H-InvDB x AHG DB
DiseaseInfo Viewer
H-InvDB_8.3 released on March 26, 2013.
Search by for Advanced Search
Home Quick guide Navi BLAST Site map Download Contact us Help

DiseaseInfo Viewer : HIX0201124

TranscriptsHIT000007694
HIT000007695
HIT000007740
HIT000007768
HIT000009898
HIT000015325
HIT000029390
HIT000048746
HIT000059085
HIT000076232
HIT000273493
HIT000496035
UCSC Genome browserchr7:100450341-100464634
G-integrachr7:100450341-100464634
Map position7q22.1

SymbolSLC12A9
OMIMNA
Disease nameNA
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 $