Summary

Gene name
stn-1
Sequence name
F30A10.8
Gene ID
WBGene00006062
Gene type
Protein Coding
RNAi library location
I-4P05
Gene information
Is an ortholog of human SNTA1 (syntrophin alpha 1)\; SNTB1 (syntrophin beta 1)\; and SNTB2 (syntrophin beta 2). Exhibits acetylcholine transmembrane transporter activity and calcium channel regulator activity. Is involved in several processes, including acetylcholine transport\; muscle cell cellular homeostasis\; and negative regulation of ion transmembrane transporter activity. Localizes to the dystrophin-associated glycoprotein complex. Is expressed in the body wall musculature\; the nervous system\; and the vulval muscle. Is used to study Duchenne muscular dystrophy. Human ortholog(s) of this gene are implicated in long QT syndrome 12.

Lineage tracing results

Phenotype

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