DiseaseInfo Viewer : HIX0001613
| Transcripts | HIT000008396 HIT000008780 HIT000009763 HIT000021381 HIT000042420 HIT000053091 HIT000092439 HIT000193168 HIT000253135 HIT000291200 HIT000293177 HIT000342042 HIT000423132 HIT000426278 HIT000491336 |
|---|---|
| UCSC Genome browser | chr1:222791444-222856105 |
| G-integra | chr1:222791444-222856105 |
| Map position | 1q41 |
| Symbol | UNQ6077 |
| OMIM | NA |
| Disease name | NA |
| MutationView | - |
Orphan diseases co-localized with HIX0001613
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 | RMD1 | 600332 | 6022 | 5148 | 1q41 | 183 | rippling muscle disease 1 | OMIM |
| 2 | GUK2 | 139280 | 2988 | - | 1q321-q42 | 911 | guanylate kinase 2 | OMIM |
This database and viewer were originally developed by Dr. Boris Lenhard at Karolinska Institute.
$Revision: 1.58.2.9.2.46 $