Primary information |
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Humcfs Id | Humcfs_668 |
chromosome_number | chromosome2 |
name | FRA2A |
chrlocation | 96800001-102700000 |
cytoband | 2q11.2 |
type | Folic acid |
frequency | Rare |
gene_ensembl_id | ENST00000272602 |
gene_name | CNGA3 |
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 |