Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
T |
G |
6: 121,647,957 (GRCm39) |
L1150V |
probably damaging |
Het |
AB124611 |
A |
G |
9: 21,455,989 (GRCm39) |
D194G |
possibly damaging |
Het |
Adgrv1 |
A |
G |
13: 81,669,302 (GRCm39) |
L2418P |
probably benign |
Het |
Ap3m1 |
A |
G |
14: 21,090,152 (GRCm39) |
S213P |
probably damaging |
Het |
Apobec2 |
A |
T |
17: 48,739,531 (GRCm39) |
L36H |
|
Het |
Arrb1 |
A |
G |
7: 99,237,280 (GRCm39) |
D78G |
|
Het |
Astn1 |
A |
G |
1: 158,338,555 (GRCm39) |
Q434R |
probably damaging |
Het |
Cadps |
C |
G |
14: 12,705,676 (GRCm38) |
D240H |
probably damaging |
Het |
Cfhr4 |
A |
G |
1: 139,660,085 (GRCm39) |
I680T |
probably damaging |
Het |
Cmya5 |
A |
C |
13: 93,233,878 (GRCm39) |
D403E |
unknown |
Het |
Crxos |
A |
C |
7: 15,631,436 (GRCm39) |
I45L |
probably benign |
Het |
Dmxl1 |
C |
G |
18: 50,072,639 (GRCm39) |
N2744K |
probably damaging |
Het |
Dnah2 |
A |
G |
11: 69,313,687 (GRCm39) |
I4204T |
|
Het |
Ei24 |
A |
G |
9: 36,697,327 (GRCm39) |
S134P |
probably damaging |
Het |
Eif2ak3 |
G |
T |
6: 70,860,614 (GRCm39) |
V397F |
probably damaging |
Het |
Eif4g2 |
T |
C |
7: 110,672,969 (GRCm39) |
I134V |
|
Het |
Gcnt3 |
T |
C |
9: 69,941,939 (GRCm39) |
M210V |
probably damaging |
Het |
Gpatch8 |
A |
G |
11: 102,370,299 (GRCm39) |
S1080P |
probably benign |
Het |
Gtf3c1 |
A |
G |
7: 125,244,949 (GRCm39) |
L1695P |
possibly damaging |
Het |
Haus3 |
A |
G |
5: 34,324,994 (GRCm39) |
F222L |
probably damaging |
Het |
Kbtbd8 |
C |
T |
6: 95,099,825 (GRCm39) |
Q445* |
probably null |
Het |
Kcnc3 |
A |
G |
7: 44,240,592 (GRCm39) |
N95D |
probably damaging |
Het |
Krt40 |
C |
T |
11: 99,430,693 (GRCm39) |
|
probably null |
Het |
Lgi1 |
A |
G |
19: 38,289,746 (GRCm39) |
T271A |
probably benign |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Map3k21 |
A |
G |
8: 126,665,463 (GRCm39) |
T551A |
possibly damaging |
Het |
Muc5ac |
T |
C |
7: 141,363,529 (GRCm39) |
I2280T |
unknown |
Het |
Mug1 |
C |
A |
6: 121,851,390 (GRCm39) |
D762E |
probably damaging |
Het |
Myo1e |
A |
T |
9: 70,266,605 (GRCm39) |
N615I |
probably damaging |
Het |
Or4k36 |
T |
C |
2: 111,145,827 (GRCm39) |
M1T |
probably null |
Het |
Or51f23 |
T |
C |
7: 102,453,339 (GRCm39) |
L218P |
probably damaging |
Het |
Pld5 |
T |
C |
1: 175,803,104 (GRCm39) |
E387G |
possibly damaging |
Het |
Pld5 |
A |
G |
1: 175,902,003 (GRCm39) |
V195A |
probably benign |
Het |
Rad54l |
T |
C |
4: 115,980,349 (GRCm39) |
|
probably benign |
Het |
Rnf123 |
A |
T |
9: 107,940,227 (GRCm39) |
|
probably benign |
Het |
Rnf213 |
A |
G |
11: 119,331,574 (GRCm39) |
E2262G |
|
Het |
Rp1 |
C |
A |
1: 4,234,161 (GRCm39) |
V910L |
unknown |
Het |
Rpp21 |
A |
T |
17: 36,568,407 (GRCm39) |
C23S |
probably benign |
Het |
Scn11a |
T |
C |
9: 119,588,989 (GRCm39) |
M1306V |
possibly damaging |
Het |
Scn2b |
C |
T |
9: 45,036,734 (GRCm39) |
L81F |
possibly damaging |
Het |
Sco2 |
T |
C |
15: 89,256,363 (GRCm39) |
D97G |
probably damaging |
Het |
Slc25a54 |
T |
C |
3: 109,001,548 (GRCm39) |
V112A |
probably benign |
Het |
Slc5a11 |
A |
T |
7: 122,864,492 (GRCm39) |
K363* |
probably null |
Het |
Smg1 |
G |
T |
7: 117,753,884 (GRCm39) |
T2563K |
unknown |
Het |
Snap47 |
A |
T |
11: 59,319,290 (GRCm39) |
S283T |
probably damaging |
Het |
Speer4a3 |
CTTT |
C |
5: 26,155,857 (GRCm39) |
|
probably benign |
Het |
Stat1 |
G |
T |
1: 52,178,388 (GRCm39) |
R274L |
probably damaging |
Het |
Stoml1 |
A |
G |
9: 58,164,409 (GRCm39) |
T166A |
|
Het |
Svs5 |
G |
T |
2: 164,079,509 (GRCm39) |
Q133K |
probably benign |
Het |
Tas2r107 |
T |
A |
6: 131,636,422 (GRCm39) |
H209L |
probably benign |
Het |
Tmco3 |
T |
A |
8: 13,360,228 (GRCm39) |
V477D |
possibly damaging |
Het |
Tmem131 |
A |
T |
1: 36,880,767 (GRCm39) |
S168T |
possibly damaging |
Het |
Tmem41a |
T |
C |
16: 21,755,859 (GRCm39) |
N149S |
probably damaging |
Het |
Ttll4 |
T |
C |
1: 74,719,225 (GRCm39) |
F359L |
probably benign |
Het |
Ttn |
T |
A |
2: 76,785,162 (GRCm39) |
M784L |
unknown |
Het |
Ubr1 |
A |
G |
2: 120,703,603 (GRCm39) |
|
probably null |
Het |
Ubxn2b |
C |
T |
4: 6,214,646 (GRCm39) |
P227S |
probably damaging |
Het |
Upb1 |
C |
T |
10: 75,265,961 (GRCm39) |
L263F |
probably benign |
Het |
Usp15 |
T |
A |
10: 122,949,553 (GRCm39) |
T935S |
probably benign |
Het |
Zscan4-ps3 |
G |
A |
7: 11,347,164 (GRCm39) |
C400Y |
probably damaging |
Het |
|
Other mutations in Fam186a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00588:Fam186a
|
APN |
15 |
99,825,572 (GRCm39) |
splice site |
probably benign |
|
IGL03047:Fam186a
|
UTSW |
15 |
99,843,589 (GRCm39) |
missense |
unknown |
|
R0172:Fam186a
|
UTSW |
15 |
99,852,768 (GRCm39) |
missense |
unknown |
|
R0194:Fam186a
|
UTSW |
15 |
99,839,644 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0381:Fam186a
|
UTSW |
15 |
99,840,055 (GRCm39) |
missense |
probably damaging |
0.97 |
R0799:Fam186a
|
UTSW |
15 |
99,839,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R1295:Fam186a
|
UTSW |
15 |
99,837,670 (GRCm39) |
splice site |
probably benign |
|
R1366:Fam186a
|
UTSW |
15 |
99,841,270 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1519:Fam186a
|
UTSW |
15 |
99,845,536 (GRCm39) |
missense |
unknown |
|
R1592:Fam186a
|
UTSW |
15 |
99,838,199 (GRCm39) |
missense |
probably benign |
0.01 |
R1636:Fam186a
|
UTSW |
15 |
99,839,539 (GRCm39) |
missense |
unknown |
|
R1719:Fam186a
|
UTSW |
15 |
99,840,227 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1759:Fam186a
|
UTSW |
15 |
99,864,762 (GRCm39) |
nonsense |
probably null |
|
R1856:Fam186a
|
UTSW |
15 |
99,838,183 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2131:Fam186a
|
UTSW |
15 |
99,831,557 (GRCm39) |
unclassified |
probably benign |
|
R2192:Fam186a
|
UTSW |
15 |
99,838,192 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2239:Fam186a
|
UTSW |
15 |
99,852,745 (GRCm39) |
missense |
unknown |
|
R2251:Fam186a
|
UTSW |
15 |
99,842,978 (GRCm39) |
missense |
probably benign |
0.02 |
R2902:Fam186a
|
UTSW |
15 |
99,843,049 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3037:Fam186a
|
UTSW |
15 |
99,841,675 (GRCm39) |
missense |
probably damaging |
0.99 |
R3744:Fam186a
|
UTSW |
15 |
99,845,416 (GRCm39) |
missense |
unknown |
|
R4021:Fam186a
|
UTSW |
15 |
99,839,680 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4183:Fam186a
|
UTSW |
15 |
99,831,566 (GRCm39) |
unclassified |
probably benign |
|
R4238:Fam186a
|
UTSW |
15 |
99,841,523 (GRCm39) |
missense |
probably benign |
0.05 |
R4667:Fam186a
|
UTSW |
15 |
99,842,413 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4817:Fam186a
|
UTSW |
15 |
99,831,419 (GRCm39) |
unclassified |
probably benign |
|
R4835:Fam186a
|
UTSW |
15 |
99,843,689 (GRCm39) |
missense |
unknown |
|
R4837:Fam186a
|
UTSW |
15 |
99,838,678 (GRCm39) |
missense |
unknown |
|
R4897:Fam186a
|
UTSW |
15 |
99,843,158 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4902:Fam186a
|
UTSW |
15 |
99,844,723 (GRCm39) |
missense |
unknown |
|
R4950:Fam186a
|
UTSW |
15 |
99,839,534 (GRCm39) |
missense |
unknown |
|
R4995:Fam186a
|
UTSW |
15 |
99,842,980 (GRCm39) |
missense |
probably benign |
0.27 |
R5062:Fam186a
|
UTSW |
15 |
99,842,527 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5124:Fam186a
|
UTSW |
15 |
99,840,977 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5133:Fam186a
|
UTSW |
15 |
99,853,374 (GRCm39) |
missense |
unknown |
|
R5424:Fam186a
|
UTSW |
15 |
99,843,644 (GRCm39) |
missense |
unknown |
|
R5624:Fam186a
|
UTSW |
15 |
99,839,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5628:Fam186a
|
UTSW |
15 |
99,839,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5637:Fam186a
|
UTSW |
15 |
99,839,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5639:Fam186a
|
UTSW |
15 |
99,844,931 (GRCm39) |
missense |
unknown |
|
R5652:Fam186a
|
UTSW |
15 |
99,843,253 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5673:Fam186a
|
UTSW |
15 |
99,839,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5799:Fam186a
|
UTSW |
15 |
99,864,705 (GRCm39) |
nonsense |
probably null |
|
R5965:Fam186a
|
UTSW |
15 |
99,842,978 (GRCm39) |
missense |
probably benign |
0.37 |
R6044:Fam186a
|
UTSW |
15 |
99,839,878 (GRCm39) |
missense |
probably damaging |
0.97 |
R6077:Fam186a
|
UTSW |
15 |
99,840,584 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6120:Fam186a
|
UTSW |
15 |
99,838,244 (GRCm39) |
missense |
probably benign |
0.00 |
R6185:Fam186a
|
UTSW |
15 |
99,845,530 (GRCm39) |
missense |
unknown |
|
R6186:Fam186a
|
UTSW |
15 |
99,845,206 (GRCm39) |
missense |
unknown |
|
R6242:Fam186a
|
UTSW |
15 |
99,837,788 (GRCm39) |
missense |
unknown |
|
R6351:Fam186a
|
UTSW |
15 |
99,839,623 (GRCm39) |
missense |
probably damaging |
0.97 |
R6368:Fam186a
|
UTSW |
15 |
99,841,198 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6369:Fam186a
|
UTSW |
15 |
99,845,212 (GRCm39) |
missense |
unknown |
|
R6559:Fam186a
|
UTSW |
15 |
99,842,356 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6855:Fam186a
|
UTSW |
15 |
99,852,756 (GRCm39) |
missense |
unknown |
|
R6867:Fam186a
|
UTSW |
15 |
99,843,731 (GRCm39) |
missense |
unknown |
|
R6957:Fam186a
|
UTSW |
15 |
99,844,357 (GRCm39) |
missense |
unknown |
|
R6961:Fam186a
|
UTSW |
15 |
99,838,082 (GRCm39) |
missense |
probably benign |
0.16 |
R6994:Fam186a
|
UTSW |
15 |
99,840,347 (GRCm39) |
missense |
probably benign |
0.35 |
R6996:Fam186a
|
UTSW |
15 |
99,853,374 (GRCm39) |
missense |
unknown |
|
R7062:Fam186a
|
UTSW |
15 |
99,831,521 (GRCm39) |
unclassified |
probably benign |
|
R7064:Fam186a
|
UTSW |
15 |
99,839,557 (GRCm39) |
missense |
unknown |
|
R7173:Fam186a
|
UTSW |
15 |
99,843,531 (GRCm39) |
missense |
unknown |
|
R7244:Fam186a
|
UTSW |
15 |
99,844,273 (GRCm39) |
missense |
unknown |
|
R7270:Fam186a
|
UTSW |
15 |
99,842,033 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7410:Fam186a
|
UTSW |
15 |
99,844,826 (GRCm39) |
nonsense |
probably null |
|
R7437:Fam186a
|
UTSW |
15 |
99,840,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R7475:Fam186a
|
UTSW |
15 |
99,845,395 (GRCm39) |
missense |
unknown |
|
R7487:Fam186a
|
UTSW |
15 |
99,840,017 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7526:Fam186a
|
UTSW |
15 |
99,839,796 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7650:Fam186a
|
UTSW |
15 |
99,837,788 (GRCm39) |
missense |
unknown |
|
R7658:Fam186a
|
UTSW |
15 |
99,837,725 (GRCm39) |
missense |
unknown |
|
R7663:Fam186a
|
UTSW |
15 |
99,842,950 (GRCm39) |
missense |
probably benign |
0.00 |
R7703:Fam186a
|
UTSW |
15 |
99,852,678 (GRCm39) |
missense |
unknown |
|
R7814:Fam186a
|
UTSW |
15 |
99,842,545 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7958:Fam186a
|
UTSW |
15 |
99,841,189 (GRCm39) |
missense |
probably damaging |
0.99 |
R7970:Fam186a
|
UTSW |
15 |
99,831,467 (GRCm39) |
missense |
unknown |
|
R8076:Fam186a
|
UTSW |
15 |
99,841,351 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8087:Fam186a
|
UTSW |
15 |
99,839,725 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8130:Fam186a
|
UTSW |
15 |
99,841,914 (GRCm39) |
frame shift |
probably null |
|
R8239:Fam186a
|
UTSW |
15 |
99,839,191 (GRCm39) |
missense |
unknown |
|
R8246:Fam186a
|
UTSW |
15 |
99,838,428 (GRCm39) |
missense |
unknown |
|
R8446:Fam186a
|
UTSW |
15 |
99,845,335 (GRCm39) |
missense |
unknown |
|
R8469:Fam186a
|
UTSW |
15 |
99,845,186 (GRCm39) |
missense |
unknown |
|
R8676:Fam186a
|
UTSW |
15 |
99,845,023 (GRCm39) |
missense |
unknown |
|
R8790:Fam186a
|
UTSW |
15 |
99,841,024 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8808:Fam186a
|
UTSW |
15 |
99,842,604 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8848:Fam186a
|
UTSW |
15 |
99,838,034 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9083:Fam186a
|
UTSW |
15 |
99,843,079 (GRCm39) |
missense |
probably benign |
0.27 |
R9106:Fam186a
|
UTSW |
15 |
99,844,107 (GRCm39) |
small deletion |
probably benign |
|
R9116:Fam186a
|
UTSW |
15 |
99,840,472 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9227:Fam186a
|
UTSW |
15 |
99,853,384 (GRCm39) |
missense |
unknown |
|
R9250:Fam186a
|
UTSW |
15 |
99,845,330 (GRCm39) |
missense |
unknown |
|
R9282:Fam186a
|
UTSW |
15 |
99,839,879 (GRCm39) |
missense |
probably damaging |
0.97 |
R9495:Fam186a
|
UTSW |
15 |
99,844,766 (GRCm39) |
missense |
unknown |
|
R9514:Fam186a
|
UTSW |
15 |
99,844,766 (GRCm39) |
missense |
unknown |
|
R9521:Fam186a
|
UTSW |
15 |
99,841,471 (GRCm39) |
missense |
probably damaging |
0.97 |
R9553:Fam186a
|
UTSW |
15 |
99,844,561 (GRCm39) |
missense |
unknown |
|
R9641:Fam186a
|
UTSW |
15 |
99,838,244 (GRCm39) |
missense |
probably benign |
0.00 |
R9655:Fam186a
|
UTSW |
15 |
99,840,973 (GRCm39) |
missense |
probably damaging |
0.99 |
R9661:Fam186a
|
UTSW |
15 |
99,842,492 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9673:Fam186a
|
UTSW |
15 |
99,841,024 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9762:Fam186a
|
UTSW |
15 |
99,842,393 (GRCm39) |
missense |
possibly damaging |
0.66 |
X0021:Fam186a
|
UTSW |
15 |
99,843,316 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Fam186a
|
UTSW |
15 |
99,843,875 (GRCm39) |
missense |
unknown |
|
|