DiseaseInfo Viewer : HIX0019600

Transcripts	HIT000012451 HIT000050928 HIT000251532 HIT000260883 HIT000387945 HIT000425447 HIT000425502
UCSC Genome browser	chr16:50700211-50715264
G-integra	chr16:50700211-50715264
Map position	16q12.1
Symbol	SLIC1
OMIM	NA
Disease name	NA
MutationView	-

Orphan diseases co-localized with HIX0019600

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	HYD2	602639	8137	29072	16q121	87	hypodontia, autosomal recessive (2)	OMIM
2	DYT10	128200	50818	33183	16p112-q121	354	dystonia 10	OMIM
3	DYT10	128200	50818	33965	16p112-q121	354	dystonia 10	OMIM
4	AA2	610753	100034703	-	16q11-q22	456	Alopecia areata 2	OMIM
5	DUPC1	126900	780895	35116	16q111-q22	456	Dupuytren contracture 1	OMIM
6	BFIC2	605751	81865	-	16p12-q12	645	Benign familial infantile convulsions-2	OMIM
7	ICCA	602066	3387	27338	16p12-q12	645	infantile convulsions and paroxysmal choreoathetosis	OMIM
8	MRT10	611096	100101425	-	16p12-q12	645	Mental retardation, autosomal recessive, 10	OMIM
9	PSORS8	610707	140454	-	16q	754	psoriasis susceptibility 8	OMIM
10	SLI1	606711	171013	35233	16q	754	Specific language impairment QTL, 1	OMIM
11	WT3	194090	8136	-	16q	754	Wilms tumor-3	OMIM

---

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

$Revision: 1.58.2.9.2.46 $