Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adprhl1 |
T |
C |
8: 13,296,114 (GRCm39) |
K144E |
probably benign |
Het |
Bcdin3d |
A |
G |
15: 99,368,614 (GRCm39) |
L195P |
probably damaging |
Het |
Bltp1 |
A |
G |
3: 37,012,830 (GRCm39) |
|
probably null |
Het |
Col11a1 |
T |
A |
3: 113,901,965 (GRCm39) |
S553R |
unknown |
Het |
Cp |
A |
T |
3: 20,020,517 (GRCm39) |
D170V |
probably damaging |
Het |
Dnah17 |
C |
T |
11: 117,915,994 (GRCm39) |
A4303T |
probably benign |
Het |
Dpp4 |
G |
A |
2: 62,217,484 (GRCm39) |
R38C |
possibly damaging |
Het |
Dusp6 |
C |
T |
10: 99,099,786 (GRCm39) |
T78M |
probably damaging |
Het |
Exoc1 |
A |
G |
5: 76,689,866 (GRCm39) |
|
probably benign |
Het |
Fbxl13 |
A |
T |
5: 21,787,051 (GRCm39) |
C295* |
probably null |
Het |
Gpsm1 |
G |
A |
2: 26,209,843 (GRCm39) |
|
probably benign |
Het |
Gstm4 |
T |
A |
3: 107,950,644 (GRCm39) |
D85V |
possibly damaging |
Het |
Hectd4 |
A |
G |
5: 121,488,544 (GRCm39) |
N3612D |
possibly damaging |
Het |
Izumo3 |
T |
C |
4: 92,035,136 (GRCm39) |
D27G |
probably damaging |
Het |
Kcna4 |
T |
A |
2: 107,125,718 (GRCm39) |
C151S |
probably benign |
Het |
Lrrc10 |
A |
G |
10: 116,881,719 (GRCm39) |
N131S |
probably damaging |
Het |
Madd |
A |
G |
2: 90,997,932 (GRCm39) |
S699P |
probably damaging |
Het |
Mcpt4 |
A |
T |
14: 56,297,993 (GRCm39) |
V186D |
probably damaging |
Het |
Mrgprx3-ps |
T |
C |
7: 46,959,746 (GRCm39) |
|
noncoding transcript |
Het |
Mrm1 |
G |
T |
11: 84,710,054 (GRCm39) |
R49S |
possibly damaging |
Het |
Nav2 |
T |
A |
7: 49,047,857 (GRCm39) |
N91K |
probably benign |
Het |
Noct |
C |
T |
3: 51,157,756 (GRCm39) |
R365W |
probably damaging |
Het |
Ntn1 |
C |
T |
11: 68,276,736 (GRCm39) |
G71S |
probably damaging |
Het |
Or10x1 |
T |
C |
1: 174,197,040 (GRCm39) |
S186P |
probably damaging |
Het |
Plekhg3 |
A |
C |
12: 76,624,538 (GRCm39) |
T1127P |
probably damaging |
Het |
Rhbdl2 |
A |
T |
4: 123,703,880 (GRCm39) |
M52L |
probably benign |
Het |
Saxo5 |
T |
A |
8: 3,533,529 (GRCm39) |
H278Q |
probably damaging |
Het |
Slc10a1 |
T |
C |
12: 81,004,906 (GRCm39) |
N212S |
probably benign |
Het |
Sohlh2 |
C |
A |
3: 55,104,423 (GRCm39) |
T264K |
probably damaging |
Het |
Syn3 |
C |
A |
10: 85,891,456 (GRCm39) |
|
probably benign |
Het |
Taf5 |
T |
A |
19: 47,059,453 (GRCm39) |
V199D |
probably damaging |
Het |
Tas2r136 |
C |
A |
6: 132,754,972 (GRCm39) |
V52L |
probably damaging |
Het |
Tnk2 |
C |
T |
16: 32,488,319 (GRCm39) |
R191C |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,556,120 (GRCm39) |
I21968T |
probably damaging |
Het |
Ubxn6 |
A |
T |
17: 56,376,303 (GRCm39) |
V311E |
probably damaging |
Het |
Usp7 |
C |
A |
16: 8,526,778 (GRCm39) |
D187Y |
probably damaging |
Het |
Vmn1r115 |
C |
T |
7: 20,578,207 (GRCm39) |
R235K |
probably benign |
Het |
Vmn2r50 |
A |
C |
7: 9,784,235 (GRCm39) |
F80V |
probably damaging |
Het |
Vmn2r58 |
T |
A |
7: 41,511,360 (GRCm39) |
K481M |
possibly damaging |
Het |
Vmn2r86 |
A |
G |
10: 130,288,469 (GRCm39) |
I344T |
possibly damaging |
Het |
Vmn2r99 |
T |
A |
17: 19,599,522 (GRCm39) |
V402E |
probably damaging |
Het |
Zfp462 |
A |
G |
4: 55,012,672 (GRCm39) |
D1546G |
probably damaging |
Het |
|
Other mutations in Srrm2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00421:Srrm2
|
APN |
17 |
24,031,452 (GRCm39) |
missense |
probably benign |
0.23 |
IGL00484:Srrm2
|
APN |
17 |
24,037,492 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01413:Srrm2
|
APN |
17 |
24,034,999 (GRCm39) |
unclassified |
probably benign |
|
IGL02272:Srrm2
|
APN |
17 |
24,034,756 (GRCm39) |
unclassified |
probably benign |
|
IGL02279:Srrm2
|
APN |
17 |
24,034,306 (GRCm39) |
unclassified |
probably benign |
|
IGL02325:Srrm2
|
APN |
17 |
24,029,453 (GRCm39) |
unclassified |
probably benign |
|
IGL02947:Srrm2
|
APN |
17 |
24,029,720 (GRCm39) |
missense |
probably benign |
0.23 |
IGL03002:Srrm2
|
APN |
17 |
24,034,708 (GRCm39) |
unclassified |
probably benign |
|
BB009:Srrm2
|
UTSW |
17 |
24,037,501 (GRCm39) |
missense |
probably benign |
0.23 |
BB019:Srrm2
|
UTSW |
17 |
24,037,501 (GRCm39) |
missense |
probably benign |
0.23 |
R0173:Srrm2
|
UTSW |
17 |
24,034,103 (GRCm39) |
unclassified |
probably benign |
|
R1018:Srrm2
|
UTSW |
17 |
24,041,514 (GRCm39) |
missense |
probably damaging |
0.98 |
R1109:Srrm2
|
UTSW |
17 |
24,038,591 (GRCm39) |
unclassified |
probably benign |
|
R1199:Srrm2
|
UTSW |
17 |
24,036,725 (GRCm39) |
unclassified |
probably benign |
|
R1471:Srrm2
|
UTSW |
17 |
24,039,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R1478:Srrm2
|
UTSW |
17 |
24,034,876 (GRCm39) |
missense |
probably benign |
0.23 |
R1618:Srrm2
|
UTSW |
17 |
24,037,906 (GRCm39) |
unclassified |
probably benign |
|
R1678:Srrm2
|
UTSW |
17 |
24,037,960 (GRCm39) |
missense |
probably benign |
0.23 |
R1853:Srrm2
|
UTSW |
17 |
24,039,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R1968:Srrm2
|
UTSW |
17 |
24,040,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R2094:Srrm2
|
UTSW |
17 |
24,031,403 (GRCm39) |
unclassified |
probably benign |
|
R2102:Srrm2
|
UTSW |
17 |
24,036,722 (GRCm39) |
unclassified |
probably benign |
|
R2156:Srrm2
|
UTSW |
17 |
24,037,237 (GRCm39) |
missense |
probably benign |
0.23 |
R2214:Srrm2
|
UTSW |
17 |
24,035,719 (GRCm39) |
unclassified |
probably benign |
|
R2913:Srrm2
|
UTSW |
17 |
24,034,658 (GRCm39) |
unclassified |
probably benign |
|
R3721:Srrm2
|
UTSW |
17 |
24,041,549 (GRCm39) |
small deletion |
probably benign |
|
R4411:Srrm2
|
UTSW |
17 |
24,029,442 (GRCm39) |
unclassified |
probably benign |
|
R4412:Srrm2
|
UTSW |
17 |
24,029,442 (GRCm39) |
unclassified |
probably benign |
|
R4583:Srrm2
|
UTSW |
17 |
24,038,593 (GRCm39) |
unclassified |
probably benign |
|
R4682:Srrm2
|
UTSW |
17 |
24,034,666 (GRCm39) |
missense |
probably benign |
0.23 |
R4910:Srrm2
|
UTSW |
17 |
24,034,362 (GRCm39) |
unclassified |
probably benign |
|
R4943:Srrm2
|
UTSW |
17 |
24,041,389 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5023:Srrm2
|
UTSW |
17 |
24,038,291 (GRCm39) |
unclassified |
probably benign |
|
R5033:Srrm2
|
UTSW |
17 |
24,039,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R5163:Srrm2
|
UTSW |
17 |
24,038,524 (GRCm39) |
unclassified |
probably benign |
|
R5186:Srrm2
|
UTSW |
17 |
24,035,561 (GRCm39) |
missense |
probably benign |
0.23 |
R5197:Srrm2
|
UTSW |
17 |
24,036,358 (GRCm39) |
missense |
probably benign |
0.23 |
R5366:Srrm2
|
UTSW |
17 |
24,037,678 (GRCm39) |
missense |
probably benign |
0.23 |
R5483:Srrm2
|
UTSW |
17 |
24,040,246 (GRCm39) |
missense |
probably damaging |
0.96 |
R5551:Srrm2
|
UTSW |
17 |
24,037,450 (GRCm39) |
unclassified |
probably benign |
|
R5602:Srrm2
|
UTSW |
17 |
24,038,311 (GRCm39) |
unclassified |
probably benign |
|
R5733:Srrm2
|
UTSW |
17 |
24,040,360 (GRCm39) |
missense |
probably damaging |
0.98 |
R5774:Srrm2
|
UTSW |
17 |
24,037,249 (GRCm39) |
unclassified |
probably benign |
|
R5909:Srrm2
|
UTSW |
17 |
24,040,291 (GRCm39) |
missense |
probably benign |
0.27 |
R5961:Srrm2
|
UTSW |
17 |
24,039,083 (GRCm39) |
unclassified |
probably benign |
|
R6122:Srrm2
|
UTSW |
17 |
24,039,330 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6906:Srrm2
|
UTSW |
17 |
24,039,337 (GRCm39) |
missense |
probably damaging |
0.97 |
R7084:Srrm2
|
UTSW |
17 |
24,039,290 (GRCm39) |
missense |
probably damaging |
0.99 |
R7177:Srrm2
|
UTSW |
17 |
24,035,747 (GRCm39) |
missense |
unknown |
|
R7197:Srrm2
|
UTSW |
17 |
24,037,198 (GRCm39) |
missense |
unknown |
|
R7442:Srrm2
|
UTSW |
17 |
24,039,091 (GRCm39) |
missense |
unknown |
|
R7644:Srrm2
|
UTSW |
17 |
24,038,294 (GRCm39) |
missense |
unknown |
|
R7664:Srrm2
|
UTSW |
17 |
24,039,955 (GRCm39) |
missense |
probably damaging |
0.99 |
R7874:Srrm2
|
UTSW |
17 |
24,034,652 (GRCm39) |
missense |
unknown |
|
R7932:Srrm2
|
UTSW |
17 |
24,037,501 (GRCm39) |
missense |
probably benign |
0.23 |
R7950:Srrm2
|
UTSW |
17 |
24,027,084 (GRCm39) |
missense |
unknown |
|
R7958:Srrm2
|
UTSW |
17 |
24,040,286 (GRCm39) |
missense |
probably benign |
0.25 |
R8081:Srrm2
|
UTSW |
17 |
24,039,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R8118:Srrm2
|
UTSW |
17 |
24,027,057 (GRCm39) |
missense |
unknown |
|
R8174:Srrm2
|
UTSW |
17 |
24,034,297 (GRCm39) |
missense |
unknown |
|
R8191:Srrm2
|
UTSW |
17 |
24,039,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R8334:Srrm2
|
UTSW |
17 |
24,027,330 (GRCm39) |
missense |
unknown |
|
R8523:Srrm2
|
UTSW |
17 |
24,027,489 (GRCm39) |
unclassified |
probably benign |
|
R8728:Srrm2
|
UTSW |
17 |
24,038,831 (GRCm39) |
missense |
unknown |
|
R8912:Srrm2
|
UTSW |
17 |
24,038,575 (GRCm39) |
missense |
probably benign |
0.23 |
R9209:Srrm2
|
UTSW |
17 |
24,039,880 (GRCm39) |
missense |
probably benign |
0.05 |
RF006:Srrm2
|
UTSW |
17 |
24,031,562 (GRCm39) |
missense |
unknown |
|
Z1176:Srrm2
|
UTSW |
17 |
24,036,157 (GRCm39) |
missense |
unknown |
|
Z1177:Srrm2
|
UTSW |
17 |
24,036,484 (GRCm39) |
missense |
unknown |
|
|