Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
T |
C |
11: 119,900,562 (GRCm39) |
T1195A |
probably benign |
Het |
Abca12 |
A |
T |
1: 71,283,930 (GRCm39) |
N2547K |
probably benign |
Het |
Abca16 |
A |
C |
7: 120,139,868 (GRCm39) |
E1510A |
probably damaging |
Het |
Adam5 |
A |
G |
8: 25,234,161 (GRCm39) |
|
probably benign |
Het |
Akna |
G |
A |
4: 63,313,397 (GRCm39) |
P242L |
probably benign |
Het |
Akr1b7 |
G |
A |
6: 34,395,929 (GRCm39) |
A144T |
possibly damaging |
Het |
Ankhd1 |
T |
A |
18: 36,767,361 (GRCm39) |
S1167T |
probably damaging |
Het |
Arf5 |
C |
T |
6: 28,424,783 (GRCm39) |
Q71* |
probably null |
Het |
Ark2n |
T |
C |
18: 77,762,168 (GRCm39) |
D48G |
possibly damaging |
Het |
Arl15 |
C |
T |
13: 114,104,196 (GRCm39) |
S111F |
probably damaging |
Het |
Atxn1l |
C |
T |
8: 110,459,240 (GRCm39) |
A341T |
probably benign |
Het |
Birc7 |
C |
A |
2: 180,572,642 (GRCm39) |
Q138K |
possibly damaging |
Het |
Blvra |
G |
T |
2: 126,927,989 (GRCm39) |
E80* |
probably null |
Het |
Ccdc148 |
T |
C |
2: 58,892,128 (GRCm39) |
E188G |
probably damaging |
Het |
Chad |
C |
T |
11: 94,459,052 (GRCm39) |
A318V |
probably benign |
Het |
Cntfr |
A |
G |
4: 41,663,534 (GRCm39) |
|
probably null |
Het |
Dnah17 |
C |
T |
11: 118,010,628 (GRCm39) |
C230Y |
probably benign |
Het |
Dnmt3l |
C |
A |
10: 77,899,130 (GRCm39) |
L110I |
probably damaging |
Het |
Dusp11 |
T |
C |
6: 85,935,651 (GRCm39) |
D74G |
probably damaging |
Het |
Duxf4 |
T |
C |
10: 58,072,073 (GRCm39) |
D47G |
possibly damaging |
Het |
Eif3m |
T |
C |
2: 104,837,141 (GRCm39) |
T61A |
probably damaging |
Het |
Esyt1 |
T |
A |
10: 128,357,973 (GRCm39) |
D212V |
probably damaging |
Het |
Exoc4 |
T |
A |
6: 33,324,760 (GRCm39) |
N351K |
possibly damaging |
Het |
F13a1 |
A |
T |
13: 37,172,831 (GRCm39) |
I183N |
probably damaging |
Het |
Fam83f |
T |
G |
15: 80,576,468 (GRCm39) |
V373G |
possibly damaging |
Het |
Fam83h |
A |
T |
15: 75,874,146 (GRCm39) |
Y1064N |
probably damaging |
Het |
Flrt3 |
G |
T |
2: 140,503,423 (GRCm39) |
N68K |
probably damaging |
Het |
Fut7 |
C |
A |
2: 25,315,343 (GRCm39) |
Y153* |
probably null |
Het |
Gm10277 |
TC |
T |
11: 77,676,828 (GRCm39) |
|
probably null |
Het |
Gm1527 |
T |
C |
3: 28,972,098 (GRCm39) |
L405P |
probably benign |
Het |
Heatr6 |
T |
A |
11: 83,648,281 (GRCm39) |
|
probably benign |
Het |
Herc2 |
T |
C |
7: 55,835,576 (GRCm39) |
|
probably benign |
Het |
Ints14 |
T |
G |
9: 64,887,077 (GRCm39) |
L336R |
probably damaging |
Het |
Irak1 |
G |
T |
X: 73,066,218 (GRCm39) |
P197Q |
possibly damaging |
Het |
Kat7 |
C |
T |
11: 95,194,120 (GRCm39) |
R60Q |
probably benign |
Het |
Katnal2 |
T |
C |
18: 77,067,787 (GRCm39) |
R385G |
probably damaging |
Het |
Kcnt2 |
G |
T |
1: 140,480,701 (GRCm39) |
L755F |
probably damaging |
Het |
Kif4 |
A |
G |
X: 99,709,323 (GRCm39) |
S315G |
probably benign |
Het |
Krit1 |
A |
T |
5: 3,872,108 (GRCm39) |
R378* |
probably null |
Het |
L3mbtl1 |
T |
A |
2: 162,801,990 (GRCm39) |
|
probably null |
Het |
Lama3 |
C |
A |
18: 12,535,906 (GRCm39) |
T204N |
possibly damaging |
Het |
Lama5 |
A |
G |
2: 179,828,678 (GRCm39) |
C2090R |
probably damaging |
Het |
Mb |
G |
T |
15: 76,906,759 (GRCm39) |
Q9K |
probably benign |
Het |
Mipep |
T |
C |
14: 61,024,829 (GRCm39) |
V90A |
probably damaging |
Het |
Myo3a |
A |
T |
2: 22,250,342 (GRCm39) |
I70F |
probably damaging |
Het |
Napa |
A |
G |
7: 15,848,134 (GRCm39) |
D217G |
possibly damaging |
Het |
Nectin2 |
T |
C |
7: 19,451,489 (GRCm39) |
D515G |
probably damaging |
Het |
Nkx2-6 |
T |
A |
14: 69,409,288 (GRCm39) |
V13E |
probably damaging |
Het |
Nmi |
T |
C |
2: 51,838,719 (GRCm39) |
T272A |
probably benign |
Het |
Nptx2 |
G |
C |
5: 144,492,216 (GRCm39) |
G331A |
probably damaging |
Het |
Or2q1 |
A |
G |
6: 42,794,431 (GRCm39) |
T9A |
possibly damaging |
Het |
Or4c122 |
T |
C |
2: 89,079,874 (GRCm39) |
I55V |
probably damaging |
Het |
Or5h17 |
T |
C |
16: 58,820,783 (GRCm39) |
L245P |
possibly damaging |
Het |
Or7g34 |
T |
C |
9: 19,478,618 (GRCm39) |
T18A |
probably benign |
Het |
Parp14 |
T |
C |
16: 35,678,904 (GRCm39) |
T355A |
probably benign |
Het |
Pcdh12 |
T |
C |
18: 38,417,039 (GRCm39) |
T29A |
probably damaging |
Het |
Pced1b |
T |
A |
15: 97,282,505 (GRCm39) |
C181* |
probably null |
Het |
Phka1 |
C |
T |
X: 101,653,807 (GRCm39) |
R290H |
probably damaging |
Het |
Pick1 |
T |
A |
15: 79,139,781 (GRCm39) |
|
probably benign |
Het |
Pitrm1 |
A |
T |
13: 6,607,809 (GRCm39) |
Y268F |
probably damaging |
Het |
Polr2h |
T |
C |
16: 20,537,737 (GRCm39) |
|
probably benign |
Het |
Ppfia2 |
A |
T |
10: 106,597,972 (GRCm39) |
K178N |
probably damaging |
Het |
Prkag1 |
T |
C |
15: 98,712,433 (GRCm39) |
Y133C |
probably damaging |
Het |
Ptk2 |
A |
G |
15: 73,114,255 (GRCm39) |
V701A |
possibly damaging |
Het |
Ptpra |
G |
T |
2: 130,381,655 (GRCm39) |
R372L |
probably damaging |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Qrich2 |
A |
G |
11: 116,337,982 (GRCm39) |
V1887A |
probably damaging |
Het |
Ralgapa1 |
T |
C |
12: 55,833,134 (GRCm39) |
|
probably null |
Het |
Rassf9 |
A |
G |
10: 102,380,806 (GRCm39) |
T63A |
probably benign |
Het |
Rdh11 |
G |
T |
12: 79,222,996 (GRCm39) |
Q292K |
probably benign |
Het |
Rere |
C |
A |
4: 150,697,018 (GRCm39) |
|
probably benign |
Het |
Rgs18 |
G |
T |
1: 144,629,629 (GRCm39) |
T210K |
possibly damaging |
Het |
Rnf213 |
A |
G |
11: 119,318,839 (GRCm39) |
N1099S |
probably benign |
Het |
Ros1 |
T |
C |
10: 52,004,651 (GRCm39) |
I969V |
probably benign |
Het |
Rrh |
T |
C |
3: 129,604,336 (GRCm39) |
I288M |
probably damaging |
Het |
Rrp12 |
C |
T |
19: 41,879,533 (GRCm39) |
V174I |
probably benign |
Het |
Rtf1 |
T |
A |
2: 119,535,999 (GRCm39) |
H184Q |
probably benign |
Het |
Sbk3 |
A |
G |
7: 4,970,415 (GRCm39) |
L318S |
possibly damaging |
Het |
Scn9a |
T |
C |
2: 66,314,396 (GRCm39) |
E1774G |
probably damaging |
Het |
Sec11c |
A |
T |
18: 65,933,720 (GRCm39) |
T9S |
probably benign |
Het |
Sec23ip |
G |
A |
7: 128,364,185 (GRCm39) |
V488I |
probably benign |
Het |
Serpine3 |
T |
C |
14: 62,910,459 (GRCm39) |
L184P |
probably damaging |
Het |
Slc26a2 |
T |
C |
18: 61,331,896 (GRCm39) |
T512A |
possibly damaging |
Het |
Slc49a4 |
T |
C |
16: 35,518,309 (GRCm39) |
D468G |
probably benign |
Het |
Smpd4 |
T |
C |
16: 17,444,729 (GRCm39) |
Y118H |
probably benign |
Het |
Tcof1 |
T |
C |
18: 60,965,857 (GRCm39) |
E415G |
possibly damaging |
Het |
Ttc33 |
G |
A |
15: 5,241,534 (GRCm39) |
V120I |
probably benign |
Het |
Usp20 |
T |
A |
2: 30,906,317 (GRCm39) |
C562S |
probably damaging |
Het |
Utp20 |
T |
C |
10: 88,621,865 (GRCm39) |
D1136G |
probably benign |
Het |
Vgll1 |
A |
C |
X: 56,137,790 (GRCm39) |
K53T |
probably damaging |
Het |
Yars1 |
T |
G |
4: 129,101,716 (GRCm39) |
|
probably null |
Het |
Zfp472 |
A |
G |
17: 33,196,988 (GRCm39) |
I354M |
possibly damaging |
Het |
Zfp786 |
A |
G |
6: 47,803,931 (GRCm39) |
V37A |
probably damaging |
Het |
|
Other mutations in Kifc3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00720:Kifc3
|
APN |
8 |
95,864,644 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01904:Kifc3
|
APN |
8 |
95,864,585 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02019:Kifc3
|
APN |
8 |
95,834,168 (GRCm39) |
splice site |
probably benign |
|
IGL02090:Kifc3
|
APN |
8 |
95,829,108 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02355:Kifc3
|
APN |
8 |
95,836,507 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02362:Kifc3
|
APN |
8 |
95,836,507 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02620:Kifc3
|
APN |
8 |
95,836,582 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02720:Kifc3
|
APN |
8 |
95,834,993 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03030:Kifc3
|
APN |
8 |
95,829,040 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03327:Kifc3
|
APN |
8 |
95,835,060 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03390:Kifc3
|
APN |
8 |
95,835,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R0233:Kifc3
|
UTSW |
8 |
95,828,100 (GRCm39) |
splice site |
probably null |
|
R0281:Kifc3
|
UTSW |
8 |
95,830,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R0302:Kifc3
|
UTSW |
8 |
95,830,098 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0619:Kifc3
|
UTSW |
8 |
95,829,293 (GRCm39) |
missense |
probably benign |
0.13 |
R0731:Kifc3
|
UTSW |
8 |
95,832,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R1017:Kifc3
|
UTSW |
8 |
95,832,413 (GRCm39) |
missense |
probably damaging |
0.99 |
R1147:Kifc3
|
UTSW |
8 |
95,864,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R1147:Kifc3
|
UTSW |
8 |
95,864,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R1257:Kifc3
|
UTSW |
8 |
95,832,400 (GRCm39) |
missense |
probably damaging |
0.98 |
R1472:Kifc3
|
UTSW |
8 |
95,864,541 (GRCm39) |
critical splice donor site |
probably null |
|
R1480:Kifc3
|
UTSW |
8 |
95,836,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R1553:Kifc3
|
UTSW |
8 |
95,833,170 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2071:Kifc3
|
UTSW |
8 |
95,834,981 (GRCm39) |
critical splice donor site |
probably null |
|
R3703:Kifc3
|
UTSW |
8 |
95,830,656 (GRCm39) |
splice site |
probably benign |
|
R3704:Kifc3
|
UTSW |
8 |
95,830,656 (GRCm39) |
splice site |
probably benign |
|
R3705:Kifc3
|
UTSW |
8 |
95,830,656 (GRCm39) |
splice site |
probably benign |
|
R4223:Kifc3
|
UTSW |
8 |
95,836,610 (GRCm39) |
missense |
probably damaging |
0.96 |
R4463:Kifc3
|
UTSW |
8 |
95,828,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R4508:Kifc3
|
UTSW |
8 |
95,834,048 (GRCm39) |
splice site |
probably null |
|
R4980:Kifc3
|
UTSW |
8 |
95,853,177 (GRCm39) |
missense |
probably benign |
|
R5032:Kifc3
|
UTSW |
8 |
95,829,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R5068:Kifc3
|
UTSW |
8 |
95,836,844 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5421:Kifc3
|
UTSW |
8 |
95,836,473 (GRCm39) |
missense |
probably damaging |
0.99 |
R5556:Kifc3
|
UTSW |
8 |
95,835,087 (GRCm39) |
nonsense |
probably null |
|
R6845:Kifc3
|
UTSW |
8 |
95,835,307 (GRCm39) |
missense |
probably benign |
0.28 |
R7136:Kifc3
|
UTSW |
8 |
95,830,077 (GRCm39) |
missense |
probably benign |
0.10 |
R7196:Kifc3
|
UTSW |
8 |
95,833,239 (GRCm39) |
missense |
probably benign |
0.02 |
R7404:Kifc3
|
UTSW |
8 |
95,830,092 (GRCm39) |
missense |
probably benign |
0.02 |
R7441:Kifc3
|
UTSW |
8 |
95,864,615 (GRCm39) |
missense |
probably benign |
0.00 |
R7784:Kifc3
|
UTSW |
8 |
95,837,320 (GRCm39) |
critical splice donor site |
probably null |
|
R7861:Kifc3
|
UTSW |
8 |
95,834,165 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8440:Kifc3
|
UTSW |
8 |
95,836,422 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8754:Kifc3
|
UTSW |
8 |
95,829,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R8983:Kifc3
|
UTSW |
8 |
95,833,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R9035:Kifc3
|
UTSW |
8 |
95,853,195 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9149:Kifc3
|
UTSW |
8 |
95,853,317 (GRCm39) |
missense |
probably benign |
|
R9464:Kifc3
|
UTSW |
8 |
95,830,622 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9589:Kifc3
|
UTSW |
8 |
95,861,372 (GRCm39) |
missense |
possibly damaging |
0.87 |
X0023:Kifc3
|
UTSW |
8 |
95,835,926 (GRCm39) |
missense |
probably benign |
0.00 |
|