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 : HIX0002607

TranscriptsHIT000022755
HIT000027187
HIT000031286
HIT000055416
HIT000063073
HIT000069497
HIT000098062
HIT000286367
HIT000297980
HIT000300842
HIT000301733
HIT000324186
HIT000339463
HIT000495895
HIT000498818
UCSC Genome browserchr2:175424302-175547627
G-integrachr2:175424302-175547627
Map position2q31.1

SymbolWASPIP
OMIMNA
Disease nameNA
MutationView-

Orphan diseases co-localized with HIX0002607

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 IDDM7 600321 3406 12477 2q31 278 insulin-dependent diabetes mellitus 7 OMIM
2 PNKD2 611147 100188328 - 2q31 278 paroxysmal nonkinesigenic dyskinesia 2 OMIM
3 SHFM5 606708 171157 12504 2q31 278 split hand/foot malformation (ectrodactyly) type 5 OMIM
4 INTLQ2 610295 100462723 - 2q241-q311 368 Intelligence QTL3 OMIM
5 RP26 - 23681 30396 2q31-q33 669 retinitis pigmentosa 26,autosomal recessive GenAtlas
6 FGQTL1 612108 100499165 - 2q24-q32 595 Fasting plasma glucose level QTL 1 OMIM
7 MMDK 156232 10305 30148 2q24-q32 595 Mesomelic dysplasia, Kantaputra type OMIM
8 AUTS5 606053 94313 34014 2q 2627 Autism, susceptibility to, 5 OMIM
9 COPD 606963 260431 - 2q 2627 Pulmonary disease, chronic obstructive, severe early-onset OMIM

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

$Revision: 1.58.2.9.2.46 $