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 : HIX0203299

TranscriptsHIT000035924
HIT000086195
HIT000218100
HIT000218536
HIT000271049
HIT000284807
HIT000285049
UCSC Genome browserchrX:48534985-48549816
G-integrachrX:48534985-48549816
Map positionXp11.23

SymbolWAS
OMIM300392 Protein title: WAS GENE
Disease name
  • Neutropenia, severe congenital, X-linked (300299)
  • Thrombocytopenia, X-linked (313900)
  • Thrombocytopenia, X-linked, intermittent (313900)
  • Wiskott-Aldrich syndrome (301000)
MutationView-

Orphan diseases co-localized with HIX0203299

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 MRX51 - 4414 33793 Xp113-p1123 225 mental retardation,X-linked 51 GenAtlas
2 MRX57 - 4420 26557 Xp113-p1123 225 mental retardation,X-linked 57 GenAtlas
3 MRX78 - 170530 34206 Xp114-p1123 300 mental retardation,X-linked,non specific GenAtlas
4 MRX44 - 4408 33790 Xp113-p1121 384 mental retardation,X-linked 44 GenAtlas
5 MRX45 - 4409 33791 Xp113-p1121 384 mental retardation,X-linked 45 GenAtlas
6 MRX50 300115 4413 33792 Xp113-p1121 384 mental retardation, X-linked 50 OMIM
7 OPA2 311050 4977 27347 Xp114-p112 459 optic atrophy 2 (obscure) OMIM
8 MRX17 - 4381 22376 Xp1123-q12 429 mental retardation mild,X-linked 17,with hyperactivity and slow speech development GenAtlas
9 MRX81 300433 266678 34438 Xp112-Xq12 429 mental retardation, X-linked 81 OMIM
10 GRDX 300351 117189 33722 Xp11 459 Graves disease, susceptibility to, X-linked OMIM
11 IDDMX 300136 8245 29504 Xp11 459 Diabetes mellitus, insulin-dependent, X-linked, susceptibility to OMIM
12 LOAS 308905 100188775 - Xp11 459 Leber optic atrophy, susceptibility to OMIM
13 MRX55 - 4418 29089 Xp11 459 mental retardation,X-linked 55 GenAtlas
14 MRXS12 309545 8246 22381 Xp11 459 Mental retardation, X-linked, syndromic 12 OMIM
15 MRXS12 309545 8246 34156 Xp11 459 Mental retardation, X-linked, syndromic 12 OMIM
16 MRX15 - 4379 22433 Xp211-p1122 466 mental retardation,X-linked 15,severe,with hypotonia in infancy GenAtlas
17 MRX18 - 4382 22377 Xp211-p1122 466 mental retardation,mild,X-linked 18,with seizures,brachycephaly and limitation of elbow extension GenAtlas
18 AGSPX 300652 100188767 - Xp113-q12 465 Angio serpiginosum OMIM
19 MRXSBCS - - 30792 Xp113-q12 465 X-linked neurodegenerative syndrome characterized by mental retardation,blindness,convulsions,spasticity and early death with mild hypomyelination GenAtlas
20 CEPA - 1064 20565 Xp11-q11 510 congenital failure of autonomic control of ventilation (Ondine-like) GenAtlas
21 CLBMX - - 33954 Xp11-q11 510 colobomatous microphthalmia,X linked GenAtlas
22 MRX26 - 4390 20692 Xp11-q11 510 mental retardation,X-linked 26 GenAtlas
23 TARPS 311900 613260 34505 Xp1123-q133 600 Talipes equinovarus, atrial septal defect, Robin sequence, and persistence of left superior vena cava OMIM
24 MRX14 300062 4378 22367 Xp113-q133 636 mental retardation, X-linked 14 OMIM
25 MRX12 - 4376 21550 Xp212-q1121 563 mental retardation,X-linked 12,mild-moderate,prematurity,low birth weight GenAtlas
26 PRS 309610 5640 22520 Xp21-p11 574 Prieto X-linked mental retardation syndrome OMIM
27 MRX1 309530 4365 20421 Xp11-q13 711 mental retardation, X-linked 1 (non-dysmorphic) OMIM
28 MRX78 300551 170530 34206 Xp114-q211 790 mental retardation, X-linked 78 OMIM
29 XS 309050 7523 - Xp212-q211 843 X-linked suppressor of LU antigens OMIM
30 MRX65 - 4428 33796 Xp113-q2133 793 mental retardation,X-linked 65 GenAtlas
31 WTS 309585 7492 20433 Xp113-q21 793 Wilson-Turner X-linked mental retardation syndrome OMIM
32 MRXS7 300218 4429 21559 Xp113-Xq221 928 mental retardation, X-linked, syndromic 7 OMIM
33 MRX20 300047 4384 20616 Xp11-q21 868 mental retardation, X-linked 20 OMIM
34 MRXS24 - - 29090 Xp114-q21 868 X-linked,syndromic mental retardation,with spastic diplegia GenAtlas
35 MRHD - - 22379 Xp213-q213 983 mental retardation,congenital heart defect,cleft palate,short stature GenAtlas
36 MRX13 - 4377 21551 Xp2122-q223 1131 mental retardation,X-linked 13 GenAtlas
37 AMCBX2 300645 100188766 - Xp212-q263 1548 Atypical mycobacteriosis, familial, X-linked 2 OMIM
38 MRX74 - 23693 34235 X 2261 mental retardation, X-linked 74 GenAtlas
39 MRX77 - 93991 34237 X 2261 mental retardation, X-linked 77 GenAtlas

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

$Revision: 1.58.2.9.2.46 $