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SPG30 spastic paraplegia 30 (autosomal recessive) [ Homo sapiens (human) ]

Gene ID: 654843, discontinued on 1-Apr-2012

Summary

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Official Symbol
SPG30provided by HGNC
Official Full Name
spastic paraplegia 30 (autosomal recessive)provided by HGNC
Primary source
HGNC:HGNC:30017
See related
MIM:610357
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:
2q37.3

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
spastic paraplegia 30 (autosomal recessive)
GeneReviews: Not available

General gene information

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Property

  • phenotype only

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Research Materials