DiseaseInfo Viewer : HIX0201124
| Transcripts | HIT000007694 HIT000007695 HIT000007740 HIT000007768 HIT000009898 HIT000015325 HIT000029390 HIT000048746 HIT000059085 HIT000076232 HIT000273493 HIT000496035 |
|---|---|
| UCSC Genome browser | chr7:100450341-100464634 |
| G-integra | chr7:100450341-100464634 |
| Map position | 7q22.1 |
| Symbol | SLC12A9 |
| OMIM | NA |
| Disease name | NA |
| MutationView | - |
Orphan diseases co-localized with HIX0201124
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 | MYH16 | 608580 | 84176 | - | 7q221 | 271 | myosin, heavy chain 16 pseudogene | OMIM |
| 2 | AUTS1 | 209850 | 100188832 | 28737 | 7q22 | 326 | Autism, susceptibility to, 1 | OMIM |
| 3 | AUTS1 | 209850 | 100188832 | 31441 | 7q22 | 326 | Autism, susceptibility to, 1 | OMIM |
| 4 | AUTS1 | 209850 | 100188832 | 33984 | 7q22 | 326 | Autism, susceptibility to, 1 | OMIM |
| 5 | AUTS1 | 209850 | 100188832 | 34070 | 7q22 | 326 | Autism, susceptibility to, 1 | OMIM |
| 6 | AUTS1 | 209850 | 100188832 | 34078 | 7q22 | 326 | Autism, susceptibility to, 1 | OMIM |
| 7 | EKV3 | 609313 | 574017 | 34897 | 7q22 | 326 | erythrokeratodermia variabilis 3 (Kamouraska type) | OMIM |
| 8 | PAPA4 | 608562 | 450096 | 34462 | 7q22 | 326 | Polydactyly, postaxial, type A4 | OMIM |
| 9 | NM | 162820 | 4827 | - | 7q22-qter | 1233 | neutrophil migration | OMIM |
| 10 | HRX | 145290 | 7974 | - | 7q | 1856 | Hyperreflexia | OMIM |
| 11 | LGMD1D | 603511 | 9186 | 31058 | 7q | 1856 | limb girdle muscular dystrophy 1D (autosomal dominant) | OMIM |
| 12 | 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 $