H-InvDB x AHG DB
DiseaseInfo Viewer
H-InvDB_8.3 released on March 26, 2013.
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DiseaseInfo Viewer : HIX0012738

TranscriptsHIT000000030
HIT000008853
HIT000009177
HIT000028584
HIT000052524
HIT000054297
HIT000055735
HIT000058444
HIT000058461
HIT000058462
HIT000058463
HIT000058464
HIT000058465
HIT000058466
HIT000072068
HIT000073771
HIT000086907
HIT000087202
HIT000090192
HIT000091467
        :
(show all transcripts)
UCSC Genome browserchr16:2802330-2821413
G-integrachr16:2802330-2821413
Map position16p13.3

SymbolSRRM2
OMIMNA
Disease nameNA
MutationView-

Orphan diseases co-localized with HIX0012738

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 CATM 156850 8130 2078 16p133 366 cataract, congenital, with microphthalmia OMIM
2 ADHD1 608903 450087 - 16p13 507 Attention deficit-hyperactivity disorder, susceptibility to, 1 OMIM
3 BMIQ5 608558 449016 - 16p13 507 body mass index QTL 5 OMIM
4 CHDS1 607339 338334 34352 16pter-p13 507 Coronary heart disease, susceptibility to, 1 OMIM
5 CHDS1 607339 338334 34664 16pter-p13 507 Coronary heart disease, susceptibility to, 1 OMIM
6 EIM 605021 54119 33688 16p13 507 Infantile myoclonic epilepsy OMIM
7 EIM 605021 54119 34536 16p13 507 Infantile myoclonic epilepsy OMIM
8 IHPS2 610260 780923 35374 16p13-p12 742 Pyloric stenosis, infantile hypertrophic, 2 OMIM
9 MHAC 605013 53341 33694 16p133-p121 742 microhydranencephaly OMIM
10 IBD8 606668 170595 34095 16p 962 inflammatory bowel disease 8 OMIM

This database and viewer were originally developed by Dr. Boris Lenhard at Karolinska Institute.

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