Version: 8.0.0Date: Tue Jan 28 2025
Gene
MAGEE1
- Species
- Homo sapiens
- Symbol
- MAGEE1
- Name
- MAGE family member E1
- Synonyms
- alpha-dystrobrevin-associated MAGE Protein
- DAMAGE
- Biotype
- protein coding gene
- Automated Description
- Predicted to be involved in negative regulation of transcription by RNA polymerase II. Predicted to be located in dendrite; perinuclear region of cytoplasm; and postsynaptic membrane. Predicted to be active in nucleus.
- RGD Description
- This gene encodes an alpha-dystrobrevin-associated MAGE (melanoma-associated antigen) protein, which is a member of the MAGE family. The protein contains a nuclear localization signal in the N-terminus, 30 12-amino acid repeats beginning at nt 60 with the consensus sequence ASEGPSTSVLPT, and two MAGE domains in the C-terminus. It may play a signaling role in brain, muscle, and peripheral nerve. This gene is located on X chromosome in a region containing loci linked to cognitive disability. [provided by RefSeq, Mar 2010]
- Cross References
- Additional Information
- Literature
Orthology
- Gene tree
- PANTHER:PTHR11736
Links to orthology data in JBrowse by filter level: Stringent, Moderate, No filter, Best and Best Reverse
Disease Associations
Cases where the expected disease association was NOT found
Cell color indicative of annotation volume
Gene | Association | Disease Qualifier | Disease | Evidence | Source | Based On | References |
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Sequence Feature Viewer
- Genome location
- ChrX:76427710...76431342 + (3.63 kb)
- Assembly version
- GRCh38
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