Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010B08Rik |
A |
T |
2: 173,719,913 |
H5L |
unknown |
Het |
Aatk |
A |
G |
11: 120,010,907 |
S888P |
probably damaging |
Het |
Ahnak |
A |
T |
19: 9,008,422 |
K2357* |
probably null |
Het |
Arl9 |
T |
A |
5: 77,007,292 |
L90Q |
probably damaging |
Het |
Atxn2 |
T |
C |
5: 121,810,992 |
V1144A |
probably damaging |
Het |
Batf3 |
C |
T |
1: 191,098,426 |
|
probably benign |
Het |
Brpf3 |
G |
A |
17: 28,818,623 |
E822K |
probably benign |
Het |
Cabin1 |
T |
A |
10: 75,739,405 |
Q602L |
probably damaging |
Het |
Cadps |
T |
C |
14: 12,597,418 |
E424G |
probably damaging |
Het |
Camta1 |
A |
G |
4: 151,131,547 |
L972P |
possibly damaging |
Het |
Ccdc159 |
A |
G |
9: 21,929,376 |
N80D |
possibly damaging |
Het |
Cdh1 |
A |
C |
8: 106,661,972 |
E553D |
possibly damaging |
Het |
Cdk14 |
T |
A |
5: 5,373,477 |
E35V |
probably benign |
Het |
Cfap70 |
A |
G |
14: 20,400,478 |
L995P |
probably damaging |
Het |
Col18a1 |
T |
A |
10: 77,080,839 |
E334V |
unknown |
Het |
Colec12 |
T |
A |
18: 9,877,000 |
I741K |
unknown |
Het |
Crot |
A |
G |
5: 8,974,170 |
V342A |
probably benign |
Het |
Ctnnal1 |
A |
G |
4: 56,865,036 |
S27P |
possibly damaging |
Het |
Cyp2j9 |
A |
G |
4: 96,571,956 |
S437P |
probably damaging |
Het |
Dennd4c |
A |
T |
4: 86,824,923 |
T1001S |
probably benign |
Het |
Dffa |
G |
A |
4: 149,117,819 |
V227I |
probably benign |
Het |
Dnaaf5 |
T |
A |
5: 139,174,154 |
H602Q |
probably benign |
Het |
Efcab7 |
G |
T |
4: 99,904,705 |
K397N |
probably damaging |
Het |
Egfl6 |
C |
T |
X: 166,536,239 |
V379I |
probably benign |
Het |
Fadd |
G |
A |
7: 144,580,647 |
T167I |
probably benign |
Het |
Fam184b |
T |
C |
5: 45,639,142 |
D33G |
probably damaging |
Het |
Fam214a |
A |
G |
9: 75,017,067 |
D864G |
possibly damaging |
Het |
Fam83h |
G |
A |
15: 76,006,127 |
R141W |
probably damaging |
Het |
Fam84a |
T |
C |
12: 14,150,189 |
N179S |
probably benign |
Het |
Fanci |
G |
A |
7: 79,427,206 |
R564Q |
probably damaging |
Het |
Fat3 |
A |
T |
9: 15,996,758 |
D2649E |
possibly damaging |
Het |
Fcrl1 |
A |
G |
3: 87,384,611 |
T46A |
possibly damaging |
Het |
Fig4 |
C |
T |
10: 41,267,767 |
G232D |
probably benign |
Het |
Frem3 |
A |
T |
8: 80,614,516 |
H1146L |
probably damaging |
Het |
Fyttd1 |
T |
A |
16: 32,895,102 |
F133L |
probably benign |
Het |
Gata2 |
A |
G |
6: 88,202,523 |
N326D |
probably damaging |
Het |
Gm10093 |
A |
T |
17: 78,491,646 |
Y22F |
probably benign |
Het |
Gm13084 |
A |
G |
4: 143,816,039 |
C4R |
probably damaging |
Het |
Gm21964 |
T |
C |
8: 110,110,948 |
F375L |
probably damaging |
Het |
Gm7298 |
A |
T |
6: 121,787,532 |
T1457S |
probably damaging |
Het |
Gm8773 |
C |
T |
5: 5,575,549 |
Q82* |
probably null |
Het |
Heatr5b |
C |
T |
17: 78,834,095 |
|
probably null |
Het |
Hfm1 |
T |
A |
5: 106,918,463 |
D33V |
possibly damaging |
Het |
Hmcn2 |
G |
A |
2: 31,402,438 |
A2447T |
possibly damaging |
Het |
Hs3st3b1 |
A |
G |
11: 63,921,505 |
F128S |
probably benign |
Het |
Hs3st6 |
G |
T |
17: 24,753,252 |
R56L |
possibly damaging |
Het |
Hsd17b3 |
C |
T |
13: 64,064,357 |
M168I |
probably damaging |
Het |
Ighv1-34 |
G |
T |
12: 114,851,265 |
D92E |
possibly damaging |
Het |
Itgb4 |
A |
T |
11: 115,994,345 |
I1018F |
possibly damaging |
Het |
Itih3 |
T |
C |
14: 30,915,648 |
D518G |
possibly damaging |
Het |
Kcnma1 |
C |
T |
14: 23,451,598 |
|
probably null |
Het |
Klhl11 |
A |
T |
11: 100,472,680 |
S17T |
probably benign |
Het |
Lilra6 |
T |
C |
7: 3,914,522 |
E158G |
possibly damaging |
Het |
Loxl1 |
A |
G |
9: 58,312,754 |
W45R |
probably damaging |
Het |
Lrfn1 |
G |
T |
7: 28,466,830 |
V550F |
probably damaging |
Het |
Lrp1 |
T |
C |
10: 127,573,499 |
K1584E |
probably benign |
Het |
Lrp4 |
C |
G |
2: 91,508,569 |
P1782A |
possibly damaging |
Het |
Map3k1 |
A |
G |
13: 111,748,944 |
S1480P |
probably damaging |
Het |
Mark4 |
G |
T |
7: 19,426,090 |
N748K |
probably benign |
Het |
Mrpl38 |
G |
A |
11: 116,135,074 |
T142M |
probably damaging |
Het |
Mrpl41 |
T |
C |
2: 24,974,469 |
T64A |
probably benign |
Het |
Mrps2 |
G |
A |
2: 28,469,752 |
R207K |
possibly damaging |
Het |
Myo5a |
A |
T |
9: 75,192,444 |
E96D |
|
Het |
Nbas |
A |
T |
12: 13,583,416 |
E2274V |
probably damaging |
Het |
Olfr1022 |
T |
C |
2: 85,868,934 |
L114P |
possibly damaging |
Het |
Olfr1022 |
T |
A |
2: 85,869,475 |
N294K |
probably damaging |
Het |
Olfr1274-ps |
T |
C |
2: 90,400,994 |
F111S |
probably damaging |
Het |
Olfr570 |
T |
C |
7: 102,900,445 |
I26T |
probably benign |
Het |
Olfr616 |
T |
C |
7: 103,564,643 |
D212G |
probably damaging |
Het |
Olfr781 |
T |
A |
10: 129,333,499 |
I206N |
possibly damaging |
Het |
Pcdhga12 |
T |
A |
18: 37,767,235 |
D373E |
probably damaging |
Het |
Pgd |
A |
C |
4: 149,151,139 |
F395V |
probably damaging |
Het |
Pi16 |
A |
G |
17: 29,319,389 |
M59V |
possibly damaging |
Het |
Pik3r5 |
A |
T |
11: 68,490,894 |
T255S |
probably benign |
Het |
Plch2 |
A |
T |
4: 154,984,059 |
V1370E |
probably benign |
Het |
Plec |
A |
G |
15: 76,182,953 |
I1309T |
unknown |
Het |
Ppp2r3d |
A |
T |
9: 124,440,831 |
S22R |
|
Het |
Ptk2b |
C |
A |
14: 66,175,705 |
E342* |
probably null |
Het |
Ptpn23 |
T |
C |
9: 110,386,158 |
|
probably null |
Het |
Rfx8 |
A |
C |
1: 39,683,690 |
S256A |
probably damaging |
Het |
Rnf115 |
C |
T |
3: 96,758,021 |
T69I |
probably damaging |
Het |
Rnf213 |
A |
G |
11: 119,479,631 |
Y4753C |
|
Het |
S100a10 |
A |
C |
3: 93,564,283 |
D58A |
possibly damaging |
Het |
Serpina12 |
T |
C |
12: 104,038,058 |
K105R |
probably benign |
Het |
Slc20a2 |
G |
A |
8: 22,538,884 |
G124S |
probably damaging |
Het |
Stab2 |
ACC |
AC |
10: 86,856,697 |
|
probably null |
Het |
Stxbp5 |
T |
A |
10: 9,899,194 |
I72F |
probably damaging |
Het |
Sumf2 |
T |
A |
5: 129,862,641 |
M282K |
possibly damaging |
Het |
Tmem135 |
G |
C |
7: 89,147,978 |
L357V |
probably benign |
Het |
Tmem185b |
G |
T |
1: 119,526,883 |
V125L |
probably benign |
Het |
Tmtc1 |
A |
G |
6: 148,243,216 |
M887T |
probably damaging |
Het |
Tnfaip8 |
C |
T |
18: 50,090,445 |
Q83* |
probably null |
Het |
Tnks |
A |
G |
8: 34,838,935 |
V1162A |
probably damaging |
Het |
Tomm70a |
T |
A |
16: 57,140,709 |
Y342N |
possibly damaging |
Het |
Tpo |
T |
A |
12: 30,075,876 |
D828V |
probably damaging |
Het |
Ugt8a |
A |
T |
3: 125,914,689 |
N257K |
probably damaging |
Het |
Uhrf1bp1l |
C |
A |
10: 89,790,731 |
T429K |
probably benign |
Het |
Unc13d |
AATGCCTCCCATGCC |
AATGCCTCCCATGCCTCCCATGCC |
11: 116,068,172 |
|
probably benign |
Het |
Vim |
T |
A |
2: 13,574,892 |
M154K |
probably damaging |
Het |
Virma |
G |
T |
4: 11,486,045 |
M1I |
probably null |
Het |
Zfp715 |
A |
T |
7: 43,301,229 |
M100K |
probably benign |
Het |
Zfp748 |
A |
T |
13: 67,542,528 |
C204* |
probably null |
Het |
Zmynd8 |
A |
T |
2: 165,838,852 |
D236E |
probably damaging |
Het |
|