Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6030468B19Rik |
T |
G |
11: 117,693,793 (GRCm39) |
S87A |
probably damaging |
Het |
Abca16 |
T |
C |
7: 120,126,290 (GRCm39) |
F1149L |
probably benign |
Het |
Abcf1 |
A |
T |
17: 36,270,146 (GRCm39) |
D637E |
probably benign |
Het |
Ankrd34c |
A |
G |
9: 89,611,927 (GRCm39) |
L138P |
probably damaging |
Het |
Cdh23 |
A |
G |
10: 60,256,819 (GRCm39) |
|
probably null |
Het |
Cep44 |
T |
C |
8: 56,998,457 (GRCm39) |
T74A |
probably benign |
Het |
Colq |
T |
A |
14: 31,279,824 (GRCm39) |
M1L |
probably benign |
Het |
Cym |
A |
T |
3: 107,127,065 (GRCm39) |
L30Q |
probably damaging |
Het |
Gbe1 |
G |
T |
16: 70,280,715 (GRCm39) |
G372V |
possibly damaging |
Het |
Hdc |
T |
A |
2: 126,443,738 (GRCm39) |
M314L |
probably benign |
Het |
Ino80b |
A |
G |
6: 83,101,121 (GRCm39) |
S149P |
probably benign |
Het |
Itpr2 |
C |
T |
6: 146,327,008 (GRCm39) |
V120I |
probably damaging |
Het |
Morc3 |
G |
A |
16: 93,670,227 (GRCm39) |
D801N |
probably benign |
Het |
Mpped1 |
A |
G |
15: 83,680,910 (GRCm39) |
|
probably benign |
Het |
Nek5 |
G |
A |
8: 22,601,178 (GRCm39) |
T181M |
probably damaging |
Het |
Nlrp4a |
T |
G |
7: 26,149,365 (GRCm39) |
F324C |
probably damaging |
Het |
Nop56 |
T |
C |
2: 130,118,593 (GRCm39) |
|
probably null |
Het |
Or6c6c |
T |
C |
10: 129,541,668 (GRCm39) |
L307S |
probably benign |
Het |
Or8u9 |
A |
T |
2: 86,001,759 (GRCm39) |
V134D |
possibly damaging |
Het |
Pcdhb3 |
A |
G |
18: 37,435,093 (GRCm39) |
N353S |
probably benign |
Het |
Pde8a |
T |
A |
7: 80,932,555 (GRCm39) |
|
probably null |
Het |
Pramel29 |
A |
T |
4: 143,936,173 (GRCm39) |
L29H |
probably damaging |
Het |
Ryr2 |
C |
T |
13: 11,707,568 (GRCm39) |
R2823H |
probably damaging |
Het |
Scart2 |
T |
C |
7: 139,877,823 (GRCm39) |
V935A |
probably damaging |
Het |
Sec22a |
A |
G |
16: 35,139,202 (GRCm39) |
F232S |
probably damaging |
Het |
Slc7a1 |
T |
C |
5: 148,278,867 (GRCm39) |
T302A |
probably damaging |
Het |
Sult2a2 |
A |
T |
7: 13,468,708 (GRCm39) |
Q58L |
probably benign |
Het |
Tek |
T |
C |
4: 94,737,920 (GRCm39) |
S657P |
probably damaging |
Het |
Trim5 |
A |
G |
7: 103,914,947 (GRCm39) |
L374P |
probably damaging |
Het |
Tspan18 |
C |
A |
2: 93,142,291 (GRCm39) |
|
probably null |
Het |
Vmn2r37 |
T |
A |
7: 9,213,092 (GRCm39) |
|
probably null |
Het |
Zbbx |
T |
C |
3: 75,046,905 (GRCm39) |
T121A |
probably benign |
Het |
Zfp35 |
A |
C |
18: 24,135,766 (GRCm39) |
I37L |
probably benign |
Het |
|
Other mutations in Dpp6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00310:Dpp6
|
APN |
5 |
27,928,441 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01137:Dpp6
|
APN |
5 |
27,919,486 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01386:Dpp6
|
APN |
5 |
27,869,760 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01409:Dpp6
|
APN |
5 |
27,762,599 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01721:Dpp6
|
APN |
5 |
27,836,518 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02149:Dpp6
|
APN |
5 |
27,743,022 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02174:Dpp6
|
APN |
5 |
27,926,085 (GRCm39) |
nonsense |
probably null |
|
IGL02176:Dpp6
|
APN |
5 |
27,928,575 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02326:Dpp6
|
APN |
5 |
27,869,755 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02336:Dpp6
|
APN |
5 |
27,674,409 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02339:Dpp6
|
APN |
5 |
27,857,228 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02402:Dpp6
|
APN |
5 |
27,839,541 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02884:Dpp6
|
APN |
5 |
27,839,554 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02885:Dpp6
|
APN |
5 |
27,923,471 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02938:Dpp6
|
APN |
5 |
27,928,365 (GRCm39) |
splice site |
probably benign |
|
IGL03083:Dpp6
|
APN |
5 |
27,914,548 (GRCm39) |
critical splice donor site |
probably null |
|
I0000:Dpp6
|
UTSW |
5 |
27,603,920 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03052:Dpp6
|
UTSW |
5 |
27,914,506 (GRCm39) |
missense |
probably benign |
0.03 |
PIT4431001:Dpp6
|
UTSW |
5 |
27,836,496 (GRCm39) |
missense |
probably benign |
0.03 |
R0060:Dpp6
|
UTSW |
5 |
27,803,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R0360:Dpp6
|
UTSW |
5 |
27,857,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R0486:Dpp6
|
UTSW |
5 |
27,866,640 (GRCm39) |
missense |
probably benign |
0.39 |
R0501:Dpp6
|
UTSW |
5 |
27,930,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R1028:Dpp6
|
UTSW |
5 |
27,871,425 (GRCm39) |
missense |
probably benign |
0.01 |
R1164:Dpp6
|
UTSW |
5 |
27,926,103 (GRCm39) |
missense |
probably benign |
0.02 |
R1177:Dpp6
|
UTSW |
5 |
27,868,471 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1993:Dpp6
|
UTSW |
5 |
27,604,004 (GRCm39) |
missense |
probably benign |
0.00 |
R2024:Dpp6
|
UTSW |
5 |
27,914,457 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2100:Dpp6
|
UTSW |
5 |
27,869,742 (GRCm39) |
missense |
probably damaging |
0.96 |
R2329:Dpp6
|
UTSW |
5 |
27,656,286 (GRCm39) |
splice site |
probably null |
|
R3619:Dpp6
|
UTSW |
5 |
27,926,118 (GRCm39) |
missense |
possibly damaging |
0.74 |
R3871:Dpp6
|
UTSW |
5 |
27,674,463 (GRCm39) |
missense |
probably benign |
0.03 |
R3872:Dpp6
|
UTSW |
5 |
27,926,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R4403:Dpp6
|
UTSW |
5 |
27,923,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R4599:Dpp6
|
UTSW |
5 |
27,839,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R4736:Dpp6
|
UTSW |
5 |
27,917,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R4929:Dpp6
|
UTSW |
5 |
27,254,785 (GRCm39) |
missense |
probably benign |
0.25 |
R4967:Dpp6
|
UTSW |
5 |
27,871,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R5162:Dpp6
|
UTSW |
5 |
27,604,013 (GRCm39) |
unclassified |
probably benign |
|
R5270:Dpp6
|
UTSW |
5 |
27,839,532 (GRCm39) |
missense |
probably damaging |
0.98 |
R5334:Dpp6
|
UTSW |
5 |
27,914,538 (GRCm39) |
missense |
probably benign |
0.30 |
R5437:Dpp6
|
UTSW |
5 |
27,868,499 (GRCm39) |
nonsense |
probably null |
|
R5663:Dpp6
|
UTSW |
5 |
27,254,620 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6023:Dpp6
|
UTSW |
5 |
27,928,545 (GRCm39) |
missense |
probably damaging |
0.96 |
R6244:Dpp6
|
UTSW |
5 |
27,254,626 (GRCm39) |
missense |
probably damaging |
0.99 |
R6312:Dpp6
|
UTSW |
5 |
27,930,669 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6442:Dpp6
|
UTSW |
5 |
27,923,507 (GRCm39) |
critical splice donor site |
probably null |
|
R6942:Dpp6
|
UTSW |
5 |
27,674,457 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6956:Dpp6
|
UTSW |
5 |
27,803,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R7210:Dpp6
|
UTSW |
5 |
27,803,801 (GRCm39) |
missense |
probably damaging |
0.99 |
R7342:Dpp6
|
UTSW |
5 |
27,919,552 (GRCm39) |
missense |
probably benign |
|
R7702:Dpp6
|
UTSW |
5 |
27,857,274 (GRCm39) |
missense |
probably benign |
0.00 |
R7727:Dpp6
|
UTSW |
5 |
27,656,242 (GRCm39) |
missense |
probably benign |
0.30 |
R7899:Dpp6
|
UTSW |
5 |
27,926,077 (GRCm39) |
missense |
probably benign |
0.03 |
R7966:Dpp6
|
UTSW |
5 |
27,928,370 (GRCm39) |
missense |
probably benign |
0.06 |
R8015:Dpp6
|
UTSW |
5 |
27,022,808 (GRCm39) |
start gained |
probably benign |
|
R8084:Dpp6
|
UTSW |
5 |
27,836,397 (GRCm39) |
missense |
probably benign |
0.32 |
R8178:Dpp6
|
UTSW |
5 |
27,803,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R8384:Dpp6
|
UTSW |
5 |
27,923,472 (GRCm39) |
missense |
probably benign |
0.18 |
R8816:Dpp6
|
UTSW |
5 |
27,930,711 (GRCm39) |
missense |
probably benign |
0.07 |
R8936:Dpp6
|
UTSW |
5 |
27,926,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R9090:Dpp6
|
UTSW |
5 |
27,803,832 (GRCm39) |
nonsense |
probably null |
|
R9164:Dpp6
|
UTSW |
5 |
27,656,286 (GRCm39) |
splice site |
probably null |
|
R9271:Dpp6
|
UTSW |
5 |
27,803,832 (GRCm39) |
nonsense |
probably null |
|
R9310:Dpp6
|
UTSW |
5 |
27,930,642 (GRCm39) |
missense |
probably benign |
0.11 |
R9310:Dpp6
|
UTSW |
5 |
27,836,439 (GRCm39) |
missense |
probably damaging |
0.97 |
R9320:Dpp6
|
UTSW |
5 |
27,868,521 (GRCm39) |
critical splice donor site |
probably null |
|
R9667:Dpp6
|
UTSW |
5 |
27,930,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R9761:Dpp6
|
UTSW |
5 |
27,869,743 (GRCm39) |
missense |
probably benign |
0.38 |
Z1176:Dpp6
|
UTSW |
5 |
27,603,996 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Dpp6
|
UTSW |
5 |
27,917,640 (GRCm39) |
missense |
probably damaging |
0.99 |
|