33961781
Intra
LECT2 O14960 NPM1 Homo sapiens P06748 30021884
Intra
LECT2 O14960 RANBP9 Homo sapiens Q96S59 33961781
Intra
LECT2 O14960 CSPG4 Homo sapiens Q6UVK1 33961781
Intra
LECT2 O14960 AKAP11 Homo sapiens Q9UKA4 33961781
Intra
LECT2 O14960 KIAA0232 Homo sapiens Q92628 33961781
Intra
LECT2 O14960 FREM2 Homo sapiens Q5SZK8 33961781
Intra
LECT2 O14960 MKLN1 Homo sapiens Q9UL63 33961781
Intra
LECT2 O14960 RSL1D1 Homo sapiens O76021 30021884
Intra
LECT2 O14960 RMND5A Homo sapiens Q9H871 33961781
Intra
LECT2 O14960 MAEA Homo sapiens Q7L5Y9 33961781
Intra
LECT2 O14960 DICER1 Homo sapiens Q9UPY3 33961781
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Amyloidosis, Familial Visceral
  • Ostertag Type Amyloidosis

  • German Type Amyloidosis

  • Familial Renal Amyloidosis

  • Amyloidosis Viii

  • Amyloidosis, 3 Or More Types

  • Familial Visceral Amyloidosis

  • Familial Amyloid Nephropathy

  • Hereditary Amyloid Nephropathy

  • Amyloidosis, Familial Renal

  • Amyloidosis, Systemic Nonneuropathic

  • Amyloidosis Familial Visceral

  • Amyloidosis 8

  • Amyloidosis, Ostertag Type

  • Hereditary Amyloidosis With Primary Renal Involvement

  • Hereditary Renal Amyloidosis

  • Renal Amyloidosis

  • Amyloidosis, Renal

  • Systemic Nonneuropathic Amyloidosis

  • Amyloidosis Familial Renal

  • Amyloidosis Systemic Nonneuropathic

  • Hereditary Amyloidosis With Primary Renal Involement

  • AMYL8

  • Systemic Non-Neuropathic Amyloidosis

  • Amyloid Nephropathy

Immunoglobulin Heavy Chain Amyloidosis
  • Ah Amyloidosis

  • Heavy Chain Amyloidosis

  • Amyloidosis Derived From Immunoglobulin Heavy Chain

  • Ig Heavy-Chain-Associated Amyloidosis

Amyloidosis
  • Amyloid Disease

  • Amyloid

  • Amyloid Degeneration

  • Amyloidosis Nos

  • Amyloid Deposition

  • Amyloid Infiltration

  • Idiopathic Amyloidosis

  • Hyaloid Degeneration

  • Lardaceous Degeneration

Immunoglobulin Light Chain Amyloidosis
  • Al Amyloidosis

  • Primary Amyloidosis

  • Primary Systemic Amyloidosis

  • Light Chain Amyloidosis

  • Amyloidosis Al

  • Amyloidosis Primary Systemic

  • Primary Al Amyloidosis

  • Primary Systemic Al Amyloidosis

  • Systemic Al Amyloidsis

  • Systemic Al Amyloidosis

  • Light-Chain Amyloidosis

  • Alys Amyloidosis

  • Familial Amyloid Nephropathy Due To Lysozyme Variant

  • Familial Renal Amyloidosis Due To Lysozyme Variant

  • Hereditary Amyloid Nephropathy Due To Lysozyme Variant

  • Hereditary Renal Amyloidosis Due To Lysozyme Variant

  • Lysozyme Amyloidosis

  • Amyloidosis Primary

  • Immunoglobulin Deposition Disease

  • Immunoglobulinic Amyloidosis

  • Amyloid Al

Amyloidosis, Finnish Type
  • Finnish Type Amyloidosis

  • Meretoja Syndrome

  • Amyloidosis V

  • Amyloidosis, Meretoja Type

  • Amyloid Cranial Neuropathy With Lattice Corneal Dystrophy

  • Lattice Corneal Dystrophy Type Ii

  • Familial Amyloidosis, Finnish Type

  • Familial Amyloid Polyneuropathy Type Iv

  • Amyloidosis Due To Mutant Gelsolin

  • Agel Amyloidosis

  • Gelsolin Amyloidosis

  • Hereditary Gelsolin Amyloidosis

  • Lattice Corneal Dystrophy Type Ii Finnish

  • Gelsolin-Related Amyloidosis

  • Kymenlaakso Syndrome

  • Lattice Corneal Dystrophy, Gelsolin Type

  • Hereditary Amyloidosis, Finnish Type

  • Lattice Corneal Dystrophy Type 2

  • Amyloidosis 5

  • AMYL5

  • Agel

  • Familial Amyloidosis Finnish Type

  • Meretoja Type Amyloidosis

  • Type Iv Familial Amyloid Polyneuropathy

  • Familial Amyloid Polyneuropathy, Type V

  • Familial Amyloid Polyneuropathy, Type Iv

Rheumatoid Arthritis
  • RA

  • Arthritis, Rheumatoid

  • Rheumatoid Arthritis, Susceptibility To

  • Arthritis Or Polyarthritis, Rheumatic

  • Atrophic Arthritis

  • Rheumatism Arthritis

  • Rheumatoid Polyarthritis

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

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
Bos taurus LECT2 VGNC VGNC:30832
Macaca mulatta LECT2 VGNC VGNC:74250
Canis familiaris LECT2 VGNC VGNC:42629
Mus musculus LECT2 MGD MGI:1278342
Rattus norvegicus LECT2 RGD RGD:1305404
Felis catus LECT2 VGNC VGNC:68033
Others LECT2 NCBI