DiseaseInfo Viewer : HIX0002608
| Transcripts | HIT000004564 HIT000098375 |
|---|---|
| UCSC Genome browser | chr2:175411869-175639555 |
| G-integra | chr2:175411869-175639555 |
| Map position | 2q31.1 |
| Symbol | - |
| OMIM | NA |
| Disease name | NA |
| MutationView | - |
Orphan diseases co-localized with HIX0002608
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 | IDDM7 | 600321 | 3406 | 12477 | 2q31 | 278 | insulin-dependent diabetes mellitus 7 | OMIM |
| 2 | PNKD2 | 611147 | 100188328 | - | 2q31 | 278 | paroxysmal nonkinesigenic dyskinesia 2 | OMIM |
| 3 | SHFM5 | 606708 | 171157 | 12504 | 2q31 | 278 | split hand/foot malformation (ectrodactyly) type 5 | OMIM |
| 4 | INTLQ2 | 610295 | 100462723 | - | 2q241-q311 | 368 | Intelligence QTL3 | OMIM |
| 5 | RP26 | - | 23681 | 30396 | 2q31-q33 | 669 | retinitis pigmentosa 26,autosomal recessive | GenAtlas |
| 6 | FGQTL1 | 612108 | 100499165 | - | 2q24-q32 | 595 | Fasting plasma glucose level QTL 1 | OMIM |
| 7 | MMDK | 156232 | 10305 | 30148 | 2q24-q32 | 595 | Mesomelic dysplasia, Kantaputra type | OMIM |
| 8 | AUTS5 | 606053 | 94313 | 34014 | 2q | 2627 | Autism, susceptibility to, 5 | OMIM |
| 9 | COPD | 606963 | 260431 | - | 2q | 2627 | Pulmonary disease, chronic obstructive, severe early-onset | OMIM |
This database and viewer were originally developed by Dr. Boris Lenhard at Karolinska Institute.
$Revision: 1.58.2.9.2.46 $