DiseaseInfo Viewer : HIX0005509
| Transcripts | HIT000020521 HIT000029437 HIT000029557 HIT000034815 HIT000036604 HIT000036857 HIT000037922 HIT000038545 HIT000038660 HIT000039335 HIT000041407 HIT000044050 HIT000091997 HIT000093916 HIT000101227 HIT000194920 HIT000251907 HIT000267828 HIT000268779 HIT000269209 :
(show all transcripts) |
|---|---|
| UCSC Genome browser | chr5:180663909-180670924 |
| G-integra | chr5:180663909-180670924 |
| Map position | 5q35.3 |
| Symbol | GNB2L1 |
| OMIM | NA |
| Disease name | NA |
| MutationView | - |
Orphan diseases co-localized with HIX0005509
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 | AMCN | 208100 | 261 | 26551 | 5q35 | 314 | arthrogryposis multiplex congenita, neurogenic | OMIM |
| 2 | CHR | 118840 | 1125 | - | 5q35 | 314 | chromate resistance; sulfate transport | OMIM |
| 3 | BSZQTL2 | 609657 | 100188794 | - | 5q | 1598 | Bone size QTL | OMIM |
| 4 | GLC1M | 610535 | 777643 | - | 5q | 1598 | glaucoma 1, open angle, M (juvenile-onset) | OMIM |
| 5 | MPD2 | 606070 | 89879 | 30938 | 5q | 1598 | myopathy, distal 2 | OMIM |
This database and viewer were originally developed by Dr. Boris Lenhard at Karolinska Institute.
$Revision: 1.58.2.9.2.46 $