This gene represents a nuclear retinoic acid receptor. The encoded protein, retinoic acid receptor alpha, regulates transcription in a ligand-dependent manner. This gene has been implicated in regulation of development, differentiation, apoptosis, granulopoeisis, and transcription of clock genes. Translocations between this locus and several other loci have been associated with acute promyelocytic leukemia. Alternatively spliced transcript variants have been found for this locus.[provided by RefSeq, Sep 2010]
Subcellular localization of RARA (and its protein):
Gene Ontology (GO) terms for RARA:
| Interacting Gene | Interaction | Source/Score |
| Name |
|---|
| 5200 Pathways in cancer [PATH:hsa05200] |
| 5202 Transcriptional misregulation in cancers [PATH:hsa05202] |
| 5221 Acute myeloid leukemia [PATH:hsa05221] |
| Name |
|---|
| Gene Expression |
| Generic Transcription Pathway |
| Nuclear Receptor transcription pathway |
| Signaling by Retinoic Acid |
| Disease | Score | NofPmids | NofSnps | Source |
| Acute Promyelocytic Leukemia | 0.347243502 | 399 | 1 | BeFree_CTD_human_LHGDN_ORPHANET |
| Mammary Neoplasms | 0.127077352 | 9 | 0 | BeFree_CTD_human_LHGDN |
| Liver carcinoma | 0.121085767 | 5 | 0 | BeFree_CTD_human |
| Phyllodes Tumor | 0.12 | 1 | 0 | CTD_human |
| Neoplasms, Second Primary | 0.12 | 1 | 0 | CTD_human |
| Sciatic Neuropathy | 0.12 | 1 | 0 | CTD_human |
| Fibroadenoma | 0.12 | 1 | 0 | CTD_human |
| Amyotrophic Lateral Sclerosis | 0.08 | 1 | 0 | RGD |
| Promyelocytic leukemia | 0.025244094 | 93 | 0 | BeFree |
| leukemia | 0.020397866 | 39 | 0 | BeFree_LHGDN |
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