Summary

Gene name
rtel-1
Sequence name
F25H2.13
Gene ID
WBGene00009124
Gene type
Protein Coding
RNAi library location
I-5G10
Gene information
Is an ortholog of human RTEL1 (regulator of telomere elongation helicase 1). Is predicted to have ATP binding activity\; ATP-dependent DNA helicase activity\; and DNA polymerase binding activity. Is involved in regulation of double-strand break repair via homologous recombination. Human ortholog(s) of this gene are implicated in autosomal dominant dyskeratosis congenita 4 and autosomal recessive dyskeratosis congenita 5.

Lineage tracing results

Phenotype

Cell
cycle		 Division
asynchrony		 Division
asymmetry		 CND-1
expression		 Division
angle
(A-P)		 Cell
position		 Phenotypic
measurement		 Phenotypic
detection
RTEL-1_emb1 1 1 1 0 0 0
RTEL-1_emb2 0 0 0 1 0 0
RTEL-1_emb3 0 0 0 0 0 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