Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca1 |
A |
C |
4: 53,083,733 (GRCm39) |
L700R |
probably damaging |
Het |
Arpc1a |
C |
A |
5: 145,038,032 (GRCm39) |
|
probably null |
Het |
Baz2b |
G |
T |
2: 59,755,234 (GRCm39) |
P241Q |
probably damaging |
Het |
Cd6 |
T |
A |
19: 10,771,973 (GRCm39) |
T414S |
probably benign |
Het |
Ces2b |
A |
T |
8: 105,563,501 (GRCm39) |
E409D |
probably benign |
Het |
Cfap54 |
A |
G |
10: 92,656,981 (GRCm39) |
Y3024H |
probably benign |
Het |
Chrm1 |
A |
G |
19: 8,655,912 (GRCm39) |
T206A |
probably benign |
Het |
Clptm1l |
T |
C |
13: 73,766,635 (GRCm39) |
W512R |
probably damaging |
Het |
Col15a1 |
T |
A |
4: 47,247,552 (GRCm39) |
|
probably null |
Het |
Cox15 |
A |
G |
19: 43,725,228 (GRCm39) |
S392P |
probably damaging |
Het |
Cplx3 |
A |
G |
9: 57,521,355 (GRCm39) |
|
probably null |
Het |
Cr2 |
T |
C |
1: 194,837,508 (GRCm39) |
M1197V |
probably damaging |
Het |
Ddx60 |
A |
G |
8: 62,453,723 (GRCm39) |
K1281E |
probably benign |
Het |
Dnah11 |
A |
G |
12: 118,009,381 (GRCm39) |
F2094L |
probably damaging |
Het |
Ear2 |
T |
A |
14: 44,340,416 (GRCm39) |
C25S |
probably damaging |
Het |
Ect2l |
T |
C |
10: 18,016,012 (GRCm39) |
D802G |
probably damaging |
Het |
Eftud2 |
G |
A |
11: 102,729,449 (GRCm39) |
Q84* |
probably null |
Het |
Eif4g3 |
T |
A |
4: 137,903,143 (GRCm39) |
|
probably null |
Het |
Ephb2 |
T |
C |
4: 136,384,813 (GRCm39) |
D866G |
probably damaging |
Het |
Farsb |
A |
G |
1: 78,449,134 (GRCm39) |
M99T |
probably damaging |
Het |
Foxs1 |
T |
A |
2: 152,774,640 (GRCm39) |
S138C |
probably damaging |
Het |
Frem1 |
T |
G |
4: 82,932,069 (GRCm39) |
S211R |
probably damaging |
Het |
Gm19410 |
G |
A |
8: 36,274,730 (GRCm39) |
R1517Q |
probably benign |
Het |
Gria2 |
T |
C |
3: 80,709,611 (GRCm39) |
I27M |
probably benign |
Het |
H2-Q7 |
A |
G |
17: 35,661,654 (GRCm39) |
E299G |
probably benign |
Het |
Hao2 |
T |
G |
3: 98,784,451 (GRCm39) |
I305L |
probably benign |
Het |
Hectd4 |
C |
T |
5: 121,445,444 (GRCm39) |
Q122* |
probably null |
Het |
Hivep1 |
T |
A |
13: 42,317,760 (GRCm39) |
C2079S |
probably damaging |
Het |
Hoxb1 |
C |
A |
11: 96,257,813 (GRCm39) |
Q248K |
probably damaging |
Het |
Hspb6 |
A |
G |
7: 30,253,772 (GRCm39) |
D95G |
probably benign |
Het |
Ighv5-2 |
T |
A |
12: 113,542,126 (GRCm39) |
R117S |
probably damaging |
Het |
Ino80d |
A |
C |
1: 63,097,769 (GRCm39) |
S708R |
probably damaging |
Het |
Mmp15 |
A |
G |
8: 96,091,942 (GRCm39) |
N51D |
probably benign |
Het |
Naip1 |
T |
C |
13: 100,559,585 (GRCm39) |
M1140V |
probably benign |
Het |
Niban2 |
T |
A |
2: 32,795,838 (GRCm39) |
V22D |
probably damaging |
Het |
Or1e1f |
A |
G |
11: 73,856,291 (GRCm39) |
N286D |
probably damaging |
Het |
Or2y8 |
A |
G |
11: 52,035,520 (GRCm39) |
V279A |
probably benign |
Het |
Or8b41 |
T |
A |
9: 38,054,449 (GRCm39) |
M1K |
probably null |
Het |
Or8k21 |
A |
G |
2: 86,145,409 (GRCm39) |
S74P |
probably damaging |
Het |
Pard3b |
A |
T |
1: 62,198,629 (GRCm39) |
N239I |
probably damaging |
Het |
Parvb |
C |
T |
15: 84,182,180 (GRCm39) |
R237W |
probably damaging |
Het |
Pcdha9 |
T |
C |
18: 37,131,122 (GRCm39) |
S64P |
probably damaging |
Het |
Pdcd1 |
T |
C |
1: 93,969,114 (GRCm39) |
N68S |
probably benign |
Het |
Pi4ka |
G |
T |
16: 17,143,916 (GRCm39) |
|
probably null |
Het |
Plekha4 |
A |
T |
7: 45,190,310 (GRCm39) |
D359V |
possibly damaging |
Het |
Serpinb13 |
A |
G |
1: 106,921,792 (GRCm39) |
I78V |
probably benign |
Het |
Slc39a7 |
T |
A |
17: 34,249,082 (GRCm39) |
T269S |
probably benign |
Het |
Sltm |
T |
G |
9: 70,480,992 (GRCm39) |
D281E |
probably damaging |
Het |
Zfp708 |
T |
C |
13: 67,219,496 (GRCm39) |
Y76C |
probably damaging |
Het |
Zfp990 |
T |
A |
4: 145,263,497 (GRCm39) |
V165D |
possibly damaging |
Het |
|
Other mutations in 1700013G24Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01547:1700013G24Rik
|
APN |
4 |
137,182,573 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02646:1700013G24Rik
|
APN |
4 |
137,182,101 (GRCm39) |
nonsense |
probably null |
|
R0526:1700013G24Rik
|
UTSW |
4 |
137,182,535 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1449:1700013G24Rik
|
UTSW |
4 |
137,182,666 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3743:1700013G24Rik
|
UTSW |
4 |
137,182,348 (GRCm39) |
missense |
probably damaging |
0.96 |
R5357:1700013G24Rik
|
UTSW |
4 |
137,182,463 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6265:1700013G24Rik
|
UTSW |
4 |
137,181,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R6586:1700013G24Rik
|
UTSW |
4 |
137,182,639 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6988:1700013G24Rik
|
UTSW |
4 |
137,181,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R7640:1700013G24Rik
|
UTSW |
4 |
137,181,905 (GRCm39) |
missense |
probably damaging |
0.99 |
R7825:1700013G24Rik
|
UTSW |
4 |
137,182,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R8905:1700013G24Rik
|
UTSW |
4 |
137,182,553 (GRCm39) |
missense |
probably benign |
|
R9536:1700013G24Rik
|
UTSW |
4 |
137,182,623 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:1700013G24Rik
|
UTSW |
4 |
137,182,303 (GRCm39) |
missense |
probably damaging |
1.00 |
|