Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9830107B12Rik |
T |
C |
17: 48,452,605 (GRCm39) |
I111M |
probably damaging |
Het |
Arid2 |
A |
G |
15: 96,259,715 (GRCm39) |
I292V |
probably damaging |
Het |
Atl3 |
T |
C |
19: 7,509,408 (GRCm39) |
S379P |
probably benign |
Het |
Btbd16 |
C |
T |
7: 130,417,516 (GRCm39) |
R344C |
probably damaging |
Het |
Ccnt1 |
G |
A |
15: 98,441,688 (GRCm39) |
H527Y |
probably damaging |
Het |
Ces1d |
T |
A |
8: 93,912,707 (GRCm39) |
I244F |
probably damaging |
Het |
Clec16a |
C |
A |
16: 10,428,964 (GRCm39) |
S449R |
probably damaging |
Het |
Cngb3 |
T |
A |
4: 19,375,190 (GRCm39) |
|
probably benign |
Het |
Col15a1 |
G |
C |
4: 47,288,200 (GRCm39) |
|
probably benign |
Het |
Cubn |
A |
T |
2: 13,337,276 (GRCm39) |
|
probably benign |
Het |
Dsp |
C |
A |
13: 38,377,337 (GRCm39) |
S1707R |
probably benign |
Het |
E330034G19Rik |
A |
T |
14: 24,347,004 (GRCm39) |
Q162L |
possibly damaging |
Het |
F830045P16Rik |
T |
C |
2: 129,316,502 (GRCm39) |
N69S |
probably benign |
Het |
Galnt10 |
C |
T |
11: 57,612,146 (GRCm39) |
T62I |
probably benign |
Het |
Gm19668 |
T |
C |
10: 77,634,960 (GRCm39) |
D3G |
unknown |
Het |
Hace1 |
T |
A |
10: 45,562,764 (GRCm39) |
F760I |
probably damaging |
Het |
Il20rb |
A |
G |
9: 100,356,936 (GRCm39) |
Y65H |
probably damaging |
Het |
Insl5 |
C |
A |
4: 102,883,841 (GRCm39) |
V27L |
probably benign |
Het |
Jade2 |
T |
C |
11: 51,715,930 (GRCm39) |
D425G |
probably benign |
Het |
Lipg |
T |
C |
18: 75,087,272 (GRCm39) |
K183R |
probably benign |
Het |
Lrrc59 |
T |
A |
11: 94,525,456 (GRCm39) |
L84Q |
probably damaging |
Het |
Lyst |
T |
A |
13: 13,835,750 (GRCm39) |
F1811I |
probably damaging |
Het |
Mcf2l |
A |
G |
8: 13,062,883 (GRCm39) |
|
probably benign |
Het |
Nfil3 |
A |
G |
13: 53,121,792 (GRCm39) |
S371P |
probably benign |
Het |
Nin |
A |
G |
12: 70,137,349 (GRCm39) |
S76P |
|
Het |
Nuak1 |
C |
T |
10: 84,213,951 (GRCm39) |
|
probably null |
Het |
Or8b47 |
A |
T |
9: 38,427,917 (GRCm39) |
|
probably benign |
Het |
Or8g19 |
A |
T |
9: 39,055,722 (GRCm39) |
I109F |
possibly damaging |
Het |
Pld1 |
A |
G |
3: 28,132,643 (GRCm39) |
|
probably benign |
Het |
Rcvrn |
T |
C |
11: 67,590,890 (GRCm39) |
F158S |
possibly damaging |
Het |
Skap2 |
T |
C |
6: 51,885,409 (GRCm39) |
T200A |
probably benign |
Het |
Slc6a1 |
G |
T |
6: 114,292,503 (GRCm39) |
|
probably benign |
Het |
Stxbp1 |
A |
G |
2: 32,688,157 (GRCm39) |
S503P |
probably damaging |
Het |
Susd5 |
A |
T |
9: 113,924,879 (GRCm39) |
E254V |
possibly damaging |
Het |
Sv2a |
T |
C |
3: 96,097,983 (GRCm39) |
S529P |
possibly damaging |
Het |
Tigd2 |
T |
A |
6: 59,188,310 (GRCm39) |
N392K |
probably benign |
Het |
Tmem131l |
A |
G |
3: 83,842,220 (GRCm39) |
L525P |
probably benign |
Het |
Tonsl |
T |
C |
15: 76,514,824 (GRCm39) |
M1127V |
probably damaging |
Het |
Top2a |
T |
A |
11: 98,900,705 (GRCm39) |
E585V |
probably benign |
Het |
Usp19 |
T |
G |
9: 108,375,398 (GRCm39) |
L847R |
probably damaging |
Het |
Vta1 |
T |
C |
10: 14,551,776 (GRCm39) |
H141R |
possibly damaging |
Het |
Zfp950 |
G |
T |
19: 61,108,778 (GRCm39) |
P102T |
probably benign |
Het |
Zzz3 |
T |
C |
3: 152,163,908 (GRCm39) |
I869T |
probably benign |
Het |
|
Other mutations in Spag17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01096:Spag17
|
APN |
3 |
99,970,691 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01143:Spag17
|
APN |
3 |
99,846,614 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01329:Spag17
|
APN |
3 |
100,002,865 (GRCm39) |
missense |
probably benign |
0.16 |
IGL01393:Spag17
|
APN |
3 |
99,934,926 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01617:Spag17
|
APN |
3 |
100,016,824 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL01705:Spag17
|
APN |
3 |
99,930,046 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01928:Spag17
|
APN |
3 |
99,847,390 (GRCm39) |
splice site |
probably benign |
|
IGL01981:Spag17
|
APN |
3 |
99,966,149 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02435:Spag17
|
APN |
3 |
99,889,760 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02452:Spag17
|
APN |
3 |
99,934,707 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02465:Spag17
|
APN |
3 |
99,983,187 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02615:Spag17
|
APN |
3 |
99,979,401 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02751:Spag17
|
APN |
3 |
99,918,110 (GRCm39) |
nonsense |
probably null |
|
IGL02803:Spag17
|
APN |
3 |
100,016,713 (GRCm39) |
missense |
probably benign |
|
IGL02898:Spag17
|
APN |
3 |
100,008,702 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03037:Spag17
|
APN |
3 |
99,979,486 (GRCm39) |
splice site |
probably null |
|
IGL03068:Spag17
|
APN |
3 |
99,987,521 (GRCm39) |
missense |
probably benign |
0.35 |
IGL03131:Spag17
|
APN |
3 |
99,918,075 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03224:Spag17
|
APN |
3 |
99,918,156 (GRCm39) |
missense |
possibly damaging |
0.53 |
FR4342:Spag17
|
UTSW |
3 |
99,963,568 (GRCm39) |
small insertion |
probably benign |
|
FR4342:Spag17
|
UTSW |
3 |
99,963,565 (GRCm39) |
small insertion |
probably benign |
|
FR4548:Spag17
|
UTSW |
3 |
99,963,570 (GRCm39) |
small insertion |
probably benign |
|
FR4589:Spag17
|
UTSW |
3 |
99,963,574 (GRCm39) |
small insertion |
probably benign |
|
FR4589:Spag17
|
UTSW |
3 |
99,963,561 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Spag17
|
UTSW |
3 |
99,963,573 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Spag17
|
UTSW |
3 |
99,963,571 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Spag17
|
UTSW |
3 |
99,963,570 (GRCm39) |
small insertion |
probably benign |
|
N/A:Spag17
|
UTSW |
3 |
99,889,570 (GRCm39) |
splice site |
probably benign |
|
PIT4504001:Spag17
|
UTSW |
3 |
100,010,426 (GRCm39) |
critical splice acceptor site |
probably null |
|
PIT4514001:Spag17
|
UTSW |
3 |
99,920,527 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0107:Spag17
|
UTSW |
3 |
99,958,103 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0230:Spag17
|
UTSW |
3 |
100,014,143 (GRCm39) |
missense |
probably benign |
0.08 |
R0243:Spag17
|
UTSW |
3 |
99,992,684 (GRCm39) |
missense |
probably benign |
0.04 |
R0321:Spag17
|
UTSW |
3 |
100,008,719 (GRCm39) |
missense |
probably damaging |
0.99 |
R0375:Spag17
|
UTSW |
3 |
99,934,906 (GRCm39) |
missense |
probably benign |
|
R0417:Spag17
|
UTSW |
3 |
99,972,870 (GRCm39) |
missense |
probably benign |
0.11 |
R0490:Spag17
|
UTSW |
3 |
99,889,727 (GRCm39) |
missense |
probably damaging |
0.97 |
R0537:Spag17
|
UTSW |
3 |
100,032,618 (GRCm39) |
missense |
probably damaging |
0.98 |
R0714:Spag17
|
UTSW |
3 |
99,987,472 (GRCm39) |
missense |
probably damaging |
0.97 |
R0844:Spag17
|
UTSW |
3 |
99,912,101 (GRCm39) |
missense |
probably benign |
|
R0919:Spag17
|
UTSW |
3 |
99,979,259 (GRCm39) |
splice site |
probably benign |
|
R0926:Spag17
|
UTSW |
3 |
99,979,432 (GRCm39) |
missense |
probably benign |
|
R1037:Spag17
|
UTSW |
3 |
100,010,433 (GRCm39) |
missense |
probably benign |
0.01 |
R1075:Spag17
|
UTSW |
3 |
100,000,992 (GRCm39) |
missense |
probably damaging |
0.99 |
R1109:Spag17
|
UTSW |
3 |
99,934,667 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1213:Spag17
|
UTSW |
3 |
100,002,954 (GRCm39) |
missense |
probably benign |
0.01 |
R1221:Spag17
|
UTSW |
3 |
99,889,584 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1576:Spag17
|
UTSW |
3 |
99,846,679 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1586:Spag17
|
UTSW |
3 |
99,929,068 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1768:Spag17
|
UTSW |
3 |
99,934,668 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1782:Spag17
|
UTSW |
3 |
99,918,070 (GRCm39) |
missense |
probably benign |
0.02 |
R1789:Spag17
|
UTSW |
3 |
99,846,672 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1945:Spag17
|
UTSW |
3 |
99,847,298 (GRCm39) |
missense |
probably benign |
|
R2065:Spag17
|
UTSW |
3 |
99,920,524 (GRCm39) |
missense |
probably benign |
0.03 |
R2118:Spag17
|
UTSW |
3 |
99,956,556 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2265:Spag17
|
UTSW |
3 |
99,969,182 (GRCm39) |
splice site |
probably null |
|
R2266:Spag17
|
UTSW |
3 |
99,969,182 (GRCm39) |
splice site |
probably null |
|
R2267:Spag17
|
UTSW |
3 |
99,969,182 (GRCm39) |
splice site |
probably null |
|
R2268:Spag17
|
UTSW |
3 |
99,969,182 (GRCm39) |
splice site |
probably null |
|
R2271:Spag17
|
UTSW |
3 |
100,014,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R2389:Spag17
|
UTSW |
3 |
100,014,153 (GRCm39) |
missense |
probably benign |
0.27 |
R2420:Spag17
|
UTSW |
3 |
99,934,935 (GRCm39) |
missense |
probably benign |
|
R2422:Spag17
|
UTSW |
3 |
99,934,935 (GRCm39) |
missense |
probably benign |
|
R2423:Spag17
|
UTSW |
3 |
100,010,772 (GRCm39) |
missense |
probably benign |
|
R3407:Spag17
|
UTSW |
3 |
99,992,615 (GRCm39) |
missense |
probably benign |
0.09 |
R3801:Spag17
|
UTSW |
3 |
99,961,169 (GRCm39) |
missense |
possibly damaging |
0.53 |
R3856:Spag17
|
UTSW |
3 |
100,014,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R4021:Spag17
|
UTSW |
3 |
99,956,546 (GRCm39) |
missense |
probably benign |
0.00 |
R4022:Spag17
|
UTSW |
3 |
99,956,546 (GRCm39) |
missense |
probably benign |
0.00 |
R4408:Spag17
|
UTSW |
3 |
100,010,694 (GRCm39) |
missense |
probably benign |
|
R4468:Spag17
|
UTSW |
3 |
99,992,682 (GRCm39) |
missense |
probably damaging |
0.98 |
R4540:Spag17
|
UTSW |
3 |
99,995,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R4621:Spag17
|
UTSW |
3 |
100,010,559 (GRCm39) |
missense |
probably benign |
0.08 |
R4622:Spag17
|
UTSW |
3 |
100,010,559 (GRCm39) |
missense |
probably benign |
0.08 |
R4756:Spag17
|
UTSW |
3 |
100,010,701 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4797:Spag17
|
UTSW |
3 |
99,891,795 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4855:Spag17
|
UTSW |
3 |
99,970,649 (GRCm39) |
missense |
probably benign |
0.02 |
R4887:Spag17
|
UTSW |
3 |
99,958,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R4962:Spag17
|
UTSW |
3 |
99,934,939 (GRCm39) |
missense |
probably benign |
|
R5030:Spag17
|
UTSW |
3 |
99,992,657 (GRCm39) |
nonsense |
probably null |
|
R5042:Spag17
|
UTSW |
3 |
99,979,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R5074:Spag17
|
UTSW |
3 |
99,987,434 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5195:Spag17
|
UTSW |
3 |
100,008,704 (GRCm39) |
missense |
probably benign |
0.16 |
R5200:Spag17
|
UTSW |
3 |
99,970,787 (GRCm39) |
nonsense |
probably null |
|
R5267:Spag17
|
UTSW |
3 |
99,969,264 (GRCm39) |
missense |
probably damaging |
0.98 |
R5360:Spag17
|
UTSW |
3 |
100,016,726 (GRCm39) |
missense |
probably benign |
0.00 |
R5444:Spag17
|
UTSW |
3 |
99,963,468 (GRCm39) |
missense |
probably benign |
0.06 |
R5498:Spag17
|
UTSW |
3 |
100,010,661 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5503:Spag17
|
UTSW |
3 |
99,934,560 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5540:Spag17
|
UTSW |
3 |
99,963,588 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5547:Spag17
|
UTSW |
3 |
99,963,468 (GRCm39) |
missense |
probably benign |
0.06 |
R5575:Spag17
|
UTSW |
3 |
99,961,138 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5629:Spag17
|
UTSW |
3 |
99,987,435 (GRCm39) |
missense |
probably benign |
0.33 |
R5639:Spag17
|
UTSW |
3 |
99,963,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R5842:Spag17
|
UTSW |
3 |
99,846,566 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5976:Spag17
|
UTSW |
3 |
100,003,107 (GRCm39) |
nonsense |
probably null |
|
R6082:Spag17
|
UTSW |
3 |
100,031,501 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6228:Spag17
|
UTSW |
3 |
99,929,918 (GRCm39) |
missense |
probably benign |
0.33 |
R6254:Spag17
|
UTSW |
3 |
99,972,901 (GRCm39) |
missense |
probably benign |
0.03 |
R6321:Spag17
|
UTSW |
3 |
99,995,743 (GRCm39) |
missense |
probably benign |
0.05 |
R6446:Spag17
|
UTSW |
3 |
100,010,448 (GRCm39) |
missense |
probably benign |
|
R6687:Spag17
|
UTSW |
3 |
100,000,266 (GRCm39) |
missense |
probably benign |
0.07 |
R6853:Spag17
|
UTSW |
3 |
99,920,551 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6946:Spag17
|
UTSW |
3 |
99,911,999 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6953:Spag17
|
UTSW |
3 |
99,942,291 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7038:Spag17
|
UTSW |
3 |
99,891,925 (GRCm39) |
missense |
probably benign |
0.00 |
R7084:Spag17
|
UTSW |
3 |
99,846,586 (GRCm39) |
missense |
probably benign |
0.18 |
R7126:Spag17
|
UTSW |
3 |
100,008,751 (GRCm39) |
missense |
probably benign |
0.00 |
R7144:Spag17
|
UTSW |
3 |
99,934,717 (GRCm39) |
splice site |
probably null |
|
R7198:Spag17
|
UTSW |
3 |
100,002,888 (GRCm39) |
missense |
probably benign |
0.02 |
R7318:Spag17
|
UTSW |
3 |
99,847,299 (GRCm39) |
missense |
probably benign |
0.00 |
R7403:Spag17
|
UTSW |
3 |
99,846,691 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7409:Spag17
|
UTSW |
3 |
99,941,475 (GRCm39) |
missense |
probably benign |
0.00 |
R7409:Spag17
|
UTSW |
3 |
99,934,547 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7537:Spag17
|
UTSW |
3 |
99,846,563 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7609:Spag17
|
UTSW |
3 |
100,002,911 (GRCm39) |
nonsense |
probably null |
|
R7772:Spag17
|
UTSW |
3 |
99,987,434 (GRCm39) |
missense |
probably damaging |
0.98 |
R7842:Spag17
|
UTSW |
3 |
99,961,174 (GRCm39) |
missense |
probably benign |
0.18 |
R7963:Spag17
|
UTSW |
3 |
99,929,954 (GRCm39) |
missense |
probably benign |
0.02 |
R8168:Spag17
|
UTSW |
3 |
99,942,300 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8291:Spag17
|
UTSW |
3 |
99,968,166 (GRCm39) |
missense |
probably benign |
|
R8347:Spag17
|
UTSW |
3 |
99,934,957 (GRCm39) |
missense |
probably benign |
|
R8383:Spag17
|
UTSW |
3 |
99,992,708 (GRCm39) |
missense |
probably damaging |
0.98 |
R8474:Spag17
|
UTSW |
3 |
99,934,586 (GRCm39) |
missense |
probably benign |
0.00 |
R8528:Spag17
|
UTSW |
3 |
100,031,501 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8804:Spag17
|
UTSW |
3 |
99,874,506 (GRCm39) |
missense |
probably benign |
|
R8809:Spag17
|
UTSW |
3 |
99,889,738 (GRCm39) |
missense |
probably benign |
0.33 |
R8818:Spag17
|
UTSW |
3 |
99,920,543 (GRCm39) |
missense |
probably benign |
0.02 |
R8830:Spag17
|
UTSW |
3 |
100,032,751 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8890:Spag17
|
UTSW |
3 |
99,911,994 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9008:Spag17
|
UTSW |
3 |
99,934,942 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9095:Spag17
|
UTSW |
3 |
99,912,092 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9182:Spag17
|
UTSW |
3 |
99,966,158 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9211:Spag17
|
UTSW |
3 |
100,032,614 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R9344:Spag17
|
UTSW |
3 |
100,010,793 (GRCm39) |
missense |
probably benign |
0.01 |
R9354:Spag17
|
UTSW |
3 |
99,934,905 (GRCm39) |
missense |
probably benign |
|
R9527:Spag17
|
UTSW |
3 |
99,970,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R9658:Spag17
|
UTSW |
3 |
99,934,932 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9738:Spag17
|
UTSW |
3 |
99,934,526 (GRCm39) |
missense |
possibly damaging |
0.53 |
X0025:Spag17
|
UTSW |
3 |
100,008,767 (GRCm39) |
missense |
probably benign |
0.31 |
Z1088:Spag17
|
UTSW |
3 |
100,002,946 (GRCm39) |
missense |
probably benign |
0.09 |
Z1176:Spag17
|
UTSW |
3 |
99,920,309 (GRCm39) |
missense |
probably benign |
0.18 |
Z1177:Spag17
|
UTSW |
3 |
99,995,715 (GRCm39) |
missense |
probably damaging |
1.00 |
|