DiseaseInfo Viewer : HIX0016834

Transcripts	HIT000004979 HIT000028226 HIT000046804 HIT000093678 HIT000097663 HIT000340479
UCSC Genome browser	chrX:62519126-62571218
G-integra	chrX:62519126-62571218
Map position	Xq11.1
Symbol	LOC139886
OMIM	NA
Disease name	NA
MutationView	-

Orphan diseases co-localized with HIX0016834

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	AGA2	300710	100188771	-	Xq11-q12	81	Alopecia, androgenetic, 2	OMIM
2	MRX17	-	4381	22376	Xp1123-q12	429	mental retardation mild,X-linked 17,with hyperactivity and slow speech development	GenAtlas
3	MRX81	300433	266678	34438	Xp112-Xq12	429	mental retardation, X-linked 81	OMIM
4	AGSPX	300652	100188767	-	Xp113-q12	465	Angio serpiginosum	OMIM
5	MRXSBCS	-	-	30792	Xp113-q12	465	X-linked neurodegenerative syndrome characterized by mental retardation,blindness,convulsions,spasticity and early death with mild hypomyelination	GenAtlas
6	CEPA	-	1064	20565	Xp11-q11	510	congenital failure of autonomic control of ventilation (Ondine-like)	GenAtlas
7	CLBMX	-	-	33954	Xp11-q11	510	colobomatous microphthalmia,X linked	GenAtlas
8	MRX26	-	4390	20692	Xp11-q11	510	mental retardation,X-linked 26	GenAtlas
9	TARPS	311900	613260	34505	Xp1123-q133	600	Talipes equinovarus, atrial septal defect, Robin sequence, and persistence of left superior vena cava	OMIM
10	MRX14	300062	4378	22367	Xp113-q133	636	mental retardation, X-linked 14	OMIM
11	MRX12	-	4376	21550	Xp212-q1121	563	mental retardation,X-linked 12,mild-moderate,prematurity,low birth weight	GenAtlas
12	MPDMRS	300519	574047	-	Xq11-q21	409	Martin-Probst deafness-mental retardation syndrome	OMIM
13	MRX1	309530	4365	20421	Xp11-q13	711	mental retardation, X-linked 1 (non-dysmorphic)	OMIM
14	MRX52	300504	4415	26558	Xp1121-q2133	483	mental retardation, X-linked 52	OMIM
15	MRX52	-	4415	26558	Xp1121-q2133	483	mental retardation,X-linked 52down-slanting palpebral fissures and midface hypoplasia	GenAtlas
16	SCAX1	302500	1166	35217	Xp1121-q213	483	spinocerebellar ataxia, X-linked 1	OMIM
17	MRX78	300551	170530	34206	Xp114-q211	790	mental retardation, X-linked 78	OMIM
18	MRX69	-	23697	34234	Xp1121-q221	618	mental retardation, X-linked 69	GenAtlas
19	WWS	314580	7493	20488	Xq11-q22	619	Wieacker-Wolff syndrome	OMIM
20	XS	309050	7523	-	Xp212-q211	843	X-linked suppressor of LU antigens	OMIM
21	MRX65	-	4428	33796	Xp113-q2133	793	mental retardation,X-linked 65	GenAtlas
22	WTS	309585	7492	20433	Xp113-q21	793	Wilson-Turner X-linked mental retardation syndrome	OMIM
23	MRXS7	300218	4429	21559	Xp113-Xq221	928	mental retardation, X-linked, syndromic 7	OMIM
24	MRX20	300047	4384	20616	Xp11-q21	868	mental retardation, X-linked 20	OMIM
25	MRXS24	-	-	29090	Xp114-q21	868	X-linked,syndromic mental retardation,with spastic diplegia	GenAtlas
26	MRHD	-	-	22379	Xp213-q213	983	mental retardation,congenital heart defect,cleft palate,short stature	GenAtlas
27	MRX13	-	4377	21551	Xp2122-q223	1131	mental retardation,X-linked 13	GenAtlas
28	MGR2	300125	8249	28720	Xq	1384	Migraine, familial typical, susceptibility to	OMIM
29	CGF1	300082	1083	29125	Xp1122-qter	1604	cognitive function 1, social	OMIM
30	AMCBX2	300645	100188766	-	Xp212-q263	1548	Atypical mycobacteriosis, familial, X-linked 2	OMIM
31	MRX74	-	23693	34235	X	2261	mental retardation, X-linked 74	GenAtlas
32	MRX77	-	93991	34237	X	2261	mental retardation, X-linked 77	GenAtlas

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

$Revision: 1.58.2.9.2.46 $