symbol withdrawn SPG13

Preferred Label : symbol withdrawn SPG13;

Obsolete resource : true;

Approved symbol HGNC : SPG13;

Chromosome HGNC : 2q24-q34;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:11228;

Automatic exact mappings (from CISMeF team)
- Spastic paraplegia 13, autosomal dominant [OMIM Phenotype]
Replaced by
- heat shock protein family D (Hsp60) member 1 [HGNC gene]

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