Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg2 |
T |
C |
6: 58,667,525 (GRCm39) |
V129A |
probably benign |
Het |
Adh1 |
A |
G |
3: 137,992,676 (GRCm39) |
D264G |
probably damaging |
Het |
Ahnak2 |
T |
A |
12: 112,748,626 (GRCm39) |
D407V |
probably benign |
Het |
Alas1 |
T |
C |
9: 106,118,489 (GRCm39) |
E211G |
probably damaging |
Het |
Alkbh1 |
C |
T |
12: 87,490,520 (GRCm39) |
|
probably benign |
Het |
Ankmy1 |
T |
C |
1: 92,809,553 (GRCm39) |
I662V |
possibly damaging |
Het |
Ano1 |
A |
G |
7: 144,201,789 (GRCm39) |
V334A |
probably damaging |
Het |
Apc |
A |
G |
18: 34,449,481 (GRCm39) |
R2092G |
probably damaging |
Het |
Arhgap18 |
C |
T |
10: 26,730,904 (GRCm39) |
T122I |
probably benign |
Het |
Atp2b4 |
G |
T |
1: 133,654,275 (GRCm39) |
Q777K |
probably benign |
Het |
Brap |
G |
A |
5: 121,801,529 (GRCm39) |
G95S |
probably damaging |
Het |
Cbfa2t2 |
G |
A |
2: 154,377,077 (GRCm39) |
A587T |
probably damaging |
Het |
Ccdc180 |
A |
G |
4: 45,932,477 (GRCm39) |
I1308V |
probably benign |
Het |
Ccser1 |
T |
A |
6: 61,399,936 (GRCm39) |
|
probably null |
Het |
Cd84 |
A |
G |
1: 171,700,317 (GRCm39) |
T145A |
possibly damaging |
Het |
Cmtm4 |
A |
C |
8: 105,081,920 (GRCm39) |
F156V |
probably damaging |
Het |
Cntln |
G |
A |
4: 84,967,911 (GRCm39) |
R710K |
probably benign |
Het |
Csn1s1 |
A |
T |
5: 87,819,387 (GRCm39) |
T15S |
possibly damaging |
Het |
Cul9 |
T |
C |
17: 46,854,298 (GRCm39) |
T135A |
probably benign |
Het |
Cyp2d10 |
T |
A |
15: 82,288,015 (GRCm39) |
I363F |
probably damaging |
Het |
Dhx38 |
G |
T |
8: 110,289,352 (GRCm39) |
|
probably benign |
Het |
Dis3 |
A |
T |
14: 99,336,251 (GRCm39) |
I85N |
possibly damaging |
Het |
Dmbt1 |
G |
A |
7: 130,707,900 (GRCm39) |
A1381T |
possibly damaging |
Het |
Dscaml1 |
A |
G |
9: 45,661,430 (GRCm39) |
D1776G |
probably damaging |
Het |
Erbin |
A |
G |
13: 103,966,824 (GRCm39) |
S1209P |
probably benign |
Het |
Fat4 |
T |
A |
3: 38,945,319 (GRCm39) |
M1404K |
possibly damaging |
Het |
Fbxo45 |
G |
T |
16: 32,057,346 (GRCm39) |
Q183K |
possibly damaging |
Het |
Frmd4b |
C |
T |
6: 97,389,448 (GRCm39) |
|
probably null |
Het |
Fzd7 |
A |
G |
1: 59,523,361 (GRCm39) |
S415G |
probably benign |
Het |
Gpd2 |
T |
A |
2: 57,229,025 (GRCm39) |
|
probably null |
Het |
Gsk3b |
T |
A |
16: 38,008,271 (GRCm39) |
D192E |
probably benign |
Het |
Gstcd |
T |
C |
3: 132,787,814 (GRCm39) |
I295V |
probably benign |
Het |
Gucy1a1 |
A |
G |
3: 82,016,592 (GRCm39) |
L132P |
possibly damaging |
Het |
Il12b |
A |
C |
11: 44,298,727 (GRCm39) |
T61P |
probably damaging |
Het |
Il7 |
A |
T |
3: 7,638,975 (GRCm39) |
N130K |
probably damaging |
Het |
Itih3 |
A |
C |
14: 30,631,481 (GRCm39) |
|
probably null |
Het |
Kdm5b |
T |
A |
1: 134,540,952 (GRCm39) |
D681E |
probably benign |
Het |
Kng2 |
TATGACCATGACCATGACCATGACCATGACCATGACCAT |
TATGACCATGACCATGACCATGACCATGACCAT |
16: 22,806,703 (GRCm39) |
|
probably benign |
Het |
Kremen2 |
T |
C |
17: 23,961,691 (GRCm39) |
E272G |
possibly damaging |
Het |
Krt9 |
G |
T |
11: 100,082,321 (GRCm39) |
N201K |
probably damaging |
Het |
Lmbr1 |
G |
A |
5: 29,438,092 (GRCm39) |
P304L |
probably benign |
Het |
Lrrfip1 |
A |
G |
1: 91,043,539 (GRCm39) |
N648S |
probably benign |
Het |
Mab21l3 |
C |
A |
3: 101,722,469 (GRCm39) |
V386L |
possibly damaging |
Het |
Mamdc4 |
T |
C |
2: 25,454,180 (GRCm39) |
Q1149R |
probably benign |
Het |
Mast1 |
A |
G |
8: 85,646,995 (GRCm39) |
F677L |
possibly damaging |
Het |
Mcoln3 |
A |
G |
3: 145,833,979 (GRCm39) |
D173G |
probably benign |
Het |
Mmrn1 |
C |
T |
6: 60,921,789 (GRCm39) |
T82I |
probably benign |
Het |
Mtcl2 |
C |
T |
2: 156,864,747 (GRCm39) |
G1154S |
probably benign |
Het |
Muc5ac |
A |
G |
7: 141,345,772 (GRCm39) |
T203A |
probably benign |
Het |
Myo9b |
T |
C |
8: 71,812,334 (GRCm39) |
I2035T |
possibly damaging |
Het |
Ndst3 |
T |
C |
3: 123,465,534 (GRCm39) |
N146S |
probably damaging |
Het |
Neu4 |
A |
G |
1: 93,950,172 (GRCm39) |
T21A |
possibly damaging |
Het |
Nos1ap |
G |
A |
1: 170,155,215 (GRCm39) |
L267F |
probably damaging |
Het |
Or14c40 |
A |
T |
7: 86,313,591 (GRCm39) |
K240N |
probably damaging |
Het |
Or3a4 |
A |
T |
11: 73,944,819 (GRCm39) |
Y255* |
probably null |
Het |
Or4p8 |
A |
G |
2: 88,727,105 (GRCm39) |
F279L |
probably damaging |
Het |
Phc1 |
T |
C |
6: 122,310,299 (GRCm39) |
N136S |
probably damaging |
Het |
Prkdc |
A |
G |
16: 15,545,469 (GRCm39) |
T1862A |
probably benign |
Het |
Psd2 |
A |
G |
18: 36,139,744 (GRCm39) |
D596G |
possibly damaging |
Het |
Psmc3 |
T |
C |
2: 90,888,433 (GRCm39) |
F315L |
probably benign |
Het |
Rerg |
G |
A |
6: 137,034,878 (GRCm39) |
T42I |
probably benign |
Het |
Rif1 |
T |
A |
2: 51,983,588 (GRCm39) |
M577K |
probably damaging |
Het |
Sap30 |
T |
C |
8: 57,940,282 (GRCm39) |
|
probably null |
Het |
Scn2b |
T |
C |
9: 45,036,815 (GRCm39) |
Y108H |
probably damaging |
Het |
Senp2 |
C |
T |
16: 21,832,949 (GRCm39) |
T79I |
probably damaging |
Het |
Serpinb2 |
T |
C |
1: 107,451,543 (GRCm39) |
V232A |
probably damaging |
Het |
Sgpp2 |
T |
A |
1: 78,393,588 (GRCm39) |
L197Q |
probably damaging |
Het |
Slc27a4 |
T |
C |
2: 29,700,953 (GRCm39) |
W320R |
probably damaging |
Het |
Spmip4 |
T |
C |
6: 50,550,725 (GRCm39) |
R575G |
possibly damaging |
Het |
Tgm4 |
T |
C |
9: 122,890,835 (GRCm39) |
I54T |
probably damaging |
Het |
Thbs4 |
T |
A |
13: 92,927,387 (GRCm39) |
D34V |
probably benign |
Het |
Tlcd4 |
T |
G |
3: 121,001,070 (GRCm39) |
I188L |
probably benign |
Het |
Tmem176b |
G |
A |
6: 48,813,267 (GRCm39) |
T64I |
probably damaging |
Het |
Tmod2 |
T |
C |
9: 75,484,524 (GRCm39) |
E248G |
probably benign |
Het |
Ttc6 |
T |
A |
12: 57,784,479 (GRCm39) |
D1849E |
probably benign |
Het |
Ttn |
T |
C |
2: 76,615,882 (GRCm39) |
D8360G |
possibly damaging |
Het |
Unc80 |
A |
G |
1: 66,679,711 (GRCm39) |
E2094G |
possibly damaging |
Het |
Vmn2r18 |
A |
T |
5: 151,508,160 (GRCm39) |
D321E |
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 |
|
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 |
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 |
|