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 |
Spag17 |
C |
T |
3: 99,934,906 (GRCm39) |
T704M |
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 |
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 Tigd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02304:Tigd2
|
APN |
6 |
59,188,683 (GRCm39) |
nonsense |
probably null |
|
IGL03356:Tigd2
|
APN |
6 |
59,188,690 (GRCm39) |
missense |
probably benign |
0.04 |
PIT1430001:Tigd2
|
UTSW |
6 |
59,188,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R0048:Tigd2
|
UTSW |
6 |
59,188,369 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0387:Tigd2
|
UTSW |
6 |
59,188,143 (GRCm39) |
missense |
probably benign |
0.00 |
R0523:Tigd2
|
UTSW |
6 |
59,187,358 (GRCm39) |
missense |
probably benign |
0.30 |
R0636:Tigd2
|
UTSW |
6 |
59,188,272 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1171:Tigd2
|
UTSW |
6 |
59,188,361 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2440:Tigd2
|
UTSW |
6 |
59,186,980 (GRCm39) |
start gained |
probably benign |
|
R4327:Tigd2
|
UTSW |
6 |
59,187,562 (GRCm39) |
missense |
probably benign |
0.36 |
R4731:Tigd2
|
UTSW |
6 |
59,188,400 (GRCm39) |
missense |
probably benign |
0.00 |
R4732:Tigd2
|
UTSW |
6 |
59,188,400 (GRCm39) |
missense |
probably benign |
0.00 |
R4733:Tigd2
|
UTSW |
6 |
59,188,400 (GRCm39) |
missense |
probably benign |
0.00 |
R5005:Tigd2
|
UTSW |
6 |
59,188,131 (GRCm39) |
missense |
probably benign |
0.06 |
R5028:Tigd2
|
UTSW |
6 |
59,188,205 (GRCm39) |
nonsense |
probably null |
|
R5248:Tigd2
|
UTSW |
6 |
59,188,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R6006:Tigd2
|
UTSW |
6 |
59,187,762 (GRCm39) |
missense |
possibly damaging |
0.45 |
R7099:Tigd2
|
UTSW |
6 |
59,187,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R7261:Tigd2
|
UTSW |
6 |
59,188,052 (GRCm39) |
missense |
probably benign |
0.02 |
R7553:Tigd2
|
UTSW |
6 |
59,188,564 (GRCm39) |
missense |
probably benign |
0.04 |
R7688:Tigd2
|
UTSW |
6 |
59,187,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R8002:Tigd2
|
UTSW |
6 |
59,187,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R8734:Tigd2
|
UTSW |
6 |
59,187,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R9007:Tigd2
|
UTSW |
6 |
59,187,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R9095:Tigd2
|
UTSW |
6 |
59,187,509 (GRCm39) |
nonsense |
probably null |
|
Z1177:Tigd2
|
UTSW |
6 |
59,188,515 (GRCm39) |
missense |
probably benign |
|
|