1. Gene
  2. CSPG4 - chondroitin sulfate proteoglycan 4 Gene

CSPG4 - chondroitin sulfate proteoglycan 4 Gene

Homo sapiens

Also known as NG2; MCSP; MCSPG; MSK16; CSPG4A; HMW-MAA; MEL-CSPG

Gene ID: 1464 | Gene type: protein coding

About CSPG4

Cytogenetic location: 15q24.2 Genomic coordinates (GRCh38): 15:75,674,322-75,713,466 (from NCBI)

This gene has 1 transcript (splice variant) and 193 orthologues. Broad expression in fat (RPKM 18.8), placenta (RPKM 10.9) and 19 other tissues.

Summary

A human melanoma-associated chondroitin sulfate proteoglycan plays a role in stabilizing cell-substratum interactions during early events of melanoma cell spreading on endothelial basement membranes. CSPG4 represents an integral membrane chondroitin sulfate proteoglycan expressed by human malignant melanoma cells. [provided by RefSeq, Jul 2008]

CSPG4 Products(1)

mRNA Protein Name
NM_001897.5 NP_001888.2 chondroitin sulfate proteoglycan 4 precursor

CSPG4 Protein Structure

Laminin_G_1

Laminin_G_1: Laminin G domain (55 - 180)

Laminin_G_2

Laminin_G_2: Laminin G domain (231 - 363)

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  • 2322 a.a.
Protein Preferred Names Protein Names

chondroitin sulfate proteoglycan 4

chondroitin sulfate proteoglycan 4 (melanoma-associated)

Related Diseases

Diseases Alias
Melanoma

Malignant Melanoma

Cutaneous Melanoma

Naevocarcinoma

Malignant Melanomas

Demyelinating Disease

Demyelinating Diseases

Demyelinating Disorder

Chordoma

CHDM

Notochordoma

Notochordal Sarcoma

Chordoma, Susceptibility To

Chordocarcinoma

Chordoepithelioma

Acral Lentiginous Melanoma

Acral Lentiginous Melanoma, Malignant

Malignant Acral Lentiginous Melanoma

Alm

Acral Lentiginous Malignant Melanoma Of Skin

Palmar/Plantar Melanoma

Subungual Melanoma

Acral Lentiginous Malignant Melanoma

Ullrich Congenital Muscular Dystrophy 1

Ullrich Congenital Muscular Dystrophy

Ullrich Disease

Ucmd

Ullrich Scleroatonic Muscular Dystrophy

Scleroatonic Muscular Dystrophy

UCMD1

Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 22

Lgmdr22

Muscular Dystrophy, Scleroatonic

Late Onset Scleroatonic Familial Myopathy

Congenital Muscular Dystrophy, Ullrich Type

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 CSPG4 RGD RGD:619942
Mus musculus CSPG4 MGD MGI:2153093
Bos taurus CSPG4 VGNC VGNC:57158
Felis catus CSPG4 VGNC VGNC:61227
Macaca mulatta CSPG4 VGNC VGNC:71525
Canis familiaris CSPG4 VGNC VGNC:59107
Macaca fascicularis CSPG4 NCBI
Others CSPG4 NCBI