Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310033P09Rik |
A |
G |
11: 59,099,528 (GRCm39) |
|
probably benign |
Het |
A730015C16Rik |
G |
A |
4: 108,705,205 (GRCm39) |
V40M |
probably damaging |
Het |
Abcg2 |
A |
G |
6: 58,655,322 (GRCm39) |
D419G |
probably benign |
Het |
Adamts17 |
A |
C |
7: 66,725,091 (GRCm39) |
E777A |
probably damaging |
Het |
Ak1 |
A |
G |
2: 32,523,478 (GRCm39) |
K166R |
probably benign |
Het |
Ankrd12 |
T |
C |
17: 66,293,300 (GRCm39) |
K711R |
probably damaging |
Het |
Ate1 |
A |
T |
7: 130,020,301 (GRCm39) |
|
probably null |
Het |
Atp5f1a |
A |
G |
18: 77,869,625 (GRCm39) |
H519R |
probably benign |
Het |
Best1 |
G |
T |
19: 9,967,853 (GRCm39) |
Y284* |
probably null |
Het |
C2cd6 |
A |
G |
1: 59,115,887 (GRCm39) |
|
probably benign |
Het |
Casz1 |
G |
T |
4: 149,030,628 (GRCm39) |
V1216L |
probably benign |
Het |
Cdc42bpg |
A |
G |
19: 6,363,812 (GRCm39) |
D493G |
probably damaging |
Het |
Ces2f |
A |
G |
8: 105,679,134 (GRCm39) |
D317G |
possibly damaging |
Het |
Chst15 |
A |
T |
7: 131,872,002 (GRCm39) |
M93K |
possibly damaging |
Het |
Cntnap5a |
T |
C |
1: 115,828,750 (GRCm39) |
L58P |
probably damaging |
Het |
Crip3 |
T |
C |
17: 46,741,702 (GRCm39) |
|
probably benign |
Het |
Csmd2 |
G |
A |
4: 128,380,794 (GRCm39) |
E2117K |
probably benign |
Het |
Cstf3 |
A |
G |
2: 104,478,564 (GRCm39) |
D212G |
possibly damaging |
Het |
Cttnbp2 |
T |
C |
6: 18,434,220 (GRCm39) |
K546R |
probably damaging |
Het |
Cubn |
A |
G |
2: 13,480,931 (GRCm39) |
I308T |
probably benign |
Het |
Cxcl9 |
T |
A |
5: 92,472,972 (GRCm39) |
D75V |
probably damaging |
Het |
Dcdc5 |
C |
T |
2: 106,188,977 (GRCm39) |
|
noncoding transcript |
Het |
Defa30 |
C |
A |
8: 21,624,752 (GRCm39) |
T25K |
possibly damaging |
Het |
Dock7 |
A |
T |
4: 98,967,672 (GRCm39) |
H239Q |
possibly damaging |
Het |
Fam83a |
T |
C |
15: 57,873,341 (GRCm39) |
M390T |
probably benign |
Het |
Fem1c |
A |
G |
18: 46,657,552 (GRCm39) |
L54P |
probably damaging |
Het |
Fntb |
T |
A |
12: 76,957,007 (GRCm39) |
M282K |
probably benign |
Het |
Galnt2l |
A |
G |
8: 122,996,323 (GRCm39) |
|
probably benign |
Het |
Gm11099 |
G |
A |
2: 58,749,482 (GRCm39) |
|
probably benign |
Het |
Gm1527 |
T |
C |
3: 28,980,705 (GRCm39) |
S602P |
probably benign |
Het |
Gm5478 |
T |
A |
15: 101,553,080 (GRCm39) |
I331F |
probably damaging |
Het |
Gm7853 |
C |
A |
14: 35,811,540 (GRCm39) |
|
noncoding transcript |
Het |
Gsta2 |
A |
T |
9: 78,249,147 (GRCm39) |
C18S |
probably benign |
Het |
H1f8 |
T |
C |
6: 115,924,701 (GRCm39) |
V69A |
possibly damaging |
Het |
Hecw1 |
T |
C |
13: 14,480,671 (GRCm39) |
E465G |
probably damaging |
Het |
Herc1 |
A |
G |
9: 66,415,548 (GRCm39) |
D4841G |
probably damaging |
Het |
Hus1b |
A |
G |
13: 31,130,984 (GRCm39) |
V225A |
probably benign |
Het |
Keg1 |
A |
T |
19: 12,693,387 (GRCm39) |
M137L |
probably benign |
Het |
Kmt2a |
C |
T |
9: 44,735,932 (GRCm39) |
|
probably benign |
Het |
Megf6 |
G |
T |
4: 154,261,578 (GRCm39) |
V68L |
probably benign |
Het |
Mga |
T |
A |
2: 119,772,156 (GRCm39) |
V1672E |
probably damaging |
Het |
Mios |
T |
C |
6: 8,234,237 (GRCm39) |
S803P |
probably benign |
Het |
Mrtfa |
T |
C |
15: 80,902,409 (GRCm39) |
|
probably benign |
Het |
Msh4 |
A |
T |
3: 153,569,021 (GRCm39) |
Y851N |
probably damaging |
Het |
Mybl1 |
A |
C |
1: 9,742,886 (GRCm39) |
|
probably null |
Het |
Myo5c |
A |
G |
9: 75,183,221 (GRCm39) |
Y865C |
probably damaging |
Het |
Naip1 |
T |
C |
13: 100,563,378 (GRCm39) |
S596G |
probably benign |
Het |
Nek5 |
G |
T |
8: 22,586,747 (GRCm39) |
Q355K |
possibly damaging |
Het |
Nphp3 |
G |
T |
9: 103,903,126 (GRCm39) |
R701L |
possibly damaging |
Het |
Or52n2 |
A |
T |
7: 104,542,444 (GRCm39) |
Y130* |
probably null |
Het |
Or5j3 |
T |
C |
2: 86,128,823 (GRCm39) |
I221T |
probably damaging |
Het |
Or5m10 |
T |
A |
2: 85,717,592 (GRCm39) |
Y149* |
probably null |
Het |
Or5t9 |
T |
C |
2: 86,659,542 (GRCm39) |
S149P |
probably benign |
Het |
Or9g4 |
T |
A |
2: 85,505,262 (GRCm39) |
T78S |
possibly damaging |
Het |
Palm |
A |
G |
10: 79,651,021 (GRCm39) |
N149D |
possibly damaging |
Het |
Pot1b |
T |
C |
17: 55,960,451 (GRCm39) |
I626M |
possibly damaging |
Het |
Ptprt |
T |
A |
2: 161,769,404 (GRCm39) |
D487V |
probably damaging |
Het |
Qpct |
A |
G |
17: 79,378,201 (GRCm39) |
I124V |
probably benign |
Het |
Rbm12b1 |
T |
A |
4: 12,145,817 (GRCm39) |
D596E |
possibly damaging |
Het |
Rnf157 |
A |
G |
11: 116,245,585 (GRCm39) |
C277R |
probably damaging |
Het |
Rnf169 |
A |
G |
7: 99,574,535 (GRCm39) |
S687P |
possibly damaging |
Het |
Sfxn1 |
T |
A |
13: 54,246,469 (GRCm39) |
|
probably null |
Het |
Slc6a21 |
T |
C |
7: 44,922,052 (GRCm39) |
V649A |
probably benign |
Het |
Slit3 |
A |
T |
11: 35,577,126 (GRCm39) |
T1120S |
probably damaging |
Het |
Spem2 |
A |
T |
11: 69,708,896 (GRCm39) |
M58K |
probably benign |
Het |
Sprr2k |
T |
A |
3: 92,340,703 (GRCm39) |
|
probably benign |
Het |
Sspo |
T |
C |
6: 48,440,334 (GRCm39) |
|
probably null |
Het |
Sv2b |
A |
T |
7: 74,769,791 (GRCm39) |
F584I |
possibly damaging |
Het |
Tkfc |
A |
T |
19: 10,572,690 (GRCm39) |
M317K |
probably null |
Het |
Tnni3k |
C |
T |
3: 154,735,942 (GRCm39) |
G134S |
probably benign |
Het |
Ttn |
C |
T |
2: 76,570,124 (GRCm39) |
R26923H |
probably damaging |
Het |
Tuba3b |
T |
C |
6: 145,564,179 (GRCm39) |
V75A |
possibly damaging |
Het |
Unc79 |
T |
C |
12: 103,149,784 (GRCm39) |
L2626P |
probably damaging |
Het |
Usp24 |
A |
T |
4: 106,219,130 (GRCm39) |
I491F |
probably damaging |
Het |
V1ra8 |
A |
T |
6: 90,180,132 (GRCm39) |
I112F |
probably damaging |
Het |
Vmn1r29 |
T |
G |
6: 58,284,663 (GRCm39) |
F128V |
probably benign |
Het |
Wdr87-ps |
A |
G |
7: 29,234,315 (GRCm39) |
|
noncoding transcript |
Het |
Zfp157 |
T |
A |
5: 138,453,357 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Dpp4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00492:Dpp4
|
APN |
2 |
62,209,646 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02205:Dpp4
|
APN |
2 |
62,182,601 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02276:Dpp4
|
APN |
2 |
62,187,295 (GRCm39) |
splice site |
probably benign |
|
IGL02335:Dpp4
|
APN |
2 |
62,164,988 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02615:Dpp4
|
APN |
2 |
62,189,672 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02639:Dpp4
|
APN |
2 |
62,182,584 (GRCm39) |
missense |
probably benign |
|
IGL02972:Dpp4
|
APN |
2 |
62,182,569 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03366:Dpp4
|
APN |
2 |
62,187,301 (GRCm39) |
splice site |
probably null |
|
caribou
|
UTSW |
2 |
62,178,245 (GRCm39) |
missense |
possibly damaging |
0.69 |
PIT4449001:Dpp4
|
UTSW |
2 |
62,186,988 (GRCm39) |
missense |
probably benign |
0.00 |
R0502:Dpp4
|
UTSW |
2 |
62,195,332 (GRCm39) |
missense |
probably damaging |
0.99 |
R0581:Dpp4
|
UTSW |
2 |
62,187,020 (GRCm39) |
missense |
probably benign |
|
R1004:Dpp4
|
UTSW |
2 |
62,162,984 (GRCm39) |
missense |
probably benign |
0.08 |
R1075:Dpp4
|
UTSW |
2 |
62,182,630 (GRCm39) |
missense |
probably benign |
0.39 |
R1702:Dpp4
|
UTSW |
2 |
62,216,773 (GRCm39) |
critical splice donor site |
probably null |
|
R1707:Dpp4
|
UTSW |
2 |
62,189,679 (GRCm39) |
splice site |
probably benign |
|
R1733:Dpp4
|
UTSW |
2 |
62,203,213 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1899:Dpp4
|
UTSW |
2 |
62,175,394 (GRCm39) |
splice site |
probably benign |
|
R2264:Dpp4
|
UTSW |
2 |
62,208,583 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2496:Dpp4
|
UTSW |
2 |
62,217,477 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3765:Dpp4
|
UTSW |
2 |
62,216,780 (GRCm39) |
missense |
probably benign |
0.17 |
R4278:Dpp4
|
UTSW |
2 |
62,209,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R4413:Dpp4
|
UTSW |
2 |
62,217,484 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4432:Dpp4
|
UTSW |
2 |
62,175,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R4647:Dpp4
|
UTSW |
2 |
62,164,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R4710:Dpp4
|
UTSW |
2 |
62,190,659 (GRCm39) |
missense |
probably benign |
0.04 |
R4914:Dpp4
|
UTSW |
2 |
62,178,236 (GRCm39) |
missense |
probably benign |
0.20 |
R5173:Dpp4
|
UTSW |
2 |
62,217,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R5283:Dpp4
|
UTSW |
2 |
62,190,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R5698:Dpp4
|
UTSW |
2 |
62,164,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R6621:Dpp4
|
UTSW |
2 |
62,182,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R6681:Dpp4
|
UTSW |
2 |
62,178,893 (GRCm39) |
missense |
probably benign |
0.01 |
R6739:Dpp4
|
UTSW |
2 |
62,217,439 (GRCm39) |
missense |
probably benign |
|
R6962:Dpp4
|
UTSW |
2 |
62,203,174 (GRCm39) |
missense |
probably benign |
0.11 |
R7249:Dpp4
|
UTSW |
2 |
62,215,547 (GRCm39) |
missense |
probably benign |
0.14 |
R7268:Dpp4
|
UTSW |
2 |
62,178,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R7343:Dpp4
|
UTSW |
2 |
62,189,245 (GRCm39) |
nonsense |
probably null |
|
R7357:Dpp4
|
UTSW |
2 |
62,217,421 (GRCm39) |
missense |
probably benign |
|
R7366:Dpp4
|
UTSW |
2 |
62,184,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R7413:Dpp4
|
UTSW |
2 |
62,187,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R7431:Dpp4
|
UTSW |
2 |
62,182,582 (GRCm39) |
missense |
probably benign |
0.01 |
R7642:Dpp4
|
UTSW |
2 |
62,190,627 (GRCm39) |
critical splice donor site |
probably null |
|
R8004:Dpp4
|
UTSW |
2 |
62,189,172 (GRCm39) |
missense |
probably benign |
0.00 |
R8197:Dpp4
|
UTSW |
2 |
62,203,171 (GRCm39) |
missense |
probably benign |
0.31 |
R8341:Dpp4
|
UTSW |
2 |
62,178,234 (GRCm39) |
missense |
probably benign |
0.10 |
R8706:Dpp4
|
UTSW |
2 |
62,208,647 (GRCm39) |
missense |
probably benign |
0.00 |
R8977:Dpp4
|
UTSW |
2 |
62,204,747 (GRCm39) |
missense |
probably benign |
0.29 |
R8997:Dpp4
|
UTSW |
2 |
62,164,958 (GRCm39) |
missense |
probably damaging |
0.99 |
R9100:Dpp4
|
UTSW |
2 |
62,204,733 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9616:Dpp4
|
UTSW |
2 |
62,217,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R9777:Dpp4
|
UTSW |
2 |
62,195,340 (GRCm39) |
missense |
probably benign |
0.04 |
|