DiseaseInfo Viewer : HIX0033594
| Transcripts | HIT000040860 HIT000084251 HIT000261540 HIT000273421 HIT000275874 |
|---|---|
| UCSC Genome browser | chr7:73082174-73086442 |
| G-integra | chr7:73082174-73086442 |
| Map position | 7q11.23 |
| Symbol | WBSCR24 |
| OMIM | NA |
| Disease name | NA |
| MutationView | - |
Orphan diseases co-localized with HIX0033594
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 | ANIB1 | 105800 | 116833 | 34039 | 7q112 | 403 | aneurysm, intracranial berry 1 | OMIM |
| 2 | ANIB1 | 105800 | 116833 | 35332 | 7q112 | 403 | aneurysm, intracranial berry 1 | OMIM |
| 3 | ISS | - | - | 27548 | 7q112 | 403 | infantile spasms syndrome,with hysarrhythmia,mental retardation,associated in a family with a deletion in the Williams-Beuren critical region (WBS1) | GenAtlas |
| 4 | DFNB44 | 610154 | 449484 | 34816 | 7p141-q1122 | 714 | deafness, autosomal recessive 44 | OMIM |
| 5 | EEC1 | 129900 | 1913 | - | 7q112-q213 | 673 | ectrodactyly, ectodermal dysplasia and cleft lip/palate syndrome 1 | OMIM |
| 6 | CLAM | 608027 | 373073 | 34861 | 7q11-q21 | 673 | cerebellar atrophy with progressive microcephaly | OMIM |
| 7 | HPC4 | 608658 | 408260 | 34644 | 7p11-q21 | 823 | Prostate cancer, hereditary, 4 | OMIM |
| 8 | HRX | 145290 | 7974 | - | 7q | 1856 | Hyperreflexia | OMIM |
| 9 | LGMD1D | 603511 | 9186 | 31058 | 7q | 1856 | limb girdle muscular dystrophy 1D (autosomal dominant) | OMIM |
| 10 | 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 $