Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931422A03Rik |
T |
A |
2: 103,856,500 (GRCm39) |
|
probably benign |
Het |
Aadacl2fm3 |
T |
A |
3: 59,784,214 (GRCm39) |
M229K |
possibly damaging |
Het |
Adh5 |
T |
C |
3: 138,151,118 (GRCm39) |
V27A |
probably damaging |
Het |
Ank2 |
A |
T |
3: 126,781,800 (GRCm39) |
D843E |
probably damaging |
Het |
Aopep |
T |
C |
13: 63,215,906 (GRCm39) |
S393P |
probably benign |
Het |
Arid2 |
A |
G |
15: 96,268,737 (GRCm39) |
N950S |
probably damaging |
Het |
Arl1 |
A |
T |
10: 88,566,608 (GRCm39) |
|
probably benign |
Het |
Bcl3 |
T |
G |
7: 19,546,428 (GRCm39) |
I136L |
probably damaging |
Het |
Car9 |
T |
A |
4: 43,509,138 (GRCm39) |
S235R |
probably damaging |
Het |
Carnmt1 |
G |
T |
19: 18,648,451 (GRCm39) |
G30W |
probably damaging |
Het |
Casp12 |
C |
T |
9: 5,348,941 (GRCm39) |
T101I |
possibly damaging |
Het |
Cdh23 |
A |
G |
10: 60,244,823 (GRCm39) |
L1026P |
probably damaging |
Het |
Clec10a |
A |
T |
11: 70,060,806 (GRCm39) |
Y186F |
probably damaging |
Het |
Col22a1 |
G |
T |
15: 71,836,511 (GRCm39) |
A508E |
possibly damaging |
Het |
Crocc |
G |
C |
4: 140,747,088 (GRCm39) |
S1573R |
probably damaging |
Het |
Cttnbp2nl |
G |
T |
3: 104,913,191 (GRCm39) |
T231K |
possibly damaging |
Het |
Drd4 |
T |
C |
7: 140,874,392 (GRCm39) |
V319A |
probably damaging |
Het |
Ehbp1l1 |
T |
C |
19: 5,767,955 (GRCm39) |
E1116G |
possibly damaging |
Het |
Fam83d |
T |
C |
2: 158,627,142 (GRCm39) |
V277A |
possibly damaging |
Het |
Fga |
G |
T |
3: 82,938,542 (GRCm39) |
G306* |
probably null |
Het |
Fkbp9 |
A |
G |
6: 56,809,367 (GRCm39) |
Y59C |
probably damaging |
Het |
Frmpd1 |
A |
G |
4: 45,274,441 (GRCm39) |
T450A |
probably benign |
Het |
Gabbr1 |
A |
G |
17: 37,367,791 (GRCm39) |
M414V |
possibly damaging |
Het |
Gm16506 |
A |
G |
14: 43,962,572 (GRCm39) |
F112L |
unknown |
Het |
Gm27047 |
T |
C |
6: 130,607,299 (GRCm39) |
|
noncoding transcript |
Het |
Gm4353 |
T |
A |
7: 115,682,847 (GRCm39) |
K245* |
probably null |
Het |
Gm4950 |
A |
T |
18: 51,998,865 (GRCm39) |
I30N |
probably benign |
Het |
H1f5 |
A |
T |
13: 21,964,681 (GRCm39) |
V15E |
probably damaging |
Het |
H2-M10.2 |
T |
C |
17: 36,596,285 (GRCm39) |
T187A |
probably benign |
Het |
H60c |
A |
T |
10: 3,209,968 (GRCm39) |
N106K |
possibly damaging |
Het |
Hoxa6 |
T |
C |
6: 52,185,387 (GRCm39) |
|
probably null |
Het |
Ighv1-74 |
A |
G |
12: 115,766,276 (GRCm39) |
C115R |
probably damaging |
Het |
Il17a |
G |
A |
1: 20,801,217 (GRCm39) |
|
probably null |
Het |
Itga9 |
T |
C |
9: 118,672,582 (GRCm39) |
Y199H |
probably damaging |
Het |
Itpr3 |
C |
T |
17: 27,312,257 (GRCm39) |
R554C |
probably damaging |
Het |
Kcnc3 |
T |
A |
7: 44,245,240 (GRCm39) |
M510K |
probably damaging |
Het |
Kif15 |
A |
G |
9: 122,822,914 (GRCm39) |
T432A |
probably benign |
Het |
Klhl2 |
C |
A |
8: 65,207,421 (GRCm39) |
G313W |
probably damaging |
Het |
Klhl32 |
C |
T |
4: 24,629,339 (GRCm39) |
S476N |
probably benign |
Het |
Krt1 |
C |
T |
15: 101,756,063 (GRCm39) |
E386K |
possibly damaging |
Het |
Lats1 |
T |
C |
10: 7,567,510 (GRCm39) |
S94P |
probably benign |
Het |
Ltf |
G |
A |
9: 110,852,001 (GRCm39) |
C146Y |
probably damaging |
Het |
Mars1 |
A |
G |
10: 127,136,322 (GRCm39) |
L501P |
probably damaging |
Het |
Myh2 |
A |
C |
11: 67,080,244 (GRCm39) |
I1153L |
probably benign |
Het |
Ncstn |
A |
T |
1: 171,895,823 (GRCm39) |
Y522* |
probably null |
Het |
Nipal4 |
A |
G |
11: 46,042,156 (GRCm39) |
V175A |
probably damaging |
Het |
Or7e169 |
T |
C |
9: 19,756,987 (GRCm39) |
I309M |
probably benign |
Het |
Pcdha1 |
C |
G |
18: 37,064,959 (GRCm39) |
A541G |
possibly damaging |
Het |
Pex11g |
A |
G |
8: 3,514,043 (GRCm39) |
Y40H |
probably damaging |
Het |
Pira13 |
T |
A |
7: 3,825,154 (GRCm39) |
Y496F |
possibly damaging |
Het |
Qrfprl |
T |
C |
6: 65,424,408 (GRCm39) |
|
probably null |
Het |
Rin2 |
G |
T |
2: 145,702,825 (GRCm39) |
R507L |
probably benign |
Het |
Sh2b2 |
T |
C |
5: 136,260,616 (GRCm39) |
D200G |
probably damaging |
Het |
Smg7 |
C |
A |
1: 152,716,052 (GRCm39) |
|
probably null |
Het |
Snx17 |
T |
C |
5: 31,355,857 (GRCm39) |
|
probably benign |
Het |
Sos1 |
T |
C |
17: 80,741,255 (GRCm39) |
Y510C |
probably benign |
Het |
Spata31d1c |
T |
A |
13: 65,183,427 (GRCm39) |
L323* |
probably null |
Het |
Supt16 |
C |
T |
14: 52,411,046 (GRCm39) |
G686D |
probably damaging |
Het |
Szt2 |
C |
T |
4: 118,229,878 (GRCm39) |
R2751H |
unknown |
Het |
Tnfsf8 |
A |
G |
4: 63,755,337 (GRCm39) |
L95P |
probably damaging |
Het |
Vmn2r17 |
A |
G |
5: 109,577,428 (GRCm39) |
H493R |
probably benign |
Het |
Zfp770 |
C |
T |
2: 114,027,251 (GRCm39) |
A273T |
possibly damaging |
Het |
|
Other mutations in Kif26b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00337:Kif26b
|
APN |
1 |
178,743,213 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00425:Kif26b
|
APN |
1 |
178,743,866 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00952:Kif26b
|
APN |
1 |
178,759,770 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01100:Kif26b
|
APN |
1 |
178,744,809 (GRCm39) |
missense |
probably benign |
|
IGL01347:Kif26b
|
APN |
1 |
178,698,240 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01543:Kif26b
|
APN |
1 |
178,506,526 (GRCm39) |
missense |
probably benign |
0.41 |
IGL01938:Kif26b
|
APN |
1 |
178,743,603 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02100:Kif26b
|
APN |
1 |
178,743,512 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02262:Kif26b
|
APN |
1 |
178,743,633 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02576:Kif26b
|
APN |
1 |
178,743,912 (GRCm39) |
missense |
probably benign |
|
IGL02673:Kif26b
|
APN |
1 |
178,649,170 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03078:Kif26b
|
APN |
1 |
178,698,291 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03155:Kif26b
|
APN |
1 |
178,701,693 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03157:Kif26b
|
APN |
1 |
178,743,930 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03162:Kif26b
|
APN |
1 |
178,744,497 (GRCm39) |
missense |
probably benign |
|
IGL03220:Kif26b
|
APN |
1 |
178,692,434 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03299:Kif26b
|
APN |
1 |
178,649,125 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03368:Kif26b
|
APN |
1 |
178,743,773 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03370:Kif26b
|
APN |
1 |
178,742,946 (GRCm39) |
missense |
probably benign |
0.39 |
PIT4449001:Kif26b
|
UTSW |
1 |
178,745,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R0142:Kif26b
|
UTSW |
1 |
178,742,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R0621:Kif26b
|
UTSW |
1 |
178,743,218 (GRCm39) |
missense |
probably benign |
0.02 |
R0987:Kif26b
|
UTSW |
1 |
178,649,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R1107:Kif26b
|
UTSW |
1 |
178,745,238 (GRCm39) |
missense |
probably benign |
0.03 |
R1367:Kif26b
|
UTSW |
1 |
178,744,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R1386:Kif26b
|
UTSW |
1 |
178,743,209 (GRCm39) |
missense |
probably benign |
|
R1619:Kif26b
|
UTSW |
1 |
178,744,043 (GRCm39) |
missense |
probably benign |
0.00 |
R1664:Kif26b
|
UTSW |
1 |
178,759,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R2240:Kif26b
|
UTSW |
1 |
178,543,488 (GRCm39) |
missense |
probably benign |
0.00 |
R2264:Kif26b
|
UTSW |
1 |
178,756,407 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2443:Kif26b
|
UTSW |
1 |
178,742,579 (GRCm39) |
missense |
probably damaging |
0.99 |
R3023:Kif26b
|
UTSW |
1 |
178,692,433 (GRCm39) |
missense |
probably damaging |
0.99 |
R3744:Kif26b
|
UTSW |
1 |
178,506,595 (GRCm39) |
missense |
probably benign |
0.00 |
R3831:Kif26b
|
UTSW |
1 |
178,744,181 (GRCm39) |
frame shift |
probably null |
|
R3832:Kif26b
|
UTSW |
1 |
178,744,181 (GRCm39) |
frame shift |
probably null |
|
R3833:Kif26b
|
UTSW |
1 |
178,744,181 (GRCm39) |
frame shift |
probably null |
|
R3843:Kif26b
|
UTSW |
1 |
178,755,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R4108:Kif26b
|
UTSW |
1 |
178,744,530 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4181:Kif26b
|
UTSW |
1 |
178,742,991 (GRCm39) |
missense |
probably damaging |
0.98 |
R4551:Kif26b
|
UTSW |
1 |
178,711,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R4552:Kif26b
|
UTSW |
1 |
178,711,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R4599:Kif26b
|
UTSW |
1 |
178,358,024 (GRCm39) |
missense |
unknown |
|
R4610:Kif26b
|
UTSW |
1 |
178,506,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R4746:Kif26b
|
UTSW |
1 |
178,701,546 (GRCm39) |
nonsense |
probably null |
|
R4873:Kif26b
|
UTSW |
1 |
178,742,892 (GRCm39) |
missense |
probably benign |
0.38 |
R4875:Kif26b
|
UTSW |
1 |
178,742,892 (GRCm39) |
missense |
probably benign |
0.38 |
R5015:Kif26b
|
UTSW |
1 |
178,755,895 (GRCm39) |
missense |
probably damaging |
0.99 |
R5060:Kif26b
|
UTSW |
1 |
178,358,195 (GRCm39) |
missense |
unknown |
|
R5301:Kif26b
|
UTSW |
1 |
178,358,233 (GRCm39) |
missense |
unknown |
|
R5368:Kif26b
|
UTSW |
1 |
178,743,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R5387:Kif26b
|
UTSW |
1 |
178,742,441 (GRCm39) |
missense |
probably benign |
0.01 |
R5589:Kif26b
|
UTSW |
1 |
178,743,864 (GRCm39) |
missense |
probably benign |
0.05 |
R6150:Kif26b
|
UTSW |
1 |
178,743,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R6259:Kif26b
|
UTSW |
1 |
178,744,970 (GRCm39) |
missense |
probably damaging |
0.97 |
R6355:Kif26b
|
UTSW |
1 |
178,743,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R6408:Kif26b
|
UTSW |
1 |
178,745,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R6488:Kif26b
|
UTSW |
1 |
178,357,138 (GRCm39) |
missense |
unknown |
|
R6546:Kif26b
|
UTSW |
1 |
178,755,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R6702:Kif26b
|
UTSW |
1 |
178,744,852 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6886:Kif26b
|
UTSW |
1 |
178,701,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R6953:Kif26b
|
UTSW |
1 |
178,701,637 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7262:Kif26b
|
UTSW |
1 |
178,745,219 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7291:Kif26b
|
UTSW |
1 |
178,506,611 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7346:Kif26b
|
UTSW |
1 |
178,358,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R7383:Kif26b
|
UTSW |
1 |
178,358,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R7448:Kif26b
|
UTSW |
1 |
178,742,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R7506:Kif26b
|
UTSW |
1 |
178,357,064 (GRCm39) |
start gained |
probably benign |
|
R7562:Kif26b
|
UTSW |
1 |
178,742,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R7583:Kif26b
|
UTSW |
1 |
178,358,010 (GRCm39) |
nonsense |
probably null |
|
R7585:Kif26b
|
UTSW |
1 |
178,744,061 (GRCm39) |
missense |
probably benign |
0.01 |
R7644:Kif26b
|
UTSW |
1 |
178,506,839 (GRCm39) |
missense |
probably benign |
0.04 |
R7759:Kif26b
|
UTSW |
1 |
178,506,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R7775:Kif26b
|
UTSW |
1 |
178,692,441 (GRCm39) |
missense |
probably benign |
0.15 |
R7954:Kif26b
|
UTSW |
1 |
178,696,944 (GRCm39) |
missense |
probably damaging |
0.99 |
R7960:Kif26b
|
UTSW |
1 |
178,506,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R8012:Kif26b
|
UTSW |
1 |
178,743,815 (GRCm39) |
missense |
probably benign |
0.20 |
R8152:Kif26b
|
UTSW |
1 |
178,506,794 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8320:Kif26b
|
UTSW |
1 |
178,711,641 (GRCm39) |
critical splice donor site |
probably null |
|
R8360:Kif26b
|
UTSW |
1 |
178,743,938 (GRCm39) |
missense |
probably benign |
0.18 |
R8428:Kif26b
|
UTSW |
1 |
178,744,923 (GRCm39) |
missense |
probably benign |
0.09 |
R8670:Kif26b
|
UTSW |
1 |
178,741,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R8737:Kif26b
|
UTSW |
1 |
178,692,430 (GRCm39) |
missense |
probably damaging |
0.99 |
R8788:Kif26b
|
UTSW |
1 |
178,357,090 (GRCm39) |
start gained |
probably benign |
|
R8854:Kif26b
|
UTSW |
1 |
178,743,948 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8870:Kif26b
|
UTSW |
1 |
178,692,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R8963:Kif26b
|
UTSW |
1 |
178,743,714 (GRCm39) |
missense |
probably benign |
0.00 |
R9232:Kif26b
|
UTSW |
1 |
178,742,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R9297:Kif26b
|
UTSW |
1 |
178,543,374 (GRCm39) |
nonsense |
probably null |
|
R9338:Kif26b
|
UTSW |
1 |
178,744,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R9572:Kif26b
|
UTSW |
1 |
178,745,042 (GRCm39) |
missense |
probably benign |
|
R9580:Kif26b
|
UTSW |
1 |
178,506,643 (GRCm39) |
nonsense |
probably null |
|
R9694:Kif26b
|
UTSW |
1 |
178,743,815 (GRCm39) |
missense |
probably benign |
0.20 |
X0021:Kif26b
|
UTSW |
1 |
178,755,724 (GRCm39) |
missense |
probably damaging |
1.00 |
X0024:Kif26b
|
UTSW |
1 |
178,506,647 (GRCm39) |
missense |
probably benign |
0.14 |
X0025:Kif26b
|
UTSW |
1 |
178,742,948 (GRCm39) |
missense |
possibly damaging |
0.70 |
X0025:Kif26b
|
UTSW |
1 |
178,742,831 (GRCm39) |
nonsense |
probably null |
|
Z1177:Kif26b
|
UTSW |
1 |
178,742,970 (GRCm39) |
nonsense |
probably null |
|
Z1177:Kif26b
|
UTSW |
1 |
178,649,115 (GRCm39) |
nonsense |
probably null |
|
Z1177:Kif26b
|
UTSW |
1 |
178,649,113 (GRCm39) |
missense |
probably benign |
0.11 |
|