Summary

Gene name
dhc-1
Sequence name
T21E12.4
Gene ID
WBGene00000962
Gene type
Protein Coding
RNAi library location
I-1P04
Gene information
Is an ortholog of human DYNC1H1 (dynein cytoplasmic 1 heavy chain 1). Is predicted to have several functions, including ATP-dependent microtubule motor activity, minus-end-directed\; dynein intermediate chain binding activity\; and dynein light chain binding activity. Is involved in several processes, including GABAergic synaptic transmission\; cytoskeleton-dependent intracellular transport\; and generation of neurons. Localizes to the cell cortex\; intracellular non-membrane-bounded organelle\; and nuclear envelope. Is expressed in germ cells\; the head\; the somatic cell\; and the tail. Is used to study lissencephaly. Human ortholog(s) of this gene are implicated in Charcot-Marie-Tooth disease axonal type 2O and autosomal dominant non-syndromic intellectual disability 13.

Lineage tracing results

Phenotype

Cell
cycle
Division
asynchrony
Division
asymmetry
CND-1
expression
Division
angle
(A/P)
Cell
position
Phenotype
detection
DHC-1_emb1 34 0 1 1 0 0
DHC-1_emb2 0 0 0 0 0 0
DHC-1_emb3 20 0 0 0 2 0
With cellular defects No No No No No No

Early embryonic arrest

Arrest embryo: DHC-1_emb4

Cell Proliferation

Proliferation speed

Cell cycle length

No defects

Division asynchrony

No defects

Division asymmetry(A/P)

No defects

Tissue Marker Expression (CND-1)

CND-1 expression

No defects

Morphogenesis

Division angle(A/P)

No defects

Relative cell position

No defects