Other mutations in this stock |
Total: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
A |
T |
13: 77,471,525 (GRCm39) |
S977C |
possibly damaging |
Het |
Abca8a |
T |
A |
11: 109,960,305 (GRCm39) |
D646V |
probably damaging |
Het |
Adss2 |
T |
A |
1: 177,597,526 (GRCm39) |
Y378F |
probably damaging |
Het |
Akap6 |
C |
T |
12: 53,188,319 (GRCm39) |
A1911V |
probably benign |
Het |
Alg2 |
T |
C |
4: 47,474,159 (GRCm39) |
Y43C |
probably benign |
Het |
Alk |
A |
C |
17: 72,202,758 (GRCm39) |
V1159G |
probably damaging |
Het |
Alx3 |
A |
T |
3: 107,508,010 (GRCm39) |
Q173L |
probably damaging |
Het |
Aqp9 |
A |
G |
9: 71,069,593 (GRCm39) |
|
probably benign |
Het |
Atf7ip |
C |
A |
6: 136,564,141 (GRCm39) |
L787I |
probably benign |
Het |
Bbs9 |
A |
T |
9: 22,590,234 (GRCm39) |
E657D |
possibly damaging |
Het |
Bean1 |
G |
A |
8: 104,908,752 (GRCm39) |
|
probably null |
Het |
Cactin |
G |
T |
10: 81,157,082 (GRCm39) |
R13L |
unknown |
Het |
Ccdc178 |
T |
C |
18: 22,200,721 (GRCm39) |
E412G |
probably damaging |
Het |
Ccdc30 |
A |
G |
4: 119,181,759 (GRCm39) |
I583T |
probably damaging |
Het |
Ccl8 |
T |
C |
11: 82,006,933 (GRCm39) |
Y49H |
probably damaging |
Het |
Clptm1 |
T |
A |
7: 19,372,932 (GRCm39) |
K199N |
probably damaging |
Het |
Cnbp |
G |
A |
6: 87,822,646 (GRCm39) |
S39L |
probably benign |
Het |
Cnih3 |
T |
A |
1: 181,237,437 (GRCm39) |
|
probably benign |
Het |
Cnksr3 |
A |
T |
10: 7,090,201 (GRCm39) |
|
probably benign |
Het |
Cntn1 |
A |
G |
15: 92,159,380 (GRCm39) |
I512V |
probably benign |
Het |
Col20a1 |
A |
G |
2: 180,640,296 (GRCm39) |
|
probably benign |
Het |
Col28a1 |
A |
T |
6: 8,127,360 (GRCm39) |
|
probably benign |
Het |
Col6a2 |
A |
T |
10: 76,450,741 (GRCm39) |
Y63* |
probably null |
Het |
Copa |
T |
G |
1: 171,925,312 (GRCm39) |
F190V |
probably damaging |
Het |
Crisp4 |
A |
C |
1: 18,207,148 (GRCm39) |
|
probably benign |
Het |
Cxcl2 |
C |
T |
5: 91,052,085 (GRCm39) |
Q64* |
probably null |
Het |
Cxcr5 |
T |
C |
9: 44,425,549 (GRCm39) |
D36G |
probably benign |
Het |
Cyp20a1 |
T |
A |
1: 60,411,765 (GRCm39) |
V271E |
possibly damaging |
Het |
D430041D05Rik |
T |
C |
2: 104,071,538 (GRCm39) |
Y570C |
probably damaging |
Het |
Ddi1 |
T |
G |
9: 6,266,198 (GRCm39) |
D57A |
probably benign |
Het |
Ddx11 |
T |
A |
17: 66,450,460 (GRCm39) |
S492T |
probably benign |
Het |
Dhx34 |
C |
T |
7: 15,950,376 (GRCm39) |
R264H |
probably damaging |
Het |
Dnah3 |
T |
A |
7: 119,561,375 (GRCm39) |
I328F |
|
Het |
Dnah5 |
C |
T |
15: 28,327,886 (GRCm39) |
R2087C |
probably damaging |
Het |
Dnah8 |
C |
G |
17: 30,927,286 (GRCm39) |
S1314W |
possibly damaging |
Het |
Dock2 |
T |
C |
11: 34,260,396 (GRCm39) |
N982D |
probably benign |
Het |
Dync1h1 |
A |
G |
12: 110,583,172 (GRCm39) |
D423G |
probably damaging |
Het |
Ect2l |
A |
C |
10: 18,048,583 (GRCm39) |
L213V |
probably damaging |
Het |
Fam210a |
T |
C |
18: 68,409,215 (GRCm39) |
I32V |
probably benign |
Het |
Fancg |
A |
G |
4: 43,007,266 (GRCm39) |
|
probably null |
Het |
Fastkd5 |
T |
C |
2: 130,457,111 (GRCm39) |
E493G |
probably benign |
Het |
Fbxo38 |
T |
C |
18: 62,659,272 (GRCm39) |
M342V |
probably damaging |
Het |
Flnc |
A |
C |
6: 29,455,410 (GRCm39) |
K2020Q |
probably damaging |
Het |
Flt4 |
A |
G |
11: 49,527,160 (GRCm39) |
|
probably benign |
Het |
Frmd4b |
G |
T |
6: 97,389,480 (GRCm39) |
P129T |
probably benign |
Het |
Galnt13 |
C |
A |
2: 54,770,138 (GRCm39) |
A310E |
probably benign |
Het |
Gm4884 |
T |
A |
7: 40,694,108 (GRCm39) |
Y692* |
probably null |
Het |
Gm6309 |
T |
A |
5: 146,105,103 (GRCm39) |
D270V |
probably damaging |
Het |
Grip1 |
G |
T |
10: 119,290,192 (GRCm39) |
|
probably benign |
Het |
Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
Kdf1 |
G |
T |
4: 133,255,505 (GRCm39) |
C74F |
probably damaging |
Het |
Kdm1b |
T |
A |
13: 47,207,184 (GRCm39) |
C169* |
probably null |
Het |
Kmt2c |
G |
T |
5: 25,520,077 (GRCm39) |
T2011K |
probably benign |
Het |
Lama1 |
G |
A |
17: 68,080,779 (GRCm39) |
G1269E |
|
Het |
Lamb3 |
C |
T |
1: 193,017,182 (GRCm39) |
A791V |
probably benign |
Het |
Leng9 |
G |
T |
7: 4,151,774 (GRCm39) |
R301S |
possibly damaging |
Het |
Lgr6 |
C |
A |
1: 134,915,342 (GRCm39) |
V746L |
probably benign |
Het |
Lrp5 |
T |
A |
19: 3,702,170 (GRCm39) |
S216C |
probably damaging |
Het |
Ltn1 |
T |
C |
16: 87,178,433 (GRCm39) |
T1599A |
probably damaging |
Het |
Map2k1 |
G |
T |
9: 64,094,606 (GRCm39) |
N345K |
probably damaging |
Het |
Map4k1 |
T |
A |
7: 28,688,862 (GRCm39) |
D304E |
probably benign |
Het |
Mcpt1 |
C |
T |
14: 56,256,522 (GRCm39) |
T86I |
probably damaging |
Het |
Mcpt9 |
T |
C |
14: 56,265,153 (GRCm39) |
K116R |
probably benign |
Het |
Morc2a |
G |
T |
11: 3,628,584 (GRCm39) |
A346S |
probably damaging |
Het |
Mybpc3 |
A |
T |
2: 90,954,237 (GRCm39) |
Q370L |
probably benign |
Het |
Nars2 |
T |
C |
7: 96,652,095 (GRCm39) |
S229P |
probably damaging |
Het |
Ndufa10 |
A |
T |
1: 92,397,693 (GRCm39) |
Y118N |
probably damaging |
Het |
Nek11 |
A |
T |
9: 105,172,571 (GRCm39) |
|
probably null |
Het |
Notch4 |
T |
C |
17: 34,803,470 (GRCm39) |
V1463A |
possibly damaging |
Het |
Nrcam |
T |
C |
12: 44,610,908 (GRCm39) |
I536T |
probably benign |
Het |
Or6c202 |
T |
C |
10: 128,996,334 (GRCm39) |
Y173C |
probably benign |
Het |
Pbld1 |
A |
T |
10: 62,912,226 (GRCm39) |
T285S |
probably benign |
Het |
Pcdhgb8 |
A |
T |
18: 37,896,177 (GRCm39) |
T416S |
possibly damaging |
Het |
Plekhg6 |
T |
C |
6: 125,351,523 (GRCm39) |
D242G |
probably damaging |
Het |
Pnmt |
T |
A |
11: 98,278,580 (GRCm39) |
V182D |
probably benign |
Het |
Ppp1r13b |
G |
T |
12: 111,799,871 (GRCm39) |
N758K |
probably damaging |
Het |
Prex2 |
A |
G |
1: 11,240,799 (GRCm39) |
|
probably benign |
Het |
Prss3 |
A |
T |
6: 41,354,512 (GRCm39) |
L7Q |
probably damaging |
Het |
Prss43 |
T |
A |
9: 110,660,046 (GRCm39) |
L370Q |
probably damaging |
Het |
Rac1 |
A |
T |
5: 143,493,885 (GRCm39) |
V104E |
probably damaging |
Het |
Rgs9 |
T |
C |
11: 109,166,449 (GRCm39) |
Y107C |
probably damaging |
Het |
Rrp1b |
G |
A |
17: 32,270,688 (GRCm39) |
V216I |
possibly damaging |
Het |
Serinc1 |
A |
G |
10: 57,395,864 (GRCm39) |
S309P |
probably benign |
Het |
Serpine3 |
T |
A |
14: 62,902,587 (GRCm39) |
L66Q |
probably damaging |
Het |
Smc5 |
C |
T |
19: 23,191,234 (GRCm39) |
V924M |
probably damaging |
Het |
Spmip4 |
A |
T |
6: 50,551,028 (GRCm39) |
Y474N |
possibly damaging |
Het |
Srgap1 |
A |
T |
10: 121,761,545 (GRCm39) |
|
probably benign |
Het |
Stab1 |
T |
C |
14: 30,883,771 (GRCm39) |
E262G |
possibly damaging |
Het |
Ston2 |
A |
G |
12: 91,606,498 (GRCm39) |
*896R |
probably null |
Het |
Syt6 |
A |
G |
3: 103,532,941 (GRCm39) |
M442V |
probably benign |
Het |
Tap1 |
T |
C |
17: 34,408,536 (GRCm39) |
|
probably null |
Het |
Tbx3 |
A |
C |
5: 119,818,624 (GRCm39) |
S420R |
probably benign |
Het |
Tespa1 |
A |
T |
10: 130,198,316 (GRCm39) |
Q446L |
probably benign |
Het |
Tifab |
T |
C |
13: 56,324,108 (GRCm39) |
M112V |
probably benign |
Het |
Trpv5 |
A |
T |
6: 41,630,192 (GRCm39) |
S633T |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,684,236 (GRCm39) |
K838R |
unknown |
Het |
Ttn |
A |
T |
2: 76,744,810 (GRCm39) |
V5413E |
probably damaging |
Het |
Tub |
C |
A |
7: 108,628,793 (GRCm39) |
N415K |
|
Het |
Vmn2r3 |
T |
C |
3: 64,182,383 (GRCm39) |
M439V |
probably benign |
Het |
Vps13c |
A |
G |
9: 67,850,736 (GRCm39) |
D2231G |
probably benign |
Het |
Wbp1 |
C |
T |
6: 83,096,913 (GRCm39) |
C118Y |
unknown |
Het |
Zdhhc20 |
C |
T |
14: 58,127,671 (GRCm39) |
|
probably benign |
Het |
Zfp217 |
T |
A |
2: 169,956,391 (GRCm39) |
N869I |
probably benign |
Het |
Zfp677 |
T |
C |
17: 21,618,350 (GRCm39) |
I469T |
probably benign |
Het |
Zmym2 |
T |
A |
14: 57,185,329 (GRCm39) |
|
probably benign |
Het |
Zzef1 |
T |
G |
11: 72,687,402 (GRCm39) |
S94A |
probably benign |
Het |
|