Detailed description page of humcfs
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Humcfs_1256 details |
| Primary information | |
|---|---|
| Humcfs Id | Humcfs_1256 |
| chromosome_number | chromosome3 |
| name | FRA3D |
| chrlocation | 148900001-160700000 |
| cytoband | 3p25 |
| type | Aphidicolin |
| frequency | Common |
| gene_ensembl_id | ENSG00000163646 |
| gene_name | CLRN1 |
| havana_transcript_id | OTTHUMT00000277060 |
| gene_location | 150926567-150972999 |
| gene_orientation | - |
| exon_id | ENSE00001342698, ENSE00003573924, ENSE00001230843 |
| exon_number | 3 |
| gene_description | clarin 1 |
| disease_description | Retinal Degeneration,Ear Diseases,Retinitis Pigmentosa,RETINITIS PIGMENTOSA 61,Usher Syndrome, Type III,Congenital cataract,Usher Syndrome,Hearing Loss, Mixed Conductive-Sensorineural,Autosomal recessive retinitis pigmentosa,Bilateral cataracts (disorder),Cataract |
| miRNA_location | NA |
| miRNA_strand | NA |
| miRNA_id | NA |
| miRNA_name | NA |
| miRNA_derived | NA |
| Technique | Karyotyping |
| PMID | 17567780 |
| Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |