Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130401M01Rik |
C |
A |
15: 57,892,223 (GRCm39) |
S128I |
probably damaging |
Het |
Aadacl2 |
A |
C |
3: 59,932,181 (GRCm39) |
H232P |
possibly damaging |
Het |
Abcc3 |
A |
G |
11: 94,265,661 (GRCm39) |
Y125H |
probably benign |
Het |
Adgrb3 |
A |
G |
1: 25,865,592 (GRCm39) |
S84P |
probably damaging |
Het |
Adgrd1 |
A |
T |
5: 129,192,142 (GRCm39) |
K71* |
probably null |
Het |
Ap2m1 |
T |
A |
16: 20,361,468 (GRCm39) |
W381R |
probably damaging |
Het |
Ascc3 |
A |
G |
10: 50,521,762 (GRCm39) |
I426V |
probably benign |
Het |
BC024063 |
T |
A |
10: 81,943,733 (GRCm39) |
D31E |
possibly damaging |
Het |
C3ar1 |
G |
A |
6: 122,827,591 (GRCm39) |
H209Y |
possibly damaging |
Het |
Ccp110 |
T |
C |
7: 118,321,644 (GRCm39) |
V433A |
possibly damaging |
Het |
Cfap54 |
A |
G |
10: 92,830,540 (GRCm39) |
S1199P |
probably benign |
Het |
Cyp24a1 |
T |
G |
2: 170,329,866 (GRCm39) |
D362A |
probably benign |
Het |
Dapk2 |
C |
G |
9: 66,161,904 (GRCm39) |
R271G |
probably benign |
Het |
Dnmt1 |
G |
T |
9: 20,829,822 (GRCm39) |
Q633K |
probably benign |
Het |
Ercc4 |
T |
A |
16: 12,948,550 (GRCm39) |
V499D |
probably damaging |
Het |
Ier3ip1 |
C |
G |
18: 77,027,309 (GRCm39) |
P46R |
probably damaging |
Het |
Ifi211 |
T |
C |
1: 173,733,832 (GRCm39) |
T110A |
probably damaging |
Het |
Isoc1 |
A |
G |
18: 58,804,374 (GRCm39) |
D134G |
possibly damaging |
Het |
Klhl33 |
T |
A |
14: 51,128,973 (GRCm39) |
D752V |
possibly damaging |
Het |
Lcn4 |
A |
G |
2: 26,559,367 (GRCm39) |
Y133H |
probably benign |
Het |
Mrs2 |
C |
A |
13: 25,185,771 (GRCm39) |
V134L |
probably benign |
Het |
Muc16 |
T |
C |
9: 18,551,825 (GRCm39) |
T4823A |
probably benign |
Het |
Ogfod3 |
A |
G |
11: 121,093,824 (GRCm39) |
I62T |
probably benign |
Het |
Or2m13 |
C |
T |
16: 19,226,278 (GRCm39) |
V164I |
probably benign |
Het |
Or2y10 |
A |
G |
11: 49,455,117 (GRCm39) |
Y123C |
probably damaging |
Het |
Or6c204 |
A |
T |
10: 129,022,474 (GRCm39) |
M272K |
probably benign |
Het |
Or7e175 |
A |
T |
9: 20,049,299 (GRCm39) |
I296L |
probably benign |
Het |
Papln |
G |
A |
12: 83,828,659 (GRCm39) |
W788* |
probably null |
Het |
Pcdhac2 |
A |
G |
18: 37,277,479 (GRCm39) |
Q153R |
probably benign |
Het |
Pcdhgb2 |
C |
T |
18: 37,823,807 (GRCm39) |
T266I |
possibly damaging |
Het |
Pcdhgc5 |
C |
A |
18: 37,953,514 (GRCm39) |
R263S |
possibly damaging |
Het |
Phactr4 |
T |
C |
4: 132,104,662 (GRCm39) |
T185A |
possibly damaging |
Het |
Plcxd2 |
T |
C |
16: 45,800,882 (GRCm39) |
D114G |
probably damaging |
Het |
Polr2a |
A |
T |
11: 69,632,537 (GRCm39) |
I987N |
probably damaging |
Het |
Prl3d3 |
A |
G |
13: 27,345,029 (GRCm39) |
M134V |
probably benign |
Het |
Pum2 |
T |
A |
12: 8,778,779 (GRCm39) |
|
probably null |
Het |
Racgap1 |
T |
C |
15: 99,524,210 (GRCm39) |
E399G |
probably damaging |
Het |
Sbspon |
A |
T |
1: 15,930,519 (GRCm39) |
S156T |
probably damaging |
Het |
Scn1a |
T |
C |
2: 66,149,813 (GRCm39) |
T927A |
probably damaging |
Het |
Sec23ip |
C |
A |
7: 128,354,520 (GRCm39) |
S78* |
probably null |
Het |
Serpina1d |
G |
A |
12: 103,733,989 (GRCm39) |
T105I |
probably benign |
Het |
Slc25a21 |
T |
A |
12: 57,205,954 (GRCm39) |
N26Y |
probably benign |
Het |
Smim20 |
T |
A |
5: 53,435,258 (GRCm39) |
D64E |
probably damaging |
Het |
Spag17 |
T |
G |
3: 99,942,291 (GRCm39) |
I772S |
possibly damaging |
Het |
Tars2 |
T |
C |
3: 95,660,426 (GRCm39) |
T99A |
possibly damaging |
Het |
Tdrd1 |
C |
T |
19: 56,819,803 (GRCm39) |
T101I |
probably damaging |
Het |
Tldc2 |
T |
G |
2: 156,931,198 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
G |
2: 76,601,929 (GRCm39) |
Y10251H |
probably damaging |
Het |
Ush2a |
A |
G |
1: 187,995,342 (GRCm39) |
R38G |
possibly damaging |
Het |
Usp19 |
T |
C |
9: 108,376,130 (GRCm39) |
L991P |
possibly damaging |
Het |
Vmn2r109 |
G |
A |
17: 20,760,973 (GRCm39) |
P795S |
possibly damaging |
Het |
Vmn2r26 |
T |
C |
6: 124,016,741 (GRCm39) |
Y402H |
probably benign |
Het |
Vmn2r-ps117 |
T |
G |
17: 19,045,095 (GRCm39) |
I504R |
probably benign |
Het |
Zfp551 |
A |
T |
7: 12,150,715 (GRCm39) |
C231* |
probably null |
Het |
Zfp607a |
T |
A |
7: 27,577,790 (GRCm39) |
C287S |
possibly damaging |
Het |
Zim1 |
T |
A |
7: 6,690,706 (GRCm39) |
T40S |
unknown |
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 |
R4597:Kif26b
|
UTSW |
1 |
178,744,358 (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 |
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 |
|