DiseaseInfo Viewer : HIX0021590
| Transcripts | HIT000006868 HIT000008007 HIT000037826 HIT000041201 HIT000085086 HIT000241990 HIT000276533 HIT000280142 HIT000283422 HIT000300698 HIT000338855 HIT000422402 |
|---|---|
| UCSC Genome browser | chr1:245912644-246670620 |
| G-integra | chr1:245912644-246670620 |
| Map position | 1q44 |
| Symbol | SMYD3 |
| OMIM | NA |
| Disease name | NA |
| MutationView | - |
Orphan diseases co-localized with HIX0021590
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 | DFNB45 | 612433 | 449483 | - | 1q43-q44 | 285 | deafness, autosomal recessive 45 | OMIM |
This database and viewer were originally developed by Dr. Boris Lenhard at Karolinska Institute.
$Revision: 1.58.2.9.2.46 $