DiseaseInfo Viewer : HIX0031484
| Transcripts | HIT000191212 HIT000270152 HIT000386063 HIT000398785 HIT000435328 |
|---|---|
| UCSC Genome browser | chr4:3768075-3770253 |
| G-integra | chr4:3768075-3770253 |
| Map position | 4p16.3 |
| Symbol | - |
| OMIM | NA |
| Disease name | NA |
| MutationView | 104250
(JRE version 1.4.0 or later is required.) |
Orphan diseases co-localized with HIX0031484
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 | LOC619409 | 609456 | 619409 | 34998 | 4p163 | 157 | muscular dystrophy, congenital, merosin-positive | OMIM |
| 2 | PLSA1 | 611637 | 100240702 | - | 4p16 | 355 | Primary lateral sclerosis, adult, 1 | OMIM |
| 3 | SLEB3 | 605480 | 64695 | 33890 | 4p16-p152 | 473 | systemic lupus erythematosus susceptibility 3 | OMIM |
| 4 | SLEB3 | 605480 | 64695 | 33969 | 4p16-p152 | 473 | systemic lupus erythematosus susceptibility 3 | OMIM |
| 5 | MNDEC | 611863 | 100188855 | - | 4p16-p15 | 492 | Microtia with nasolacrimal duct imperforation and eye coloboma | OMIM |
| 6 | SPG38 | 612335 | 100049707 | - | 4p16-p15 | 492 | spastic paraplegia 38 (autosomal dominant, Silver syndrome) | OMIM |
| 7 | MHW1 | 603663 | 10386 | 30953 | 4p | 653 | Mental health wellness 1 | OMIM |
| 8 | INTLQ1 | 603783 | 100462721 | - | 4p16-q34 | 1733 | Intelligence QTL1 | OMIM |
This database and viewer were originally developed by Dr. Boris Lenhard at Karolinska Institute.
$Revision: 1.58.2.9.2.46 $