Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adat3 |
C |
T |
10: 80,442,234 (GRCm39) |
A24V |
probably benign |
Het |
Agbl1 |
A |
T |
7: 76,239,241 (GRCm39) |
E832D |
unknown |
Het |
Akap8l |
G |
A |
17: 32,554,545 (GRCm39) |
S347L |
probably benign |
Het |
Ankmy1 |
G |
T |
1: 92,804,379 (GRCm39) |
A868E |
probably damaging |
Het |
Ankrd49 |
A |
T |
9: 14,693,837 (GRCm39) |
L110* |
probably null |
Het |
Aoc3 |
A |
G |
11: 101,228,229 (GRCm39) |
T679A |
probably damaging |
Het |
Ap1s3 |
A |
G |
1: 79,592,018 (GRCm39) |
Y111H |
probably damaging |
Het |
Arnt |
T |
A |
3: 95,402,659 (GRCm39) |
N777K |
probably damaging |
Het |
Atp4b |
A |
T |
8: 13,436,732 (GRCm39) |
M260K |
probably benign |
Het |
Bcl2l15 |
A |
T |
3: 103,740,729 (GRCm39) |
D65V |
probably damaging |
Het |
Bicdl1 |
G |
T |
5: 115,801,845 (GRCm39) |
S340* |
probably null |
Het |
Ccdc15 |
T |
C |
9: 37,226,574 (GRCm39) |
R467G |
probably benign |
Het |
Ccdc68 |
T |
A |
18: 70,102,084 (GRCm39) |
M327K |
possibly damaging |
Het |
Ccdc83 |
T |
C |
7: 89,873,138 (GRCm39) |
T406A |
probably benign |
Het |
Ccnf |
A |
T |
17: 24,468,232 (GRCm39) |
V55D |
probably damaging |
Het |
Cdcp3 |
C |
A |
7: 130,830,562 (GRCm39) |
P332Q |
probably damaging |
Het |
Cldn12 |
A |
G |
5: 5,558,008 (GRCm39) |
F140L |
probably benign |
Het |
Copb1 |
A |
C |
7: 113,844,720 (GRCm39) |
I213S |
possibly damaging |
Het |
Cps1 |
G |
A |
1: 67,179,016 (GRCm39) |
G76D |
probably damaging |
Het |
Ctrc |
A |
G |
4: 141,567,627 (GRCm39) |
W159R |
probably damaging |
Het |
Cul4a |
C |
T |
8: 13,190,279 (GRCm39) |
T572M |
possibly damaging |
Het |
Cyp2c40 |
A |
T |
19: 39,796,050 (GRCm39) |
Y109* |
probably null |
Het |
Dcc |
A |
G |
18: 71,553,317 (GRCm39) |
Y780H |
probably benign |
Het |
Dctn1 |
C |
T |
6: 83,166,887 (GRCm39) |
A283V |
possibly damaging |
Het |
Dio1 |
T |
C |
4: 107,154,874 (GRCm39) |
D134G |
probably benign |
Het |
Dlg5 |
A |
T |
14: 24,198,390 (GRCm39) |
D1514E |
probably benign |
Het |
Dlg5 |
A |
T |
14: 24,227,907 (GRCm39) |
L338Q |
probably damaging |
Het |
Dlgap2 |
A |
T |
8: 14,879,952 (GRCm39) |
K767N |
probably damaging |
Het |
Dst |
A |
T |
1: 34,313,270 (GRCm39) |
I4346F |
probably benign |
Het |
Dzip1l |
T |
C |
9: 99,543,065 (GRCm39) |
F507L |
probably benign |
Het |
Erich2 |
A |
T |
2: 70,362,109 (GRCm39) |
D300V |
probably damaging |
Het |
Fam114a2 |
C |
T |
11: 57,404,515 (GRCm39) |
G83D |
probably damaging |
Het |
Fam131a |
C |
T |
16: 20,520,444 (GRCm39) |
A299V |
probably benign |
Het |
Fbln2 |
A |
G |
6: 91,247,143 (GRCm39) |
|
probably null |
Het |
Fbn2 |
T |
C |
18: 58,204,912 (GRCm39) |
D1177G |
possibly damaging |
Het |
Fbxl6 |
T |
C |
15: 76,422,113 (GRCm39) |
|
probably null |
Het |
Frem3 |
A |
T |
8: 81,339,965 (GRCm39) |
I753F |
probably damaging |
Het |
Gfra1 |
A |
G |
19: 58,288,744 (GRCm39) |
S234P |
probably damaging |
Het |
Hdgfl3 |
T |
C |
7: 81,550,106 (GRCm39) |
N76S |
probably benign |
Het |
Herc6 |
A |
G |
6: 57,558,089 (GRCm39) |
E23G |
probably benign |
Het |
Hid1 |
T |
A |
11: 115,245,545 (GRCm39) |
H420L |
probably damaging |
Het |
Igsf21 |
G |
A |
4: 139,755,049 (GRCm39) |
T440I |
probably benign |
Het |
Ikzf4 |
T |
A |
10: 128,468,451 (GRCm39) |
H676L |
unknown |
Het |
Il18r1 |
A |
G |
1: 40,520,140 (GRCm39) |
E177G |
probably benign |
Het |
Iqch |
A |
G |
9: 63,415,599 (GRCm39) |
Y558H |
possibly damaging |
Het |
Kif11 |
A |
T |
19: 37,399,072 (GRCm39) |
N752I |
possibly damaging |
Het |
Kntc1 |
T |
A |
5: 123,925,019 (GRCm39) |
C1111S |
possibly damaging |
Het |
Krtap9-5 |
A |
G |
11: 99,839,800 (GRCm39) |
K167R |
unknown |
Het |
Lgalsl2 |
C |
T |
7: 5,362,440 (GRCm39) |
R24C |
probably benign |
Het |
Lipe |
G |
T |
7: 25,080,036 (GRCm39) |
T704K |
probably benign |
Het |
Lrrc32 |
A |
T |
7: 98,147,414 (GRCm39) |
I65F |
possibly damaging |
Het |
Mogs |
C |
T |
6: 83,093,188 (GRCm39) |
H179Y |
probably damaging |
Het |
Mtnr1b |
A |
T |
9: 15,774,590 (GRCm39) |
Y156* |
probably null |
Het |
Mtus1 |
T |
C |
8: 41,537,590 (GRCm39) |
H42R |
probably benign |
Het |
Mx2 |
T |
A |
16: 97,346,918 (GRCm39) |
D128E |
probably benign |
Het |
Myof |
A |
T |
19: 37,939,939 (GRCm39) |
L829* |
probably null |
Het |
Naip6 |
T |
C |
13: 100,420,359 (GRCm39) |
K1304E |
probably benign |
Het |
Neo1 |
A |
C |
9: 58,791,826 (GRCm39) |
S1307R |
probably benign |
Het |
Nipbl |
A |
T |
15: 8,359,779 (GRCm39) |
D1475E |
probably benign |
Het |
Nlrp9b |
T |
A |
7: 19,757,875 (GRCm39) |
F371I |
probably damaging |
Het |
Nrip1 |
A |
T |
16: 76,088,338 (GRCm39) |
M1073K |
probably damaging |
Het |
Obox6 |
T |
C |
7: 15,567,863 (GRCm39) |
N195D |
probably damaging |
Het |
Or13a18 |
T |
A |
7: 140,190,091 (GRCm39) |
I4K |
probably benign |
Het |
Or1j18 |
T |
A |
2: 36,624,650 (GRCm39) |
F106I |
probably benign |
Het |
Or5ac24 |
A |
T |
16: 59,165,687 (GRCm39) |
C126S |
probably damaging |
Het |
Or5b99 |
C |
T |
19: 12,976,922 (GRCm39) |
H191Y |
probably benign |
Het |
Or5p64 |
C |
A |
7: 107,855,045 (GRCm39) |
C100F |
probably damaging |
Het |
Pax7 |
T |
C |
4: 139,511,880 (GRCm39) |
K232E |
probably benign |
Het |
Phldb3 |
C |
T |
7: 24,310,689 (GRCm39) |
|
probably benign |
Het |
Pkd1l1 |
C |
A |
11: 8,915,148 (GRCm39) |
V131L |
|
Het |
Ppp2r5a |
A |
G |
1: 191,128,532 (GRCm39) |
S28P |
probably benign |
Het |
Prl8a1 |
A |
G |
13: 27,758,068 (GRCm39) |
S214P |
probably damaging |
Het |
Prmt2 |
A |
T |
10: 76,056,838 (GRCm39) |
C228* |
probably null |
Het |
Prpf8 |
C |
T |
11: 75,399,738 (GRCm39) |
R2266* |
probably null |
Het |
Rabl6 |
A |
G |
2: 25,474,153 (GRCm39) |
S648P |
unknown |
Het |
Ralgapa1 |
T |
C |
12: 55,759,457 (GRCm39) |
K1022R |
probably damaging |
Het |
Ralgapb |
T |
A |
2: 158,285,275 (GRCm39) |
D591E |
probably benign |
Het |
Rprd1a |
A |
G |
18: 24,639,889 (GRCm39) |
|
probably null |
Het |
Rsu1 |
T |
C |
2: 13,221,686 (GRCm39) |
R165G |
probably damaging |
Het |
Samd8 |
A |
G |
14: 21,842,491 (GRCm39) |
E334G |
probably benign |
Het |
Scn9a |
T |
A |
2: 66,364,561 (GRCm39) |
Q804L |
probably damaging |
Het |
Sez6 |
A |
G |
11: 77,864,711 (GRCm39) |
D557G |
probably benign |
Het |
Sgsm1 |
A |
T |
5: 113,427,501 (GRCm39) |
|
probably null |
Het |
Slc17a3 |
T |
A |
13: 24,039,832 (GRCm39) |
M290K |
|
Het |
Snd1 |
T |
A |
6: 28,531,449 (GRCm39) |
V330E |
probably benign |
Het |
Tceanc2 |
T |
C |
4: 107,022,852 (GRCm39) |
K45R |
probably damaging |
Het |
Tg |
A |
T |
15: 66,568,437 (GRCm39) |
I1375F |
probably benign |
Het |
Tmem116 |
T |
A |
5: 121,633,124 (GRCm39) |
I357K |
|
Het |
Tmem39a |
G |
T |
16: 38,408,658 (GRCm39) |
R407L |
possibly damaging |
Het |
Tmem74 |
A |
T |
15: 43,730,761 (GRCm39) |
M94K |
probably benign |
Het |
Tpp1 |
C |
T |
7: 105,398,751 (GRCm39) |
C226Y |
probably damaging |
Het |
Trbv21 |
T |
C |
6: 41,179,861 (GRCm39) |
I59T |
not run |
Het |
Trim11 |
A |
G |
11: 58,869,463 (GRCm39) |
D133G |
probably benign |
Het |
Uaca |
G |
A |
9: 60,753,282 (GRCm39) |
V76I |
probably damaging |
Het |
Ugt2a3 |
A |
G |
5: 87,475,539 (GRCm39) |
|
probably null |
Het |
Vmn2r104 |
G |
T |
17: 20,249,737 (GRCm39) |
H845N |
probably benign |
Het |
Wdr24 |
T |
C |
17: 26,045,101 (GRCm39) |
Y279H |
probably damaging |
Het |
Zbtb46 |
A |
G |
2: 181,065,512 (GRCm39) |
S213P |
probably benign |
Het |
Zdhhc13 |
C |
A |
7: 48,461,103 (GRCm39) |
Y346* |
probably null |
Het |
Zfp280b |
A |
T |
10: 75,875,075 (GRCm39) |
H318L |
probably damaging |
Het |
|
Other mutations in Gtse1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00990:Gtse1
|
APN |
15 |
85,753,018 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL01344:Gtse1
|
APN |
15 |
85,746,267 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01541:Gtse1
|
APN |
15 |
85,759,855 (GRCm39) |
nonsense |
probably null |
|
IGL01621:Gtse1
|
APN |
15 |
85,759,283 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01945:Gtse1
|
APN |
15 |
85,755,748 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02193:Gtse1
|
APN |
15 |
85,746,531 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02215:Gtse1
|
APN |
15 |
85,746,799 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02494:Gtse1
|
APN |
15 |
85,751,704 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02879:Gtse1
|
APN |
15 |
85,753,264 (GRCm39) |
splice site |
probably benign |
|
R0009:Gtse1
|
UTSW |
15 |
85,746,636 (GRCm39) |
missense |
probably benign |
0.06 |
R0047:Gtse1
|
UTSW |
15 |
85,746,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R0047:Gtse1
|
UTSW |
15 |
85,746,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R0576:Gtse1
|
UTSW |
15 |
85,753,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R1078:Gtse1
|
UTSW |
15 |
85,746,508 (GRCm39) |
missense |
probably damaging |
0.98 |
R1442:Gtse1
|
UTSW |
15 |
85,744,303 (GRCm39) |
splice site |
probably benign |
|
R1623:Gtse1
|
UTSW |
15 |
85,751,779 (GRCm39) |
missense |
probably benign |
|
R1925:Gtse1
|
UTSW |
15 |
85,757,939 (GRCm39) |
missense |
probably benign |
0.00 |
R1928:Gtse1
|
UTSW |
15 |
85,746,264 (GRCm39) |
splice site |
probably benign |
|
R4565:Gtse1
|
UTSW |
15 |
85,759,385 (GRCm39) |
missense |
probably damaging |
0.99 |
R5170:Gtse1
|
UTSW |
15 |
85,748,465 (GRCm39) |
critical splice donor site |
probably null |
|
R5310:Gtse1
|
UTSW |
15 |
85,757,993 (GRCm39) |
missense |
probably benign |
0.04 |
R5428:Gtse1
|
UTSW |
15 |
85,746,340 (GRCm39) |
missense |
probably benign |
0.12 |
R5748:Gtse1
|
UTSW |
15 |
85,751,778 (GRCm39) |
missense |
probably benign |
|
R5996:Gtse1
|
UTSW |
15 |
85,748,381 (GRCm39) |
missense |
probably benign |
0.00 |
R6179:Gtse1
|
UTSW |
15 |
85,753,158 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6379:Gtse1
|
UTSW |
15 |
85,748,425 (GRCm39) |
missense |
probably benign |
0.01 |
R6381:Gtse1
|
UTSW |
15 |
85,746,349 (GRCm39) |
missense |
probably benign |
0.00 |
R6434:Gtse1
|
UTSW |
15 |
85,759,370 (GRCm39) |
missense |
probably benign |
0.21 |
R7086:Gtse1
|
UTSW |
15 |
85,759,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R7304:Gtse1
|
UTSW |
15 |
85,755,748 (GRCm39) |
missense |
probably benign |
0.00 |
R7580:Gtse1
|
UTSW |
15 |
85,746,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R7856:Gtse1
|
UTSW |
15 |
85,748,342 (GRCm39) |
missense |
probably benign |
0.09 |
R8496:Gtse1
|
UTSW |
15 |
85,746,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R8674:Gtse1
|
UTSW |
15 |
85,746,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R8987:Gtse1
|
UTSW |
15 |
85,753,109 (GRCm39) |
missense |
probably benign |
0.00 |
R9491:Gtse1
|
UTSW |
15 |
85,755,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R9642:Gtse1
|
UTSW |
15 |
85,751,697 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Gtse1
|
UTSW |
15 |
85,752,947 (GRCm39) |
missense |
possibly damaging |
0.85 |
Z1177:Gtse1
|
UTSW |
15 |
85,759,938 (GRCm39) |
missense |
probably damaging |
0.96 |
|