Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
A |
G |
13: 77,471,735 (GRCm39) |
K1047E |
possibly damaging |
Het |
Aadacl2fm1 |
A |
G |
3: 59,839,110 (GRCm39) |
T11A |
possibly damaging |
Het |
Abca14 |
A |
T |
7: 119,807,191 (GRCm39) |
Y79F |
possibly damaging |
Het |
Abca2 |
T |
A |
2: 25,329,094 (GRCm39) |
M978K |
probably benign |
Het |
Adamts3 |
A |
T |
5: 89,848,269 (GRCm39) |
C684* |
probably null |
Het |
Adnp2 |
T |
C |
18: 80,172,637 (GRCm39) |
T591A |
probably benign |
Het |
Aff4 |
A |
T |
11: 53,263,306 (GRCm39) |
T109S |
probably damaging |
Het |
Agmo |
A |
G |
12: 37,293,720 (GRCm39) |
I48V |
probably benign |
Het |
Appl1 |
G |
A |
14: 26,649,784 (GRCm39) |
R581* |
probably null |
Het |
Armc9 |
A |
T |
1: 86,189,766 (GRCm39) |
M714L |
probably benign |
Het |
Atp6v0d2 |
T |
A |
4: 19,922,377 (GRCm39) |
T41S |
probably benign |
Het |
Bin1 |
A |
T |
18: 32,552,921 (GRCm39) |
Q182L |
probably damaging |
Het |
Bmp10 |
A |
G |
6: 87,410,684 (GRCm39) |
D159G |
probably benign |
Het |
Bsn |
G |
A |
9: 107,984,854 (GRCm39) |
P295S |
possibly damaging |
Het |
Cbx6 |
A |
G |
15: 79,712,606 (GRCm39) |
S274P |
probably damaging |
Het |
Cdc20b |
A |
G |
13: 113,192,631 (GRCm39) |
K108R |
probably benign |
Het |
Ces1d |
T |
A |
8: 93,912,724 (GRCm39) |
N238I |
probably damaging |
Het |
Col7a1 |
C |
T |
9: 108,787,708 (GRCm39) |
Q663* |
probably null |
Het |
Cpsf3 |
T |
C |
12: 21,358,039 (GRCm39) |
I517T |
possibly damaging |
Het |
Cyp2a5 |
C |
A |
7: 26,539,879 (GRCm39) |
T309N |
probably damaging |
Het |
Cyp2d40 |
A |
G |
15: 82,645,802 (GRCm39) |
F68L |
possibly damaging |
Het |
Cyp7b1 |
A |
T |
3: 18,150,837 (GRCm39) |
W301R |
probably damaging |
Het |
Dnah6 |
T |
A |
6: 73,189,513 (GRCm39) |
N45I |
probably benign |
Het |
Dnah7a |
A |
T |
1: 53,621,776 (GRCm39) |
H1116Q |
probably benign |
Het |
Dntt |
A |
G |
19: 41,027,356 (GRCm39) |
N141S |
probably benign |
Het |
Fbxl13 |
T |
C |
5: 21,790,201 (GRCm39) |
N281D |
probably damaging |
Het |
Frem2 |
A |
T |
3: 53,559,410 (GRCm39) |
L1699H |
probably damaging |
Het |
Gabrr3 |
T |
C |
16: 59,282,037 (GRCm39) |
V464A |
possibly damaging |
Het |
Gdap1 |
T |
A |
1: 17,227,353 (GRCm39) |
I160N |
probably damaging |
Het |
Hnrnpll |
C |
A |
17: 80,369,291 (GRCm39) |
R44L |
unknown |
Het |
Hsp90ab1 |
T |
C |
17: 45,881,680 (GRCm39) |
E187G |
probably damaging |
Het |
Ighm |
T |
A |
12: 113,386,210 (GRCm39) |
T47S |
|
Het |
Itgb7 |
A |
C |
15: 102,135,831 (GRCm39) |
|
probably null |
Het |
Kif16b |
A |
T |
2: 142,461,738 (GRCm39) |
C1293* |
probably null |
Het |
Klf11 |
C |
T |
12: 24,705,043 (GRCm39) |
R166C |
probably benign |
Het |
Lca5l |
T |
A |
16: 95,977,212 (GRCm39) |
Q198L |
probably damaging |
Het |
Lnx2 |
A |
T |
5: 146,961,180 (GRCm39) |
M584K |
probably benign |
Het |
Lpp |
A |
T |
16: 24,540,737 (GRCm39) |
M1L |
probably benign |
Het |
Lrig3 |
A |
G |
10: 125,832,953 (GRCm39) |
T276A |
probably damaging |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Megf8 |
A |
T |
7: 25,039,840 (GRCm39) |
|
probably null |
Het |
Myh1 |
A |
C |
11: 67,093,259 (GRCm39) |
T117P |
probably damaging |
Het |
Neb |
C |
A |
2: 52,134,113 (GRCm39) |
R3290L |
possibly damaging |
Het |
Neb |
A |
C |
2: 52,137,304 (GRCm39) |
V220G |
|
Het |
Nktr |
A |
T |
9: 121,577,264 (GRCm39) |
K444I |
probably damaging |
Het |
Nol11 |
A |
T |
11: 107,064,505 (GRCm39) |
M483K |
probably benign |
Het |
Npy1r |
C |
A |
8: 67,156,861 (GRCm39) |
P94T |
probably damaging |
Het |
Nsmaf |
T |
C |
4: 6,440,940 (GRCm39) |
T37A |
probably benign |
Het |
Or10ad1b |
A |
G |
15: 98,124,920 (GRCm39) |
L204P |
possibly damaging |
Het |
Or2y3 |
G |
A |
17: 38,393,056 (GRCm39) |
A271V |
possibly damaging |
Het |
Or4c119 |
T |
C |
2: 88,987,399 (GRCm39) |
N40S |
probably damaging |
Het |
Or51v8 |
A |
T |
7: 103,319,389 (GRCm39) |
M283K |
probably damaging |
Het |
Or5w14 |
C |
A |
2: 87,541,423 (GRCm39) |
V276F |
possibly damaging |
Het |
Or8a1b |
A |
G |
9: 37,623,473 (GRCm39) |
I34T |
probably damaging |
Het |
Or8b37 |
G |
A |
9: 37,958,775 (GRCm39) |
V86M |
possibly damaging |
Het |
Palld |
C |
T |
8: 61,969,691 (GRCm39) |
R1211H |
unknown |
Het |
Pclo |
G |
A |
5: 14,815,877 (GRCm39) |
V1266I |
|
Het |
Pcnx4 |
T |
C |
12: 72,602,664 (GRCm39) |
Y309H |
probably damaging |
Het |
Pde8a |
C |
T |
7: 80,982,619 (GRCm39) |
T746I |
probably damaging |
Het |
Pdzrn3 |
T |
G |
6: 101,127,772 (GRCm39) |
K965Q |
probably damaging |
Het |
Phldb1 |
G |
A |
9: 44,615,425 (GRCm39) |
A225V |
probably benign |
Het |
Pierce1 |
TCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCGGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTC |
TCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCGGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTC |
2: 28,356,122 (GRCm39) |
|
probably benign |
Het |
Plat |
A |
G |
8: 23,265,599 (GRCm39) |
Y214C |
probably damaging |
Het |
Plppr1 |
T |
A |
4: 49,325,627 (GRCm39) |
C274* |
probably null |
Het |
Poglut1 |
A |
G |
16: 38,347,133 (GRCm39) |
F345L |
possibly damaging |
Het |
Ppara |
A |
T |
15: 85,661,837 (GRCm39) |
E26V |
possibly damaging |
Het |
Ppcdc |
A |
T |
9: 57,327,571 (GRCm39) |
W79R |
probably damaging |
Het |
Prdm1 |
C |
T |
10: 44,316,150 (GRCm39) |
C662Y |
probably damaging |
Het |
Sgms2 |
G |
A |
3: 131,136,011 (GRCm39) |
|
probably benign |
Het |
Slc31a1 |
T |
A |
4: 62,306,843 (GRCm39) |
M133K |
probably damaging |
Het |
Smg1 |
G |
A |
7: 117,777,998 (GRCm39) |
Q1309* |
probably null |
Het |
Sos1 |
T |
C |
17: 80,761,239 (GRCm39) |
I152M |
probably damaging |
Het |
Stk4 |
A |
T |
2: 163,952,136 (GRCm39) |
|
probably benign |
Het |
Syne1 |
T |
G |
10: 5,200,954 (GRCm39) |
N3538T |
probably damaging |
Het |
Tbc1d16 |
A |
G |
11: 119,099,666 (GRCm39) |
F236S |
probably damaging |
Het |
Tgs1 |
T |
A |
4: 3,595,475 (GRCm39) |
M548K |
probably benign |
Het |
Twf1 |
G |
A |
15: 94,483,336 (GRCm39) |
T124I |
probably damaging |
Het |
Tyro3 |
G |
A |
2: 119,642,648 (GRCm39) |
G611R |
probably damaging |
Het |
Unc13b |
T |
A |
4: 43,173,282 (GRCm39) |
I1370K |
unknown |
Het |
Usp40 |
A |
G |
1: 87,885,032 (GRCm39) |
W939R |
probably damaging |
Het |
Vamp8 |
A |
T |
6: 72,362,554 (GRCm39) |
V82E |
probably damaging |
Het |
Vmn2r17 |
A |
G |
5: 109,575,732 (GRCm39) |
H201R |
possibly damaging |
Het |
Whrn |
T |
C |
4: 63,350,079 (GRCm39) |
H546R |
probably benign |
Het |
Yeats2 |
T |
C |
16: 20,033,228 (GRCm39) |
V1036A |
probably benign |
Het |
Zfp352 |
T |
G |
4: 90,112,575 (GRCm39) |
N238K |
probably benign |
Het |
Zfp36l3 |
TCCAGGGGCGAGGGCAGCCCCAGGAGCAAGGGCCGCCCTAGGAATGAGGGCCGCCCCAGG |
TCCAGG |
X: 52,776,521 (GRCm39) |
|
probably benign |
Het |
Zfp462 |
T |
A |
4: 55,011,510 (GRCm39) |
S1159T |
probably benign |
Het |
Zscan4-ps1 |
A |
T |
7: 10,800,192 (GRCm39) |
H232Q |
probably benign |
Het |
|
Other mutations in Pcdha3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R2497:Pcdha3
|
UTSW |
18 |
37,080,556 (GRCm39) |
missense |
probably benign |
|
R3702:Pcdha3
|
UTSW |
18 |
37,080,401 (GRCm39) |
missense |
probably benign |
0.16 |
R4090:Pcdha3
|
UTSW |
18 |
37,081,504 (GRCm39) |
missense |
probably benign |
0.04 |
R4273:Pcdha3
|
UTSW |
18 |
37,081,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R4486:Pcdha3
|
UTSW |
18 |
37,080,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R4535:Pcdha3
|
UTSW |
18 |
37,081,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R4582:Pcdha3
|
UTSW |
18 |
37,080,485 (GRCm39) |
missense |
probably benign |
|
R4712:Pcdha3
|
UTSW |
18 |
37,079,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R5160:Pcdha3
|
UTSW |
18 |
37,079,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R5302:Pcdha3
|
UTSW |
18 |
37,081,208 (GRCm39) |
missense |
probably damaging |
0.96 |
R5361:Pcdha3
|
UTSW |
18 |
37,079,752 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5535:Pcdha3
|
UTSW |
18 |
37,080,989 (GRCm39) |
missense |
probably benign |
0.02 |
R5682:Pcdha3
|
UTSW |
18 |
37,081,040 (GRCm39) |
missense |
probably damaging |
0.99 |
R6656:Pcdha3
|
UTSW |
18 |
37,080,875 (GRCm39) |
missense |
probably benign |
0.24 |
R6878:Pcdha3
|
UTSW |
18 |
37,080,416 (GRCm39) |
nonsense |
probably null |
|
R7150:Pcdha3
|
UTSW |
18 |
37,080,165 (GRCm39) |
missense |
probably benign |
0.01 |
R7167:Pcdha3
|
UTSW |
18 |
37,080,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R7299:Pcdha3
|
UTSW |
18 |
37,079,977 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7301:Pcdha3
|
UTSW |
18 |
37,079,977 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7448:Pcdha3
|
UTSW |
18 |
37,079,266 (GRCm39) |
missense |
probably benign |
0.00 |
R7467:Pcdha3
|
UTSW |
18 |
37,080,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R7542:Pcdha3
|
UTSW |
18 |
37,080,784 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7659:Pcdha3
|
UTSW |
18 |
37,081,219 (GRCm39) |
missense |
probably benign |
0.14 |
R7761:Pcdha3
|
UTSW |
18 |
37,079,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R7782:Pcdha3
|
UTSW |
18 |
37,081,193 (GRCm39) |
missense |
probably damaging |
0.98 |
R7939:Pcdha3
|
UTSW |
18 |
37,080,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R8217:Pcdha3
|
UTSW |
18 |
37,079,974 (GRCm39) |
missense |
probably damaging |
0.99 |
R8440:Pcdha3
|
UTSW |
18 |
37,080,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R8938:Pcdha3
|
UTSW |
18 |
37,080,154 (GRCm39) |
missense |
probably benign |
0.43 |
R9375:Pcdha3
|
UTSW |
18 |
37,079,353 (GRCm39) |
missense |
probably benign |
0.29 |
R9546:Pcdha3
|
UTSW |
18 |
37,079,389 (GRCm39) |
missense |
probably damaging |
1.00 |
|