Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
A |
G |
5: 77,039,551 (GRCm39) |
S253P |
probably damaging |
Het |
Adgrb1 |
A |
G |
15: 74,412,314 (GRCm39) |
D431G |
probably damaging |
Het |
Adgrv1 |
C |
T |
13: 81,522,368 (GRCm39) |
C5923Y |
probably damaging |
Het |
Akr1b10 |
T |
A |
6: 34,365,805 (GRCm39) |
I110N |
probably damaging |
Het |
Apba2 |
T |
C |
7: 64,394,378 (GRCm39) |
|
probably null |
Het |
Arhgef12 |
G |
T |
9: 42,917,152 (GRCm39) |
Q396K |
probably damaging |
Het |
Arpc1b |
A |
G |
5: 145,059,443 (GRCm39) |
T56A |
probably null |
Het |
Atoh1 |
T |
C |
6: 64,706,443 (GRCm39) |
V46A |
probably benign |
Het |
AU015836 |
T |
C |
X: 93,012,985 (GRCm39) |
|
probably benign |
Het |
Cacna1c |
C |
T |
6: 118,589,586 (GRCm39) |
R1446H |
probably damaging |
Het |
Capn13 |
T |
C |
17: 73,657,520 (GRCm39) |
E240G |
possibly damaging |
Het |
Cdh8 |
T |
C |
8: 100,006,189 (GRCm39) |
T133A |
possibly damaging |
Het |
Cep295 |
T |
C |
9: 15,243,399 (GRCm39) |
T1686A |
possibly damaging |
Het |
Col4a3 |
A |
T |
1: 82,656,829 (GRCm39) |
K749N |
unknown |
Het |
Col6a3 |
T |
A |
1: 90,731,433 (GRCm39) |
M1000L |
probably benign |
Het |
Coq8b |
G |
A |
7: 26,939,299 (GRCm39) |
V150I |
possibly damaging |
Het |
Dmxl1 |
G |
T |
18: 50,088,981 (GRCm39) |
|
probably null |
Het |
Dnah10 |
A |
G |
5: 124,835,494 (GRCm39) |
D990G |
probably benign |
Het |
Dpp7 |
G |
T |
2: 25,243,691 (GRCm39) |
|
probably null |
Het |
Eif3l |
A |
G |
15: 78,973,677 (GRCm39) |
N364S |
possibly damaging |
Het |
Epb41l5 |
T |
C |
1: 119,476,902 (GRCm39) |
D718G |
possibly damaging |
Het |
F930017D23Rik |
G |
A |
10: 43,469,440 (GRCm39) |
|
noncoding transcript |
Het |
Fam20a |
T |
C |
11: 109,564,380 (GRCm39) |
K458E |
probably benign |
Het |
Fbxo44 |
C |
G |
4: 148,240,726 (GRCm39) |
R220S |
probably damaging |
Het |
Fut2 |
A |
G |
7: 45,300,748 (GRCm39) |
F8S |
probably damaging |
Het |
Gad2 |
A |
T |
2: 22,575,440 (GRCm39) |
T515S |
probably benign |
Het |
Glmn |
T |
C |
5: 107,718,110 (GRCm39) |
D269G |
probably benign |
Het |
Gpatch4 |
A |
G |
3: 87,959,409 (GRCm39) |
Y106C |
probably damaging |
Het |
Grm3 |
A |
G |
5: 9,562,123 (GRCm39) |
W576R |
probably damaging |
Het |
Hdac7 |
T |
C |
15: 97,694,767 (GRCm39) |
D701G |
probably damaging |
Het |
Hectd2 |
T |
A |
19: 36,591,860 (GRCm39) |
I687K |
probably damaging |
Het |
Hmcn2 |
T |
C |
2: 31,295,647 (GRCm39) |
S2619P |
probably damaging |
Het |
Ilf3 |
T |
A |
9: 21,316,063 (GRCm39) |
|
probably benign |
Het |
Kdm4b |
T |
A |
17: 56,704,340 (GRCm39) |
V272E |
probably damaging |
Het |
Kera |
A |
G |
10: 97,445,009 (GRCm39) |
K123E |
probably benign |
Het |
Kmt2c |
A |
T |
5: 25,520,152 (GRCm39) |
V1986E |
probably benign |
Het |
Lrp11 |
T |
C |
10: 7,499,540 (GRCm39) |
Y244H |
probably damaging |
Het |
Lrp1b |
T |
A |
2: 40,555,159 (GRCm39) |
D320V |
unknown |
Het |
Map4k5 |
A |
T |
12: 69,892,529 (GRCm39) |
D133E |
probably damaging |
Het |
Megf11 |
A |
T |
9: 64,586,558 (GRCm39) |
D461V |
probably damaging |
Het |
Muc5b |
A |
C |
7: 141,411,382 (GRCm39) |
T1443P |
unknown |
Het |
Mxi1 |
G |
A |
19: 53,358,775 (GRCm39) |
R236H |
probably benign |
Het |
Nav1 |
A |
T |
1: 135,386,396 (GRCm39) |
W1211R |
probably damaging |
Het |
Ncoa3 |
T |
A |
2: 165,901,097 (GRCm39) |
N896K |
possibly damaging |
Het |
Nmt2 |
T |
A |
2: 3,323,672 (GRCm39) |
I355N |
probably benign |
Het |
Nxpe5 |
T |
C |
5: 138,249,785 (GRCm39) |
V525A |
probably damaging |
Het |
Oas1f |
A |
T |
5: 120,993,648 (GRCm39) |
T287S |
probably benign |
Het |
Or1n1b |
A |
T |
2: 36,780,458 (GRCm39) |
M134K |
possibly damaging |
Het |
Or5ae1 |
T |
C |
7: 84,565,487 (GRCm39) |
S167P |
probably benign |
Het |
Or6ae1 |
T |
A |
7: 139,742,726 (GRCm39) |
I46F |
possibly damaging |
Het |
Or7a38 |
T |
A |
10: 78,752,758 (GRCm39) |
I28N |
probably damaging |
Het |
Or8b3 |
T |
A |
9: 38,314,182 (GRCm39) |
M1K |
probably null |
Het |
Pakap |
T |
C |
4: 57,638,068 (GRCm39) |
V35A |
probably benign |
Het |
Panx1 |
A |
G |
9: 14,918,822 (GRCm39) |
C346R |
probably benign |
Het |
Plekha7 |
T |
C |
7: 115,744,209 (GRCm39) |
E764G |
probably damaging |
Het |
Plet1 |
A |
G |
9: 50,415,652 (GRCm39) |
|
probably null |
Het |
Plod2 |
A |
G |
9: 92,489,188 (GRCm39) |
S707G |
probably damaging |
Het |
Plscr4 |
G |
A |
9: 92,365,889 (GRCm39) |
V120I |
probably damaging |
Het |
Pramel31 |
T |
A |
4: 144,088,435 (GRCm39) |
V77E |
probably benign |
Het |
Prob1 |
T |
A |
18: 35,785,942 (GRCm39) |
T771S |
possibly damaging |
Het |
Rasa3 |
A |
G |
8: 13,681,768 (GRCm39) |
|
probably benign |
Het |
Ror2 |
T |
C |
13: 53,285,885 (GRCm39) |
I110V |
probably damaging |
Het |
Sec24d |
A |
T |
3: 123,147,043 (GRCm39) |
H667L |
probably benign |
Het |
Sema3d |
A |
G |
5: 12,623,810 (GRCm39) |
Q573R |
probably damaging |
Het |
Serpinb2 |
T |
A |
1: 107,452,337 (GRCm39) |
V305D |
probably damaging |
Het |
Slc11a2 |
G |
A |
15: 100,301,775 (GRCm39) |
R249C |
probably benign |
Het |
Slc14a1 |
T |
C |
18: 78,152,912 (GRCm39) |
I276V |
possibly damaging |
Het |
Snx19 |
T |
A |
9: 30,343,620 (GRCm39) |
N593K |
probably damaging |
Het |
Ssh2 |
C |
G |
11: 77,340,571 (GRCm39) |
D574E |
probably damaging |
Het |
Stil |
T |
C |
4: 114,881,072 (GRCm39) |
S539P |
probably benign |
Het |
Syt4 |
T |
C |
18: 31,577,141 (GRCm39) |
K71R |
probably damaging |
Het |
Tenm4 |
A |
T |
7: 96,385,015 (GRCm39) |
H524L |
probably damaging |
Het |
Tex30 |
C |
T |
1: 44,130,564 (GRCm39) |
G68D |
probably damaging |
Het |
Tm4sf19 |
A |
G |
16: 32,226,500 (GRCm39) |
Y138C |
probably damaging |
Het |
Tmem43 |
A |
T |
6: 91,463,891 (GRCm39) |
I389F |
probably benign |
Het |
Trpm1 |
A |
T |
7: 63,873,556 (GRCm39) |
N488Y |
probably damaging |
Het |
Tshz1 |
A |
T |
18: 84,031,558 (GRCm39) |
L950Q |
probably damaging |
Het |
Vmn1r16 |
T |
C |
6: 57,299,885 (GRCm39) |
I246V |
probably benign |
Het |
Vmn1r188 |
T |
G |
13: 22,272,815 (GRCm39) |
S256R |
possibly damaging |
Het |
Zfp12 |
G |
A |
5: 143,231,133 (GRCm39) |
E487K |
probably 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 |
R0254:Kif11
|
UTSW |
19 |
37,399,957 (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 |
|
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 |
|