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Gene : MAGEA11 Homo sapiens

Name  ? MAGE family member A11 Cytological Location  Xq28
Brief Description  MAGE family member A11
description  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. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
  • synonyms:
  • uc004fdq.4,
  • CT1.11,
  • MAGEA11,
  • melanoma antigen family A11,
  • melanoma-associated antigen 11,
  • CT1.11,
  • OTTHUMG00000022633,
  • HGNC:6798,
  • MAGE-11,
  • MAGE11,
  • MAGE-11,
  • MAGEA-11,
  • NM_005366,
  • cancer/testis antigen family 1, member 11,
  • MAGE-11 antigen,
  • MGC10511,
  • MAGEA-11,
  • MAGE11
  • identifiers:
  • 4110,
  • ENSG00000185247,
  • MAGEA11

Genome feature

Region: gene ? Length: 29076  
Location: X:149688193-149717268 Cyto location: Xq28

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Orthologues


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

6 SN Ps

5 Cross References

14 Data Sets

65 Homologues

0 Located Features

97 Rna Seq Results