DiseaseInfo Viewer : HIX0056681
| Transcripts | HIT000077727 |
|---|---|
| UCSC Genome browser | chrY:23745486-23756552 |
| G-integra | chrY:23745486-23756552 |
| Map position | Yq11.223 |
| Symbol | TTTY13 |
| OMIM | NA |
| Disease name | NA |
| MutationView | - |
Orphan diseases co-localized with HIX0056681
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 | GCY | 475000 | 2656 | 22589 | Yq11 | 175 | growth control, Y chromosome influenced | OMIM |
| 2 | HEY | 425500 | 100188776 | - | Yq | 177 | unknown | OMIM |
This database and viewer were originally developed by Dr. Boris Lenhard at Karolinska Institute.
$Revision: 1.58.2.9.2.46 $