Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
A |
G |
6: 121,651,820 (GRCm39) |
N1296S |
probably damaging |
Het |
Abca5 |
A |
T |
11: 110,210,686 (GRCm39) |
D164E |
probably benign |
Het |
Adamts5 |
T |
C |
16: 85,666,956 (GRCm39) |
D512G |
probably damaging |
Het |
Ankrd11 |
G |
A |
8: 123,617,216 (GRCm39) |
T2191I |
probably benign |
Het |
Anxa3 |
T |
C |
5: 96,986,171 (GRCm39) |
F270S |
possibly damaging |
Het |
Bard1 |
A |
G |
1: 71,092,770 (GRCm39) |
|
probably null |
Het |
Ccdc142 |
T |
C |
6: 83,084,777 (GRCm39) |
V591A |
probably damaging |
Het |
Col6a3 |
C |
T |
1: 90,716,776 (GRCm39) |
E1613K |
unknown |
Het |
Dnah9 |
T |
A |
11: 65,975,492 (GRCm39) |
H1519L |
probably damaging |
Het |
Enah |
A |
C |
1: 181,763,235 (GRCm39) |
|
probably benign |
Het |
Fat3 |
A |
T |
9: 15,901,856 (GRCm39) |
N3056K |
possibly damaging |
Het |
Gm4846 |
T |
A |
1: 166,317,748 (GRCm39) |
N223Y |
probably benign |
Het |
Gm8104 |
A |
G |
14: 42,958,975 (GRCm39) |
N55S |
probably damaging |
Het |
Gpatch8 |
A |
G |
11: 102,370,404 (GRCm39) |
S1045P |
probably damaging |
Het |
Haus4 |
A |
G |
14: 54,781,251 (GRCm39) |
M275T |
probably benign |
Het |
Ighe |
T |
A |
12: 113,235,006 (GRCm39) |
T385S |
unknown |
Het |
Ipo9 |
G |
A |
1: 135,347,808 (GRCm39) |
S78L |
probably damaging |
Het |
Kif21b |
G |
A |
1: 136,099,411 (GRCm39) |
V1473M |
probably damaging |
Het |
Lama1 |
T |
A |
17: 68,052,078 (GRCm39) |
Y345* |
probably null |
Het |
Lgr6 |
C |
T |
1: 134,921,748 (GRCm39) |
A199T |
probably damaging |
Het |
Loxl3 |
A |
G |
6: 83,012,775 (GRCm39) |
T105A |
probably benign |
Het |
Map4k3 |
A |
G |
17: 80,922,599 (GRCm39) |
S441P |
probably benign |
Het |
Med12l |
C |
T |
3: 59,153,209 (GRCm39) |
T1078I |
probably damaging |
Het |
Mef2c |
T |
A |
13: 83,801,026 (GRCm39) |
M242K |
possibly damaging |
Het |
Morc2b |
A |
G |
17: 33,355,226 (GRCm39) |
Y849H |
probably benign |
Het |
Mroh2b |
T |
A |
15: 4,971,004 (GRCm39) |
V1003E |
probably benign |
Het |
Myo15a |
T |
A |
11: 60,393,674 (GRCm39) |
M1135K |
possibly damaging |
Het |
Nckap1l |
A |
T |
15: 103,392,066 (GRCm39) |
I834F |
probably benign |
Het |
Nrg1 |
T |
A |
8: 32,308,507 (GRCm39) |
Y503F |
probably damaging |
Het |
Numa1 |
T |
C |
7: 101,644,731 (GRCm39) |
S236P |
possibly damaging |
Het |
Or4f61 |
A |
T |
2: 111,922,734 (GRCm39) |
I104N |
probably benign |
Het |
Pcdhga2 |
T |
C |
18: 37,802,795 (GRCm39) |
V213A |
probably benign |
Het |
Pdzd2 |
A |
T |
15: 12,390,119 (GRCm39) |
M826K |
probably damaging |
Het |
Pdzrn3 |
C |
T |
6: 101,130,272 (GRCm39) |
D515N |
probably damaging |
Het |
Rnf38 |
T |
C |
4: 44,149,176 (GRCm39) |
Q57R |
probably benign |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Serpina6 |
T |
C |
12: 103,618,157 (GRCm39) |
T219A |
probably benign |
Het |
Spata31d1c |
T |
A |
13: 65,183,248 (GRCm39) |
N263K |
probably benign |
Het |
Spef2 |
T |
G |
15: 9,667,316 (GRCm39) |
I791L |
possibly damaging |
Het |
Sv2a |
T |
C |
3: 96,092,776 (GRCm39) |
C159R |
probably damaging |
Het |
Tbc1d31 |
T |
A |
15: 57,824,315 (GRCm39) |
L859Q |
probably damaging |
Het |
Tecta |
C |
A |
9: 42,306,239 (GRCm39) |
R63L |
probably damaging |
Het |
Tex52 |
A |
G |
6: 128,361,779 (GRCm39) |
E252G |
probably damaging |
Het |
Tnfsf13b |
A |
G |
8: 10,081,608 (GRCm39) |
I257V |
possibly damaging |
Het |
Tpk1 |
A |
G |
6: 43,400,653 (GRCm39) |
L172P |
probably damaging |
Het |
Trim3 |
T |
G |
7: 105,268,720 (GRCm39) |
N78T |
possibly damaging |
Het |
Try5 |
A |
G |
6: 41,289,312 (GRCm39) |
V88A |
probably benign |
Het |
Vmn1r222 |
T |
G |
13: 23,417,172 (GRCm39) |
M14L |
probably benign |
Het |
Wdr90 |
A |
T |
17: 26,074,277 (GRCm39) |
V678E |
probably benign |
Het |
Zan |
A |
G |
5: 137,452,340 (GRCm39) |
L1543P |
unknown |
Het |
|
Other mutations in Egf |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00272:Egf
|
APN |
3 |
129,505,098 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00579:Egf
|
APN |
3 |
129,491,447 (GRCm39) |
missense |
probably benign |
0.36 |
IGL01307:Egf
|
APN |
3 |
129,533,642 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01314:Egf
|
APN |
3 |
129,479,909 (GRCm39) |
missense |
probably benign |
0.16 |
IGL01360:Egf
|
APN |
3 |
129,533,669 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01367:Egf
|
APN |
3 |
129,496,104 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01610:Egf
|
APN |
3 |
129,499,909 (GRCm39) |
splice site |
probably benign |
|
IGL01721:Egf
|
APN |
3 |
129,491,371 (GRCm39) |
nonsense |
probably null |
|
IGL01803:Egf
|
APN |
3 |
129,530,415 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01866:Egf
|
APN |
3 |
129,529,529 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02001:Egf
|
APN |
3 |
129,510,417 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02141:Egf
|
APN |
3 |
129,533,631 (GRCm39) |
nonsense |
probably null |
|
IGL02209:Egf
|
APN |
3 |
129,500,956 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02347:Egf
|
APN |
3 |
129,472,026 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02821:Egf
|
APN |
3 |
129,496,128 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02902:Egf
|
APN |
3 |
129,474,796 (GRCm39) |
missense |
probably benign |
0.34 |
IGL03114:Egf
|
APN |
3 |
129,530,529 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4151001:Egf
|
UTSW |
3 |
129,496,198 (GRCm39) |
missense |
probably benign |
0.00 |
R0200:Egf
|
UTSW |
3 |
129,531,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R0200:Egf
|
UTSW |
3 |
129,499,882 (GRCm39) |
missense |
probably benign |
0.00 |
R0463:Egf
|
UTSW |
3 |
129,531,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R0463:Egf
|
UTSW |
3 |
129,499,882 (GRCm39) |
missense |
probably benign |
0.00 |
R0507:Egf
|
UTSW |
3 |
129,474,828 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0801:Egf
|
UTSW |
3 |
129,496,234 (GRCm39) |
splice site |
probably benign |
|
R1495:Egf
|
UTSW |
3 |
129,506,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R1535:Egf
|
UTSW |
3 |
129,484,427 (GRCm39) |
missense |
probably benign |
0.00 |
R1626:Egf
|
UTSW |
3 |
129,479,864 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1702:Egf
|
UTSW |
3 |
129,484,460 (GRCm39) |
missense |
probably benign |
0.17 |
R1906:Egf
|
UTSW |
3 |
129,518,873 (GRCm39) |
missense |
probably benign |
0.01 |
R2184:Egf
|
UTSW |
3 |
129,517,007 (GRCm39) |
nonsense |
probably null |
|
R3842:Egf
|
UTSW |
3 |
129,491,442 (GRCm39) |
nonsense |
probably null |
|
R3918:Egf
|
UTSW |
3 |
129,490,509 (GRCm39) |
missense |
probably null |
0.22 |
R4073:Egf
|
UTSW |
3 |
129,529,618 (GRCm39) |
missense |
probably benign |
0.01 |
R4074:Egf
|
UTSW |
3 |
129,529,618 (GRCm39) |
missense |
probably benign |
0.01 |
R4075:Egf
|
UTSW |
3 |
129,529,618 (GRCm39) |
missense |
probably benign |
0.01 |
R4307:Egf
|
UTSW |
3 |
129,512,744 (GRCm39) |
missense |
probably damaging |
0.99 |
R4321:Egf
|
UTSW |
3 |
129,499,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R4617:Egf
|
UTSW |
3 |
129,484,442 (GRCm39) |
missense |
probably benign |
0.02 |
R4646:Egf
|
UTSW |
3 |
129,513,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R4674:Egf
|
UTSW |
3 |
129,511,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R4798:Egf
|
UTSW |
3 |
129,510,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R4931:Egf
|
UTSW |
3 |
129,505,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R4992:Egf
|
UTSW |
3 |
129,505,179 (GRCm39) |
splice site |
probably null |
|
R5166:Egf
|
UTSW |
3 |
129,529,489 (GRCm39) |
missense |
probably benign |
|
R5179:Egf
|
UTSW |
3 |
129,479,936 (GRCm39) |
missense |
probably damaging |
0.99 |
R6043:Egf
|
UTSW |
3 |
129,530,434 (GRCm39) |
missense |
probably benign |
0.09 |
R6119:Egf
|
UTSW |
3 |
129,530,421 (GRCm39) |
missense |
probably benign |
0.00 |
R6493:Egf
|
UTSW |
3 |
129,512,737 (GRCm39) |
start gained |
probably benign |
|
R6639:Egf
|
UTSW |
3 |
129,530,481 (GRCm39) |
missense |
probably benign |
0.22 |
R6936:Egf
|
UTSW |
3 |
129,474,853 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7019:Egf
|
UTSW |
3 |
129,511,713 (GRCm39) |
splice site |
probably null |
|
R7046:Egf
|
UTSW |
3 |
129,548,607 (GRCm39) |
missense |
unknown |
|
R7463:Egf
|
UTSW |
3 |
129,533,664 (GRCm39) |
missense |
probably benign |
0.39 |
R7472:Egf
|
UTSW |
3 |
129,479,912 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7723:Egf
|
UTSW |
3 |
129,499,786 (GRCm39) |
missense |
probably benign |
0.00 |
R7920:Egf
|
UTSW |
3 |
129,529,489 (GRCm39) |
missense |
probably benign |
|
R7952:Egf
|
UTSW |
3 |
129,533,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R8098:Egf
|
UTSW |
3 |
129,484,486 (GRCm39) |
missense |
probably benign |
0.09 |
R8344:Egf
|
UTSW |
3 |
129,548,592 (GRCm39) |
missense |
unknown |
|
R8557:Egf
|
UTSW |
3 |
129,548,600 (GRCm39) |
missense |
unknown |
|
R8912:Egf
|
UTSW |
3 |
129,531,164 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9091:Egf
|
UTSW |
3 |
129,529,449 (GRCm39) |
critical splice donor site |
probably null |
|
R9159:Egf
|
UTSW |
3 |
129,472,026 (GRCm39) |
missense |
probably benign |
0.17 |
R9270:Egf
|
UTSW |
3 |
129,529,449 (GRCm39) |
critical splice donor site |
probably null |
|
R9526:Egf
|
UTSW |
3 |
129,491,421 (GRCm39) |
missense |
probably benign |
|
R9544:Egf
|
UTSW |
3 |
129,511,617 (GRCm39) |
missense |
probably benign |
0.16 |
R9588:Egf
|
UTSW |
3 |
129,511,617 (GRCm39) |
missense |
probably benign |
0.16 |
R9630:Egf
|
UTSW |
3 |
129,518,844 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9639:Egf
|
UTSW |
3 |
129,513,949 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9751:Egf
|
UTSW |
3 |
129,548,538 (GRCm39) |
missense |
probably damaging |
0.99 |
R9772:Egf
|
UTSW |
3 |
129,499,756 (GRCm39) |
missense |
probably benign |
0.01 |
R9776:Egf
|
UTSW |
3 |
129,530,514 (GRCm39) |
missense |
probably damaging |
0.99 |
X0011:Egf
|
UTSW |
3 |
129,504,947 (GRCm39) |
missense |
probably benign |
0.19 |
Z1176:Egf
|
UTSW |
3 |
129,491,366 (GRCm39) |
critical splice donor site |
probably null |
|
|