Gene

sptssa

ID
ZDB-GENE-050320-26
Name
serine palmitoyltransferase, small subunit A
Symbol
sptssa Nomenclature History
Previous Names
  • wu:fb60h11
  • zgc:112487
Type
protein_coding_gene
Location
Chr: 17 Mapping Details/Browsers
Description
Predicted to contribute to serine C-palmitoyltransferase activity. Predicted to be involved in sphingolipid metabolic process. Predicted to localize to serine C-palmitoyltransferase complex. Orthologous to human SPTSSA (serine palmitoyltransferase small subunit A).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure from Thisse et al., 2004
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With sptssa Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
hereditary spastic paraplegia 90A Alliance Spastic paraplegia 90A, autosomal dominant 620416
hereditary spastic paraplegia 90B Alliance ?Spastic paraplegia 90B, autosomal recessive 620417
Associated With sptssa Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR024512 Small subunit of serine palmitoyltransferase-like
Domain Details Per Protein
Protein Length Small subunit of serine palmitoyltransferase-like
UniProtKB:Q5BJC1 68
Transcripts
Genome Browsers
Type Name Annotation Method Length (nt) Analysis
mRNA sptssa-201 (1) Havana 1589 nt
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations