DiseaseInfo Viewer : HIX0007498

Transcripts	HIT000038216 HIT000246314
UCSC Genome browser	chr8:49984903-49988642
G-integra	chr8:49984903-49988642
Map position	8q11.21
Symbol	C8orf22
OMIM	NA
Disease name	NA
MutationView	-

Orphan diseases co-localized with HIX0007498

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	NKCD	609981	780917	-	8p1123-q1121	169	Natural killer cell deficiency, familial isolated	OMIM
2	FGD3	609197	619477	34272	8q112-q132	232	glucocorticoid deficiency 3	OMIM
3	CORD9	612775	60424	-	8p12-q11	273	cone rod dystrophy 9	OMIM
4	PAFC	128700	404715	-	8q111-q133	278	Preauricular fistulae, congenital	OMIM
5	SNAX1	608984	474386	34746	8p12-q121	339	sensory ataxia 1 (autosomal dominant)	OMIM
6	MPD3	610099	780920	-	8p22-q11	493	Myopathy, distal 3	OMIM
7	SPG37	611945	100049159	-	8p212-q133	546	spastic paraplegia 37 (autosomal dominant)	OMIM
8	AD12	611073	100188830	-	8p12-q22	743	Alzheimer disease 12	OMIM
9	CCAL1	600668	882	18973	8q	1063	chondrocalcinosis 1 (calcium pyrophosphate-deposition disease, early onset osteoarthritis)	OMIM
10	FHQTL	606789	171515	-	8q	1063	Fetal hemoglobin QTL on chromosome 8	OMIM

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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 $