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PARK11 Parkinson disease (autosomal recessive, early onset) 11 [ Homo sapiens (human) ]

Gene ID: 352908, discontinued on 18-Jun-2008

This record was replaced with Gene ID: 26058

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Summary

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Official Symbol: PARK11provided by HGNC
Official Full Name: Parkinson disease (autosomal recessive, early onset) 11provided by HGNC
Primary source: HGNC:HGNC:17963
See related: MIM:607688
Gene type: unknown
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

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Location:: 2q36-q37

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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Phenotypes

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Associated conditions

Description	Tests
Parkinson disease (autosomal recessive, early onset) 11 GeneReviews: Not available

General gene information

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Markers

D2S206 (e-PCR), detects polymorphism
- UniSTS:76156

Property

phenotype only

Additional links

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Supplemental Content

Table of contents

Summary
Genomic context
Bibliography
Phenotypes
General gene information
Markers
Additional links

Genome Browsers

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RefSeq

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PARK11 Parkinson disease (autosomal recessive, early onset) 11 [Homo sapiens]
PARK11 Parkinson disease (autosomal recessive, early onset) 11 [Homo sapiens]
Gene ID:352908

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