symbol withdrawn SPG26

Preferred Label : symbol withdrawn SPG26;

Obsolete resource : true;

Approved symbol HGNC : SPG26;

Chromosome HGNC : 12p11.1-q14;

Locus type HGNC : phenotype;

Détails

Origin ID

HGNC:22494;

Automatic exact mappings (from CISMeF team)
- Spastic paraplegia 26, autosomal recessive [OMIM Phenotype]
Replaced by
- beta-1,4-N-acetyl-galactosaminyltransferase 1 [HGNC gene]

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