DiseaseInfo Viewer : HIX0167689
| Transcripts | HIT000503383 HIT000503540 |
|---|---|
| UCSC Genome browser | chr7:123670970-123673523 |
| G-integra | chr7:123670970-123673523 |
| Map position | 7q31.32 |
| Symbol | - |
| OMIM | NA |
| Disease name | NA |
| MutationView | - |
Orphan diseases co-localized with HIX0167689
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 | STQTL2 | 606256 | 192143 | - | 7q313 | 159 | stature quantitative trait locus 2 | OMIM |
| 2 | DFNB17 | 603010 | 1709 | 29488 | 7q31 | 270 | deafness, autosomal recessive 17 | OMIM |
| 3 | SCA18 | 607458 | 94008 | 34535 | 7q31-q32 | 396 | spinocerebellar ataxia 18 (sensory with neurogenic muscular atrophy) | OMIM |
| 4 | NM | 162820 | 4827 | - | 7q22-qter | 1233 | neutrophil migration | OMIM |
| 5 | HRX | 145290 | 7974 | - | 7q | 1856 | Hyperreflexia | OMIM |
| 6 | LGMD1D | 603511 | 9186 | 31058 | 7q | 1856 | limb girdle muscular dystrophy 1D (autosomal dominant) | OMIM |
| 7 | 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 $