H-InvDB x AHG DB
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H-InvDB_8.3 released on March 26, 2013.
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DiseaseInfo Viewer : HIX0000182

TranscriptsHIT000002374
HIT000039984
HIT000058537
HIT000423304
HIT000428503
HIT000433705
UCSC Genome browserchr1:17634690-17690499
G-integrachr1:17634690-17690499
Map position1p36.13

SymbolPADI4
OMIM605347 Protein title: PEPTIDYLARGININE DEIMINASE, TYPE IV
Disease name
  • {Rheumatoid arthritis, susceptibility to} (180300)
MutationView605347
(JRE version 1.4.0 or later is required.)

Orphan diseases co-localized with HIX0000182

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 ANIB3 609122 497657 34822 1p3613-p343 816 aneurysm, intracranial berry 3 OMIM
2 ALPQTL2 612367 100196914 - 1p36 976 Alkaline phosphatase, plasma level of, QTL 2 OMIM
3 BMND3 606928 246259 29078 1p36 976 Bone mineral density variability 3 OMIM
4 BMND3 606928 246259 29079 1p36 976 Bone mineral density variability 3 OMIM
5 BMND3 606928 246259 29080 1p36 976 Bone mineral density variability 3 OMIM
6 CCV 115665 7792 6072 1p36 976 cataract, congenital, Volkmann type OMIM
7 CMM 155600 1243 123 1p36 976 cutaneous malignant melanoma/dysplastic nevus OMIM
8 CTPP 116600 10306 10888 1pter-p361 976 Cataract, posterior polar OMIM
9 CTPP 116600 10306 34568 1pter-p361 976 Cataract, posterior polar OMIM
10 DYT13 607671 93983 34130 1p36 976 dystonia 13, torsion OMIM
11 GLC3B 600975 2728 7589 1p36 976 glaucoma 3, primary infantile, B OMIM
12 IBD7 605225 57042 33908 1p36 976 inflammatory bowel disease 7 OMIM
13 LCA9 608553 619483 34461 1p36 976 Leber congenital amaurosis 9 OMIM
14 MS4 612596 100271696 - 1p36 976 Multiple sclerosis, susceptiblity to, 4 OMIM
15 MYP14 610320 100359407 - 1p36 976 myopia 14 OMIM
16 SCASI 607317 260415 34534 1p36 976 spinocerebellar ataxia with saccadic intrusions OMIM
17 DYX8 608995 406874 34708 1p36-p34 1516 dyslexia susceptibility 8 OMIM
18 DYT13 - 93983 34130 1p3132-p3613 1459 primarytorsion dystomia 13 with prominent cranial - cervical and upper limb involvement GenAtlas
19 ANON 606788 171514 34131 1p 2813 Anorexia nervosa, susceptibility to OMIM
20 ANON 606788 171514 34132 1p 2813 Anorexia nervosa, susceptibility to OMIM
21 PARK10 606852 170534 34395 1p 2813 Parkinson disease 10 OMIM
22 PSORS7 605606 65245 33842 1p 2813 psoriasis susceptibility 7 OMIM
23 SCZD12 608543 619488 - 1p 2813 schizophrenia 12 OMIM

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

$Revision: 1.58.2.9.2.46 $