Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810055G02Rik |
C |
T |
19: 3,767,100 (GRCm39) |
S229L |
possibly damaging |
Het |
Actc1 |
TGA |
T |
2: 113,879,710 (GRCm39) |
|
probably null |
Het |
Actl9 |
G |
A |
17: 33,653,004 (GRCm39) |
A355T |
probably benign |
Het |
Adamts8 |
A |
G |
9: 30,854,188 (GRCm39) |
Q19R |
probably benign |
Het |
Akr1c14 |
A |
T |
13: 4,130,695 (GRCm39) |
Y216F |
possibly damaging |
Het |
Alms1 |
T |
C |
6: 85,598,770 (GRCm39) |
C1199R |
possibly damaging |
Het |
Apc2 |
T |
C |
10: 80,150,111 (GRCm39) |
S1722P |
probably damaging |
Het |
Arid1a |
T |
C |
4: 133,409,167 (GRCm39) |
E1395G |
unknown |
Het |
Atp6v0e2 |
T |
C |
6: 48,516,190 (GRCm39) |
V46A |
possibly damaging |
Het |
Bcar3 |
A |
G |
3: 122,319,091 (GRCm39) |
R743G |
probably damaging |
Het |
Bhmt2 |
A |
G |
13: 93,805,854 (GRCm39) |
V56A |
probably damaging |
Het |
Bsn |
C |
A |
9: 107,982,686 (GRCm39) |
R917L |
|
Het |
Cabyr |
T |
G |
18: 12,887,278 (GRCm39) |
V303G |
possibly damaging |
Het |
Carmil1 |
A |
T |
13: 24,292,512 (GRCm39) |
I429N |
probably damaging |
Het |
Ccdc27 |
T |
C |
4: 154,122,174 (GRCm39) |
N235D |
unknown |
Het |
Ccdc61 |
T |
C |
7: 18,637,746 (GRCm39) |
M37V |
probably benign |
Het |
Cd40 |
A |
T |
2: 164,898,716 (GRCm39) |
I48F |
unknown |
Het |
Cdk13 |
A |
T |
13: 17,941,071 (GRCm39) |
S664R |
probably damaging |
Het |
Cel |
TTA |
TTATA |
2: 28,449,441 (GRCm39) |
|
probably null |
Het |
Cfap46 |
T |
A |
7: 139,258,416 (GRCm39) |
R286* |
probably null |
Het |
Ckap2 |
A |
C |
8: 22,659,954 (GRCm39) |
I509S |
possibly damaging |
Het |
Clptm1l |
A |
T |
13: 73,752,344 (GRCm39) |
|
probably benign |
Het |
Col11a1 |
T |
G |
3: 114,001,929 (GRCm39) |
M1591R |
unknown |
Het |
Col6a5 |
C |
A |
9: 105,814,594 (GRCm39) |
A473S |
unknown |
Het |
Cxcr2 |
T |
A |
1: 74,197,756 (GRCm39) |
D83E |
probably damaging |
Het |
Cyp2c39 |
G |
A |
19: 39,527,332 (GRCm39) |
C226Y |
probably benign |
Het |
Ddr1 |
A |
C |
17: 36,000,609 (GRCm39) |
F352C |
probably damaging |
Het |
Defb22 |
T |
A |
2: 152,327,721 (GRCm39) |
T155S |
unknown |
Het |
Dennd4c |
G |
T |
4: 86,738,170 (GRCm39) |
E935* |
probably null |
Het |
Dst |
A |
C |
1: 34,330,879 (GRCm39) |
E4889D |
probably damaging |
Het |
Efcab3 |
A |
G |
11: 104,661,801 (GRCm39) |
Q1314R |
probably benign |
Het |
Emilin1 |
T |
A |
5: 31,074,823 (GRCm39) |
C355S |
probably damaging |
Het |
Enpp3 |
C |
T |
10: 24,650,716 (GRCm39) |
V807I |
probably benign |
Het |
Fcnb |
T |
A |
2: 27,969,160 (GRCm39) |
D179V |
probably damaging |
Het |
Ficd |
T |
A |
5: 113,875,196 (GRCm39) |
D88E |
probably benign |
Het |
Fndc3b |
T |
C |
3: 27,524,450 (GRCm39) |
K437E |
possibly damaging |
Het |
Fyb2 |
T |
A |
4: 104,853,105 (GRCm39) |
W566R |
probably benign |
Het |
Gm14403 |
A |
G |
2: 177,200,336 (GRCm39) |
Q94R |
probably benign |
Het |
Gm32687 |
T |
A |
10: 81,714,866 (GRCm39) |
I86N |
probably benign |
Het |
Gpam |
T |
G |
19: 55,075,907 (GRCm39) |
D235A |
probably damaging |
Het |
Gstt4 |
T |
C |
10: 75,651,046 (GRCm39) |
E192G |
probably damaging |
Het |
H2-Q6 |
T |
G |
17: 35,644,309 (GRCm39) |
V97G |
probably benign |
Het |
Hcn1 |
G |
A |
13: 118,062,254 (GRCm39) |
G507S |
unknown |
Het |
Hydin |
T |
C |
8: 111,259,516 (GRCm39) |
I2496T |
probably benign |
Het |
Jund |
A |
G |
8: 71,151,864 (GRCm39) |
D53G |
probably damaging |
Het |
Kat6b |
T |
A |
14: 21,720,031 (GRCm39) |
M1461K |
probably benign |
Het |
Lnx1 |
T |
G |
5: 74,766,810 (GRCm39) |
K435Q |
probably benign |
Het |
Lpcat1 |
C |
A |
13: 73,658,161 (GRCm39) |
L316M |
probably damaging |
Het |
Lrrtm3 |
ATTTT |
ATTTTT |
10: 63,925,035 (GRCm39) |
|
probably null |
Het |
Ly6c1 |
T |
A |
15: 74,916,465 (GRCm39) |
T126S |
probably benign |
Het |
Macf1 |
A |
G |
4: 123,326,690 (GRCm39) |
S4938P |
probably damaging |
Het |
Map2k2 |
T |
C |
10: 80,954,008 (GRCm39) |
V158A |
possibly damaging |
Het |
Map3k4 |
A |
G |
17: 12,456,973 (GRCm39) |
V1323A |
probably damaging |
Het |
Map4k5 |
A |
T |
12: 69,939,467 (GRCm39) |
V23E |
possibly damaging |
Het |
Med30 |
T |
G |
15: 52,582,839 (GRCm39) |
L92R |
probably damaging |
Het |
Mroh8 |
C |
T |
2: 157,063,069 (GRCm39) |
G851S |
possibly damaging |
Het |
Msmb |
T |
A |
14: 31,880,060 (GRCm39) |
C83* |
probably null |
Het |
Mtif2 |
A |
T |
11: 29,494,364 (GRCm39) |
R655S |
probably benign |
Het |
Myo10 |
C |
T |
15: 25,808,081 (GRCm39) |
S1901L |
probably benign |
Het |
Myom2 |
A |
T |
8: 15,178,804 (GRCm39) |
I1279F |
possibly damaging |
Het |
Nat9 |
T |
C |
11: 115,075,441 (GRCm39) |
I67V |
probably damaging |
Het |
Ncam1 |
A |
G |
9: 49,419,995 (GRCm39) |
S774P |
probably damaging |
Het |
Ndufaf6 |
T |
C |
4: 11,062,089 (GRCm39) |
T181A |
probably damaging |
Het |
Nlrp4f |
T |
A |
13: 65,332,829 (GRCm39) |
K110* |
probably null |
Het |
Nlrp9b |
T |
C |
7: 19,753,217 (GRCm39) |
S41P |
probably benign |
Het |
Nlrp9b |
A |
G |
7: 19,757,476 (GRCm39) |
T238A |
probably benign |
Het |
Noxo1 |
A |
T |
17: 24,919,305 (GRCm39) |
E342D |
probably benign |
Het |
Nt5dc2 |
T |
C |
14: 30,857,665 (GRCm39) |
M55T |
probably benign |
Het |
Or1j14 |
A |
T |
2: 36,417,838 (GRCm39) |
Q138L |
probably benign |
Het |
Or2ag18 |
T |
C |
7: 106,405,489 (GRCm39) |
Y60C |
probably damaging |
Het |
Or2f1 |
T |
C |
6: 42,721,904 (GRCm39) |
F311S |
probably benign |
Het |
Or2h2c |
T |
C |
17: 37,422,767 (GRCm39) |
T36A |
possibly damaging |
Het |
Or5al6 |
T |
A |
2: 85,976,220 (GRCm39) |
N286I |
probably damaging |
Het |
Or6c210 |
C |
A |
10: 129,496,007 (GRCm39) |
L111M |
probably damaging |
Het |
Or6c6 |
T |
A |
10: 129,186,450 (GRCm39) |
M6K |
probably benign |
Het |
Or9s18 |
C |
T |
13: 65,300,203 (GRCm39) |
T55I |
probably damaging |
Het |
P4ha2 |
C |
T |
11: 54,009,963 (GRCm39) |
P240L |
possibly damaging |
Het |
Pcdha11 |
T |
A |
18: 37,139,073 (GRCm39) |
L234Q |
probably damaging |
Het |
Pgm3 |
C |
T |
9: 86,438,415 (GRCm39) |
A457T |
probably benign |
Het |
Pira12 |
T |
C |
7: 3,900,234 (GRCm39) |
T123A |
probably benign |
Het |
Pkp4 |
T |
C |
2: 59,144,738 (GRCm39) |
V533A |
probably benign |
Het |
Plac8l1 |
T |
C |
18: 42,325,702 (GRCm39) |
T68A |
possibly damaging |
Het |
Pou2f3 |
A |
T |
9: 43,050,694 (GRCm39) |
I222N |
probably damaging |
Het |
Ppp1r14d |
T |
C |
2: 119,060,222 (GRCm39) |
D20G |
probably benign |
Het |
Ppp1r37 |
C |
A |
7: 19,265,729 (GRCm39) |
G679V |
probably damaging |
Het |
Ppp6r2 |
T |
A |
15: 89,146,599 (GRCm39) |
I199N |
probably damaging |
Het |
Prune2 |
A |
G |
19: 17,097,393 (GRCm39) |
T966A |
probably damaging |
Het |
Ptdss2 |
T |
C |
7: 140,734,798 (GRCm39) |
V375A |
probably benign |
Het |
Rara |
TGCCCCGC |
TGCCCCGCCCCGC |
11: 98,857,236 (GRCm39) |
|
probably null |
Het |
Rin2 |
T |
A |
2: 145,720,822 (GRCm39) |
C718* |
probably null |
Het |
Rptor |
C |
T |
11: 119,785,113 (GRCm39) |
T1170I |
probably benign |
Het |
Samd5 |
T |
C |
10: 9,550,259 (GRCm39) |
Y150C |
probably damaging |
Het |
Setd1b |
T |
C |
5: 123,296,773 (GRCm39) |
S1245P |
unknown |
Het |
Sipa1l2 |
T |
C |
8: 126,218,716 (GRCm39) |
E207G |
probably damaging |
Het |
Slc29a1 |
C |
A |
17: 45,897,153 (GRCm39) |
V378L |
probably damaging |
Het |
Slc2a12 |
T |
G |
10: 22,541,261 (GRCm39) |
I372S |
possibly damaging |
Het |
Slc7a10 |
T |
A |
7: 34,894,639 (GRCm39) |
Y99* |
probably null |
Het |
Sptlc3 |
C |
T |
2: 139,336,154 (GRCm39) |
T10I |
probably benign |
Het |
Sri |
T |
A |
5: 8,113,323 (GRCm39) |
W105R |
probably damaging |
Het |
Stk35 |
T |
C |
2: 129,652,491 (GRCm39) |
Y331H |
probably damaging |
Het |
Tipin |
T |
C |
9: 64,195,430 (GRCm39) |
I12T |
probably benign |
Het |
Tlr5 |
A |
G |
1: 182,802,693 (GRCm39) |
T666A |
probably benign |
Het |
Tmprss11g |
C |
A |
5: 86,640,003 (GRCm39) |
V222L |
probably benign |
Het |
Tnfrsf11b |
T |
A |
15: 54,115,556 (GRCm39) |
Y347F |
possibly damaging |
Het |
Traf6 |
A |
G |
2: 101,527,512 (GRCm39) |
T421A |
probably benign |
Het |
Trrap |
T |
A |
5: 144,708,049 (GRCm39) |
D30E |
possibly damaging |
Het |
Ube2k |
T |
A |
5: 65,751,847 (GRCm39) |
Y162N |
probably damaging |
Het |
Uck2 |
A |
T |
1: 167,065,171 (GRCm39) |
V49E |
probably damaging |
Het |
Vcam1 |
A |
T |
3: 115,904,592 (GRCm39) |
Y718* |
probably null |
Het |
Zan |
T |
C |
5: 137,472,269 (GRCm39) |
N159S |
probably damaging |
Het |
Zfp438 |
A |
G |
18: 5,210,788 (GRCm39) |
L750P |
probably damaging |
Het |
Zfp54 |
A |
T |
17: 21,654,037 (GRCm39) |
Y177F |
probably benign |
Het |
|