Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap11 |
T |
A |
14: 78,747,477 (GRCm39) |
I1637L |
possibly damaging |
Het |
Ankrd27 |
T |
C |
7: 35,315,265 (GRCm39) |
|
probably benign |
Het |
Anxa3 |
T |
C |
5: 96,978,349 (GRCm39) |
|
probably null |
Het |
Arfgef2 |
G |
C |
2: 166,707,679 (GRCm39) |
G1025A |
probably benign |
Het |
Arhgap21 |
T |
C |
2: 20,868,037 (GRCm39) |
I829V |
possibly damaging |
Het |
Arhgap42 |
T |
C |
9: 9,035,512 (GRCm39) |
M277V |
probably benign |
Het |
Cep112 |
A |
T |
11: 108,746,671 (GRCm39) |
R176S |
probably damaging |
Het |
Chd9 |
C |
T |
8: 91,760,615 (GRCm39) |
P2120L |
probably benign |
Het |
Cnga1 |
C |
T |
5: 72,776,404 (GRCm39) |
V20I |
possibly damaging |
Het |
Cpped1 |
A |
C |
16: 11,712,745 (GRCm39) |
|
probably null |
Het |
Cr2 |
T |
C |
1: 194,839,676 (GRCm39) |
R960G |
possibly damaging |
Het |
Dbf4 |
T |
C |
5: 8,471,333 (GRCm39) |
N36S |
possibly damaging |
Het |
Dnah6 |
G |
A |
6: 73,090,564 (GRCm39) |
S2210L |
probably benign |
Het |
Dnajb12 |
C |
T |
10: 59,728,799 (GRCm39) |
T229I |
probably benign |
Het |
Dnajc28 |
G |
A |
16: 91,413,755 (GRCm39) |
T187M |
probably damaging |
Het |
Epb41l2 |
T |
C |
10: 25,364,842 (GRCm39) |
|
probably benign |
Het |
Fam178b |
A |
G |
1: 36,671,539 (GRCm39) |
L194P |
probably damaging |
Het |
Fam50b |
C |
T |
13: 34,930,823 (GRCm39) |
Q100* |
probably null |
Het |
Gimap9 |
A |
G |
6: 48,654,812 (GRCm39) |
H133R |
probably benign |
Het |
Gpbp1 |
A |
T |
13: 111,603,512 (GRCm39) |
|
probably null |
Het |
Gpr89 |
A |
G |
3: 96,804,743 (GRCm39) |
Y38H |
probably damaging |
Het |
Gsdmc3 |
T |
A |
15: 63,732,105 (GRCm39) |
Y307F |
probably benign |
Het |
H4c16 |
T |
A |
6: 136,781,299 (GRCm39) |
I27F |
probably damaging |
Het |
Hip1 |
C |
T |
5: 135,485,900 (GRCm39) |
R101K |
probably damaging |
Het |
Hsf4 |
G |
A |
8: 105,996,628 (GRCm39) |
D18N |
probably null |
Het |
Igfn1 |
T |
C |
1: 135,892,479 (GRCm39) |
K2214E |
probably damaging |
Het |
Itgal |
A |
T |
7: 126,927,919 (GRCm39) |
E1038V |
probably null |
Het |
Kank2 |
C |
A |
9: 21,681,080 (GRCm39) |
M816I |
probably damaging |
Het |
Kctd15 |
T |
C |
7: 34,344,366 (GRCm39) |
D95G |
possibly damaging |
Het |
Kif1a |
A |
T |
1: 92,996,199 (GRCm39) |
|
probably benign |
Het |
Lgi4 |
T |
G |
7: 30,760,037 (GRCm39) |
L78V |
probably damaging |
Het |
Lrrc7 |
A |
G |
3: 157,885,429 (GRCm39) |
F432L |
probably damaging |
Het |
Madd |
A |
T |
2: 90,974,028 (GRCm39) |
C1419S |
possibly damaging |
Het |
Nisch |
T |
C |
14: 30,898,803 (GRCm39) |
|
probably benign |
Het |
Or2h1b |
A |
T |
17: 37,462,145 (GRCm39) |
C239* |
probably null |
Het |
Osbpl2 |
G |
A |
2: 179,790,319 (GRCm39) |
G198S |
possibly damaging |
Het |
Pclo |
T |
A |
5: 14,764,287 (GRCm39) |
D4253E |
unknown |
Het |
Phactr1 |
A |
T |
13: 43,231,265 (GRCm39) |
S244C |
possibly damaging |
Het |
Pja2 |
T |
C |
17: 64,599,865 (GRCm39) |
S478G |
probably damaging |
Het |
Prex1 |
A |
T |
2: 166,419,875 (GRCm39) |
I79N |
probably benign |
Het |
Ptpn4 |
T |
C |
1: 119,612,321 (GRCm39) |
D24G |
probably damaging |
Het |
Rars2 |
T |
C |
4: 34,656,835 (GRCm39) |
S495P |
probably damaging |
Het |
Rhebl1 |
A |
T |
15: 98,776,167 (GRCm39) |
D162E |
probably benign |
Het |
Rhou |
T |
C |
8: 124,382,258 (GRCm39) |
V100A |
probably damaging |
Het |
Rpn2 |
A |
G |
2: 157,152,208 (GRCm39) |
T394A |
possibly damaging |
Het |
Ryr3 |
A |
T |
2: 112,479,664 (GRCm39) |
M4386K |
possibly damaging |
Het |
Scmh1 |
G |
T |
4: 120,340,869 (GRCm39) |
C185F |
probably damaging |
Het |
Sema3d |
A |
T |
5: 12,592,549 (GRCm39) |
Q326L |
possibly damaging |
Het |
Sis |
T |
A |
3: 72,821,934 (GRCm39) |
K1376* |
probably null |
Het |
Slc25a29 |
T |
C |
12: 108,792,852 (GRCm39) |
E242G |
probably benign |
Het |
Slc26a5 |
A |
G |
5: 22,028,545 (GRCm39) |
V304A |
probably benign |
Het |
Slc39a7 |
C |
T |
17: 34,250,241 (GRCm39) |
|
probably benign |
Het |
Slco1a4 |
A |
G |
6: 141,761,308 (GRCm39) |
V435A |
possibly damaging |
Het |
Syne2 |
A |
G |
12: 75,974,240 (GRCm39) |
E1146G |
possibly damaging |
Het |
Tgm5 |
T |
A |
2: 120,879,304 (GRCm39) |
|
probably benign |
Het |
Tgm7 |
A |
G |
2: 120,929,045 (GRCm39) |
S284P |
probably damaging |
Het |
Tmem132d |
G |
A |
5: 127,872,987 (GRCm39) |
R541W |
probably damaging |
Het |
Tmem170 |
C |
A |
8: 112,596,349 (GRCm39) |
V59L |
probably benign |
Het |
Tpbgl |
G |
T |
7: 99,275,233 (GRCm39) |
A208E |
possibly damaging |
Het |
Ulk1 |
T |
C |
5: 110,936,028 (GRCm39) |
E827G |
probably benign |
Het |
Vps13a |
A |
G |
19: 16,687,790 (GRCm39) |
V886A |
possibly damaging |
Het |
Wrn |
A |
T |
8: 33,814,584 (GRCm39) |
C44S |
probably benign |
Het |
Zscan22 |
T |
A |
7: 12,640,750 (GRCm39) |
C331* |
probably null |
Het |
|
Other mutations in Ttc23l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01143:Ttc23l
|
APN |
15 |
10,530,775 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01319:Ttc23l
|
APN |
15 |
10,509,492 (GRCm39) |
splice site |
probably benign |
|
IGL01562:Ttc23l
|
APN |
15 |
10,551,476 (GRCm39) |
splice site |
probably benign |
|
IGL01969:Ttc23l
|
APN |
15 |
10,551,520 (GRCm39) |
nonsense |
probably null |
|
IGL03172:Ttc23l
|
APN |
15 |
10,537,652 (GRCm39) |
missense |
probably benign |
0.06 |
R0042:Ttc23l
|
UTSW |
15 |
10,551,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R0042:Ttc23l
|
UTSW |
15 |
10,551,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R0335:Ttc23l
|
UTSW |
15 |
10,540,049 (GRCm39) |
missense |
probably benign |
0.26 |
R0554:Ttc23l
|
UTSW |
15 |
10,530,743 (GRCm39) |
missense |
probably benign |
0.12 |
R0609:Ttc23l
|
UTSW |
15 |
10,504,622 (GRCm39) |
missense |
probably benign |
|
R0631:Ttc23l
|
UTSW |
15 |
10,540,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R1703:Ttc23l
|
UTSW |
15 |
10,523,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R2106:Ttc23l
|
UTSW |
15 |
10,547,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R2220:Ttc23l
|
UTSW |
15 |
10,537,652 (GRCm39) |
missense |
probably benign |
0.06 |
R2277:Ttc23l
|
UTSW |
15 |
10,523,678 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2278:Ttc23l
|
UTSW |
15 |
10,523,678 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2279:Ttc23l
|
UTSW |
15 |
10,523,678 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2368:Ttc23l
|
UTSW |
15 |
10,537,652 (GRCm39) |
missense |
probably benign |
0.06 |
R2368:Ttc23l
|
UTSW |
15 |
10,537,648 (GRCm39) |
small insertion |
probably benign |
|
R2420:Ttc23l
|
UTSW |
15 |
10,537,652 (GRCm39) |
missense |
probably benign |
0.06 |
R2420:Ttc23l
|
UTSW |
15 |
10,537,648 (GRCm39) |
small insertion |
probably benign |
|
R2421:Ttc23l
|
UTSW |
15 |
10,537,652 (GRCm39) |
missense |
probably benign |
0.06 |
R2422:Ttc23l
|
UTSW |
15 |
10,537,652 (GRCm39) |
missense |
probably benign |
0.06 |
R2422:Ttc23l
|
UTSW |
15 |
10,537,648 (GRCm39) |
small insertion |
probably benign |
|
R2830:Ttc23l
|
UTSW |
15 |
10,537,648 (GRCm39) |
small insertion |
probably benign |
|
R2831:Ttc23l
|
UTSW |
15 |
10,537,652 (GRCm39) |
missense |
probably benign |
0.06 |
R2831:Ttc23l
|
UTSW |
15 |
10,537,648 (GRCm39) |
small insertion |
probably benign |
|
R2979:Ttc23l
|
UTSW |
15 |
10,537,652 (GRCm39) |
missense |
probably benign |
0.06 |
R2980:Ttc23l
|
UTSW |
15 |
10,537,652 (GRCm39) |
missense |
probably benign |
0.06 |
R2980:Ttc23l
|
UTSW |
15 |
10,537,648 (GRCm39) |
small insertion |
probably benign |
|
R2981:Ttc23l
|
UTSW |
15 |
10,537,652 (GRCm39) |
missense |
probably benign |
0.06 |
R2981:Ttc23l
|
UTSW |
15 |
10,537,648 (GRCm39) |
small insertion |
probably benign |
|
R2982:Ttc23l
|
UTSW |
15 |
10,537,652 (GRCm39) |
missense |
probably benign |
0.06 |
R2982:Ttc23l
|
UTSW |
15 |
10,537,648 (GRCm39) |
small insertion |
probably benign |
|
R2983:Ttc23l
|
UTSW |
15 |
10,537,648 (GRCm39) |
small insertion |
probably benign |
|
R2983:Ttc23l
|
UTSW |
15 |
10,537,652 (GRCm39) |
missense |
probably benign |
0.06 |
R3176:Ttc23l
|
UTSW |
15 |
10,547,318 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3177:Ttc23l
|
UTSW |
15 |
10,547,318 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3276:Ttc23l
|
UTSW |
15 |
10,547,318 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3277:Ttc23l
|
UTSW |
15 |
10,547,318 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3722:Ttc23l
|
UTSW |
15 |
10,537,648 (GRCm39) |
small insertion |
probably benign |
|
R3722:Ttc23l
|
UTSW |
15 |
10,537,652 (GRCm39) |
missense |
probably benign |
0.06 |
R3743:Ttc23l
|
UTSW |
15 |
10,537,648 (GRCm39) |
small insertion |
probably benign |
|
R3743:Ttc23l
|
UTSW |
15 |
10,537,652 (GRCm39) |
missense |
probably benign |
0.06 |
R3767:Ttc23l
|
UTSW |
15 |
10,530,781 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3921:Ttc23l
|
UTSW |
15 |
10,537,652 (GRCm39) |
missense |
probably benign |
0.06 |
R3921:Ttc23l
|
UTSW |
15 |
10,537,648 (GRCm39) |
small insertion |
probably benign |
|
R3921:Ttc23l
|
UTSW |
15 |
10,537,649 (GRCm39) |
small insertion |
probably benign |
|
R4091:Ttc23l
|
UTSW |
15 |
10,537,652 (GRCm39) |
missense |
probably benign |
0.06 |
R4091:Ttc23l
|
UTSW |
15 |
10,537,648 (GRCm39) |
small insertion |
probably benign |
|
R4119:Ttc23l
|
UTSW |
15 |
10,540,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R4120:Ttc23l
|
UTSW |
15 |
10,540,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R4373:Ttc23l
|
UTSW |
15 |
10,537,652 (GRCm39) |
missense |
probably benign |
0.06 |
R4373:Ttc23l
|
UTSW |
15 |
10,537,648 (GRCm39) |
small insertion |
probably benign |
|
R4375:Ttc23l
|
UTSW |
15 |
10,537,652 (GRCm39) |
missense |
probably benign |
0.06 |
R4375:Ttc23l
|
UTSW |
15 |
10,537,648 (GRCm39) |
small insertion |
probably benign |
|
R4376:Ttc23l
|
UTSW |
15 |
10,537,652 (GRCm39) |
missense |
probably benign |
0.06 |
R4376:Ttc23l
|
UTSW |
15 |
10,537,648 (GRCm39) |
small insertion |
probably benign |
|
R4377:Ttc23l
|
UTSW |
15 |
10,537,648 (GRCm39) |
small insertion |
probably benign |
|
R4377:Ttc23l
|
UTSW |
15 |
10,537,652 (GRCm39) |
missense |
probably benign |
0.06 |
R5002:Ttc23l
|
UTSW |
15 |
10,551,636 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5106:Ttc23l
|
UTSW |
15 |
10,551,636 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5107:Ttc23l
|
UTSW |
15 |
10,551,636 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5109:Ttc23l
|
UTSW |
15 |
10,551,636 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5156:Ttc23l
|
UTSW |
15 |
10,551,636 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5157:Ttc23l
|
UTSW |
15 |
10,551,636 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5160:Ttc23l
|
UTSW |
15 |
10,551,636 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5161:Ttc23l
|
UTSW |
15 |
10,551,636 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5259:Ttc23l
|
UTSW |
15 |
10,515,236 (GRCm39) |
missense |
probably damaging |
0.99 |
R5307:Ttc23l
|
UTSW |
15 |
10,533,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R5728:Ttc23l
|
UTSW |
15 |
10,551,636 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5756:Ttc23l
|
UTSW |
15 |
10,551,636 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5772:Ttc23l
|
UTSW |
15 |
10,551,555 (GRCm39) |
missense |
probably benign |
0.01 |
R5793:Ttc23l
|
UTSW |
15 |
10,551,636 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5794:Ttc23l
|
UTSW |
15 |
10,551,636 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5847:Ttc23l
|
UTSW |
15 |
10,537,682 (GRCm39) |
missense |
probably benign |
0.07 |
R6976:Ttc23l
|
UTSW |
15 |
10,537,666 (GRCm39) |
nonsense |
probably null |
|
R7010:Ttc23l
|
UTSW |
15 |
10,515,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R7342:Ttc23l
|
UTSW |
15 |
10,551,583 (GRCm39) |
missense |
probably benign |
0.01 |
R7404:Ttc23l
|
UTSW |
15 |
10,551,663 (GRCm39) |
missense |
probably damaging |
0.98 |
R7453:Ttc23l
|
UTSW |
15 |
10,533,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R7584:Ttc23l
|
UTSW |
15 |
10,533,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R7599:Ttc23l
|
UTSW |
15 |
10,533,766 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8710:Ttc23l
|
UTSW |
15 |
10,540,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R8927:Ttc23l
|
UTSW |
15 |
10,530,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R8928:Ttc23l
|
UTSW |
15 |
10,530,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R9101:Ttc23l
|
UTSW |
15 |
10,537,661 (GRCm39) |
missense |
probably benign |
0.16 |
R9746:Ttc23l
|
UTSW |
15 |
10,523,729 (GRCm39) |
missense |
probably benign |
0.01 |
R9782:Ttc23l
|
UTSW |
15 |
10,530,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R9792:Ttc23l
|
UTSW |
15 |
10,537,731 (GRCm39) |
missense |
probably benign |
|
R9793:Ttc23l
|
UTSW |
15 |
10,537,731 (GRCm39) |
missense |
probably benign |
|
R9795:Ttc23l
|
UTSW |
15 |
10,537,731 (GRCm39) |
missense |
probably benign |
|
Z1088:Ttc23l
|
UTSW |
15 |
10,533,753 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ttc23l
|
UTSW |
15 |
10,533,719 (GRCm39) |
missense |
probably damaging |
1.00 |
|