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SPG9 spastic paraplegia 9 (autosomal dominant) [ Homo sapiens (human) ]

Gene ID: 9193, discontinued on 27-Sep-2017

Summary

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Official Symbol
SPG9provided by HGNC
Official Full Name
spastic paraplegia 9 (autosomal dominant)provided by HGNC
Primary source
HGNC:HGNC:11239
See related
MIM:601162
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:
10q23.3-q24.2

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
spastic paraplegia 9 (autosomal dominant)
GeneReviews: Not available

General gene information

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Other Names

  • Spastic paraplegia-9 (spastic paraparesis with amyotrophy, cataracts and gastroesophageal reflux)

Property

  • phenotype only

Gene LinkOut

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