1. Gene
  2. MAGEA10 - MAGE family member A10 Gene

MAGEA10 - MAGE family member A10 Gene

Homo sapiens

Also known as CT1.10; MAGE10

Gene ID: 4109 | Gene type: protein coding

About MAGEA10

Cytogenetic location: Xq28 Genomic coordinates (GRCh38): X:152,133,310-152,138,577 (from NCBI)

This gene has 6 transcripts (splice variants), 208 orthologues and 37 paralogues. Biased expression in placenta (RPKM 4.9) and testis (RPKM 1.2).

Summary

This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream melanoma antigen family A, 5 (MAGEA5) gene.[provided by RefSeq, Oct 2011]

MAGEA10 Products(3)

mRNA Protein Name
NM_001011543.3 NP_001011543.3 melanoma-associated antigen 10
NM_001251828.2 NP_001238757.2 melanoma-associated antigen 10
NM_021048.5 NP_066386.3 melanoma-associated antigen 10

MAGEA10 Protein Structure

MAGE_N

MAGE_N: Melanoma associated antigen family N terminal (3 - 60)

MAGE_N

MAGE_N: Melanoma associated antigen family N terminal (58 - 119)

MAGE

MAGE: MAGE family (141 - 311)

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

melanoma-associated antigen 10

MAGE-10 antigen

Related Diseases

Diseases Alias
Melanoma

Malignant Melanoma

Cutaneous Melanoma

Naevocarcinoma

Malignant Melanomas

Dyskeratosis Congenita

Dyskeratosis Congenita Autosomal Dominant

Dc

Dkc

Zinsser-Engman-Cole Syndrome

Dyskeratosis Congenita, Autosomal Dominant

Autosomal Dominant Dyskeratosis Congenita

Dkca

Dyskeratosis Congenita Scoggins Type

Zinsser-Cole-Engman Syndrome

X-Linked Dyskeratosis Congenita

Hoyeraal-Hreidarsson Syndrome

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 MAGEA10 RGD RGD:1563693