| Primary information |
|---|
| gene_name | CNGA3 |
| Humcfs Id | Humcfs_668 |
| chromosome_number | chromosome2 |
| name | FRA2A |
| chrlocation | 96800001-102700000 |
| cytoband | 2q11.2 |
| type | Folic acid |
| frequency | Rare |
| gene_ensembl_id | ENST00000272602 |
| havana_transcript_id | OTTHUMT00000252986 |
| gene_location | 98369937-98398601 |
| gene_orientation | + |
| exon_id | ENSE00000963912, ENSE00003460052, ENSE00000963915, ENSE00000963916, ENSE00000963918, ENSE00000963919, ENSE00001472196 |
| exon_number | 7 |
| gene_description | cyclic nucleotide gated channel alpha 3 |
| disease_description | Photophobia,Retinal Degeneration,Cone dystrophy,Achromatopsia,Retinitis Pigmentosa,Retinal Diseases,Nystagmus,Alkaline Phosphatase Adverse Event,Achromatopsia 2,Retinal Dystrophies,Progressive cone-rod dystrophy,Achromatopsia 1,Color blindness,Color vision defect,Achromatopsia 3 |
| miRNA_location | 102432336-102432357 |
| miRNA_strand | + |
| miRNA_id | MIMAT0019927 |
| miRNA_name | hsa-miR-4772-3p |
| miRNA_derived | MI0017414 |
| Technique | Karyotyping |
| PMID | 20198338 |
| Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |