DiseaseInfo Viewer : HIX0006611
| Transcripts | HIT000013457 HIT000040375 HIT000051430 HIT000052239 HIT000066724 HIT000071588 HIT000089438 HIT000092147 HIT000095525 HIT000194211 HIT000194476 HIT000195131_03 HIT000195132 HIT000195393 HIT000215938 HIT000260652 HIT000264559 HIT000264832 HIT000264841 HIT000284373 :
(show all transcripts) |
|---|---|
| UCSC Genome browser | chr7:38279180-38403119 |
| G-integra | chr7:38279180-38403119 |
| Map position | 7p14.1 |
| Symbol | TRGC2 |
| OMIM | NA |
| Disease name | NA |
| MutationView | - |
Orphan diseases co-localized with HIX0006611
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 | HHT4 | 610655 | 791087 | 35551 | 7p14 | 303 | Telangiectasia, hereditary hemorrhagic, type 4 | OMIM |
| 2 | DFNB44 | 610154 | 449484 | 34816 | 7p141-q1122 | 714 | deafness, autosomal recessive 44 | OMIM |
| 3 | 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 $