Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl6a |
C |
T |
3: 32,766,263 (GRCm39) |
T39M |
possibly damaging |
Het |
Arhgdib |
T |
C |
6: 136,901,156 (GRCm39) |
N191S |
probably benign |
Het |
Arhgef39 |
A |
G |
4: 43,497,353 (GRCm39) |
|
probably benign |
Het |
Baz1a |
G |
A |
12: 54,947,233 (GRCm39) |
R1139C |
probably damaging |
Het |
Cdhr5 |
A |
T |
7: 140,852,752 (GRCm39) |
I78N |
probably damaging |
Het |
Cfap97 |
T |
A |
8: 46,645,698 (GRCm39) |
N525K |
probably benign |
Het |
Cntn2 |
T |
A |
1: 132,455,481 (GRCm39) |
Y252F |
probably benign |
Het |
Cyp3a57 |
G |
A |
5: 145,286,207 (GRCm39) |
G48S |
probably damaging |
Het |
Cyp4v3 |
A |
C |
8: 45,781,260 (GRCm39) |
F73V |
possibly damaging |
Het |
Ear10 |
T |
C |
14: 44,160,404 (GRCm39) |
D141G |
probably benign |
Het |
Fbn2 |
T |
C |
18: 58,168,411 (GRCm39) |
I2309V |
probably damaging |
Het |
Fcrl5 |
A |
G |
3: 87,349,531 (GRCm39) |
D102G |
probably benign |
Het |
Fdxacb1 |
A |
T |
9: 50,683,879 (GRCm39) |
Q614L |
probably damaging |
Het |
Gm10267 |
T |
C |
18: 44,290,331 (GRCm39) |
T59A |
probably damaging |
Het |
Gm5581 |
C |
T |
6: 131,144,519 (GRCm39) |
|
noncoding transcript |
Het |
Gm5592 |
G |
T |
7: 40,808,336 (GRCm39) |
|
probably benign |
Het |
Gtf2a1l |
A |
G |
17: 89,001,884 (GRCm39) |
T200A |
probably damaging |
Het |
Hspg2 |
C |
T |
4: 137,246,251 (GRCm39) |
R1010C |
probably damaging |
Het |
Ift122 |
T |
C |
6: 115,900,852 (GRCm39) |
C1057R |
probably damaging |
Het |
Kirrel3 |
A |
T |
9: 34,934,769 (GRCm39) |
N73I |
probably benign |
Het |
Kndc1 |
A |
G |
7: 139,490,798 (GRCm39) |
I433M |
probably benign |
Het |
Mks1 |
T |
C |
11: 87,747,530 (GRCm39) |
|
probably benign |
Het |
Mmp14 |
A |
T |
14: 54,673,665 (GRCm39) |
K110* |
probably null |
Het |
Mms19 |
A |
G |
19: 41,933,992 (GRCm39) |
L938P |
probably damaging |
Het |
Mrpl36 |
A |
T |
13: 73,479,777 (GRCm39) |
|
probably null |
Het |
Mypn |
T |
C |
10: 62,966,961 (GRCm39) |
E905G |
probably damaging |
Het |
Ncam1 |
G |
T |
9: 49,468,472 (GRCm39) |
T329N |
probably damaging |
Het |
Nfkbie |
T |
C |
17: 45,869,516 (GRCm39) |
L157P |
probably damaging |
Het |
Or14c45 |
T |
A |
7: 86,176,262 (GRCm39) |
I99N |
probably damaging |
Het |
Or4f47 |
T |
A |
2: 111,972,319 (GRCm39) |
S10T |
probably benign |
Het |
Pappa |
C |
T |
4: 65,074,100 (GRCm39) |
A218V |
probably benign |
Het |
Plekhg5 |
T |
C |
4: 152,196,884 (GRCm39) |
Y737H |
probably benign |
Het |
Plod2 |
G |
A |
9: 92,485,041 (GRCm39) |
R514Q |
possibly damaging |
Het |
Plxnb1 |
C |
T |
9: 108,943,420 (GRCm39) |
R1888W |
probably damaging |
Het |
Prss45 |
A |
G |
9: 110,669,997 (GRCm39) |
T269A |
probably benign |
Het |
Ptpn13 |
A |
G |
5: 103,681,151 (GRCm39) |
T784A |
probably damaging |
Het |
Pycr3 |
T |
C |
15: 75,790,655 (GRCm39) |
N68S |
probably benign |
Het |
Rbis |
T |
C |
3: 14,674,714 (GRCm39) |
M1V |
probably null |
Het |
Rdh14 |
A |
T |
12: 10,444,949 (GRCm39) |
N267Y |
probably benign |
Het |
Rph3a |
G |
A |
5: 121,111,368 (GRCm39) |
R71C |
probably damaging |
Het |
Sall2 |
C |
A |
14: 52,551,260 (GRCm39) |
R643L |
probably damaging |
Het |
Spata13 |
T |
A |
14: 60,928,523 (GRCm39) |
V27E |
probably damaging |
Het |
Tbc1d1 |
T |
A |
5: 64,417,771 (GRCm39) |
S312T |
probably damaging |
Het |
Trdn |
C |
T |
10: 33,340,578 (GRCm39) |
S604L |
probably benign |
Het |
Ttn |
T |
C |
2: 76,640,742 (GRCm39) |
T13669A |
probably benign |
Het |
Tyw3 |
A |
T |
3: 154,302,645 (GRCm39) |
F30I |
probably damaging |
Het |
Vmn1r227 |
G |
T |
17: 20,956,092 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r74 |
C |
T |
7: 85,606,562 (GRCm39) |
M261I |
probably benign |
Het |
Zfp217 |
C |
T |
2: 169,956,707 (GRCm39) |
G764S |
probably benign |
Het |
Zfp267 |
A |
G |
3: 36,213,747 (GRCm39) |
N27S |
possibly damaging |
Het |
Zfp748 |
T |
A |
13: 67,689,202 (GRCm39) |
H686L |
probably damaging |
Het |
|
Other mutations in Tcp11l2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00725:Tcp11l2
|
APN |
10 |
84,430,574 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL00845:Tcp11l2
|
APN |
10 |
84,440,847 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02375:Tcp11l2
|
APN |
10 |
84,440,932 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02418:Tcp11l2
|
APN |
10 |
84,449,470 (GRCm39) |
nonsense |
probably null |
|
IGL03325:Tcp11l2
|
APN |
10 |
84,440,764 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0031:Tcp11l2
|
UTSW |
10 |
84,427,004 (GRCm39) |
missense |
probably damaging |
0.98 |
R0591:Tcp11l2
|
UTSW |
10 |
84,440,458 (GRCm39) |
missense |
probably benign |
0.05 |
R1563:Tcp11l2
|
UTSW |
10 |
84,420,808 (GRCm39) |
missense |
probably damaging |
0.96 |
R1607:Tcp11l2
|
UTSW |
10 |
84,449,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R1840:Tcp11l2
|
UTSW |
10 |
84,440,463 (GRCm39) |
missense |
probably damaging |
0.98 |
R2144:Tcp11l2
|
UTSW |
10 |
84,449,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R2251:Tcp11l2
|
UTSW |
10 |
84,440,933 (GRCm39) |
critical splice donor site |
probably null |
|
R4639:Tcp11l2
|
UTSW |
10 |
84,420,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R4844:Tcp11l2
|
UTSW |
10 |
84,449,555 (GRCm39) |
missense |
probably benign |
0.00 |
R4973:Tcp11l2
|
UTSW |
10 |
84,427,027 (GRCm39) |
missense |
probably damaging |
0.98 |
R5264:Tcp11l2
|
UTSW |
10 |
84,449,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R5970:Tcp11l2
|
UTSW |
10 |
84,430,661 (GRCm39) |
splice site |
probably benign |
|
R6966:Tcp11l2
|
UTSW |
10 |
84,427,133 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7250:Tcp11l2
|
UTSW |
10 |
84,423,105 (GRCm39) |
critical splice donor site |
probably null |
|
R7535:Tcp11l2
|
UTSW |
10 |
84,430,523 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7565:Tcp11l2
|
UTSW |
10 |
84,422,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R7619:Tcp11l2
|
UTSW |
10 |
84,430,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R7774:Tcp11l2
|
UTSW |
10 |
84,440,847 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8145:Tcp11l2
|
UTSW |
10 |
84,444,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R8379:Tcp11l2
|
UTSW |
10 |
84,449,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R8458:Tcp11l2
|
UTSW |
10 |
84,449,396 (GRCm39) |
nonsense |
probably null |
|
R8821:Tcp11l2
|
UTSW |
10 |
84,449,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R8831:Tcp11l2
|
UTSW |
10 |
84,449,522 (GRCm39) |
missense |
probably damaging |
1.00 |
RF008:Tcp11l2
|
UTSW |
10 |
84,449,388 (GRCm39) |
missense |
probably damaging |
0.99 |
|