YEL048C

Return home


WT_vs_xrn1_delta
lithium
TS_control


Description : Protein that interacts with subunits of the TRAPP complex and may play a role its assembly or stability; mutation is synthetically lethal with gcs1 deletion; Sedlin_N family member; human Sedlin mutations cause the skeletal disorder SEDT

ID gene Alias Chr Start Stop Strand orf_classification
YEL048C TCA17 TCA17 5 64709 65167 - Verified

Sequence read density, YEL048C, TCA17, (5:57438..72437)



A tool by Marc Descrimes