DiseaseInfo Viewer : HIX0176523

Transcripts	HIT000028509_03 HIT000031053_03 HIT000192815_03 HIT000192816_03 HIT000196130_03 HIT000196286_03 HIT000222660_03 HIT000264650_03 HIT000321625_03 HIT000321946_03 HIT000425883_03 HIT000428496_03 HIT000468608_03 HIT000496019_01
UCSC Genome browser	chrX:1387693-1428981
G-integra	chrX:1387693-1428981
Map position	Xp22.33
Symbol	CSF2RA
OMIM	NA
Disease name	NA
MutationView	-

Orphan diseases co-localized with HIX0176523

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	MRXS16	-	-	20689	Xp2233	67	mental retardation,X-linked syndromic,with ataxia,hypotonia,late onset progressive myoclonic encephalopathy and macular degeneration	GenAtlas
2	VSPA	313000	59332	-	Xp2233	67	Visuospatial/perceptual abilities	OMIM
3	HDPA	300221	50829	-	Xpter-p2232	83	Hodgkin disease, susceptibility, pseudoautosomal	OMIM
4	EMWX	300211	10118	32421	Xp223	134	episodic muscle weakness, X-linked	OMIM
5	FGS3	300406	93985	34276	Xp223	134	FG syndrome 3	OMIM
6	LCDX	-	-	33951	Xp223	134	Lisch corneal dystrophy (microcystic dystrophy of the corneal epithelium)	GenAtlas
7	WTRS	300421	619509	-	Xp223	134	Wittwer syndrome	OMIM
8	FCP1	305435	2221	21249	Xp223-p222	241	F-cell production 1	OMIM
9	MRX2	300428	4367	34231	Xp223-p222	241	mental retardation, X-linked 2 (non-dysmorphic)	OMIM
10	MRX2	-	4367	34231	Xp223-p222	241	mental retardation, X-linked 2 (non-dysmorphic)	GenAtlas
11	MRX49	300114	4412	33978	Xp223-p222	241	mental retardation, X-linked 49	OMIM
12	MRX56	-	4419	26555	Xp223-p222	241	mental retardation,X-linked 56	GenAtlas
13	AGMX2	300310	179	-	Xp22	332	agammaglobulinemia, X-linked 2 (with growth hormone deficiency)	OMIM
14	AIC	304050	192	21367	Xp22	332	Aicardi syndrome	OMIM
15	CMTX2	302801	1253	21514	Xp22	332	Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive)	OMIM
16	DFN6	300066	1682	20716	Xp22	332	deafness, X-linked 6, sensorineural	OMIM
17	MNG2	300273	59081	33843	Xp22	332	multinodular goiter 2	OMIM
18	MRXS21	-	-	26938	Xp22	332	mental retardation,X-linked,syndromic,with hydrocephalus,facial dysmorphism,spastic diplegia,calcification of the basal ganglia,Fried syndrome	GenAtlas
19	RP23	300424	6115	33931	Xp22	332	retinitis pigmentosa 23 (X-linked recessive)	OMIM
20	MRX76	-	57193	34236	Xp223-p213	378	mental retardation, X-linked 76	GenAtlas
21	CCXNS	-	-	34080	Xp223-p211	450	X-linked non syndromic congenital cataract	GenAtlas
22	NSX	310465	4906	21231	Xp223-p211	450	N syndrome (mental retardation, malformations, chromosome breakage)	OMIM
23	PDR	301220	5171	25482	Xp22-p21	450	pigment disorder, reticulate	OMIM
24	MRX74	-	23693	34235	X	2261	mental retardation, X-linked 74	GenAtlas
25	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 $