| Primary information |
|---|
| Humcfs Id | Humcfs_4700 |
| chromosome_number | chromosome19 |
| name | FRA19B |
| chrlocation | 1-20000000 |
| cytoband | 19p13 |
| type | Folic acid |
| frequency | Rare |
| gene_ensembl_id | ENSG00000142303 |
| gene_name | ADAMTS10 |
| havana_transcript_id | OTTHUMT00000460202 |
| gene_location | 8580242-8592196 |
| gene_orientation | - |
| exon_id | ENSE00001316649, ENSE00003640808, ENSE00003515336, ENSE00003499041, ENSE00003560582, ENSE00003693258, ENSE00003642256, ENSE00003679958, ENSE00003597227, ENSE00003193876, ENSE00003642073, ENSE000036784 |
| exon_number | 13 |
| gene_description | ADAM metallopeptidase with thrombospondin type 1 motif, 10 |
| disease_description | Dermatitis, Atopic,Intraocular pressure disorder,Mental Depression,Aqueous Humor Disorders,Glaucoma,Glaucoma, Primary Open Angle,Weill-Marchesani syndrome,Schizophrenia,Depressive disorder,Delirium,Weill-Marchesani Syndrome, Autosomal Recessive,Microspherophakia |
| miRNA_location | NA |
| miRNA_strand | NA |
| miRNA_id | NA |
| miRNA_name | NA |
| miRNA_derived | NA |
| Technique | FISH |
| PMID | 3568428 |
| Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |