Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim1 |
G |
T |
19: 57,025,691 (GRCm39) |
R851S |
probably damaging |
Het |
Acap2 |
C |
A |
16: 30,929,763 (GRCm39) |
A407S |
probably damaging |
Het |
Adam26a |
A |
T |
8: 44,021,635 (GRCm39) |
S618R |
probably benign |
Het |
Adamtsl5 |
T |
C |
10: 80,180,896 (GRCm39) |
Y89C |
probably damaging |
Het |
Aebp2 |
T |
A |
6: 140,588,021 (GRCm39) |
S364T |
probably damaging |
Het |
Ankfy1 |
A |
G |
11: 72,621,401 (GRCm39) |
E229G |
probably benign |
Het |
Arhgap27 |
G |
T |
11: 103,251,511 (GRCm39) |
D72E |
probably benign |
Het |
Arhgap33 |
T |
C |
7: 30,230,950 (GRCm39) |
E191G |
probably null |
Het |
Atp6v0a1 |
C |
T |
11: 100,946,427 (GRCm39) |
H807Y |
possibly damaging |
Het |
Ccdc113 |
A |
C |
8: 96,272,605 (GRCm39) |
E237D |
probably benign |
Het |
Cd200r2 |
T |
A |
16: 44,729,420 (GRCm39) |
I25K |
probably benign |
Het |
Cd300c2 |
A |
G |
11: 114,887,775 (GRCm39) |
V209A |
probably damaging |
Het |
Cdkn2d |
T |
A |
9: 21,200,383 (GRCm39) |
E129D |
probably benign |
Het |
Cfap251 |
A |
G |
5: 123,460,533 (GRCm39) |
Y1165C |
probably damaging |
Het |
Chd9 |
A |
T |
8: 91,712,741 (GRCm39) |
N855Y |
unknown |
Het |
Cntn3 |
A |
G |
6: 102,254,196 (GRCm39) |
C249R |
probably damaging |
Het |
Col12a1 |
T |
C |
9: 79,527,266 (GRCm39) |
E2688G |
possibly damaging |
Het |
Copb2 |
C |
T |
9: 98,464,901 (GRCm39) |
T612I |
probably benign |
Het |
Cplx1 |
A |
T |
5: 108,673,378 (GRCm39) |
D29E |
possibly damaging |
Het |
Cracd |
A |
G |
5: 77,006,555 (GRCm39) |
K972R |
unknown |
Het |
Ctdp1 |
A |
T |
18: 80,492,550 (GRCm39) |
Y648* |
probably null |
Het |
Daam1 |
T |
A |
12: 71,990,855 (GRCm39) |
D156E |
unknown |
Het |
Dbn1 |
G |
A |
13: 55,622,824 (GRCm39) |
P599L |
probably damaging |
Het |
Diaph1 |
C |
A |
18: 37,987,589 (GRCm39) |
V1056F |
probably damaging |
Het |
Dzip3 |
A |
T |
16: 48,748,707 (GRCm39) |
D870E |
probably damaging |
Het |
Efcab12 |
T |
C |
6: 115,800,331 (GRCm39) |
T231A |
possibly damaging |
Het |
Efl1 |
A |
C |
7: 82,412,596 (GRCm39) |
D995A |
probably benign |
Het |
Fam186a |
T |
C |
15: 99,842,393 (GRCm39) |
T1284A |
possibly damaging |
Het |
Fbxo33 |
T |
C |
12: 59,251,708 (GRCm39) |
E269G |
probably benign |
Het |
Foxj3 |
T |
A |
4: 119,483,540 (GRCm39) |
M604K |
unknown |
Het |
Gabra4 |
A |
G |
5: 71,814,463 (GRCm39) |
S86P |
unknown |
Het |
Gnas |
G |
A |
2: 174,140,639 (GRCm39) |
W269* |
probably null |
Het |
Gpc6 |
T |
G |
14: 118,202,258 (GRCm39) |
N489K |
probably damaging |
Het |
Gprin3 |
T |
C |
6: 59,331,236 (GRCm39) |
K357R |
possibly damaging |
Het |
Grip1 |
G |
T |
10: 119,811,906 (GRCm39) |
A286S |
possibly damaging |
Het |
Grm4 |
A |
T |
17: 27,721,688 (GRCm39) |
V151E |
probably damaging |
Het |
Gucy1b1 |
A |
T |
3: 81,942,065 (GRCm39) |
S565T |
possibly damaging |
Het |
Hace1 |
T |
C |
10: 45,525,014 (GRCm39) |
V260A |
probably benign |
Het |
Hepacam2 |
A |
G |
6: 3,486,940 (GRCm39) |
I139T |
probably damaging |
Het |
Hspa4l |
T |
C |
3: 40,727,057 (GRCm39) |
I486T |
probably benign |
Het |
Igkv8-19 |
T |
C |
6: 70,317,866 (GRCm39) |
Y120C |
probably damaging |
Het |
Iglv2 |
C |
T |
16: 19,079,548 (GRCm39) |
|
probably benign |
Het |
Igsf10 |
A |
T |
3: 59,237,106 (GRCm39) |
L1025H |
probably damaging |
Het |
Itpkb |
A |
G |
1: 180,161,752 (GRCm39) |
N626S |
probably benign |
Het |
Jarid2 |
C |
T |
13: 45,068,253 (GRCm39) |
R1092W |
possibly damaging |
Het |
Klc3 |
C |
T |
7: 19,132,023 (GRCm39) |
W118* |
probably null |
Het |
Klhl25 |
C |
T |
7: 75,516,741 (GRCm39) |
T549I |
probably damaging |
Het |
Krtap6-2 |
T |
A |
16: 89,216,763 (GRCm39) |
Y68F |
unknown |
Het |
Mtcl1 |
T |
C |
17: 66,673,347 (GRCm39) |
N1121D |
probably benign |
Het |
Ncbp3 |
A |
G |
11: 72,961,668 (GRCm39) |
K314R |
probably benign |
Het |
Nop2 |
T |
C |
6: 125,121,272 (GRCm39) |
W685R |
probably benign |
Het |
Orc1 |
T |
A |
4: 108,447,874 (GRCm39) |
D40E |
probably benign |
Het |
Pappa2 |
G |
T |
1: 158,684,948 (GRCm39) |
N730K |
probably damaging |
Het |
Parpbp |
A |
G |
10: 87,960,815 (GRCm39) |
S224P |
possibly damaging |
Het |
Pdgfc |
A |
G |
3: 80,944,792 (GRCm39) |
R17G |
probably benign |
Het |
Pfpl |
G |
C |
19: 12,406,297 (GRCm39) |
E183Q |
probably damaging |
Het |
Pik3r6 |
T |
A |
11: 68,424,358 (GRCm39) |
L321* |
probably null |
Het |
Pnp2 |
T |
C |
14: 51,197,006 (GRCm39) |
W31R |
probably damaging |
Het |
Prr12 |
T |
C |
7: 44,696,954 (GRCm39) |
Y987C |
unknown |
Het |
Prr27 |
C |
A |
5: 87,990,994 (GRCm39) |
P202Q |
probably benign |
Het |
Prss23 |
T |
C |
7: 89,159,683 (GRCm39) |
I129V |
probably damaging |
Het |
Rhno1 |
T |
C |
6: 128,336,119 (GRCm39) |
T39A |
probably damaging |
Het |
Rps2 |
A |
T |
17: 24,940,810 (GRCm39) |
R279* |
probably null |
Het |
Ski |
T |
C |
4: 155,244,344 (GRCm39) |
K427R |
probably damaging |
Het |
Slc23a3 |
ATT |
ATTT |
1: 75,109,925 (GRCm39) |
|
probably null |
Het |
Slc26a7 |
C |
T |
4: 14,546,372 (GRCm39) |
G319D |
probably damaging |
Het |
Slc7a6os |
A |
G |
8: 106,937,523 (GRCm39) |
V8A |
probably damaging |
Het |
Smim8 |
A |
C |
4: 34,771,265 (GRCm39) |
I43S |
probably damaging |
Het |
Sox5 |
T |
C |
6: 143,819,842 (GRCm39) |
K400R |
probably damaging |
Het |
Tab1 |
G |
A |
15: 80,032,943 (GRCm39) |
V76M |
probably damaging |
Het |
Taf2 |
A |
C |
15: 54,894,440 (GRCm39) |
|
probably null |
Het |
Taf5 |
G |
A |
19: 47,059,434 (GRCm39) |
V193M |
probably damaging |
Het |
Tm2d1 |
A |
T |
4: 98,246,261 (GRCm39) |
S180R |
probably damaging |
Het |
Ttc12 |
A |
G |
9: 49,368,166 (GRCm39) |
F287S |
probably damaging |
Het |
Ubqln4 |
G |
A |
3: 88,473,185 (GRCm39) |
|
probably null |
Het |
Ubr3 |
T |
C |
2: 69,839,497 (GRCm39) |
V1537A |
probably benign |
Het |
Ugt8a |
A |
G |
3: 125,708,900 (GRCm39) |
L70P |
probably damaging |
Het |
Vps26a |
A |
T |
10: 62,316,433 (GRCm39) |
N51K |
probably benign |
Het |
Xkr5 |
T |
A |
8: 18,990,749 (GRCm39) |
T173S |
probably benign |
Het |
Zfp354c |
A |
G |
11: 50,706,239 (GRCm39) |
C279R |
probably damaging |
Het |
Zfp65 |
T |
A |
13: 67,856,478 (GRCm39) |
H267L |
probably damaging |
Het |
|
Other mutations in Cstf3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01911:Cstf3
|
APN |
2 |
104,476,976 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02734:Cstf3
|
APN |
2 |
104,439,539 (GRCm39) |
splice site |
probably benign |
|
IGL03025:Cstf3
|
APN |
2 |
104,439,276 (GRCm39) |
missense |
possibly damaging |
0.82 |
Amanita
|
UTSW |
2 |
104,420,926 (GRCm39) |
start gained |
probably benign |
|
Ptomaine
|
UTSW |
2 |
104,479,807 (GRCm39) |
missense |
probably benign |
|
R0043:Cstf3
|
UTSW |
2 |
104,475,430 (GRCm39) |
splice site |
probably benign |
|
R0189:Cstf3
|
UTSW |
2 |
104,482,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R0332:Cstf3
|
UTSW |
2 |
104,476,812 (GRCm39) |
critical splice donor site |
probably null |
|
R0499:Cstf3
|
UTSW |
2 |
104,479,950 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1476:Cstf3
|
UTSW |
2 |
104,478,564 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1677:Cstf3
|
UTSW |
2 |
104,494,623 (GRCm39) |
intron |
probably benign |
|
R1881:Cstf3
|
UTSW |
2 |
104,484,563 (GRCm39) |
missense |
probably benign |
|
R1916:Cstf3
|
UTSW |
2 |
104,486,101 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3720:Cstf3
|
UTSW |
2 |
104,483,431 (GRCm39) |
splice site |
probably benign |
|
R3813:Cstf3
|
UTSW |
2 |
104,439,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R5155:Cstf3
|
UTSW |
2 |
104,482,830 (GRCm39) |
missense |
probably benign |
|
R5304:Cstf3
|
UTSW |
2 |
104,493,735 (GRCm39) |
nonsense |
probably null |
|
R5564:Cstf3
|
UTSW |
2 |
104,439,347 (GRCm39) |
intron |
probably benign |
|
R5869:Cstf3
|
UTSW |
2 |
104,489,585 (GRCm39) |
splice site |
probably null |
|
R6172:Cstf3
|
UTSW |
2 |
104,481,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R6747:Cstf3
|
UTSW |
2 |
104,477,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R6841:Cstf3
|
UTSW |
2 |
104,486,076 (GRCm39) |
missense |
probably benign |
0.22 |
R6959:Cstf3
|
UTSW |
2 |
104,479,807 (GRCm39) |
missense |
probably benign |
|
R7139:Cstf3
|
UTSW |
2 |
104,483,409 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7143:Cstf3
|
UTSW |
2 |
104,476,961 (GRCm39) |
missense |
probably benign |
0.01 |
R7350:Cstf3
|
UTSW |
2 |
104,439,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R7794:Cstf3
|
UTSW |
2 |
104,420,926 (GRCm39) |
start gained |
probably benign |
|
R8315:Cstf3
|
UTSW |
2 |
104,420,926 (GRCm39) |
start gained |
probably benign |
|
R8873:Cstf3
|
UTSW |
2 |
104,475,355 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9188:Cstf3
|
UTSW |
2 |
104,439,223 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9339:Cstf3
|
UTSW |
2 |
104,493,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R9612:Cstf3
|
UTSW |
2 |
104,483,370 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9801:Cstf3
|
UTSW |
2 |
104,421,024 (GRCm39) |
missense |
possibly damaging |
0.73 |
X0013:Cstf3
|
UTSW |
2 |
104,489,622 (GRCm39) |
missense |
possibly damaging |
0.58 |
|