Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts10 |
T |
A |
17: 33,756,316 (GRCm39) |
S320T |
probably benign |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Als2 |
T |
C |
1: 59,257,226 (GRCm39) |
E12G |
probably benign |
Het |
Arhgef10 |
A |
T |
8: 14,997,157 (GRCm39) |
D321V |
probably damaging |
Het |
Atp8a1 |
T |
G |
5: 67,906,395 (GRCm39) |
|
probably null |
Het |
Avil |
A |
G |
10: 126,846,494 (GRCm39) |
|
probably null |
Het |
Cdhr18 |
C |
T |
14: 13,829,796 (GRCm38) |
E649K |
probably damaging |
Het |
Col18a1 |
G |
A |
10: 76,895,131 (GRCm39) |
P1177S |
probably damaging |
Het |
Copb2 |
T |
A |
9: 98,462,213 (GRCm39) |
F428L |
probably benign |
Het |
Cpa1 |
A |
G |
6: 30,640,923 (GRCm39) |
E138G |
probably damaging |
Het |
Ctsm |
T |
C |
13: 61,686,249 (GRCm39) |
I12V |
possibly damaging |
Het |
Dctn1 |
A |
G |
6: 83,174,578 (GRCm39) |
Q967R |
possibly damaging |
Het |
Dok2 |
T |
C |
14: 71,014,393 (GRCm39) |
Y194H |
probably damaging |
Het |
Ezh2 |
C |
T |
6: 47,554,592 (GRCm39) |
M1I |
probably null |
Het |
Fkbp8 |
T |
A |
8: 70,984,282 (GRCm39) |
L210Q |
probably damaging |
Het |
Fpr1 |
T |
A |
17: 18,097,263 (GRCm39) |
Q242L |
probably benign |
Het |
Gal3st2b |
T |
A |
1: 93,868,505 (GRCm39) |
D243E |
probably damaging |
Het |
Gm5422 |
A |
G |
10: 31,125,802 (GRCm39) |
|
noncoding transcript |
Het |
Gucy1a2 |
A |
G |
9: 3,533,052 (GRCm39) |
N84D |
probably damaging |
Het |
Hsd3b5 |
A |
C |
3: 98,529,393 (GRCm39) |
V79G |
probably damaging |
Het |
Htr6 |
A |
T |
4: 138,788,804 (GRCm39) |
V417E |
probably benign |
Het |
Ifnar2 |
G |
A |
16: 91,188,755 (GRCm39) |
V79I |
probably benign |
Het |
Ighv10-1 |
T |
C |
12: 114,443,102 (GRCm39) |
|
probably benign |
Het |
Itpr2 |
A |
G |
6: 146,081,788 (GRCm39) |
F182L |
probably damaging |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Lama3 |
A |
G |
18: 12,540,551 (GRCm39) |
Y285C |
probably damaging |
Het |
Lamc2 |
C |
A |
1: 153,034,680 (GRCm39) |
V108L |
possibly damaging |
Het |
Lrrc14b |
A |
G |
13: 74,509,373 (GRCm39) |
|
probably null |
Het |
Magi3 |
T |
C |
3: 103,958,493 (GRCm39) |
T531A |
probably benign |
Het |
Mapre2 |
A |
G |
18: 23,966,011 (GRCm39) |
Y32C |
probably damaging |
Het |
Med1 |
C |
T |
11: 98,046,452 (GRCm39) |
|
probably benign |
Het |
Mslnl |
G |
A |
17: 25,961,908 (GRCm39) |
V128M |
probably damaging |
Het |
Nt5el |
C |
A |
13: 105,218,749 (GRCm39) |
Q28K |
probably benign |
Het |
Or10a3b |
A |
C |
7: 108,445,064 (GRCm39) |
L51R |
probably damaging |
Het |
Or51h1 |
A |
G |
7: 102,308,408 (GRCm39) |
I127V |
probably damaging |
Het |
Or5h23 |
G |
A |
16: 58,906,408 (GRCm39) |
T146I |
probably benign |
Het |
Or7a35 |
A |
T |
10: 78,853,239 (GRCm39) |
I28L |
probably benign |
Het |
Pde1b |
A |
G |
15: 103,430,099 (GRCm39) |
T143A |
probably damaging |
Het |
Pkhd1 |
T |
C |
1: 20,593,121 (GRCm39) |
D1664G |
probably benign |
Het |
Plod3 |
C |
T |
5: 137,017,847 (GRCm39) |
R208W |
probably damaging |
Het |
Pstk |
G |
A |
7: 130,986,271 (GRCm39) |
A277T |
possibly damaging |
Het |
Qrich1 |
T |
C |
9: 108,411,684 (GRCm39) |
V403A |
probably damaging |
Het |
Rad21 |
C |
A |
15: 51,833,436 (GRCm39) |
V348F |
probably damaging |
Het |
Sacs |
T |
A |
14: 61,448,181 (GRCm39) |
L3409* |
probably null |
Het |
Setd4 |
T |
A |
16: 93,390,136 (GRCm39) |
K98* |
probably null |
Het |
Skint5 |
A |
G |
4: 113,341,123 (GRCm39) |
V1385A |
probably benign |
Het |
Stam |
C |
A |
2: 14,151,059 (GRCm39) |
S472* |
probably null |
Het |
Stx2 |
A |
G |
5: 129,069,289 (GRCm39) |
F141L |
probably damaging |
Het |
Tia1 |
A |
G |
6: 86,397,330 (GRCm39) |
D101G |
probably damaging |
Het |
Ttc21a |
T |
A |
9: 119,783,228 (GRCm39) |
|
probably null |
Het |
Usp34 |
T |
A |
11: 23,410,651 (GRCm39) |
N2700K |
probably damaging |
Het |
|
Other mutations in C2cd3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00540:C2cd3
|
APN |
7 |
100,040,335 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01420:C2cd3
|
APN |
7 |
100,104,065 (GRCm39) |
missense |
probably benign |
0.35 |
IGL01775:C2cd3
|
APN |
7 |
100,092,638 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01832:C2cd3
|
APN |
7 |
100,076,421 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01883:C2cd3
|
APN |
7 |
100,023,693 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02664:C2cd3
|
APN |
7 |
100,068,922 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02697:C2cd3
|
APN |
7 |
100,076,376 (GRCm39) |
unclassified |
probably benign |
|
IGL02852:C2cd3
|
APN |
7 |
100,079,396 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03158:C2cd3
|
APN |
7 |
100,023,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R0012:C2cd3
|
UTSW |
7 |
100,067,729 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0012:C2cd3
|
UTSW |
7 |
100,067,729 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0013:C2cd3
|
UTSW |
7 |
100,065,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:C2cd3
|
UTSW |
7 |
100,065,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R0032:C2cd3
|
UTSW |
7 |
100,093,652 (GRCm39) |
unclassified |
probably benign |
|
R0032:C2cd3
|
UTSW |
7 |
100,093,652 (GRCm39) |
unclassified |
probably benign |
|
R0124:C2cd3
|
UTSW |
7 |
100,118,725 (GRCm39) |
missense |
probably benign |
|
R0387:C2cd3
|
UTSW |
7 |
100,071,714 (GRCm39) |
splice site |
probably benign |
|
R0522:C2cd3
|
UTSW |
7 |
100,044,429 (GRCm39) |
missense |
probably benign |
0.14 |
R1124:C2cd3
|
UTSW |
7 |
100,071,888 (GRCm39) |
missense |
probably benign |
0.00 |
R1484:C2cd3
|
UTSW |
7 |
100,089,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R1533:C2cd3
|
UTSW |
7 |
100,055,284 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1875:C2cd3
|
UTSW |
7 |
100,056,232 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2059:C2cd3
|
UTSW |
7 |
100,104,700 (GRCm39) |
unclassified |
probably benign |
|
R2060:C2cd3
|
UTSW |
7 |
100,104,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R2348:C2cd3
|
UTSW |
7 |
100,062,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R3103:C2cd3
|
UTSW |
7 |
100,044,459 (GRCm39) |
missense |
possibly damaging |
0.47 |
R3405:C2cd3
|
UTSW |
7 |
100,039,373 (GRCm39) |
missense |
probably benign |
0.01 |
R3687:C2cd3
|
UTSW |
7 |
100,085,040 (GRCm39) |
missense |
probably benign |
0.28 |
R3775:C2cd3
|
UTSW |
7 |
100,081,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R3854:C2cd3
|
UTSW |
7 |
100,103,808 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4359:C2cd3
|
UTSW |
7 |
100,090,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R4403:C2cd3
|
UTSW |
7 |
100,081,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R4446:C2cd3
|
UTSW |
7 |
100,023,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R4646:C2cd3
|
UTSW |
7 |
100,021,657 (GRCm39) |
unclassified |
probably benign |
|
R4705:C2cd3
|
UTSW |
7 |
100,044,395 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4770:C2cd3
|
UTSW |
7 |
100,092,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R4777:C2cd3
|
UTSW |
7 |
100,065,539 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4816:C2cd3
|
UTSW |
7 |
100,040,226 (GRCm39) |
missense |
probably benign |
0.01 |
R4842:C2cd3
|
UTSW |
7 |
100,065,397 (GRCm39) |
missense |
probably benign |
0.00 |
R4858:C2cd3
|
UTSW |
7 |
100,104,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R4871:C2cd3
|
UTSW |
7 |
100,062,581 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4898:C2cd3
|
UTSW |
7 |
100,055,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R5026:C2cd3
|
UTSW |
7 |
100,109,049 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5112:C2cd3
|
UTSW |
7 |
100,092,692 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5242:C2cd3
|
UTSW |
7 |
100,039,373 (GRCm39) |
missense |
probably benign |
0.01 |
R5538:C2cd3
|
UTSW |
7 |
100,104,700 (GRCm39) |
critical splice donor site |
probably null |
|
R5861:C2cd3
|
UTSW |
7 |
100,093,682 (GRCm39) |
unclassified |
probably benign |
|
R6110:C2cd3
|
UTSW |
7 |
100,090,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R6326:C2cd3
|
UTSW |
7 |
100,065,635 (GRCm39) |
missense |
probably benign |
0.02 |
R6429:C2cd3
|
UTSW |
7 |
100,081,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R6610:C2cd3
|
UTSW |
7 |
100,104,505 (GRCm39) |
missense |
probably benign |
|
R6613:C2cd3
|
UTSW |
7 |
100,044,448 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6631:C2cd3
|
UTSW |
7 |
100,067,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R6787:C2cd3
|
UTSW |
7 |
100,104,553 (GRCm39) |
missense |
probably benign |
|
R6837:C2cd3
|
UTSW |
7 |
100,097,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R6849:C2cd3
|
UTSW |
7 |
100,056,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R6860:C2cd3
|
UTSW |
7 |
100,039,448 (GRCm39) |
missense |
probably benign |
0.28 |
R6929:C2cd3
|
UTSW |
7 |
100,100,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R7026:C2cd3
|
UTSW |
7 |
100,081,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R7088:C2cd3
|
UTSW |
7 |
100,065,388 (GRCm39) |
missense |
|
|
R7174:C2cd3
|
UTSW |
7 |
100,081,405 (GRCm39) |
missense |
|
|
R7241:C2cd3
|
UTSW |
7 |
100,056,257 (GRCm39) |
missense |
|
|
R7335:C2cd3
|
UTSW |
7 |
100,071,810 (GRCm39) |
missense |
|
|
R7357:C2cd3
|
UTSW |
7 |
100,079,310 (GRCm39) |
missense |
|
|
R7493:C2cd3
|
UTSW |
7 |
100,076,433 (GRCm39) |
missense |
|
|
R7567:C2cd3
|
UTSW |
7 |
100,080,022 (GRCm39) |
missense |
|
|
R7573:C2cd3
|
UTSW |
7 |
100,068,914 (GRCm39) |
missense |
|
|
R7869:C2cd3
|
UTSW |
7 |
100,118,698 (GRCm39) |
missense |
probably damaging |
0.99 |
R7999:C2cd3
|
UTSW |
7 |
100,109,096 (GRCm39) |
critical splice donor site |
probably null |
|
R8134:C2cd3
|
UTSW |
7 |
100,067,711 (GRCm39) |
missense |
|
|
R8369:C2cd3
|
UTSW |
7 |
100,044,465 (GRCm39) |
missense |
probably benign |
0.03 |
R8372:C2cd3
|
UTSW |
7 |
100,104,487 (GRCm39) |
nonsense |
probably null |
|
R8753:C2cd3
|
UTSW |
7 |
100,049,024 (GRCm39) |
critical splice donor site |
probably null |
|
R8893:C2cd3
|
UTSW |
7 |
100,104,004 (GRCm39) |
missense |
probably benign |
|
R8905:C2cd3
|
UTSW |
7 |
100,074,132 (GRCm39) |
critical splice donor site |
probably null |
|
R8945:C2cd3
|
UTSW |
7 |
100,040,286 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8970:C2cd3
|
UTSW |
7 |
100,068,971 (GRCm39) |
missense |
|
|
R9000:C2cd3
|
UTSW |
7 |
100,065,281 (GRCm39) |
missense |
|
|
R9064:C2cd3
|
UTSW |
7 |
100,059,608 (GRCm39) |
missense |
|
|
R9072:C2cd3
|
UTSW |
7 |
100,040,291 (GRCm39) |
missense |
probably benign |
0.07 |
R9126:C2cd3
|
UTSW |
7 |
100,081,430 (GRCm39) |
missense |
|
|
R9160:C2cd3
|
UTSW |
7 |
100,075,236 (GRCm39) |
missense |
|
|
R9234:C2cd3
|
UTSW |
7 |
100,049,012 (GRCm39) |
missense |
|
|
R9258:C2cd3
|
UTSW |
7 |
100,098,026 (GRCm39) |
missense |
|
|
R9295:C2cd3
|
UTSW |
7 |
100,081,734 (GRCm39) |
missense |
|
|
R9411:C2cd3
|
UTSW |
7 |
100,065,704 (GRCm39) |
missense |
|
|
R9420:C2cd3
|
UTSW |
7 |
100,065,262 (GRCm39) |
missense |
|
|
R9589:C2cd3
|
UTSW |
7 |
100,081,756 (GRCm39) |
missense |
|
|
R9628:C2cd3
|
UTSW |
7 |
100,097,961 (GRCm39) |
missense |
|
|
R9629:C2cd3
|
UTSW |
7 |
100,029,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R9681:C2cd3
|
UTSW |
7 |
100,023,662 (GRCm39) |
missense |
probably benign |
0.32 |
R9775:C2cd3
|
UTSW |
7 |
100,076,458 (GRCm39) |
missense |
|
|
X0002:C2cd3
|
UTSW |
7 |
100,089,442 (GRCm39) |
missense |
possibly damaging |
0.50 |
|