DiseaseInfo Viewer : HIX0016764

Transcripts	HIT000029962 HIT000033047 HIT000081889 HIT000194171 HIT000195909 HIT000216243 HIT000267135 HIT000268851 HIT000269767 HIT000272546 HIT000281285 HIT000320936 HIT000320964 HIT000426088 HIT000429072 HIT000430803 HIT000490740
UCSC Genome browser	chrX:47441690-47446190
G-integra	chrX:47441690-47446190
Map position	Xp11.23
Symbol	TIMP1
OMIM	NA
Disease name	NA
MutationView	-

Orphan diseases co-localized with HIX0016764

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

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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 $