DiseaseInfo Viewer : HIX0201992
| Transcripts | HIT000018099 HIT000021848 HIT000038977 HIT000066932 HIT000098447 |
|---|---|
| UCSC Genome browser | chr13:41371127-41495910 |
| G-integra | chr13:41371127-41495910 |
| Map position | 13q14.11 |
| Symbol | LOC283507 |
| OMIM | NA |
| Disease name | NA |
| MutationView | - |
Orphan diseases co-localized with HIX0201992
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 | AUTS3 | 608049 | 387577 | 34286 | 13q142-q141 | 232 | Autism, susceptibility to, 3 | OMIM |
| 2 | BMIQ2 | 606643 | 192149 | - | 13q14 | 285 | body mass index QTL 2 | OMIM |
| 3 | BMND9 | 612110 | 100188882 | - | 13q14 | 285 | Bone mineral density QTL 9 | OMIM |
| 4 | D13S25 | 109543 | 8101 | - | 13q14 | 285 | Disrupted in B-cell neoplasia | OMIM |
| 5 | GER | 109350 | 59330 | 33799 | 13q14 | 285 | Gastroesophageal reflux | OMIM |
| 6 | RIEG2 | 601499 | 6012 | 7376 | 13q14 | 285 | Rieger syndrome 2 | OMIM |
| 7 | SPG24 | 607584 | 338090 | 35479 | 13q14 | 285 | spastic paraplegia 24 (autosomal recessive) | OMIM |
| 8 | XRS | 194370 | 8102 | - | 13q14 | 285 | X-ray sensitivity | OMIM |
| 9 | ENUR1 | 600631 | 2031 | 8547 | 13q13-q143 | 465 | enuresis, nocturnal 1 | OMIM |
| 10 | AUNA1 | 609129 | 378942 | 34825 | 13q14-q21 | 411 | auditory neuropathy, autosomal dominant 1 | OMIM |
| 11 | ATOD5 | 605844 | 117188 | - | 13q12-q14 | 773 | Dermatitis, atopic, 5 | OMIM |
| 12 | CLF | 604595 | 54501 | 33624 | 13q | 1392 | cholesterol-lowering factor | OMIM |
This database and viewer were originally developed by Dr. Boris Lenhard at Karolinska Institute.
$Revision: 1.58.2.9.2.46 $