| Primary information |
|---|
| Humcfs Id | Humcfs_1675 |
| chromosome_number | chromosome6 |
| name | FRA6D |
| chrlocation | 70000001-75900000 |
| cytoband | 6q13 |
| type | BrdU |
| frequency | Common |
| gene_ensembl_id | ENSG00000185760 |
| gene_name | KCNQ5 |
| havana_transcript_id | OTTHUMT00000484423 |
| gene_location | 72622172-73195454 |
| gene_orientation | + |
| exon_id | ENSE00003770362, ENSE00001303421, ENSE00001297383, ENSE00001315454, ENSE00001295584, ENSE00002021875, ENSE00002099238, ENSE00001326399, ENSE00001376844, ENSE00001303940, ENSE00001315237, ENSE000013048 |
| exon_number | 13 |
| gene_description | potassium channel, voltage gated KQT-like subfamily Q, member 5 |
| disease_description | Myopia,Craniosynostosis,Irritable Bowel Syndrome,Epilepsy,Diarrhea,Tobacco Use Disorder,Schizophrenia,Refractive Errors,Bladder outflow obstruction,Periodontitis |
| miRNA_location | 71403595-71403616 |
| miRNA_strand | - |
| miRNA_id | MIMAT0000087 |
| miRNA_name | hsa-miR-30a-5p |
| miRNA_derived | MI0000088 |
| Technique | Karyotyping |
| PMID | 2579891 |
| Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |