DiseaseInfo Viewer : HIX0028852
| Transcripts | HIT000326949 HIT000390117 HIT000426408 HIT000492861 HIT000500501 HIT000503499 |
|---|---|
| UCSC Genome browser | chr1:117544372-117579173 |
| G-integra | chr1:117544372-117579173 |
| Map position | 1p13.1 |
| Symbol | IGSF2 |
| OMIM | NA |
| Disease name | NA |
| MutationView | - |
Orphan diseases co-localized with HIX0028852
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 | VUR | 193000 | 54113 | 33673 | 1p13 | 306 | Vesicoureteral reflux | OMIM |
| 2 | SCA19 | 607346 | 140452 | 34273 | 1p21-q21 | 1112 | spinocerebellar ataxia 19 | OMIM |
| 3 | SCA19 | 607346 | 140452 | 34745 | 1p21-q21 | 1112 | spinocerebellar ataxia 19 | OMIM |
| 4 | ARCODS | 602483 | 100381211 | - | 1p211-q233 | 1315 | Ariculocondylar syndrome | OMIM |
| 5 | ANON | 606788 | 171514 | 34131 | 1p | 2813 | Anorexia nervosa, susceptibility to | OMIM |
| 6 | ANON | 606788 | 171514 | 34132 | 1p | 2813 | Anorexia nervosa, susceptibility to | OMIM |
| 7 | PARK10 | 606852 | 170534 | 34395 | 1p | 2813 | Parkinson disease 10 | OMIM |
| 8 | PSORS7 | 605606 | 65245 | 33842 | 1p | 2813 | psoriasis susceptibility 7 | OMIM |
| 9 | SCZD12 | 608543 | 619488 | - | 1p | 2813 | schizophrenia 12 | OMIM |
This database and viewer were originally developed by Dr. Boris Lenhard at Karolinska Institute.
$Revision: 1.58.2.9.2.46 $