Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aldh1a1 |
T |
A |
19: 20,602,117 (GRCm39) |
Y225* |
probably null |
Het |
Bard1 |
T |
C |
1: 71,114,099 (GRCm39) |
K294R |
probably benign |
Het |
Bcap29 |
A |
T |
12: 31,667,080 (GRCm39) |
S194T |
probably benign |
Het |
Ccdc40 |
G |
A |
11: 119,155,107 (GRCm39) |
V1116M |
probably damaging |
Het |
Cntnap5a |
A |
G |
1: 115,987,979 (GRCm39) |
E170G |
probably damaging |
Het |
Crygs |
C |
T |
16: 22,624,301 (GRCm39) |
G102D |
possibly damaging |
Het |
Cyp2c54 |
T |
C |
19: 40,060,867 (GRCm39) |
D92G |
probably benign |
Het |
Filip1l |
G |
T |
16: 57,333,649 (GRCm39) |
K147N |
probably damaging |
Het |
Hrnr |
T |
A |
3: 93,239,181 (GRCm39) |
S3140T |
unknown |
Het |
Igfn1 |
G |
T |
1: 135,896,574 (GRCm39) |
H1331N |
probably benign |
Het |
Kalrn |
C |
T |
16: 34,024,226 (GRCm39) |
|
probably null |
Het |
Kmt2d |
TTGCTGCTGCTGCTGCTGCTGCTGC |
TTGCTGCTGCTGCTGCTGC |
15: 98,748,902 (GRCm39) |
|
probably benign |
Het |
Mfng |
A |
G |
15: 78,640,821 (GRCm39) |
L308P |
probably damaging |
Het |
Nt5e |
C |
A |
9: 88,246,746 (GRCm39) |
N327K |
probably benign |
Het |
Or5m13 |
T |
G |
2: 85,748,926 (GRCm39) |
|
probably null |
Het |
Pgbd1 |
C |
T |
13: 21,618,540 (GRCm39) |
R39H |
possibly damaging |
Het |
Phactr4 |
T |
C |
4: 132,104,560 (GRCm39) |
T256A |
probably benign |
Het |
Rab24 |
T |
C |
13: 55,468,992 (GRCm39) |
D63G |
probably damaging |
Het |
Rubcnl |
C |
T |
14: 75,278,356 (GRCm39) |
P380L |
probably benign |
Het |
Satb2 |
A |
G |
1: 56,930,379 (GRCm39) |
S215P |
probably damaging |
Het |
Serpina3b |
A |
T |
12: 104,105,047 (GRCm39) |
I408F |
probably damaging |
Het |
Setx |
A |
G |
2: 29,035,753 (GRCm39) |
D746G |
probably damaging |
Het |
Sf3a2 |
A |
C |
10: 80,640,527 (GRCm39) |
|
probably benign |
Het |
Snx33 |
T |
C |
9: 56,834,024 (GRCm39) |
N15S |
probably benign |
Het |
Snx9 |
C |
T |
17: 5,942,056 (GRCm39) |
P61L |
probably benign |
Het |
Sult2a6 |
T |
C |
7: 13,988,701 (GRCm39) |
K20E |
probably benign |
Het |
Tas2r122 |
A |
G |
6: 132,688,543 (GRCm39) |
S117P |
probably benign |
Het |
Tmem26 |
G |
A |
10: 68,614,562 (GRCm39) |
E326K |
probably benign |
Het |
Tnpo2 |
T |
A |
8: 85,781,380 (GRCm39) |
C789S |
probably null |
Het |
Togaram1 |
A |
C |
12: 65,049,419 (GRCm39) |
E1285D |
probably benign |
Het |
Ubxn7 |
T |
A |
16: 32,200,248 (GRCm39) |
S335T |
possibly damaging |
Het |
Unc119b |
G |
A |
5: 115,268,567 (GRCm39) |
T106M |
probably damaging |
Het |
Usp14 |
A |
G |
18: 10,002,370 (GRCm39) |
S314P |
possibly damaging |
Het |
Usp32 |
T |
C |
11: 84,971,982 (GRCm39) |
D129G |
probably null |
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 |
R3872:Dpp6
|
UTSW |
5 |
27,926,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R4114:Dpp6
|
UTSW |
5 |
27,674,485 (GRCm39) |
critical splice donor site |
probably null |
|
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 |
|