Gene

iba57

ID
ZDB-GENE-060929-712
Name
iron-sulfur cluster assembly factor IBA57
Symbol
iba57 Nomenclature History
Previous Names
  • zgc:153540
Type
protein_coding_gene
Location
Chr: 2 Mapping Details/Browsers
Description
Involved in heme biosynthetic process. Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 74 and multiple mitochondrial dysfunctions syndrome 3. Is expressed in intermediate cell mass of mesoderm. Orthologous to human IBA57 (iron-sulfur cluster assembly factor IBA57).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure from Nilsson et al., 2009
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
1 Figure from Nilsson et al., 2009
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With iba57 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
hereditary spastic paraplegia 74 Alliance ?Spastic paraplegia 74, autosomal recessive 616451
multiple mitochondrial dysfunctions syndrome 3 Alliance Multiple mitochondrial dysfunctions syndrome 3 615330
Associated With iba57 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Conserved_site IPR017703 YgfZ/GcvT conserved site
Family IPR045179 YgfZ/GcvT
Homologous_superfamily IPR027266 GTP-binding protein TrmE/Aminomethyltransferase GcvT, domain 1
Domain Details Per Protein
Protein Length GTP-binding protein TrmE/Aminomethyltransferase GcvT, domain 1 YgfZ/GcvT YgfZ/GcvT conserved site
UniProtKB:B8JMH0
Transcripts
Genome Browsers
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