Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
T |
C |
3: 121,941,497 (GRCm39) |
V447A |
probably benign |
Het |
Adam6b |
A |
G |
12: 113,454,122 (GRCm39) |
D313G |
probably damaging |
Het |
Adcy10 |
G |
T |
1: 165,367,443 (GRCm39) |
C571F |
probably damaging |
Het |
Anxa1 |
A |
G |
19: 20,352,635 (GRCm39) |
V313A |
probably benign |
Het |
Bpifb6 |
A |
T |
2: 153,750,733 (GRCm39) |
|
probably null |
Het |
Cacna1c |
C |
A |
6: 118,578,124 (GRCm39) |
C1713F |
probably benign |
Het |
Cep135 |
A |
G |
5: 76,754,585 (GRCm39) |
N354S |
probably benign |
Het |
Cers2 |
A |
G |
3: 95,228,965 (GRCm39) |
D200G |
probably damaging |
Het |
Cpne1 |
A |
G |
2: 155,920,727 (GRCm39) |
L133P |
probably damaging |
Het |
Ddhd1 |
A |
G |
14: 45,840,138 (GRCm39) |
Y16H |
probably damaging |
Het |
Depp1 |
T |
C |
6: 116,629,254 (GRCm39) |
L199P |
probably damaging |
Het |
Fastkd2 |
T |
C |
1: 63,771,009 (GRCm39) |
F122L |
probably benign |
Het |
Fastkd5 |
A |
T |
2: 130,457,431 (GRCm39) |
D386E |
probably damaging |
Het |
Gm5134 |
T |
A |
10: 75,828,292 (GRCm39) |
C291S |
probably damaging |
Het |
Gria2 |
T |
C |
3: 80,596,634 (GRCm39) |
S811G |
probably damaging |
Het |
Hcn1 |
C |
T |
13: 118,111,998 (GRCm39) |
P654L |
unknown |
Het |
Hrnr |
C |
A |
3: 93,230,461 (GRCm39) |
S233* |
probably null |
Het |
Hspa5 |
C |
T |
2: 34,663,204 (GRCm39) |
P127L |
probably damaging |
Het |
Itgal |
A |
T |
7: 126,895,573 (GRCm39) |
|
probably benign |
Het |
L3mbtl4 |
G |
T |
17: 68,768,561 (GRCm39) |
R223L |
probably benign |
Het |
Mical1 |
A |
G |
10: 41,358,246 (GRCm39) |
R420G |
possibly damaging |
Het |
Mllt6 |
T |
A |
11: 97,564,637 (GRCm39) |
L481Q |
probably damaging |
Het |
Mtdh |
T |
A |
15: 34,131,311 (GRCm39) |
N174K |
probably damaging |
Het |
Nhsl1 |
A |
G |
10: 18,407,386 (GRCm39) |
M1507V |
probably damaging |
Het |
Npm3 |
A |
T |
19: 45,737,994 (GRCm39) |
M1K |
probably null |
Het |
Or1e21 |
C |
T |
11: 73,344,430 (GRCm39) |
G203R |
probably damaging |
Het |
Pold1 |
A |
T |
7: 44,190,795 (GRCm39) |
W290R |
possibly damaging |
Het |
Prss52 |
C |
T |
14: 64,350,021 (GRCm39) |
T216I |
probably damaging |
Het |
Psme4 |
T |
C |
11: 30,763,904 (GRCm39) |
|
probably null |
Het |
Pwwp2a |
T |
A |
11: 43,597,018 (GRCm39) |
F453I |
probably damaging |
Het |
Rttn |
A |
G |
18: 89,082,340 (GRCm39) |
N1422S |
probably damaging |
Het |
Scaf4 |
A |
C |
16: 90,057,075 (GRCm39) |
I92R |
unknown |
Het |
Slc12a1 |
A |
G |
2: 125,013,177 (GRCm39) |
K345E |
probably benign |
Het |
Slc22a28 |
A |
T |
19: 8,049,270 (GRCm39) |
N326K |
probably benign |
Het |
Smgc |
A |
G |
15: 91,744,576 (GRCm39) |
E311G |
possibly damaging |
Het |
Snx7 |
C |
T |
3: 117,633,680 (GRCm39) |
R90H |
possibly damaging |
Het |
Tex101 |
A |
G |
7: 24,367,683 (GRCm39) |
I223T |
probably benign |
Het |
Tnik |
A |
T |
3: 28,715,853 (GRCm39) |
K1093* |
probably null |
Het |
Tnxb |
T |
G |
17: 34,936,242 (GRCm39) |
|
probably null |
Het |
Trio |
T |
C |
15: 27,749,885 (GRCm39) |
N2272S |
possibly damaging |
Het |
Vmn2r4 |
C |
T |
3: 64,296,550 (GRCm39) |
G745D |
probably benign |
Het |
Vps9d1 |
A |
T |
8: 123,973,882 (GRCm39) |
Y300* |
probably null |
Het |
Zfp646 |
T |
A |
7: 127,479,199 (GRCm39) |
C459S |
possibly damaging |
Het |
|
Other mutations in Tubal3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00595:Tubal3
|
APN |
13 |
3,983,015 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02053:Tubal3
|
APN |
13 |
3,983,159 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02120:Tubal3
|
APN |
13 |
3,980,675 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02426:Tubal3
|
APN |
13 |
3,982,750 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02548:Tubal3
|
APN |
13 |
3,980,554 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02981:Tubal3
|
APN |
13 |
3,983,257 (GRCm39) |
missense |
probably benign |
0.02 |
R0458:Tubal3
|
UTSW |
13 |
3,983,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R1626:Tubal3
|
UTSW |
13 |
3,982,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R1657:Tubal3
|
UTSW |
13 |
3,983,011 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2084:Tubal3
|
UTSW |
13 |
3,978,192 (GRCm39) |
missense |
possibly damaging |
0.62 |
R3545:Tubal3
|
UTSW |
13 |
3,983,560 (GRCm39) |
makesense |
probably null |
|
R3976:Tubal3
|
UTSW |
13 |
3,982,946 (GRCm39) |
missense |
probably benign |
|
R4700:Tubal3
|
UTSW |
13 |
3,983,514 (GRCm39) |
missense |
probably damaging |
0.99 |
R4722:Tubal3
|
UTSW |
13 |
3,978,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R5617:Tubal3
|
UTSW |
13 |
3,983,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R6474:Tubal3
|
UTSW |
13 |
3,983,107 (GRCm39) |
missense |
probably benign |
0.10 |
R7082:Tubal3
|
UTSW |
13 |
3,983,050 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7273:Tubal3
|
UTSW |
13 |
3,980,675 (GRCm39) |
missense |
probably damaging |
0.96 |
R7586:Tubal3
|
UTSW |
13 |
3,978,198 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8805:Tubal3
|
UTSW |
13 |
3,983,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R8921:Tubal3
|
UTSW |
13 |
3,983,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R9043:Tubal3
|
UTSW |
13 |
3,982,708 (GRCm39) |
nonsense |
probably null |
|
R9173:Tubal3
|
UTSW |
13 |
3,983,050 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9487:Tubal3
|
UTSW |
13 |
3,980,674 (GRCm39) |
missense |
probably benign |
0.03 |
Z1088:Tubal3
|
UTSW |
13 |
3,983,511 (GRCm39) |
missense |
probably benign |
0.06 |
|