Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aox1 |
T |
A |
1: 58,343,644 (GRCm39) |
D442E |
probably benign |
Het |
Arl6ip4 |
G |
A |
5: 124,254,665 (GRCm39) |
G53R |
probably damaging |
Het |
Asns |
T |
C |
6: 7,675,344 (GRCm39) |
T553A |
probably benign |
Het |
Atp1a1 |
T |
A |
3: 101,493,614 (GRCm39) |
N497Y |
possibly damaging |
Het |
Birc2 |
T |
C |
9: 7,836,966 (GRCm39) |
|
probably benign |
Het |
Catsperd |
C |
A |
17: 56,961,426 (GRCm39) |
|
probably null |
Het |
Dchs1 |
G |
T |
7: 105,406,210 (GRCm39) |
Q2341K |
possibly damaging |
Het |
Dydc2 |
C |
A |
14: 40,771,296 (GRCm39) |
V128L |
probably benign |
Het |
Dync2i2 |
A |
G |
2: 29,923,284 (GRCm39) |
|
probably null |
Het |
Efna3 |
C |
T |
3: 89,223,769 (GRCm39) |
|
probably null |
Het |
Fbn2 |
C |
T |
18: 58,143,686 (GRCm39) |
E2790K |
probably benign |
Het |
Fhip1a |
A |
T |
3: 85,579,865 (GRCm39) |
L780* |
probably null |
Het |
Gm11569 |
C |
A |
11: 99,689,657 (GRCm39) |
|
probably benign |
Het |
Gprc6a |
C |
T |
10: 51,507,412 (GRCm39) |
G39D |
probably damaging |
Het |
Igkv6-17 |
A |
G |
6: 70,348,692 (GRCm39) |
D21G |
probably benign |
Het |
Klra4 |
T |
C |
6: 130,039,182 (GRCm39) |
Q70R |
probably damaging |
Het |
Lingo4 |
G |
T |
3: 94,306,662 (GRCm39) |
|
probably benign |
Het |
Lrp2bp |
A |
G |
8: 46,466,151 (GRCm39) |
K87E |
possibly damaging |
Het |
Macf1 |
A |
T |
4: 123,266,231 (GRCm39) |
M5333K |
probably damaging |
Het |
Mmp13 |
A |
T |
9: 7,272,781 (GRCm39) |
Y47F |
probably benign |
Het |
Muc16 |
G |
A |
9: 18,471,282 (GRCm39) |
P7261S |
probably benign |
Het |
Nostrin |
G |
T |
2: 69,005,856 (GRCm39) |
M212I |
probably benign |
Het |
Nr1h5 |
G |
A |
3: 102,865,677 (GRCm39) |
T8M |
possibly damaging |
Het |
Nup153 |
A |
T |
13: 46,870,792 (GRCm39) |
L41H |
probably damaging |
Het |
Or10b1 |
T |
C |
10: 78,355,802 (GRCm39) |
L120P |
noncoding transcript |
Het |
Or5b97 |
T |
A |
19: 12,878,653 (GRCm39) |
I164L |
probably benign |
Het |
Pappa |
A |
T |
4: 65,099,278 (GRCm39) |
D599V |
probably damaging |
Het |
Pcdh18 |
G |
A |
3: 49,710,364 (GRCm39) |
T317I |
probably benign |
Het |
Pcsk5 |
T |
A |
19: 17,434,150 (GRCm39) |
N1406I |
possibly damaging |
Het |
Pik3c2a |
A |
T |
7: 115,961,419 (GRCm39) |
Y1027N |
probably damaging |
Het |
Prpf6 |
T |
A |
2: 181,257,844 (GRCm39) |
Y105* |
probably null |
Het |
Rab5a |
C |
T |
17: 53,804,650 (GRCm39) |
P87S |
probably damaging |
Het |
Rnf8 |
T |
A |
17: 29,854,843 (GRCm39) |
W433R |
probably damaging |
Het |
Slc18b1 |
T |
A |
10: 23,692,227 (GRCm39) |
V232D |
probably benign |
Het |
Taf11 |
C |
A |
17: 28,126,492 (GRCm39) |
A52S |
probably benign |
Het |
Thoc2l |
T |
C |
5: 104,665,555 (GRCm39) |
F26L |
probably benign |
Het |
Trav9-2 |
T |
C |
14: 53,828,819 (GRCm39) |
L63P |
possibly damaging |
Het |
Zfat |
T |
C |
15: 67,956,235 (GRCm39) |
Y1199C |
probably damaging |
Het |
|
Other mutations in Krtap31-2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02511:Krtap31-2
|
APN |
11 |
99,827,518 (GRCm39) |
missense |
possibly damaging |
0.71 |
PIT4378001:Krtap31-2
|
UTSW |
11 |
99,827,542 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0243:Krtap31-2
|
UTSW |
11 |
99,827,572 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4751:Krtap31-2
|
UTSW |
11 |
99,827,402 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4987:Krtap31-2
|
UTSW |
11 |
99,827,396 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5500:Krtap31-2
|
UTSW |
11 |
99,827,173 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7519:Krtap31-2
|
UTSW |
11 |
99,827,501 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7614:Krtap31-2
|
UTSW |
11 |
99,827,429 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7890:Krtap31-2
|
UTSW |
11 |
99,827,377 (GRCm39) |
missense |
possibly damaging |
0.71 |
|