MAGEC3
Melanoma-associated antigen C3
Also known as: CT7.2, HCA2, MAGC3_HUMAN, MAGE-C3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8TD91
- Gene
- MAGEC3
- Ensembl
- ENSG00000165509
- Chromosome
- X
- Canonical length
- 643 aa
- Protein class
- Cancer-related genes, Predicted intracellular proteins
OverviewNCBI Gene
This gene is a member of the MAGEC gene family. The members of this family are not expressed in normal tissues, except for testis, and are expressed in tumors of various histological types. The MAGEC genes are clustered on chromosome Xq26-q27. Two transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
643 residues, UniProt reviewed canonical sequence.
>Q8TD91|MAGEC3
1 MLLPCHWVLD ATFSDGSLGQ WVKNTCATYA LSPVVLPPQP QPRKKATDKD YSAFHLGHLR
61 EVRLFLRGGT SDQRMDSLVL CPTYFKLWRT LSGSPGLQLS DLHFGSQPEG KFSLRRAVSV
121 KQREEPQDWP LNEKRTLWKD SDLPTWRRGT GYTLSLPAVS PGKRLWGEKA GSLPESEPLF
181 TYTLDEKVDK LVQFLLLKYQ AKEPLTRAEM QMNVINTYTG YFPMIFRKAR EFIEILFGIS
241 LTEVDPDHFY VFVNTLDLTC EGSLSDEQGM PQNRLLILIL SVIFIKGNCA SEEVIWEVLN
301 AIGPWSALAG FADVLSRLAL WESEGPEAFC EESGLRSAEG SVLDLANPQG LAGHRQEDGR
361 RGLTEASPQQ KKGGEDEDMP AAGMPPLPQS PPEIPPQGPP KISPQGPPQS PPQSPLDSCS
421 SPLLWTRLDE ESSSEEEDTA TWHALPESES LPRYALDEKV AELVQFLLLK YQTKEPVTKA
481 EMLTTVIKKY KDYFPMIFGK AHEFIELIFG IALTDMDPDN HSYFFEDTLD LTYEGSLIDD
541 QGMPKNCLLI LILSMIFIKG SCVPEEVIWE VLSAIGPIQR PAREVLEFLS KLSSIIPSAF
601 PSWYMDALKD MEDRAQAIID TTDDATAMAS ASPSVMSTNF CPELocalizationUniProt · AlphaFold · HPA
Whether an antibody against MAGEC3 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.52
- Highest tissue expression
- 3.6 nTPM
Expression across tissuesHPA
Tissue
- spinal cord: 3.6 nTPM
- hippocampal formation: 2.4 nTPM
- blood vessel: 2 nTPM
- midbrain: 1.9 nTPM
- basal ganglia: 1.8 nTPM
- cerebral cortex: 1.5 nTPM
Single-cell type
- oligodendrocytes: 34 nCPM
- brain inhibitory neurons: 13 nCPM
- brain excitatory neurons: 13 nCPM
- undifferentiated spermatogonia: 12 nCPM
- somatotrophs: 11 nCPM
- adrenal medulla cells: 11 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- white matter: 8.7 nTPM
- cerebral cortex: 3.5 nTPM
- hypothalamus: 3.4 nTPM
- pons: 3 nTPM
- medulla oblongata: 2.8 nTPM
- basal ganglia: 2.6 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.72
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.95
- DepMap mean gene effect
- 0.11
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads MAGEC3 as an antibody target. Whether an autoantibody or antibody against MAGEC3 could matter depends on whether native MAGEC3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MAGEC3 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label MAGEC3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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