DiseaseInfo Viewer : HIX0003480
| Transcripts | HIT000024554 HIT000032300 HIT000053852 HIT000097182_03 HIT000243799 HIT000250392 HIT000267704 |
|---|---|
| UCSC Genome browser | chr3:88101100-88199035 |
| G-integra | chr3:88101100-88199035 |
| Map position | 3p11.1 |
| Symbol | CGGBP1 |
| OMIM | NA |
| Disease name | NA |
| MutationView | - |
Orphan diseases co-localized with HIX0003480
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 | NRC1 | 604442 | 27182 | - | 3p12 | 75 | nonpapillry renal carcinoma 1 | OMIM |
| 2 | HYT7 | 610948 | 100188825 | - | 3p141-q123 | 281 | Hypertension, essential, susceptibility to, 7 | OMIM |
| 3 | DYX5 | 606896 | 171089 | 33957 | 3p12-q13 | 377 | dyslexia susceptibility 5 | OMIM |
| 4 | SSD | 608445 | 404713 | - | 3p12-q13 | 377 | Speech-sound disorder | OMIM |
| 5 | DFNB42 | 609646 | 449482 | 34899 | 3p13-q13 | 430 | deafness, autosomal recessive 42 | OMIM |
| 6 | KTCN3 | 608586 | 406215 | 34652 | 3p14-q13 | 575 | Keratoconus 3 | OMIM |
| 7 | CRCL | 607135 | 261727 | - | 3p | 1351 | Creatinine clearance QTL | OMIM |
| 8 | DFNB15 | 601869 | 1707 | 27117 | 3or19 | 2751 | deafness, autosomal recessive 15 | OMIM |
This database and viewer were originally developed by Dr. Boris Lenhard at Karolinska Institute.
$Revision: 1.58.2.9.2.46 $