DiseaseInfo Viewer : HIX0019573
| Transcripts | HIT000011318 HIT000026379 HIT000026389 HIT000052316 HIT000087307 HIT000243735 HIT000266175 |
|---|---|
| UCSC Genome browser | chr7:192969-300711 |
| G-integra | chr7:192969-300711 |
| Map position | 7p22.3 |
| Symbol | FAM20C |
| OMIM | NA |
| Disease name | NA |
| MutationView | 611061
(JRE version 1.4.0 or later is required.) |
Orphan diseases co-localized with HIX0019573
The number of co-localized H-Inv loci was computed by converting each cytogenetic band into a physical range on the chromosome, with additional 1000000 bp added on each side.
| Symbol | OMIM phenotype | Entrez Gene | GenAtlas |
Cytogenetic band (Link to the latest human genome on UCSC Genome Browser) |
Number-of co-localized H-Inv loci (Click for list) | Description | Source | |
|---|---|---|---|---|---|---|---|---|
| 1 | FHA2 | 605635 | 79179 | 34476 | 7p22 | 231 | Hyperaldosteronism, familial, type II | OMIM |
| 2 | UD7PA | - | - | 19343 | 7 | 2979 | uniparental disomy,paternal,with cystic fibrosis,complete situs inversus,immotile cilia,including any cases of congenital chloride diarrhea | GenAtlas |
This database and viewer were originally developed by Dr. Boris Lenhard at Karolinska Institute.
$Revision: 1.58.2.9.2.46 $