H-InvDB x AHG DB
DiseaseInfo Viewer
H-InvDB_8.3 released on March 26, 2013.
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DiseaseInfo Viewer : HIX0010103

TranscriptsHIT000041216
HIT000246170
UCSC Genome browserchr11:111338255-111383064
G-integrachr11:111338255-111383064
Map position11q23.1

SymbolBTG4
OMIMNA
Disease nameNA
MutationView-

Orphan diseases co-localized with HIX0010103

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 BMND5 609354 554315 - 11q23 253 Bone mineral density variation QTL 5 OMIM
2 BRCATA 600048 8068 - 11q23 253 Breast cancer, 11;22 translocation associated OMIM
3 CRCS7 612232 100187711 - 11q23 253 colorectal cancer, susceptibility to, 7 OMIM
4 TSG11 603040 50970 - 11q23 253 Tumor suppressor gene on chromosome 11 OMIM
5 ADIPQTL4 612629 100271698 - 11q23-q24 442 Adiponectin, serum level of, QTL4 OMIM
6 IHPS3 612017 100188876 - 11q14-q22 338 Pyloric stenosis, infantile hypertrophic, 3 OMIM
7 ANC 105580 8066 - 11q22-qter 574 Anal canal carcinoma OMIM
8 ST3 191181 6762 - 11q13-q23 1080 suppression of tumorigenicity 3 OMIM
9 HPC11 - - 33686 11 2837 prostate cancer 11,hereditary,susceptibility locus GenAtlas

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

$Revision: 1.58.2.9.2.46 $