Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
T |
C |
5: 8,957,267 (GRCm39) |
V132A |
possibly damaging |
Het |
Acp3 |
A |
T |
9: 104,184,174 (GRCm39) |
V292E |
probably damaging |
Het |
Adamts10 |
T |
C |
17: 33,747,870 (GRCm39) |
V102A |
possibly damaging |
Het |
Add2 |
A |
G |
6: 86,073,728 (GRCm39) |
T206A |
probably benign |
Het |
Alg12 |
A |
T |
15: 88,700,391 (GRCm39) |
L15Q |
probably damaging |
Het |
Ankrd27 |
T |
A |
7: 35,307,800 (GRCm39) |
D346E |
probably damaging |
Het |
Armc2 |
A |
T |
10: 41,799,790 (GRCm39) |
N689K |
probably damaging |
Het |
Best3 |
T |
A |
10: 116,860,460 (GRCm39) |
D573E |
probably benign |
Het |
Bltp1 |
T |
G |
3: 37,020,086 (GRCm39) |
N2108K |
probably damaging |
Het |
Ccdc80 |
A |
T |
16: 44,916,261 (GRCm39) |
Q339L |
probably benign |
Het |
Cdh9 |
T |
C |
15: 16,778,242 (GRCm39) |
V19A |
probably benign |
Het |
Cimap1a |
G |
A |
7: 140,428,398 (GRCm39) |
|
probably benign |
Het |
Cnksr1 |
A |
T |
4: 133,956,986 (GRCm39) |
|
probably null |
Het |
Col7a1 |
T |
A |
9: 108,786,345 (GRCm39) |
V525E |
unknown |
Het |
Cplane1 |
T |
C |
15: 8,251,421 (GRCm39) |
S1898P |
probably benign |
Het |
Crebrf |
T |
C |
17: 26,961,394 (GRCm39) |
S172P |
possibly damaging |
Het |
Csmd1 |
T |
C |
8: 16,059,439 (GRCm39) |
I2099V |
probably benign |
Het |
Dcaf4 |
T |
A |
12: 83,586,233 (GRCm39) |
M400K |
possibly damaging |
Het |
Dnah11 |
A |
T |
12: 117,958,935 (GRCm39) |
F2983I |
probably damaging |
Het |
Dock6 |
A |
G |
9: 21,735,733 (GRCm39) |
V1005A |
possibly damaging |
Het |
Dyrk2 |
C |
A |
10: 118,704,153 (GRCm39) |
G34C |
probably damaging |
Het |
Eif4a1 |
A |
T |
11: 69,559,423 (GRCm39) |
|
probably benign |
Het |
Eno4 |
G |
T |
19: 58,952,975 (GRCm39) |
D330Y |
probably damaging |
Het |
Faf1 |
G |
A |
4: 109,699,496 (GRCm39) |
C347Y |
probably benign |
Het |
Fam169a |
A |
G |
13: 97,234,100 (GRCm39) |
Y124C |
probably damaging |
Het |
Fam227a |
G |
T |
15: 79,521,255 (GRCm39) |
F269L |
probably benign |
Het |
Fancm |
C |
A |
12: 65,122,605 (GRCm39) |
D42E |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,404,317 (GRCm39) |
I356N |
possibly damaging |
Het |
Fer1l6 |
A |
T |
15: 58,509,869 (GRCm39) |
T1444S |
probably damaging |
Het |
Galr1 |
A |
G |
18: 82,412,065 (GRCm39) |
L267P |
probably damaging |
Het |
Gbx1 |
T |
C |
5: 24,709,837 (GRCm39) |
H336R |
probably damaging |
Het |
Gimap8 |
A |
T |
6: 48,636,281 (GRCm39) |
Q682L |
possibly damaging |
Het |
Gm2396 |
T |
G |
9: 88,813,281 (GRCm39) |
|
noncoding transcript |
Het |
Gm5798 |
T |
C |
14: 41,070,614 (GRCm39) |
L8S |
probably damaging |
Het |
Hmgcll1 |
C |
T |
9: 75,963,460 (GRCm39) |
S39F |
possibly damaging |
Het |
Hspg2 |
C |
T |
4: 137,246,251 (GRCm39) |
R1010C |
probably damaging |
Het |
Il3ra |
A |
T |
14: 14,355,381 (GRCm38) |
E289D |
probably benign |
Het |
Isoc1 |
T |
A |
18: 58,806,350 (GRCm39) |
L220Q |
probably damaging |
Het |
Itga2 |
T |
A |
13: 114,990,302 (GRCm39) |
K918* |
probably null |
Het |
Kat6a |
C |
T |
8: 23,428,329 (GRCm39) |
T1228I |
probably benign |
Het |
Klhl30 |
T |
A |
1: 91,287,046 (GRCm39) |
|
probably null |
Het |
Krtap6-2 |
A |
T |
16: 89,216,806 (GRCm39) |
C54S |
unknown |
Het |
Lmf2 |
G |
A |
15: 89,236,003 (GRCm39) |
P634S |
probably benign |
Het |
Map3k4 |
A |
G |
17: 12,490,906 (GRCm39) |
V175A |
possibly damaging |
Het |
Mcm3 |
A |
C |
1: 20,890,480 (GRCm39) |
|
probably benign |
Het |
Mon1b |
T |
C |
8: 114,365,859 (GRCm39) |
S396P |
probably damaging |
Het |
Mroh2a |
T |
C |
1: 88,184,476 (GRCm39) |
V1453A |
probably benign |
Het |
Ncor2 |
A |
G |
5: 125,126,404 (GRCm39) |
|
probably null |
Het |
Nlrc5 |
T |
G |
8: 95,247,844 (GRCm39) |
|
probably benign |
Het |
Nlrp14 |
GT |
GTT |
7: 106,796,386 (GRCm39) |
|
probably null |
Het |
Nwd2 |
T |
G |
5: 63,962,151 (GRCm39) |
S578R |
probably damaging |
Het |
Or12k7 |
A |
G |
2: 36,958,422 (GRCm39) |
Y35C |
probably damaging |
Het |
Or4f4b |
G |
A |
2: 111,314,005 (GRCm39) |
V105I |
possibly damaging |
Het |
Otoa |
C |
A |
7: 120,701,902 (GRCm39) |
P194T |
probably damaging |
Het |
Pde1b |
A |
C |
15: 103,429,801 (GRCm39) |
D98A |
probably damaging |
Het |
Pi4ka |
A |
T |
16: 17,195,033 (GRCm39) |
C122S |
probably damaging |
Het |
Pole2 |
C |
T |
12: 69,269,924 (GRCm39) |
V67M |
probably damaging |
Het |
Prickle2 |
A |
T |
6: 92,393,736 (GRCm39) |
D312E |
probably benign |
Het |
Prkd1 |
T |
C |
12: 50,436,745 (GRCm39) |
D453G |
probably damaging |
Het |
Prrc1 |
T |
A |
18: 57,507,626 (GRCm39) |
V260E |
probably damaging |
Het |
Reg3g |
A |
T |
6: 78,444,793 (GRCm39) |
Y62N |
probably benign |
Het |
Reln |
C |
T |
5: 22,160,236 (GRCm39) |
G2111E |
probably damaging |
Het |
Rsph6a |
A |
T |
7: 18,791,665 (GRCm39) |
E278V |
possibly damaging |
Het |
Scpep1 |
T |
A |
11: 88,832,122 (GRCm39) |
I203F |
probably damaging |
Het |
Sec24d |
T |
C |
3: 123,148,596 (GRCm39) |
C747R |
probably damaging |
Het |
Sec31a |
A |
T |
5: 100,516,192 (GRCm39) |
N967K |
probably damaging |
Het |
Sell |
T |
C |
1: 163,890,631 (GRCm39) |
W5R |
probably benign |
Het |
Siglec1 |
C |
T |
2: 130,911,789 (GRCm39) |
V1697M |
probably benign |
Het |
Sinhcaf |
A |
G |
6: 148,834,498 (GRCm39) |
|
probably null |
Het |
Slc22a26 |
T |
A |
19: 7,768,419 (GRCm39) |
I213L |
probably benign |
Het |
Slc2a13 |
G |
A |
15: 91,296,415 (GRCm39) |
P300S |
probably benign |
Het |
Slco1a4 |
A |
G |
6: 141,761,231 (GRCm39) |
Y461H |
possibly damaging |
Het |
Slco3a1 |
G |
C |
7: 73,970,304 (GRCm39) |
C434W |
probably null |
Het |
Sp3 |
A |
T |
2: 72,768,633 (GRCm39) |
V666D |
probably benign |
Het |
Spidr |
A |
T |
16: 15,936,806 (GRCm39) |
W100R |
possibly damaging |
Het |
Stk33 |
T |
A |
7: 108,926,802 (GRCm39) |
M286L |
probably damaging |
Het |
Sult1c2 |
T |
A |
17: 54,139,163 (GRCm39) |
I183F |
probably benign |
Het |
Svep1 |
G |
T |
4: 58,087,751 (GRCm39) |
T1776K |
probably benign |
Het |
Tesk2 |
A |
G |
4: 116,660,190 (GRCm39) |
H436R |
probably benign |
Het |
Tex2 |
T |
C |
11: 106,459,230 (GRCm39) |
T67A |
probably damaging |
Het |
Timm10 |
T |
C |
2: 84,660,192 (GRCm39) |
S44P |
possibly damaging |
Het |
Tmed11 |
C |
A |
5: 108,943,048 (GRCm39) |
|
probably null |
Het |
Trim12c |
G |
A |
7: 103,990,155 (GRCm39) |
R441C |
probably damaging |
Het |
Trmt2a |
A |
G |
16: 18,070,793 (GRCm39) |
K509E |
probably damaging |
Het |
Upk3a |
A |
G |
15: 84,903,624 (GRCm39) |
T108A |
probably benign |
Het |
Usp29 |
A |
G |
7: 6,965,158 (GRCm39) |
M334V |
probably benign |
Het |
Vash1 |
A |
G |
12: 86,726,916 (GRCm39) |
D52G |
probably benign |
Het |
Vmn2r14 |
T |
G |
5: 109,368,246 (GRCm39) |
T249P |
probably benign |
Het |
Vmn2r43 |
A |
T |
7: 8,247,848 (GRCm39) |
F772I |
probably damaging |
Het |
Vmn2r75 |
G |
T |
7: 85,820,787 (GRCm39) |
S49Y |
probably benign |
Het |
Xdh |
T |
C |
17: 74,217,238 (GRCm39) |
T677A |
probably damaging |
Het |
Zan |
A |
G |
5: 137,384,718 (GRCm39) |
L5102P |
unknown |
Het |
Zfp160 |
T |
A |
17: 21,240,343 (GRCm39) |
S9T |
probably benign |
Het |
Zfp273 |
A |
T |
13: 67,973,673 (GRCm39) |
H267L |
probably damaging |
Het |
Zfp97 |
T |
A |
17: 17,365,038 (GRCm39) |
I179K |
probably benign |
Het |
|
Other mutations in Zfp975 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02008:Zfp975
|
APN |
7 |
42,312,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R0194:Zfp975
|
UTSW |
7 |
42,311,916 (GRCm39) |
missense |
probably benign |
0.02 |
R0662:Zfp975
|
UTSW |
7 |
42,311,950 (GRCm39) |
missense |
probably benign |
0.02 |
R1491:Zfp975
|
UTSW |
7 |
42,312,236 (GRCm39) |
missense |
probably benign |
0.19 |
R1573:Zfp975
|
UTSW |
7 |
42,311,507 (GRCm39) |
missense |
probably benign |
0.03 |
R1738:Zfp975
|
UTSW |
7 |
42,312,373 (GRCm39) |
missense |
probably benign |
0.05 |
R1833:Zfp975
|
UTSW |
7 |
42,311,263 (GRCm39) |
missense |
probably benign |
0.01 |
R2185:Zfp975
|
UTSW |
7 |
42,311,105 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4031:Zfp975
|
UTSW |
7 |
42,312,377 (GRCm39) |
nonsense |
probably null |
|
R4090:Zfp975
|
UTSW |
7 |
42,312,298 (GRCm39) |
missense |
probably benign |
0.10 |
R4356:Zfp975
|
UTSW |
7 |
42,311,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R4631:Zfp975
|
UTSW |
7 |
42,312,369 (GRCm39) |
missense |
probably benign |
0.09 |
R4795:Zfp975
|
UTSW |
7 |
42,314,570 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5266:Zfp975
|
UTSW |
7 |
42,311,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R5267:Zfp975
|
UTSW |
7 |
42,311,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R5580:Zfp975
|
UTSW |
7 |
42,314,513 (GRCm39) |
nonsense |
probably null |
|
R5874:Zfp975
|
UTSW |
7 |
42,312,312 (GRCm39) |
missense |
probably benign |
0.00 |
R5898:Zfp975
|
UTSW |
7 |
42,311,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R6529:Zfp975
|
UTSW |
7 |
42,311,325 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6782:Zfp975
|
UTSW |
7 |
42,311,454 (GRCm39) |
missense |
probably benign |
0.41 |
R6937:Zfp975
|
UTSW |
7 |
42,314,480 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7088:Zfp975
|
UTSW |
7 |
42,312,096 (GRCm39) |
missense |
probably benign |
0.02 |
R7233:Zfp975
|
UTSW |
7 |
42,311,918 (GRCm39) |
missense |
probably benign |
0.38 |
R7253:Zfp975
|
UTSW |
7 |
42,311,036 (GRCm39) |
makesense |
probably null |
|
R7358:Zfp975
|
UTSW |
7 |
42,312,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R7659:Zfp975
|
UTSW |
7 |
42,311,848 (GRCm39) |
missense |
probably benign |
0.00 |
R7999:Zfp975
|
UTSW |
7 |
42,312,356 (GRCm39) |
missense |
probably benign |
0.02 |
R8676:Zfp975
|
UTSW |
7 |
42,312,264 (GRCm39) |
missense |
probably benign |
0.44 |
R8957:Zfp975
|
UTSW |
7 |
42,311,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R9274:Zfp975
|
UTSW |
7 |
42,312,299 (GRCm39) |
missense |
probably benign |
0.02 |
R9326:Zfp975
|
UTSW |
7 |
42,311,837 (GRCm39) |
nonsense |
probably null |
|
R9536:Zfp975
|
UTSW |
7 |
42,312,345 (GRCm39) |
missense |
probably benign |
0.11 |
R9569:Zfp975
|
UTSW |
7 |
42,311,413 (GRCm39) |
missense |
probably benign |
0.00 |
R9717:Zfp975
|
UTSW |
7 |
42,312,332 (GRCm39) |
missense |
possibly damaging |
0.50 |
|