Summary

Gene name
F39H2.3
Sequence name
F39H2.3
Gene ID
WBGene00009563
Gene type
Protein Coding
RNAi library location
I-4C20
Gene information
Is an ortholog of human IBA57 (iron-sulfur cluster assembly factor IBA57). Human ortholog(s) of this gene are implicated in hereditary spastic paraplegia 74 and multiple mitochondrial dysfunctions syndrome 3. Human IBA57 exhibits RNA binding activity. Is predicted to encode a protein with the following domains: Aminomethyltransferase, folate-binding domain\; YgfZ\/GcvT conserved site\; GTP-binding protein TrmE\/Glycine cleavage system T protein, domain 1\; and Aminomethyltransferase-like.

Lineage tracing results

Phenotype

Cell
cycle		 Division
asynchrony		 Division
asymmetry		 CND-1
expression		 Division
angle
(A-P)		 Cell
position		 Phenotypic
measurement		 Phenotypic
detection
F39H2.3_emb1 0 0 0 0 1 0
F39H2.3_emb2 0 0 0 0 0 0
F39H2.3_emb3 0 0 0 1 2 0
With cellular defects No No No No No No

Cell Proliferation

Proliferation speed

Cell cycle length

No defects

Division asynchrony

No defects

Division asymmetry

No defects

Tissue Marker Expression (CND-1)

CND-1 expression

No defects

Morphogenesis

Division angle (A-P)

No defects

Relative cell position

No defects