CIViC Compass
Research use only — not FDA-cleared, not medical advice. Always consult FDA-approved labeling and a qualified clinician.

ROS1

CIViC ID: 4941 · Entrez: 6098

Aliases: MCF3,ROS,c-ros-1,ROS1

Description

ROS1 is a receptor tyrosine kinase that is frequently involved in genetic rearrangement in a variety of human cancers (e.g. NSCLC, gastric cancer, ovarian cancer, cholangiocarcinoma, colorectal cancer, angiosarcoma...). The resulting fusion protein harbors the constitutively active ROS1 kinase domain and drives cellular proliferation (Davies et. al.). In NSCLC about 1% harbor a ROS1 rearrangement. These patients are predominantely female and have a lower T-stage (Warth et. al.). Treatment with crizotinib leads to a reported objective response rate of appr. 70% and a median duration of response of 18 months (Shaw et. al.). Resistance mechanisms to crizotinib have been described and involve mutations in the kinase domain. More selective inhibitors of ROS1 might overcome this resistance (Davare et. al.).

Cyan = gene  ·  Slate = variant  ·  Green = drug  ·  Click variant to filter table

Variants (4)

CIViC IDNameHGVSType(s)
1271G2032R
GLY2032ARG,GLY2026ARG,GLY2028ARG,G2026R,G2028R,RS1057519788
NC_000006.11:g.117638347C>T,NM_002944.2:c.6094G>A,NP_002935.2:p.Gly2032Arg,ENST00000368508.3:c.6094G>A,NM_001378902.1:c.6076G>A,NP_001365831.1:p.Gly2026Arg,NP_001365820.1:p.Gly2028Arg,NM_001378891.1:c.6082G>A,NC_000006.12:g.117317184C>T,ENST00000368507.8:c.6076G>Amissense_variant
518G2101A
GLY2095ALA,G2095A,GLY2101ALA
NC_000006.11:g.117631376C>G,ENST00000368508.3:c.6302G>C,NM_002944.2:c.6302G>C,NP_002935.2:p.Gly2101Ala,ENST00000368507.8:c.6284G>C,NM_001378902.1:c.6284G>C,NP_001365831.1:p.Gly2095Alamissense_variant
516L2026M
LEU2026MET
NC_000006.11:g.117638365G>T,ENST00000368508.3:c.6076C>A,NM_002944.2:c.6076C>A,NP_002935.2:p.Leu2026Metmissense_variant
517L2155S
L2149S,LEU2155SER,LEU2149SER
NC_000006.11:g.117630062A>G,NM_002944.2:c.6464T>C,NP_002935.2:p.Leu2155Ser,ENST00000368508.3:c.6464T>C,ENSP00000357493.3:p.Leu2149Ser,NP_001365831.1:p.Leu2149Ser ,ENST00000368507.8:c.6446T>C,NM_001378902.1:c.6446T>Cmissense_variant