Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1a |
T |
C |
5: 8,776,873 (GRCm39) |
L857P |
probably damaging |
Het |
Adam12 |
T |
C |
7: 133,489,671 (GRCm39) |
*582W |
probably null |
Het |
Adra1d |
A |
G |
2: 131,403,007 (GRCm39) |
V361A |
probably damaging |
Het |
Ank2 |
A |
G |
3: 126,737,698 (GRCm39) |
|
probably benign |
Het |
Atxn10 |
T |
A |
15: 85,346,515 (GRCm39) |
N424K |
probably damaging |
Het |
C8b |
A |
G |
4: 104,637,860 (GRCm39) |
T111A |
probably benign |
Het |
Ccdc168 |
A |
C |
1: 44,097,139 (GRCm39) |
C1320G |
possibly damaging |
Het |
Cdc45 |
C |
T |
16: 18,614,647 (GRCm39) |
R205H |
probably damaging |
Het |
Cdr2l |
T |
C |
11: 115,284,396 (GRCm39) |
V244A |
possibly damaging |
Het |
Col11a2 |
A |
G |
17: 34,270,775 (GRCm39) |
M468V |
probably benign |
Het |
Col4a2 |
G |
A |
8: 11,495,984 (GRCm39) |
R1535H |
probably damaging |
Het |
Cryab |
A |
T |
9: 50,664,751 (GRCm39) |
S59C |
probably damaging |
Het |
Cuzd1 |
G |
A |
7: 130,917,853 (GRCm39) |
T249I |
probably damaging |
Het |
Disp2 |
G |
A |
2: 118,617,392 (GRCm39) |
V129M |
probably benign |
Het |
Dlg2 |
G |
T |
7: 91,099,011 (GRCm39) |
R31L |
probably benign |
Het |
Dthd1 |
A |
C |
5: 62,996,730 (GRCm39) |
L488F |
probably damaging |
Het |
Dusp29 |
G |
A |
14: 21,727,091 (GRCm39) |
R186W |
probably benign |
Het |
Fat2 |
T |
G |
11: 55,172,992 (GRCm39) |
I2574L |
probably damaging |
Het |
Fchsd1 |
C |
T |
18: 38,092,926 (GRCm39) |
|
probably benign |
Het |
Fryl |
T |
C |
5: 73,231,247 (GRCm39) |
D1610G |
probably damaging |
Het |
Gm10330 |
T |
A |
12: 23,830,131 (GRCm39) |
N17Y |
probably damaging |
Het |
Gm4787 |
T |
A |
12: 81,424,239 (GRCm39) |
R640* |
probably null |
Het |
H2bc13 |
A |
T |
13: 21,900,030 (GRCm39) |
I95N |
probably damaging |
Het |
Ift88 |
T |
A |
14: 57,675,699 (GRCm39) |
S71T |
probably benign |
Het |
Isoc2b |
A |
G |
7: 4,852,357 (GRCm39) |
|
probably benign |
Het |
Itgb2 |
G |
T |
10: 77,393,886 (GRCm39) |
R442L |
probably benign |
Het |
Lama5 |
A |
T |
2: 179,823,444 (GRCm39) |
N2658K |
possibly damaging |
Het |
Lemd3 |
A |
T |
10: 120,769,538 (GRCm39) |
I598K |
probably damaging |
Het |
Lrp2 |
A |
T |
2: 69,285,182 (GRCm39) |
C3825* |
probably null |
Het |
Mep1a |
T |
C |
17: 43,788,037 (GRCm39) |
D673G |
probably damaging |
Het |
Met |
A |
G |
6: 17,491,361 (GRCm39) |
Y41C |
probably damaging |
Het |
Mfn2 |
A |
G |
4: 147,979,035 (GRCm39) |
V99A |
probably damaging |
Het |
Mmadhc |
A |
G |
2: 50,181,436 (GRCm39) |
I78T |
probably benign |
Het |
Mmp9 |
C |
A |
2: 164,792,912 (GRCm39) |
P389T |
possibly damaging |
Het |
Mvk |
T |
G |
5: 114,590,499 (GRCm39) |
S7A |
probably damaging |
Het |
Nlrp1a |
T |
A |
11: 71,015,077 (GRCm39) |
T58S |
probably benign |
Het |
Nlrp1c-ps |
C |
A |
11: 71,148,839 (GRCm39) |
|
noncoding transcript |
Het |
Nr1h3 |
A |
G |
2: 91,022,253 (GRCm39) |
I125T |
possibly damaging |
Het |
Or2a55-ps1 |
C |
T |
6: 43,071,598 (GRCm39) |
|
noncoding transcript |
Het |
Or8k39 |
A |
T |
2: 86,563,680 (GRCm39) |
I92K |
probably damaging |
Het |
Parn |
A |
G |
16: 13,485,886 (GRCm39) |
I3T |
possibly damaging |
Het |
Parp8 |
A |
G |
13: 116,998,740 (GRCm39) |
|
probably null |
Het |
Parva |
T |
C |
7: 112,143,475 (GRCm39) |
|
probably null |
Het |
Pwp2 |
A |
C |
10: 78,011,378 (GRCm39) |
I672M |
possibly damaging |
Het |
Sfswap |
C |
T |
5: 129,616,810 (GRCm39) |
T418I |
probably benign |
Het |
Slc6a3 |
A |
G |
13: 73,709,078 (GRCm39) |
Y334C |
probably damaging |
Het |
Slc7a13 |
C |
A |
4: 19,839,267 (GRCm39) |
T290K |
probably benign |
Het |
Spry2 |
A |
G |
14: 106,130,712 (GRCm39) |
L158P |
probably damaging |
Het |
Usp25 |
A |
G |
16: 76,847,342 (GRCm39) |
E150G |
probably damaging |
Het |
Zfp747 |
A |
G |
7: 126,973,769 (GRCm39) |
F134L |
possibly damaging |
Het |
Zp3r |
A |
G |
1: 130,524,518 (GRCm39) |
F175S |
probably benign |
Het |
|
Other mutations in Zscan22 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01966:Zscan22
|
APN |
7 |
12,640,398 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02408:Zscan22
|
APN |
7 |
12,640,426 (GRCm39) |
missense |
probably benign |
0.09 |
PIT4378001:Zscan22
|
UTSW |
7 |
12,637,983 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0079:Zscan22
|
UTSW |
7 |
12,638,014 (GRCm39) |
critical splice donor site |
probably null |
|
R1677:Zscan22
|
UTSW |
7 |
12,640,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R1731:Zscan22
|
UTSW |
7 |
12,640,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R1944:Zscan22
|
UTSW |
7 |
12,637,767 (GRCm39) |
missense |
probably damaging |
0.98 |
R2258:Zscan22
|
UTSW |
7 |
12,637,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R2276:Zscan22
|
UTSW |
7 |
12,640,750 (GRCm39) |
nonsense |
probably null |
|
R3115:Zscan22
|
UTSW |
7 |
12,641,217 (GRCm39) |
missense |
probably benign |
0.39 |
R4064:Zscan22
|
UTSW |
7 |
12,640,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R4274:Zscan22
|
UTSW |
7 |
12,640,251 (GRCm39) |
missense |
probably benign |
0.01 |
R4691:Zscan22
|
UTSW |
7 |
12,640,488 (GRCm39) |
missense |
probably benign |
0.06 |
R5607:Zscan22
|
UTSW |
7 |
12,640,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R5608:Zscan22
|
UTSW |
7 |
12,640,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R5789:Zscan22
|
UTSW |
7 |
12,637,853 (GRCm39) |
missense |
probably benign |
|
R6293:Zscan22
|
UTSW |
7 |
12,640,834 (GRCm39) |
nonsense |
probably null |
|
R7210:Zscan22
|
UTSW |
7 |
12,640,748 (GRCm39) |
missense |
probably damaging |
0.98 |
R7475:Zscan22
|
UTSW |
7 |
12,640,664 (GRCm39) |
missense |
probably damaging |
0.99 |
R7491:Zscan22
|
UTSW |
7 |
12,640,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R8321:Zscan22
|
UTSW |
7 |
12,637,625 (GRCm39) |
missense |
probably benign |
0.28 |
R9198:Zscan22
|
UTSW |
7 |
12,641,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R9238:Zscan22
|
UTSW |
7 |
12,641,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R9566:Zscan22
|
UTSW |
7 |
12,640,866 (GRCm39) |
missense |
probably damaging |
1.00 |
|