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SPTSSA

serine palmitoyltransferase small subunit A

HCNC Approved Symbol
SPTSSA (HGNC:20361)
Genomic Coordinates
14:34,432,788 - 34,462,240 (14q13.1)
Synonyms
ssSPTa, C14orf147
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Spastic paraplegia 90B, autosomal recessive
620417AD
Spastic paraplegia 90A, autosomal dominant
620416AD

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the SPTSSA gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results