Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
G |
A |
3: 137,775,520 (GRCm39) |
V1570I |
probably damaging |
Het |
Alx4 |
A |
G |
2: 93,473,106 (GRCm39) |
R35G |
probably damaging |
Het |
Apod |
T |
C |
16: 31,116,211 (GRCm39) |
D173G |
probably benign |
Het |
Atp8b3 |
G |
A |
10: 80,361,858 (GRCm39) |
T731I |
possibly damaging |
Het |
Birc6 |
A |
C |
17: 74,947,145 (GRCm39) |
T2955P |
probably benign |
Het |
Cdh15 |
G |
A |
8: 123,587,612 (GRCm39) |
D179N |
probably damaging |
Het |
Cntnap5c |
G |
T |
17: 58,717,263 (GRCm39) |
V1282L |
probably benign |
Het |
Crocc2 |
G |
A |
1: 93,141,372 (GRCm39) |
R1175H |
probably benign |
Het |
Dbh |
A |
G |
2: 27,064,836 (GRCm39) |
D349G |
probably damaging |
Het |
Dync1h1 |
A |
G |
12: 110,605,278 (GRCm39) |
I2372V |
probably benign |
Het |
Fer1l4 |
A |
T |
2: 155,889,007 (GRCm39) |
W389R |
probably damaging |
Het |
Fndc1 |
T |
C |
17: 7,984,036 (GRCm39) |
T1297A |
unknown |
Het |
Gart |
T |
C |
16: 91,422,321 (GRCm39) |
N732S |
probably damaging |
Het |
Gas2l2 |
T |
C |
11: 83,313,924 (GRCm39) |
I463V |
probably benign |
Het |
Gm5591 |
G |
A |
7: 38,220,072 (GRCm39) |
S267L |
probably benign |
Het |
Gzmk |
A |
G |
13: 113,309,657 (GRCm39) |
V92A |
probably damaging |
Het |
Hspg2 |
C |
T |
4: 137,273,884 (GRCm39) |
R2680W |
probably damaging |
Het |
Insyn2a |
A |
G |
7: 134,520,270 (GRCm39) |
Y87H |
probably damaging |
Het |
Kcnh3 |
G |
A |
15: 99,131,982 (GRCm39) |
V646M |
probably damaging |
Het |
Kcnk7 |
A |
C |
19: 5,756,463 (GRCm39) |
I230L |
probably benign |
Het |
Klra5 |
T |
C |
6: 129,885,776 (GRCm39) |
S128G |
probably benign |
Het |
Krba1 |
C |
T |
6: 48,383,282 (GRCm39) |
R4* |
probably null |
Het |
Krt1c |
T |
A |
15: 101,726,026 (GRCm39) |
I171F |
probably damaging |
Het |
Lss |
A |
G |
10: 76,372,089 (GRCm39) |
D148G |
probably benign |
Het |
Mavs |
G |
T |
2: 131,082,370 (GRCm39) |
A85S |
probably damaging |
Het |
Mipep |
T |
C |
14: 61,140,865 (GRCm39) |
C566R |
probably damaging |
Het |
Myocd |
T |
A |
11: 65,069,254 (GRCm39) |
|
probably benign |
Het |
Ndufa9 |
C |
T |
6: 126,804,498 (GRCm39) |
|
probably null |
Het |
Nolc1 |
G |
A |
19: 46,071,959 (GRCm39) |
G583D |
probably damaging |
Het |
Nucb2 |
T |
C |
7: 116,127,059 (GRCm39) |
|
probably null |
Het |
Or1i2 |
T |
C |
10: 78,448,409 (GRCm39) |
D22G |
probably benign |
Het |
Or52e19 |
C |
T |
7: 102,959,165 (GRCm39) |
T79I |
probably benign |
Het |
Or5p63 |
A |
T |
7: 107,811,301 (GRCm39) |
I145N |
possibly damaging |
Het |
Pank4 |
C |
A |
4: 155,061,076 (GRCm39) |
D508E |
probably benign |
Het |
Phb1 |
T |
A |
11: 95,562,416 (GRCm39) |
|
probably benign |
Het |
Pign |
T |
A |
1: 105,449,715 (GRCm39) |
|
probably benign |
Het |
Plec |
T |
C |
15: 76,076,382 (GRCm39) |
K349E |
probably benign |
Het |
Ppp1r3c |
A |
T |
19: 36,711,743 (GRCm39) |
V9E |
possibly damaging |
Het |
Rap1gap |
T |
A |
4: 137,443,422 (GRCm39) |
V130D |
probably damaging |
Het |
Senp3 |
T |
A |
11: 69,567,944 (GRCm39) |
Y432F |
probably benign |
Het |
Serpina3f |
T |
C |
12: 104,183,549 (GRCm39) |
I137T |
possibly damaging |
Het |
Slc46a3 |
T |
A |
5: 147,823,540 (GRCm39) |
K101* |
probably null |
Het |
Snph |
G |
A |
2: 151,436,434 (GRCm39) |
Q96* |
probably null |
Het |
Sptb |
A |
T |
12: 76,630,581 (GRCm39) |
C2244* |
probably null |
Het |
Srbd1 |
A |
T |
17: 86,416,693 (GRCm39) |
F488L |
probably benign |
Het |
Ssc5d |
A |
T |
7: 4,932,524 (GRCm39) |
H396L |
probably damaging |
Het |
Sulf1 |
A |
C |
1: 12,856,876 (GRCm39) |
R42S |
probably damaging |
Het |
Taf1a |
T |
A |
1: 183,181,752 (GRCm39) |
|
probably benign |
Het |
Thoc5 |
T |
A |
11: 4,876,218 (GRCm39) |
M609K |
probably damaging |
Het |
Tiam2 |
A |
T |
17: 3,568,617 (GRCm39) |
I1588F |
probably damaging |
Het |
Tmcc1 |
C |
T |
6: 116,020,247 (GRCm39) |
V402I |
probably damaging |
Het |
Tmprss15 |
T |
C |
16: 78,818,358 (GRCm39) |
D524G |
probably damaging |
Het |
Trbv31 |
T |
C |
6: 41,534,901 (GRCm39) |
I21V |
probably benign |
Het |
Vmn1r74 |
A |
T |
7: 11,581,398 (GRCm39) |
T233S |
possibly damaging |
Het |
Vmn1r74 |
G |
C |
7: 11,581,403 (GRCm39) |
Q234H |
probably damaging |
Het |
Vsx1 |
A |
T |
2: 150,530,529 (GRCm39) |
S118T |
probably benign |
Het |
Wnt9b |
G |
A |
11: 103,621,949 (GRCm39) |
T236I |
probably benign |
Het |
Zbtb21 |
T |
C |
16: 97,751,092 (GRCm39) |
T1092A |
possibly damaging |
Het |
Zc3hc1 |
G |
A |
6: 30,387,523 (GRCm39) |
T52I |
probably benign |
Het |
Zfp558 |
T |
A |
9: 18,367,577 (GRCm39) |
N404Y |
possibly damaging |
Het |
Zfp735 |
A |
T |
11: 73,602,031 (GRCm39) |
D325V |
probably damaging |
Het |
Zhx3 |
A |
T |
2: 160,623,879 (GRCm39) |
M96K |
probably damaging |
Het |
|
Other mutations in Kif3b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00162:Kif3b
|
APN |
2 |
153,159,051 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00927:Kif3b
|
APN |
2 |
153,158,381 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02121:Kif3b
|
APN |
2 |
153,159,194 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02302:Kif3b
|
APN |
2 |
153,158,868 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02306:Kif3b
|
APN |
2 |
153,162,572 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02348:Kif3b
|
APN |
2 |
153,158,813 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03111:Kif3b
|
APN |
2 |
153,171,988 (GRCm39) |
missense |
probably benign |
0.00 |
R1463:Kif3b
|
UTSW |
2 |
153,172,073 (GRCm39) |
makesense |
probably null |
|
R1474:Kif3b
|
UTSW |
2 |
153,162,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R1485:Kif3b
|
UTSW |
2 |
153,164,851 (GRCm39) |
splice site |
probably null |
|
R1538:Kif3b
|
UTSW |
2 |
153,159,382 (GRCm39) |
small deletion |
probably benign |
|
R1834:Kif3b
|
UTSW |
2 |
153,159,405 (GRCm39) |
missense |
probably benign |
0.22 |
R2371:Kif3b
|
UTSW |
2 |
153,164,743 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4051:Kif3b
|
UTSW |
2 |
153,165,477 (GRCm39) |
missense |
probably damaging |
0.99 |
R4208:Kif3b
|
UTSW |
2 |
153,165,477 (GRCm39) |
missense |
probably damaging |
0.99 |
R4504:Kif3b
|
UTSW |
2 |
153,165,564 (GRCm39) |
critical splice donor site |
probably null |
|
R4806:Kif3b
|
UTSW |
2 |
153,162,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R4911:Kif3b
|
UTSW |
2 |
153,159,212 (GRCm39) |
nonsense |
probably null |
|
R7017:Kif3b
|
UTSW |
2 |
153,171,644 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7990:Kif3b
|
UTSW |
2 |
153,159,383 (GRCm39) |
missense |
probably benign |
0.01 |
R8056:Kif3b
|
UTSW |
2 |
153,171,979 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8503:Kif3b
|
UTSW |
2 |
153,162,824 (GRCm39) |
critical splice donor site |
probably null |
|
R8515:Kif3b
|
UTSW |
2 |
153,158,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R9041:Kif3b
|
UTSW |
2 |
153,159,468 (GRCm39) |
missense |
probably benign |
0.01 |
R9524:Kif3b
|
UTSW |
2 |
153,159,460 (GRCm39) |
missense |
probably benign |
0.38 |
X0026:Kif3b
|
UTSW |
2 |
153,158,241 (GRCm39) |
missense |
probably damaging |
1.00 |
|