1. Gene
  2. MRC2 - mannose receptor C type 2 Gene

MRC2 - mannose receptor C type 2 Gene

Homo sapiens

Also known as CD280; UPARAP; CLEC13E; ENDO180

Gene ID: 9902 | Gene type: protein coding

About MRC2

Cytogenetic location: 17q23.2 Genomic coordinates (GRCh38): 17:62,627,670-62,693,597 (from NCBI)

This gene has 7 transcripts (splice variants), 203 orthologues and 4 paralogues. Ubiquitous expression in gall bladder (RPKM 26.1), ovary (RPKM 24.7) and 24 other tissues.

Summary

This gene encodes a member of the Mannose Receptor family of proteins that contain a fibronectin type II domain and multiple C-type lectin-like domains. The encoded protein plays a role in extracellular matrix remodeling by mediating the internalization and lysosomal degradation of collagen ligands. Expression of this gene may play a role in the tumorigenesis and metastasis of several malignancies including breast Cancer, gliomas and metastatic bone disease. [provided by RefSeq, Feb 2012]

MRC2 Products(1)

mRNA Protein Name
NM_006039.5 NP_006030.2 C-type mannose receptor 2 precursor

MRC2 Protein Structure

fn2

fn2: Fibronectin type II domain (187 - 228)

Lectin_C

Lectin_C: Lectin C-type domain (256 - 361)

Lectin_C

Lectin_C: Lectin C-type domain (399 - 506)

Lectin_C

Lectin_C: Lectin C-type domain (539 - 645)

Lectin_C

Lectin_C: Lectin C-type domain (694 - 809)

Lectin_C

Lectin_C: Lectin C-type domain (844 - 952)

Lectin_C

Lectin_C: Lectin C-type domain (995 - 1109)

Lectin_C

Lectin_C: Lectin C-type domain (1143 - 1243)

Lectin_C

Lectin_C: Lectin C-type domain (1288 - 1394)

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  • 1479 a.a.
Protein Preferred Names Protein Names

C-type mannose receptor 2

C-type lectin domain family 13 member E

Recombinant MRC2 Proteins

Cat. No. Product Name Accession Purity
HY-P700875 MRC2 Protein, Human (HEK293, His) Q9UBG0 (G31-P530) ≥95%

Related Diseases

Diseases Alias
Bone Disease

Bone Diseases

Skeletal Disease

Skeletal Disorder

Disorder Of Skeletal System

Gliofibroma
Deafness, X-Linked 6

DFNX6

X-Linked Deafness 6

Deafness, X-Linked, 6

Deafness, X-Linked, Type 6

Breast Cancer

Breast Carcinoma

Male Breast Cancer

Breast Cancer, Familial

Malignant Neoplasm Of Breast

Breast Cancer, Susceptibility To

Breast Cancer, Early-Onset

Malignant Tumor Of Breast

Carcinoma Of Male Breast

Breast Cancer, Invasive Ductal

Breast Cancer, Protection Against

Breast Cancer, Somatic

Breast Cancer, Male

Breast Cancer, Lobular, Somatic

Breast Tumor

Mammary Cancer

Mammary Tumor

Malignant Neoplasm Of Male Breast

Mammary Carcinoma

Male Breast Carcinoma

Familial Cancer Of Breast

Invasive Ductal Breast Carcinoma

Breast Cancer Susceptibility

Breast Cancer, Male, Susceptibility To

Breast Cancer, Early-Onset, Susceptibility To

Malignant Tumor Of The Breast

Mammary Neoplasm

Primary Breast Cancer

Neoplasm Of Male Breast

Carcinoma Of Breast

Breast Cancer In Men

Familial Breast Cancer

Cancer Of Breast

BC

Breast Cancer Familial

Breast Cancer Familial Male

Breast Cancer, Familial Male

Breast Male Carcinoma

Breast Neoplasms

Breast Neoplasms, Male

Mammary Tumors

Mammary Carcinomas

Cancer, Breast

Cancer, Breast, Susceptibility

Invasive Breast Ductal Carcinoma

Breast Neoplasm

Susceptibility To Breast Cancer

Mammary Neoplasms

Animal Mammary Neoplasms

Primary Malignant Neoplasm Of Breast

Infiltrating Ductal Carcinoma Of Breast

Infiltrating Duct Carcinoma Of Unspecified Site

Infiltrating Ductular Carcinoma Of Unspecified Site

Invasive Breast Carcinoma Of No Special Type

Microinvasive Carcinoma Of Breast

Carcinoma With Apocrine Differentiation

Osteogenesis Imperfecta, Type Iii

Osteogenesis Imperfecta Type Iii

OI3

Oi, Type Iii

Osteogenesis Imperfecta Type 3

Oi Type Iii

Oi Type 3

Progressive Deforming Osteogenesis Imperfecta

Severe Osteogenesis Imperfecta

Osteogenesis Imperfecta, Progressively Deforming, With Normal Sclerae

Progressively Deforming Osteogenesis Imperfecta With Normal Sclera

Osteogenesis Imperfecta, Progressively Deforming With Normal Sclerae

Progressively Deforming Oi

Osteogenesis Imperfecta 3

Oi-Iii

Progressively Deforming Osteogenesis Imperfecta With Normal Sclerae

Cone-Rod Dystrophy 2

Cone-Rod Dystrophy

CORD2

Cone-Rod Retinal Dystrophy

Rcrd2

Cone-Rod Retinal Dystrophy 2

Crd2

Cord

Crd

Retinal Cone-Rod Dystrophy

Cone-Rod Retinal Dystrophy-2

Retinal Cone-Rod Dystrophy 2

Tapetoretinal Degeneration

Cone-Rod Degeneration

Cone Rod Dystrophy

Dystrophy, Cone-Rod

Dystrophy, Cone-Rod, Type 2

Retinitis Pigmentosa

Retinitis Pigmentosa 2

Progressive Cone-Rod Dystrophy

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
Canis familiaris MRC2 VGNC VGNC:43360
Felis catus MRC2 VGNC VGNC:63579
Rattus norvegicus MRC2 RGD RGD:1559436
Mus musculus MRC2 MGD MGI:107818
Bos taurus MRC2 VGNC VGNC:31599
Macaca mulatta MRC2 VGNC VGNC:74784
Others MRC2 NCBI