DiseaseInfo Viewer : HIX0011990
| Transcripts | HIT000037119 HIT000040268 HIT000266894 HIT000271905 HIT000274775 HIT000281736 HIT000288563 HIT000295634 HIT000300524 HIT000424665 |
|---|---|
| UCSC Genome browser | chr14:102973180-102976136 |
| G-integra | chr14:102973180-102976136 |
| Map position | 14q32.31 |
| Symbol | ANKRD9 |
| OMIM | NA |
| Disease name | NA |
| MutationView | - |
Orphan diseases co-localized with HIX0011990
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 | CHDS4 | 608318 | 387585 | - | 14q32 | 551 | Coronary heart disease, susceptibility to, 4 | OMIM |
| 2 | CKBE | 123270 | 1156 | 35326 | 14q32 | 551 | creatine kinase, ectopic expression | OMIM |
| 3 | GEVQ1 | 608875 | 474334 | - | 14q32 | 551 | gene expression, variation in, quantitative trait locus | OMIM |
| 4 | HFM | 164210 | 170474 | 34074 | 14q32 | 551 | Hemifacial microsomia | OMIM |
| 5 | IV | 270100 | 8114 | - | 14q32 | 551 | inversus situs, viscerum | OMIM |
| 6 | MCOP | 251600 | 8113 | 29115 | 14q32 | 551 | microphthalmia, autosomal recessive | OMIM |
| 7 | CTAA1 | 115650 | 1483 | 70 | 14q24-qter | 974 | cataract, anterior polar 1 | OMIM |
| 8 | IBGC1 | 213600 | 23706 | 32135 | 14q | 1654 | idiopathic basal ganglia calcification 1 | OMIM |
| 9 | MNG1 | 138800 | 4333 | 27579 | 14q | 1654 | multinodular goitre 1 | OMIM |
| 10 | SPG32 | 611252 | 724107 | - | 14q | 1654 | spastic paraplegia 32 (autosomal recessive) | OMIM |
This database and viewer were originally developed by Dr. Boris Lenhard at Karolinska Institute.
$Revision: 1.58.2.9.2.46 $