Gene
max
- ID
- ZDB-GENE-990415-152
- Name
- myc associated factor X
- Symbol
- max Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 20 Mapping Details/Browsers
- Description
- Contributes to transcription regulatory region DNA binding activity. Involved in determination of ventral identity and hemopoiesis. Localizes to SMAD protein complex. Human ortholog(s) of this gene implicated in lung small cell carcinoma and pheochromocytoma. Is expressed in central nervous system. Orthologous to human MAX (MYC associated factor X).
- Genome Resources
- Note
- None
- Comparative Information
- All Expression Data
- 8 figures from 8 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:55677 (1 image)
Wild Type Expression Summary
Phenotype Summary
Mutations
Human Disease
Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
---|---|---|---|
pheochromocytoma | Alliance | {Pheochromocytoma, susceptibility to} | 171300 |
Polydactyly-macrocephaly syndrome | 620712 |
Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Length | Helix-loop-helix DNA-binding domain superfamily | Myc-type, basic helix-loop-helix (bHLH) domain |
---|---|---|---|
UniProtKB:Q5SPG2
|
151 | ||
UniProtKB:P52161
|
165 | ||
UniProtKB:A0A8M2B7R2
|
165 | ||
UniProtKB:Q6NY29
|
160 | ||
UniProtKB:Q803J7
|
156 |
Interactions and Pathways
No data available
Plasmids