Gene

cpt1a2a

ID
ZDB-GENE-030131-590
Name
carnitine palmitoyltransferase 1A 2a
Symbol
cpt1a2a Nomenclature History
Previous Names
  • cpt1ca (1)
  • fb37e01
  • wu:fb37e01
Type
protein_coding_gene
Location
Chr: 24 Mapping Details/Browsers
Description
Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 73. Orthologous to human CPT1C (carnitine palmitoyltransferase 1C).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
No data available
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
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 cpt1a2a Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
carnitine palmitoyltransferase I deficiency Alliance CPT deficiency, hepatic, type IA 255120
Associated With cpt1a2a Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
No data available
Transcripts
Genome Browsers
No data available
No data available
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Citations