DiseaseInfo Viewer : HIX0002935
| Transcripts | HIT000004121 HIT000028283 HIT000036201 HIT000043967 HIT000249156 HIT000262545 HIT000266127 HIT000290559 HIT000303326 HIT000489736 HIT000492445 |
|---|---|
| UCSC Genome browser | chr2:234383739-234475428 |
| G-integra | chr2:234383739-234475428 |
| Map position | 2q37.1 |
| Symbol | USP40 |
| OMIM | NA |
| Disease name | NA |
| MutationView | - |
Orphan diseases co-localized with HIX0002935
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 | HPE6 | 605934 | 117190 | 35176 | 2q371 | 149 | holoprosencephaly 6 | OMIM |
| 2 | MYP12 | 609995 | 664780 | - | 2q371 | 149 | myopia 12 (high grade, autosomal dominant) | OMIM |
| 3 | BDMR | 600430 | 626 | 12271 | 2q37 | 347 | brachydactyly-mental retardation syndrome | OMIM |
| 4 | BDMR | 600430 | 626 | 31482 | 2q37 | 347 | brachydactyly-mental retardation syndrome | OMIM |
| 5 | BDMR | 600430 | 626 | 34564 | 2q37 | 347 | brachydactyly-mental retardation syndrome | OMIM |
| 6 | AUTS5 | 606053 | 94313 | 34014 | 2q | 2627 | Autism, susceptibility to, 5 | OMIM |
| 7 | 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 $