Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700034J05Rik |
T |
A |
6: 146,853,902 (GRCm39) |
M252L |
probably benign |
Het |
Abca6 |
A |
G |
11: 110,127,615 (GRCm39) |
V314A |
probably benign |
Het |
Abcb1b |
A |
T |
5: 8,877,409 (GRCm39) |
E656D |
probably benign |
Het |
Abhd4 |
T |
C |
14: 54,500,691 (GRCm39) |
I160T |
probably benign |
Het |
Aco2 |
T |
C |
15: 81,773,557 (GRCm39) |
V32A |
probably damaging |
Het |
Actl6b |
A |
G |
5: 137,552,406 (GRCm39) |
|
probably benign |
Het |
Akap13 |
T |
C |
7: 75,386,352 (GRCm39) |
|
probably benign |
Het |
Alpk3 |
A |
T |
7: 80,726,722 (GRCm39) |
T136S |
probably benign |
Het |
Ap1g1 |
G |
T |
8: 110,529,749 (GRCm39) |
M56I |
probably benign |
Het |
Arid2 |
C |
T |
15: 96,268,452 (GRCm39) |
T855I |
probably damaging |
Het |
Asprv1 |
T |
C |
6: 86,606,077 (GRCm39) |
F308L |
probably damaging |
Het |
Ass1 |
A |
T |
2: 31,404,831 (GRCm39) |
N371Y |
probably damaging |
Het |
Atp11b |
T |
A |
3: 35,866,259 (GRCm39) |
M378K |
possibly damaging |
Het |
Atp1a3 |
T |
C |
7: 24,680,937 (GRCm39) |
|
probably benign |
Het |
Blk |
C |
A |
14: 63,618,253 (GRCm39) |
A218S |
probably benign |
Het |
C4b |
T |
A |
17: 34,953,750 (GRCm39) |
T953S |
probably benign |
Het |
Cdadc1 |
T |
C |
14: 59,813,356 (GRCm39) |
|
probably benign |
Het |
Cdca2 |
C |
A |
14: 67,914,627 (GRCm39) |
L877F |
probably damaging |
Het |
Ceacam10 |
G |
T |
7: 24,477,733 (GRCm39) |
V83L |
probably damaging |
Het |
Cep290 |
A |
T |
10: 100,350,436 (GRCm39) |
I677F |
probably benign |
Het |
Clip1 |
A |
T |
5: 123,755,395 (GRCm39) |
|
probably benign |
Het |
Col11a2 |
G |
T |
17: 34,283,777 (GRCm39) |
|
probably benign |
Het |
Coro1c |
A |
T |
5: 113,983,313 (GRCm39) |
V405D |
probably benign |
Het |
Crebrf |
A |
G |
17: 26,958,568 (GRCm39) |
T13A |
probably benign |
Het |
Cspg4 |
A |
G |
9: 56,804,694 (GRCm39) |
E1835G |
probably damaging |
Het |
Cubn |
A |
T |
2: 13,480,846 (GRCm39) |
|
probably null |
Het |
Cubn |
T |
C |
2: 13,429,505 (GRCm39) |
N1332S |
probably benign |
Het |
Cubn |
T |
C |
2: 13,445,325 (GRCm39) |
T1014A |
possibly damaging |
Het |
Efnb1 |
T |
C |
X: 98,180,634 (GRCm39) |
|
probably benign |
Het |
Elf2 |
G |
T |
3: 51,215,611 (GRCm39) |
P33Q |
probably damaging |
Het |
Fap |
C |
T |
2: 62,333,746 (GRCm39) |
G633D |
probably damaging |
Het |
Gm10288 |
T |
C |
3: 146,544,675 (GRCm39) |
|
noncoding transcript |
Het |
Got2 |
T |
C |
8: 96,596,166 (GRCm39) |
N318S |
probably benign |
Het |
Guk1 |
A |
T |
11: 59,076,854 (GRCm39) |
F76L |
probably damaging |
Het |
H2-K2 |
A |
T |
17: 34,215,639 (GRCm39) |
|
probably benign |
Het |
Helz2 |
C |
A |
2: 180,874,552 (GRCm39) |
G1981C |
probably damaging |
Het |
Hinfp |
G |
A |
9: 44,209,536 (GRCm39) |
H250Y |
probably damaging |
Het |
Hnrnpm |
C |
T |
17: 33,871,242 (GRCm39) |
|
probably null |
Het |
Hsd11b2 |
T |
A |
8: 106,249,699 (GRCm39) |
V270E |
possibly damaging |
Het |
Igbp1b |
A |
T |
6: 138,635,201 (GRCm39) |
M81K |
probably damaging |
Het |
Kit |
G |
A |
5: 75,781,581 (GRCm39) |
V337I |
probably benign |
Het |
Klf11 |
T |
C |
12: 24,703,582 (GRCm39) |
S6P |
probably damaging |
Het |
Klk13 |
T |
C |
7: 43,373,245 (GRCm39) |
V193A |
probably benign |
Het |
Krt73 |
T |
A |
15: 101,708,324 (GRCm39) |
|
probably benign |
Het |
L1td1 |
T |
A |
4: 98,625,419 (GRCm39) |
L538* |
probably null |
Het |
Macf1 |
A |
G |
4: 123,326,572 (GRCm39) |
L2061P |
probably damaging |
Het |
Mcm2 |
A |
G |
6: 88,860,998 (GRCm39) |
I900T |
probably damaging |
Het |
Med16 |
A |
T |
10: 79,736,034 (GRCm39) |
N371K |
possibly damaging |
Het |
Mepce |
A |
C |
5: 137,783,698 (GRCm39) |
D209E |
possibly damaging |
Het |
Mrc2 |
C |
G |
11: 105,238,692 (GRCm39) |
P1249R |
probably benign |
Het |
Mx2 |
A |
T |
16: 97,357,295 (GRCm39) |
I463L |
probably benign |
Het |
Naaa |
A |
T |
5: 92,412,994 (GRCm39) |
N73K |
probably damaging |
Het |
Nags |
T |
A |
11: 102,038,771 (GRCm39) |
L404Q |
probably damaging |
Het |
Neb |
A |
G |
2: 52,133,402 (GRCm39) |
Y3379H |
probably damaging |
Het |
Nhsl1 |
A |
G |
10: 18,348,733 (GRCm39) |
E120G |
probably damaging |
Het |
Or11j4 |
T |
C |
14: 50,630,536 (GRCm39) |
S108P |
probably damaging |
Het |
Or4f53 |
A |
C |
2: 111,087,466 (GRCm39) |
N2T |
probably benign |
Het |
Or51a42 |
T |
C |
7: 103,708,728 (GRCm39) |
H27R |
probably benign |
Het |
Or51ah3 |
T |
A |
7: 103,209,829 (GRCm39) |
Y48* |
probably null |
Het |
Or51f5 |
C |
A |
7: 102,424,076 (GRCm39) |
S115* |
probably null |
Het |
Pcnt |
A |
G |
10: 76,228,414 (GRCm39) |
F1584L |
probably benign |
Het |
Pdgfra |
G |
A |
5: 75,328,596 (GRCm39) |
V243I |
probably damaging |
Het |
Polr2a |
T |
C |
11: 69,634,497 (GRCm39) |
I689V |
possibly damaging |
Het |
Ppfia4 |
C |
A |
1: 134,251,962 (GRCm39) |
|
probably benign |
Het |
Prmt8 |
C |
A |
6: 127,688,771 (GRCm39) |
V200L |
probably damaging |
Het |
Prpf8 |
T |
A |
11: 75,397,188 (GRCm39) |
I2007N |
possibly damaging |
Het |
Ptpn6 |
T |
C |
6: 124,705,113 (GRCm39) |
E230G |
probably damaging |
Het |
R3hcc1l |
G |
A |
19: 42,551,587 (GRCm39) |
V195I |
probably damaging |
Het |
Rb1cc1 |
C |
T |
1: 6,333,071 (GRCm39) |
T1330I |
probably damaging |
Het |
Reep3 |
G |
T |
10: 66,857,575 (GRCm39) |
T172N |
probably benign |
Het |
Rfwd3 |
A |
G |
8: 112,020,655 (GRCm39) |
V236A |
probably benign |
Het |
Rgs22 |
T |
C |
15: 36,104,698 (GRCm39) |
I121V |
probably damaging |
Het |
Robo1 |
T |
A |
16: 72,461,058 (GRCm39) |
F11I |
probably benign |
Het |
Rsrc2 |
A |
G |
5: 123,878,910 (GRCm39) |
|
probably benign |
Het |
Rubcn |
A |
G |
16: 32,668,316 (GRCm39) |
V117A |
probably benign |
Het |
Scamp1 |
T |
G |
13: 94,347,088 (GRCm39) |
N192T |
probably benign |
Het |
Scn8a |
T |
A |
15: 100,916,245 (GRCm39) |
I1218N |
probably damaging |
Het |
Serinc1 |
A |
G |
10: 57,399,304 (GRCm39) |
S200P |
probably damaging |
Het |
Serpinb9f |
T |
A |
13: 33,518,574 (GRCm39) |
F358Y |
probably damaging |
Het |
Slc12a5 |
T |
C |
2: 164,839,165 (GRCm39) |
|
probably null |
Het |
Slc5a4b |
T |
C |
10: 75,906,462 (GRCm39) |
M386V |
possibly damaging |
Het |
Smarca5 |
A |
G |
8: 81,431,329 (GRCm39) |
F963L |
probably benign |
Het |
Smchd1 |
A |
T |
17: 71,718,886 (GRCm39) |
F828I |
probably benign |
Het |
Smr2l |
A |
T |
5: 88,430,230 (GRCm39) |
H42L |
possibly damaging |
Het |
Stab2 |
G |
T |
10: 86,733,824 (GRCm39) |
Q1333K |
probably benign |
Het |
Svop |
T |
C |
5: 114,176,600 (GRCm39) |
S349G |
probably benign |
Het |
Tdrd1 |
G |
A |
19: 56,830,998 (GRCm39) |
S271N |
probably benign |
Het |
Tec |
G |
A |
5: 72,941,081 (GRCm39) |
P159S |
probably benign |
Het |
Tec |
T |
C |
5: 72,920,899 (GRCm39) |
|
probably benign |
Het |
Tfip11 |
G |
A |
5: 112,483,521 (GRCm39) |
M645I |
probably benign |
Het |
Thap12 |
A |
T |
7: 98,364,488 (GRCm39) |
T219S |
probably benign |
Het |
Tmem87a |
C |
T |
2: 120,205,988 (GRCm39) |
R329H |
probably damaging |
Het |
Tpsab1 |
A |
G |
17: 25,562,719 (GRCm39) |
Y227H |
probably damaging |
Het |
Urah |
G |
A |
7: 140,417,602 (GRCm39) |
V114I |
probably benign |
Het |
Wnt5a |
G |
A |
14: 28,244,811 (GRCm39) |
E353K |
probably damaging |
Het |
Zfp1004 |
G |
A |
2: 150,033,784 (GRCm39) |
R35K |
possibly damaging |
Het |
Zfp101 |
A |
T |
17: 33,599,952 (GRCm39) |
H601Q |
possibly damaging |
Het |
|
Other mutations in Kif11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00434:Kif11
|
APN |
19 |
37,399,857 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL00785:Kif11
|
APN |
19 |
37,392,746 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00785:Kif11
|
APN |
19 |
37,392,745 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01586:Kif11
|
APN |
19 |
37,372,681 (GRCm39) |
splice site |
probably benign |
|
IGL01883:Kif11
|
APN |
19 |
37,372,791 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02138:Kif11
|
APN |
19 |
37,373,057 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03197:Kif11
|
APN |
19 |
37,395,475 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4151001:Kif11
|
UTSW |
19 |
37,373,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R0027:Kif11
|
UTSW |
19 |
37,395,431 (GRCm39) |
splice site |
probably benign |
|
R0027:Kif11
|
UTSW |
19 |
37,395,431 (GRCm39) |
splice site |
probably benign |
|
R0104:Kif11
|
UTSW |
19 |
37,401,663 (GRCm39) |
missense |
probably benign |
0.00 |
R0631:Kif11
|
UTSW |
19 |
37,401,565 (GRCm39) |
splice site |
probably benign |
|
R1607:Kif11
|
UTSW |
19 |
37,375,648 (GRCm39) |
nonsense |
probably null |
|
R1895:Kif11
|
UTSW |
19 |
37,375,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R1983:Kif11
|
UTSW |
19 |
37,379,224 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2056:Kif11
|
UTSW |
19 |
37,390,660 (GRCm39) |
missense |
probably benign |
0.17 |
R2158:Kif11
|
UTSW |
19 |
37,399,062 (GRCm39) |
missense |
probably benign |
|
R2291:Kif11
|
UTSW |
19 |
37,395,451 (GRCm39) |
missense |
probably benign |
|
R2300:Kif11
|
UTSW |
19 |
37,399,987 (GRCm39) |
missense |
probably benign |
0.01 |
R2850:Kif11
|
UTSW |
19 |
37,397,941 (GRCm39) |
missense |
probably benign |
|
R2904:Kif11
|
UTSW |
19 |
37,392,103 (GRCm39) |
splice site |
probably benign |
|
R3035:Kif11
|
UTSW |
19 |
37,395,501 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3908:Kif11
|
UTSW |
19 |
37,379,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R4319:Kif11
|
UTSW |
19 |
37,373,033 (GRCm39) |
missense |
probably damaging |
0.99 |
R4356:Kif11
|
UTSW |
19 |
37,399,883 (GRCm39) |
missense |
probably benign |
0.00 |
R4469:Kif11
|
UTSW |
19 |
37,404,940 (GRCm39) |
missense |
probably benign |
0.05 |
R4623:Kif11
|
UTSW |
19 |
37,398,195 (GRCm39) |
missense |
probably benign |
|
R4779:Kif11
|
UTSW |
19 |
37,406,397 (GRCm39) |
missense |
probably benign |
0.00 |
R4911:Kif11
|
UTSW |
19 |
37,406,385 (GRCm39) |
missense |
probably benign |
0.00 |
R4980:Kif11
|
UTSW |
19 |
37,375,819 (GRCm39) |
nonsense |
probably null |
|
R5109:Kif11
|
UTSW |
19 |
37,373,063 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5770:Kif11
|
UTSW |
19 |
37,379,313 (GRCm39) |
missense |
probably benign |
0.03 |
R6023:Kif11
|
UTSW |
19 |
37,379,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R6666:Kif11
|
UTSW |
19 |
37,398,214 (GRCm39) |
missense |
probably benign |
|
R6755:Kif11
|
UTSW |
19 |
37,398,199 (GRCm39) |
missense |
probably benign |
0.01 |
R6845:Kif11
|
UTSW |
19 |
37,392,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R7052:Kif11
|
UTSW |
19 |
37,373,040 (GRCm39) |
nonsense |
probably null |
|
R7367:Kif11
|
UTSW |
19 |
37,408,789 (GRCm39) |
missense |
probably benign |
|
R7387:Kif11
|
UTSW |
19 |
37,398,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R7485:Kif11
|
UTSW |
19 |
37,399,072 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7502:Kif11
|
UTSW |
19 |
37,398,255 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7591:Kif11
|
UTSW |
19 |
37,372,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R7618:Kif11
|
UTSW |
19 |
37,400,008 (GRCm39) |
missense |
probably benign |
0.32 |
R7809:Kif11
|
UTSW |
19 |
37,373,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R8181:Kif11
|
UTSW |
19 |
37,379,095 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8274:Kif11
|
UTSW |
19 |
37,391,994 (GRCm39) |
missense |
probably damaging |
0.99 |
R8323:Kif11
|
UTSW |
19 |
37,372,692 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8948:Kif11
|
UTSW |
19 |
37,386,602 (GRCm39) |
missense |
probably damaging |
0.96 |
R9372:Kif11
|
UTSW |
19 |
37,399,892 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Kif11
|
UTSW |
19 |
37,401,735 (GRCm39) |
missense |
possibly damaging |
0.62 |
|