Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgef26 |
A |
G |
3: 62,288,262 (GRCm39) |
E444G |
probably damaging |
Het |
Astl |
G |
A |
2: 127,189,105 (GRCm39) |
V144M |
possibly damaging |
Het |
AW146154 |
A |
T |
7: 41,129,878 (GRCm39) |
C413S |
probably damaging |
Het |
Bicdl2 |
G |
A |
17: 23,886,519 (GRCm39) |
|
probably benign |
Het |
Cacna1h |
G |
T |
17: 25,610,925 (GRCm39) |
S624R |
probably benign |
Het |
Car9 |
G |
T |
4: 43,512,439 (GRCm39) |
|
probably null |
Het |
Cep126 |
C |
T |
9: 8,100,087 (GRCm39) |
E816K |
probably damaging |
Het |
Cyp2j13 |
T |
C |
4: 95,945,155 (GRCm39) |
K291R |
probably benign |
Het |
Defb26 |
A |
T |
2: 152,349,737 (GRCm39) |
M181K |
unknown |
Het |
Dicer1 |
G |
A |
12: 104,695,401 (GRCm39) |
R177C |
probably damaging |
Het |
Eif4g2 |
A |
G |
7: 110,673,287 (GRCm39) |
Y831H |
probably damaging |
Het |
Ermap |
C |
T |
4: 119,038,558 (GRCm39) |
|
probably null |
Het |
Fcamr |
C |
T |
1: 130,740,757 (GRCm39) |
T392I |
possibly damaging |
Het |
Fgf3 |
T |
C |
7: 144,394,517 (GRCm39) |
|
probably benign |
Het |
Gpr162 |
T |
C |
6: 124,838,161 (GRCm39) |
Y163C |
probably damaging |
Het |
Gprc5d |
T |
C |
6: 135,093,230 (GRCm39) |
R226G |
possibly damaging |
Het |
Hapln3 |
A |
C |
7: 78,771,708 (GRCm39) |
S60R |
probably damaging |
Het |
Hif1a |
T |
C |
12: 73,987,235 (GRCm39) |
S443P |
probably benign |
Het |
Irf2bpl |
A |
G |
12: 86,929,398 (GRCm39) |
M425T |
probably benign |
Het |
Mbtps1 |
A |
G |
8: 120,244,901 (GRCm39) |
L850S |
possibly damaging |
Het |
Mios |
T |
A |
6: 8,228,120 (GRCm39) |
M679K |
possibly damaging |
Het |
Mocos |
T |
C |
18: 24,793,107 (GRCm39) |
F68S |
probably damaging |
Het |
Nuf2 |
T |
C |
1: 169,338,118 (GRCm39) |
|
probably benign |
Het |
Or51k1 |
A |
G |
7: 103,661,523 (GRCm39) |
Y129H |
possibly damaging |
Het |
Orc1 |
T |
A |
4: 108,452,564 (GRCm39) |
D146E |
probably benign |
Het |
Pcdhb22 |
T |
C |
18: 37,651,627 (GRCm39) |
F32L |
probably benign |
Het |
Pde4d |
G |
T |
13: 110,087,809 (GRCm39) |
E562D |
possibly damaging |
Het |
Pgk2 |
T |
C |
17: 40,518,691 (GRCm39) |
K246E |
probably damaging |
Het |
Plekhh2 |
A |
T |
17: 84,884,574 (GRCm39) |
|
probably benign |
Het |
Pou3f2 |
A |
T |
4: 22,487,162 (GRCm39) |
C324S |
probably damaging |
Het |
Prkdc |
C |
T |
16: 15,485,564 (GRCm39) |
L464F |
possibly damaging |
Het |
Prrc2a |
T |
C |
17: 35,376,863 (GRCm39) |
H749R |
possibly damaging |
Het |
Rad18 |
T |
C |
6: 112,597,863 (GRCm39) |
N218S |
possibly damaging |
Het |
Rbm11 |
T |
C |
16: 75,393,531 (GRCm39) |
Y76H |
possibly damaging |
Het |
Rif1 |
T |
G |
2: 52,001,567 (GRCm39) |
Y1674D |
possibly damaging |
Het |
Rrp1b |
A |
G |
17: 32,275,611 (GRCm39) |
H386R |
possibly damaging |
Het |
Sacs |
T |
C |
14: 61,440,210 (GRCm39) |
V752A |
probably benign |
Het |
Sema3c |
A |
G |
5: 17,883,334 (GRCm39) |
D314G |
possibly damaging |
Het |
Spata2l |
G |
A |
8: 123,960,072 (GRCm39) |
R406C |
probably damaging |
Het |
Tacc2 |
C |
T |
7: 130,264,733 (GRCm39) |
|
probably benign |
Het |
Tent4b |
C |
A |
8: 88,927,002 (GRCm39) |
Y137* |
probably null |
Het |
Trpc4 |
A |
G |
3: 54,102,423 (GRCm39) |
E107G |
probably damaging |
Het |
Vmn2r70 |
A |
G |
7: 85,214,262 (GRCm39) |
S297P |
probably damaging |
Het |
Xdh |
A |
G |
17: 74,230,073 (GRCm39) |
I286T |
probably benign |
Het |
Zfp608 |
T |
C |
18: 55,031,463 (GRCm39) |
T826A |
probably benign |
Het |
Zfp646 |
T |
A |
7: 127,482,683 (GRCm39) |
V1620E |
probably benign |
Het |
Zfyve28 |
T |
G |
5: 34,389,549 (GRCm39) |
D217A |
probably damaging |
Het |
Zmym6 |
G |
A |
4: 127,016,798 (GRCm39) |
G768R |
probably benign |
Het |
|
Other mutations in Lrrc39 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00340:Lrrc39
|
APN |
3 |
116,364,630 (GRCm39) |
splice site |
probably benign |
|
IGL01017:Lrrc39
|
APN |
3 |
116,364,500 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01717:Lrrc39
|
APN |
3 |
116,373,146 (GRCm39) |
unclassified |
probably benign |
|
IGL01728:Lrrc39
|
APN |
3 |
116,373,149 (GRCm39) |
unclassified |
probably benign |
|
IGL02208:Lrrc39
|
APN |
3 |
116,371,923 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02801:Lrrc39
|
APN |
3 |
116,371,995 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0279:Lrrc39
|
UTSW |
3 |
116,371,952 (GRCm39) |
missense |
probably benign |
0.19 |
R1436:Lrrc39
|
UTSW |
3 |
116,373,293 (GRCm39) |
splice site |
probably null |
|
R1641:Lrrc39
|
UTSW |
3 |
116,364,562 (GRCm39) |
missense |
probably damaging |
0.99 |
R1716:Lrrc39
|
UTSW |
3 |
116,373,216 (GRCm39) |
missense |
probably benign |
0.00 |
R2199:Lrrc39
|
UTSW |
3 |
116,364,610 (GRCm39) |
missense |
probably damaging |
0.97 |
R2410:Lrrc39
|
UTSW |
3 |
116,374,899 (GRCm39) |
missense |
probably benign |
0.02 |
R4696:Lrrc39
|
UTSW |
3 |
116,363,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R4816:Lrrc39
|
UTSW |
3 |
116,362,515 (GRCm39) |
critical splice donor site |
probably null |
|
R5076:Lrrc39
|
UTSW |
3 |
116,373,189 (GRCm39) |
missense |
probably benign |
0.37 |
R6152:Lrrc39
|
UTSW |
3 |
116,364,624 (GRCm39) |
critical splice donor site |
probably null |
|
R7124:Lrrc39
|
UTSW |
3 |
116,359,562 (GRCm39) |
missense |
probably benign |
|
R8855:Lrrc39
|
UTSW |
3 |
116,363,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R8866:Lrrc39
|
UTSW |
3 |
116,363,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R8941:Lrrc39
|
UTSW |
3 |
116,359,496 (GRCm39) |
missense |
probably damaging |
0.98 |
R9480:Lrrc39
|
UTSW |
3 |
116,359,475 (GRCm39) |
missense |
probably benign |
0.03 |
X0028:Lrrc39
|
UTSW |
3 |
116,359,520 (GRCm39) |
missense |
probably damaging |
1.00 |
|