Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc4 |
A |
G |
14: 118,853,800 (GRCm39) |
V444A |
possibly damaging |
Het |
Add1 |
T |
A |
5: 34,770,622 (GRCm39) |
|
probably benign |
Het |
Adgrg3 |
A |
G |
8: 95,762,891 (GRCm39) |
|
probably benign |
Het |
Adgrl3 |
A |
C |
5: 81,842,299 (GRCm39) |
Q809P |
possibly damaging |
Het |
Ankmy2 |
T |
C |
12: 36,236,806 (GRCm39) |
C205R |
probably damaging |
Het |
Atp6v1b2 |
A |
G |
8: 69,541,476 (GRCm39) |
N11S |
|
Het |
B3gnt6 |
T |
A |
7: 97,843,958 (GRCm39) |
M1L |
not run |
Het |
Bltp1 |
A |
G |
3: 37,098,907 (GRCm39) |
K1256R |
|
Het |
Ccdc88b |
T |
C |
19: 6,833,213 (GRCm39) |
E278G |
probably damaging |
Het |
Cdca8 |
T |
C |
4: 124,830,238 (GRCm39) |
T45A |
probably benign |
Het |
Ces2b |
C |
A |
8: 105,558,221 (GRCm39) |
|
probably benign |
Het |
Clip4 |
G |
A |
17: 72,117,884 (GRCm39) |
G310R |
probably damaging |
Het |
Cmklr1 |
G |
C |
5: 113,752,043 (GRCm39) |
H319Q |
probably benign |
Het |
Cnot3 |
A |
G |
7: 3,661,192 (GRCm39) |
D567G |
probably benign |
Het |
Cnot6l |
T |
C |
5: 96,230,875 (GRCm39) |
D364G |
probably damaging |
Het |
Cpped1 |
A |
G |
16: 11,646,419 (GRCm39) |
V111A |
|
Het |
Cstdc4 |
T |
A |
16: 36,008,285 (GRCm39) |
M57K |
possibly damaging |
Het |
Cyp11b2 |
T |
C |
15: 74,722,995 (GRCm39) |
K468E |
probably damaging |
Het |
Efcab15 |
T |
C |
11: 103,090,893 (GRCm39) |
T151A |
probably benign |
Het |
Fat2 |
A |
G |
11: 55,153,347 (GRCm39) |
W3622R |
probably damaging |
Het |
Fat4 |
A |
C |
3: 39,064,803 (GRCm39) |
K4920Q |
|
Het |
Frmpd2 |
A |
G |
14: 33,252,407 (GRCm39) |
I656M |
probably benign |
Het |
Gck |
A |
G |
11: 5,856,516 (GRCm39) |
Y214H |
probably damaging |
Het |
Gde1 |
C |
T |
7: 118,294,305 (GRCm39) |
R166H |
probably benign |
Het |
Gdf7 |
A |
T |
12: 8,348,652 (GRCm39) |
F215Y |
unknown |
Het |
Gdpgp1 |
A |
G |
7: 79,888,282 (GRCm39) |
I104M |
probably benign |
Het |
Gldc |
A |
G |
19: 30,077,314 (GRCm39) |
S953P |
possibly damaging |
Het |
Golga3 |
C |
T |
5: 110,337,544 (GRCm39) |
H411Y |
probably benign |
Het |
Gpn1 |
G |
T |
5: 31,655,740 (GRCm39) |
R101I |
probably damaging |
Het |
Itgb5 |
T |
A |
16: 33,740,551 (GRCm39) |
S554T |
possibly damaging |
Het |
Klhl1 |
G |
A |
14: 96,584,364 (GRCm39) |
L289F |
probably damaging |
Het |
Klhl13 |
C |
T |
X: 23,113,733 (GRCm39) |
R95Q |
probably benign |
Het |
Kmt2d |
G |
C |
15: 98,747,832 (GRCm39) |
T3164R |
unknown |
Het |
Knl1 |
T |
C |
2: 118,899,469 (GRCm39) |
V390A |
probably benign |
Het |
Krtap5-2 |
GCCACAGCCTCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACCACAGCCCCCACAGGAACTACA |
GCCACAGCCCCCACAGGAACTACA |
7: 141,728,836 (GRCm39) |
|
probably benign |
Het |
Lamtor4 |
G |
A |
5: 138,254,595 (GRCm39) |
|
probably benign |
Het |
Lonrf1 |
AGGCGGCGGCGGCGG |
AGGCGGCGGCGG |
8: 36,715,919 (GRCm39) |
|
probably benign |
Het |
Ltbp1 |
C |
T |
17: 75,622,102 (GRCm39) |
L829F |
probably benign |
Het |
Ltbp1 |
T |
A |
17: 75,622,103 (GRCm39) |
L829H |
probably damaging |
Het |
Mrgpra1 |
C |
T |
7: 46,984,732 (GRCm39) |
E316K |
probably damaging |
Het |
Muc16 |
T |
A |
9: 18,556,966 (GRCm39) |
H3109L |
unknown |
Het |
Nck1 |
T |
C |
9: 100,377,561 (GRCm39) |
E368G |
probably damaging |
Het |
Nox4 |
G |
A |
7: 87,025,448 (GRCm39) |
R525Q |
probably benign |
Het |
Nus1 |
A |
T |
10: 52,305,287 (GRCm39) |
|
probably null |
Het |
Nxph2 |
T |
C |
2: 23,289,780 (GRCm39) |
V44A |
probably benign |
Het |
Or1e30 |
A |
G |
11: 73,678,687 (GRCm39) |
K308E |
probably benign |
Het |
Or4f56 |
A |
G |
2: 111,703,606 (GRCm39) |
M198T |
possibly damaging |
Het |
Or4k35 |
A |
G |
2: 111,100,094 (GRCm39) |
L206P |
probably benign |
Het |
Or4z4 |
G |
T |
19: 12,076,254 (GRCm39) |
H250N |
probably benign |
Het |
Or5d35 |
T |
C |
2: 87,855,330 (GRCm39) |
I88T |
probably benign |
Het |
Or5m11b |
A |
G |
2: 85,806,096 (GRCm39) |
K170E |
probably benign |
Het |
Or6d13 |
A |
T |
6: 116,517,990 (GRCm39) |
N192I |
possibly damaging |
Het |
Otof |
T |
C |
5: 30,539,696 (GRCm39) |
D1039G |
possibly damaging |
Het |
Parpbp |
T |
A |
10: 87,968,969 (GRCm39) |
Q159L |
possibly damaging |
Het |
Per2 |
A |
T |
1: 91,351,464 (GRCm39) |
L1014Q |
possibly damaging |
Het |
Pik3ap1 |
C |
G |
19: 41,312,924 (GRCm39) |
|
silent |
Het |
Pik3ca |
A |
G |
3: 32,514,168 (GRCm39) |
N885D |
probably damaging |
Het |
Pip5k1c |
T |
C |
10: 81,145,056 (GRCm39) |
V299A |
probably benign |
Het |
Polr3h |
A |
T |
15: 81,806,717 (GRCm39) |
|
probably benign |
Het |
Pramel11 |
T |
A |
4: 143,623,646 (GRCm39) |
N176I |
probably benign |
Het |
Pramel23 |
T |
G |
4: 143,425,727 (GRCm39) |
N72T |
probably benign |
Het |
Pus3 |
C |
A |
9: 35,476,946 (GRCm39) |
Q248K |
probably benign |
Het |
Sectm1a |
T |
A |
11: 120,960,569 (GRCm39) |
Q82L |
possibly damaging |
Het |
Sema3e |
A |
G |
5: 14,282,208 (GRCm39) |
Y448C |
probably damaging |
Het |
Slc12a4 |
A |
T |
8: 106,675,774 (GRCm39) |
S584T |
probably benign |
Het |
Slc25a40 |
T |
C |
5: 8,499,613 (GRCm39) |
F249L |
probably benign |
Het |
St3gal6 |
T |
A |
16: 58,306,793 (GRCm39) |
N79I |
|
Het |
Stxbp4 |
A |
T |
11: 90,426,320 (GRCm39) |
I496K |
possibly damaging |
Het |
Sulf1 |
A |
G |
1: 12,878,118 (GRCm39) |
Y202C |
probably damaging |
Het |
Swt1 |
A |
G |
1: 151,299,256 (GRCm39) |
|
probably null |
Het |
Tdrd6 |
T |
C |
17: 43,936,305 (GRCm39) |
Y1581C |
possibly damaging |
Het |
Tenm4 |
G |
C |
7: 96,495,061 (GRCm39) |
G1163A |
probably damaging |
Het |
Tlr4 |
A |
G |
4: 66,758,518 (GRCm39) |
E437G |
probably benign |
Het |
Txnrd2 |
A |
T |
16: 18,256,315 (GRCm39) |
H101L |
probably damaging |
Het |
Uba3 |
A |
T |
6: 97,163,671 (GRCm39) |
V306E |
probably damaging |
Het |
Unc5b |
T |
C |
10: 60,604,152 (GRCm39) |
Q814R |
probably damaging |
Het |
Vamp5 |
T |
G |
6: 72,347,304 (GRCm39) |
E5A |
possibly damaging |
Het |
Vmn1r69 |
T |
A |
7: 10,314,064 (GRCm39) |
R222S |
probably damaging |
Het |
Zfp507 |
G |
A |
7: 35,494,446 (GRCm39) |
T199I |
probably benign |
Het |
Zfyve19 |
T |
G |
2: 119,041,718 (GRCm39) |
L95R |
probably benign |
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 |
R1476:Dpp4
|
UTSW |
2 |
62,178,245 (GRCm39) |
missense |
possibly damaging |
0.69 |
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 |
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 |
|