Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700018F24Rik |
C |
T |
5: 144,982,333 (GRCm39) |
T306I |
probably benign |
Het |
Aurkb |
T |
C |
11: 68,941,175 (GRCm39) |
I250T |
probably damaging |
Het |
C1qtnf1 |
A |
G |
11: 118,334,672 (GRCm39) |
T51A |
probably benign |
Het |
Cd8b1 |
G |
A |
6: 71,306,777 (GRCm39) |
|
probably null |
Het |
Cep57l1 |
A |
T |
10: 41,607,082 (GRCm39) |
D160E |
probably damaging |
Het |
Ces1f |
C |
T |
8: 93,992,491 (GRCm39) |
S320N |
probably benign |
Het |
Cfap54 |
A |
G |
10: 92,656,936 (GRCm39) |
S3039P |
possibly damaging |
Het |
Chia1 |
A |
T |
3: 106,022,502 (GRCm39) |
|
probably benign |
Het |
Chka |
T |
G |
19: 3,935,953 (GRCm39) |
F220V |
possibly damaging |
Het |
Cmtm2b |
A |
G |
8: 105,048,980 (GRCm39) |
|
probably benign |
Het |
Dgcr8 |
C |
T |
16: 18,098,079 (GRCm39) |
|
probably benign |
Het |
Dhx30 |
T |
C |
9: 109,920,603 (GRCm39) |
T304A |
possibly damaging |
Het |
Dhx30 |
A |
T |
9: 109,922,189 (GRCm39) |
D164E |
probably benign |
Het |
Dip2b |
A |
T |
15: 100,071,152 (GRCm39) |
K661I |
probably damaging |
Het |
Dlgap4 |
G |
T |
2: 156,546,514 (GRCm39) |
R394L |
possibly damaging |
Het |
Dop1b |
T |
A |
16: 93,568,681 (GRCm39) |
L1581H |
probably damaging |
Het |
Fam219a |
C |
A |
4: 41,521,942 (GRCm39) |
G46V |
probably damaging |
Het |
Fer1l6 |
G |
A |
15: 58,490,766 (GRCm39) |
V1028M |
probably damaging |
Het |
Glb1 |
C |
A |
9: 114,249,558 (GRCm39) |
A129E |
probably damaging |
Het |
Heatr1 |
T |
C |
13: 12,447,608 (GRCm39) |
V1767A |
probably benign |
Het |
Ift88 |
T |
A |
14: 57,718,199 (GRCm39) |
S591T |
probably benign |
Het |
Itgb4 |
A |
G |
11: 115,885,187 (GRCm39) |
K1023R |
probably benign |
Het |
Mfng |
C |
A |
15: 78,643,457 (GRCm39) |
S250I |
probably damaging |
Het |
Mmp9 |
A |
G |
2: 164,796,800 (GRCm39) |
T723A |
probably benign |
Het |
Mzf1 |
T |
A |
7: 12,785,534 (GRCm39) |
H299L |
probably benign |
Het |
Naa40 |
T |
C |
19: 7,211,485 (GRCm39) |
K47E |
possibly damaging |
Het |
Ncdn |
A |
C |
4: 126,643,903 (GRCm39) |
F306L |
possibly damaging |
Het |
Notch3 |
A |
G |
17: 32,377,254 (GRCm39) |
C246R |
probably damaging |
Het |
Npc1l1 |
A |
T |
11: 6,168,355 (GRCm39) |
Y945* |
probably null |
Het |
Or2av9 |
T |
A |
11: 58,380,745 (GRCm39) |
I279L |
probably benign |
Het |
Or2n1d |
A |
T |
17: 38,646,320 (GRCm39) |
T91S |
possibly damaging |
Het |
Or2y14 |
C |
T |
11: 49,404,635 (GRCm39) |
P57S |
probably damaging |
Het |
Or52n5 |
T |
C |
7: 104,587,816 (GRCm39) |
W28R |
probably damaging |
Het |
Pcnx1 |
C |
A |
12: 82,028,853 (GRCm39) |
D1044E |
|
Het |
Pgm2l1 |
T |
A |
7: 99,919,629 (GRCm39) |
I575K |
probably damaging |
Het |
Plat |
T |
C |
8: 23,272,100 (GRCm39) |
I553T |
probably damaging |
Het |
Prrc2c |
A |
G |
1: 162,507,130 (GRCm39) |
V2513A |
probably benign |
Het |
Qser1 |
A |
T |
2: 104,617,593 (GRCm39) |
V983E |
possibly damaging |
Het |
Ring1 |
A |
G |
17: 34,241,547 (GRCm39) |
S190P |
possibly damaging |
Het |
Rnf150 |
A |
G |
8: 83,716,982 (GRCm39) |
E163G |
probably benign |
Het |
Scgb2b12 |
T |
C |
7: 32,026,060 (GRCm39) |
H44R |
probably benign |
Het |
Septin4 |
T |
A |
11: 87,459,792 (GRCm39) |
C513* |
probably null |
Het |
Shtn1 |
T |
C |
19: 58,998,257 (GRCm39) |
K379E |
probably damaging |
Het |
Slc52a2 |
G |
T |
15: 76,424,475 (GRCm39) |
V238L |
probably benign |
Het |
Smg1 |
T |
C |
7: 117,744,639 (GRCm39) |
H3171R |
possibly damaging |
Het |
Tada3 |
A |
G |
6: 113,347,264 (GRCm39) |
V342A |
possibly damaging |
Het |
Tbc1d20 |
T |
C |
2: 152,153,262 (GRCm39) |
V264A |
probably damaging |
Het |
Tmco5 |
G |
A |
2: 116,710,745 (GRCm39) |
A22T |
probably benign |
Het |
Tmem63b |
A |
G |
17: 45,975,697 (GRCm39) |
F549S |
probably benign |
Het |
Trav16d-dv11 |
T |
C |
14: 53,285,086 (GRCm39) |
F54S |
probably benign |
Het |
Trim7 |
A |
T |
11: 48,736,281 (GRCm39) |
K5* |
probably null |
Het |
Usp48 |
G |
A |
4: 137,340,996 (GRCm39) |
G332E |
probably benign |
Het |
Zfp78 |
T |
C |
7: 6,381,367 (GRCm39) |
I139T |
probably benign |
Het |
Zfp839 |
T |
A |
12: 110,834,878 (GRCm39) |
V711D |
probably benign |
Het |
|
Other mutations in C1rb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R3722:C1rb
|
UTSW |
6 |
124,557,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R4806:C1rb
|
UTSW |
6 |
124,551,908 (GRCm39) |
missense |
probably benign |
0.18 |
R5095:C1rb
|
UTSW |
6 |
124,557,272 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5572:C1rb
|
UTSW |
6 |
124,557,758 (GRCm39) |
missense |
probably benign |
|
R6223:C1rb
|
UTSW |
6 |
124,551,539 (GRCm39) |
missense |
probably benign |
0.06 |
R6769:C1rb
|
UTSW |
6 |
124,554,364 (GRCm39) |
missense |
probably benign |
0.00 |
R6771:C1rb
|
UTSW |
6 |
124,554,364 (GRCm39) |
missense |
probably benign |
0.00 |
R7204:C1rb
|
UTSW |
6 |
124,554,386 (GRCm39) |
missense |
probably benign |
|
R7335:C1rb
|
UTSW |
6 |
124,552,238 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7341:C1rb
|
UTSW |
6 |
124,554,411 (GRCm39) |
nonsense |
probably null |
|
R7554:C1rb
|
UTSW |
6 |
124,557,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R7604:C1rb
|
UTSW |
6 |
124,557,443 (GRCm39) |
missense |
not run |
|
R7753:C1rb
|
UTSW |
6 |
124,557,390 (GRCm39) |
missense |
probably benign |
0.00 |
R7813:C1rb
|
UTSW |
6 |
124,557,488 (GRCm39) |
missense |
probably benign |
0.00 |
R8423:C1rb
|
UTSW |
6 |
124,551,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R8549:C1rb
|
UTSW |
6 |
124,551,498 (GRCm39) |
missense |
probably benign |
0.04 |
R8835:C1rb
|
UTSW |
6 |
124,552,217 (GRCm39) |
missense |
probably benign |
0.02 |
R9056:C1rb
|
UTSW |
6 |
124,553,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R9091:C1rb
|
UTSW |
6 |
124,551,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R9270:C1rb
|
UTSW |
6 |
124,551,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R9390:C1rb
|
UTSW |
6 |
124,557,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R9460:C1rb
|
UTSW |
6 |
124,557,865 (GRCm39) |
missense |
probably benign |
0.00 |
|