Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A430093F15Rik |
T |
A |
19: 10,762,711 (GRCm39) |
|
probably benign |
Het |
Abca13 |
T |
C |
11: 9,199,749 (GRCm39) |
|
probably benign |
Het |
Abcc6 |
G |
A |
7: 45,652,034 (GRCm39) |
P611L |
possibly damaging |
Het |
Acsl6 |
A |
G |
11: 54,241,385 (GRCm39) |
E547G |
probably benign |
Het |
Aldh1b1 |
T |
C |
4: 45,803,472 (GRCm39) |
F337L |
possibly damaging |
Het |
Alg1 |
C |
T |
16: 5,062,383 (GRCm39) |
R422C |
probably benign |
Het |
Ankrd23 |
A |
G |
1: 36,573,147 (GRCm39) |
L75S |
probably damaging |
Het |
Arid5b |
T |
C |
10: 67,933,439 (GRCm39) |
H578R |
probably damaging |
Het |
Atp10a |
G |
T |
7: 58,447,310 (GRCm39) |
W684L |
probably benign |
Het |
Bzw2 |
T |
C |
12: 36,157,647 (GRCm39) |
|
probably null |
Het |
C2cd2 |
A |
T |
16: 97,671,372 (GRCm39) |
I509K |
probably damaging |
Het |
Card11 |
T |
C |
5: 140,868,057 (GRCm39) |
T864A |
possibly damaging |
Het |
Ces1f |
A |
G |
8: 93,993,948 (GRCm39) |
S278P |
possibly damaging |
Het |
Chd8 |
T |
C |
14: 52,450,111 (GRCm39) |
I208V |
probably benign |
Het |
Cxcl1 |
A |
G |
5: 91,039,436 (GRCm39) |
T60A |
probably benign |
Het |
Diaph1 |
G |
T |
18: 37,986,762 (GRCm39) |
|
probably benign |
Het |
Dnai4 |
T |
C |
4: 102,919,632 (GRCm39) |
I139V |
probably benign |
Het |
Exoc3l |
T |
G |
8: 106,019,587 (GRCm39) |
K394T |
probably benign |
Het |
Fabp4 |
T |
C |
3: 10,270,293 (GRCm39) |
|
probably benign |
Het |
Fam234b |
T |
A |
6: 135,188,903 (GRCm39) |
F169L |
possibly damaging |
Het |
Hectd1 |
C |
A |
12: 51,849,593 (GRCm39) |
D204Y |
possibly damaging |
Het |
Hephl1 |
A |
T |
9: 14,981,066 (GRCm39) |
Y789N |
probably damaging |
Het |
Igfbp6 |
C |
A |
15: 102,053,252 (GRCm39) |
N90K |
probably benign |
Het |
Khdrbs1 |
A |
T |
4: 129,619,462 (GRCm39) |
D226E |
probably benign |
Het |
Lipo4 |
T |
A |
19: 33,490,013 (GRCm39) |
Q163L |
probably damaging |
Het |
Med13l |
T |
C |
5: 118,880,472 (GRCm39) |
I1188T |
probably benign |
Het |
Mki67 |
T |
C |
7: 135,298,278 (GRCm39) |
E2252G |
probably benign |
Het |
Nepn |
G |
T |
10: 52,276,660 (GRCm39) |
R132L |
probably benign |
Het |
Nlrp9b |
T |
A |
7: 19,757,342 (GRCm39) |
L193* |
probably null |
Het |
Ntn1 |
A |
G |
11: 68,276,244 (GRCm39) |
S235P |
probably damaging |
Het |
Nup210l |
G |
T |
3: 90,061,873 (GRCm39) |
R684L |
probably damaging |
Het |
Obi1 |
T |
C |
14: 104,716,738 (GRCm39) |
D545G |
probably damaging |
Het |
Obp2b |
A |
G |
2: 25,629,293 (GRCm39) |
S154G |
possibly damaging |
Het |
Or10ag59 |
A |
G |
2: 87,406,282 (GRCm39) |
T285A |
probably benign |
Het |
Or4f57 |
A |
G |
2: 111,790,980 (GRCm39) |
V146A |
probably benign |
Het |
Or51b6b |
T |
A |
7: 103,310,053 (GRCm39) |
T135S |
probably benign |
Het |
Or5p1 |
A |
T |
7: 107,916,682 (GRCm39) |
I194F |
probably benign |
Het |
Polr3b |
A |
T |
10: 84,467,704 (GRCm39) |
R95* |
probably null |
Het |
Prelid2 |
C |
T |
18: 42,070,714 (GRCm39) |
V40M |
probably benign |
Het |
Ptprb |
T |
G |
10: 116,208,781 (GRCm39) |
L2205R |
probably damaging |
Het |
R3hcc1l |
T |
C |
19: 42,551,240 (GRCm39) |
V79A |
probably benign |
Het |
Stam2 |
A |
G |
2: 52,598,162 (GRCm39) |
I259T |
probably damaging |
Het |
Tdpoz4 |
A |
T |
3: 93,704,189 (GRCm39) |
N162I |
possibly damaging |
Het |
Tuba3a |
A |
G |
6: 125,259,721 (GRCm39) |
V75A |
possibly damaging |
Het |
Vmn2r73 |
A |
T |
7: 85,506,757 (GRCm39) |
*852K |
probably null |
Het |
Zfp7 |
C |
T |
15: 76,772,505 (GRCm39) |
Q69* |
probably null |
Het |
Zfp865 |
G |
T |
7: 5,032,875 (GRCm39) |
A287S |
probably benign |
Het |
Zmpste24 |
T |
A |
4: 120,955,081 (GRCm39) |
Q39L |
probably benign |
Het |
|
Other mutations in Cstf2t |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01739:Cstf2t
|
APN |
19 |
31,060,536 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02466:Cstf2t
|
APN |
19 |
31,061,277 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0064:Cstf2t
|
UTSW |
19 |
31,060,699 (GRCm39) |
missense |
probably damaging |
0.99 |
R0099:Cstf2t
|
UTSW |
19 |
31,061,231 (GRCm39) |
missense |
probably benign |
0.00 |
R0197:Cstf2t
|
UTSW |
19 |
31,062,026 (GRCm39) |
missense |
probably benign |
0.01 |
R0423:Cstf2t
|
UTSW |
19 |
31,061,676 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0883:Cstf2t
|
UTSW |
19 |
31,062,026 (GRCm39) |
missense |
probably benign |
0.01 |
R1753:Cstf2t
|
UTSW |
19 |
31,061,085 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2206:Cstf2t
|
UTSW |
19 |
31,061,175 (GRCm39) |
missense |
probably benign |
0.00 |
R2291:Cstf2t
|
UTSW |
19 |
31,062,264 (GRCm39) |
missense |
probably benign |
0.36 |
R3753:Cstf2t
|
UTSW |
19 |
31,060,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R4523:Cstf2t
|
UTSW |
19 |
31,060,482 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4991:Cstf2t
|
UTSW |
19 |
31,061,983 (GRCm39) |
missense |
probably damaging |
0.97 |
R5134:Cstf2t
|
UTSW |
19 |
31,061,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R5863:Cstf2t
|
UTSW |
19 |
31,060,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R6081:Cstf2t
|
UTSW |
19 |
31,060,523 (GRCm39) |
missense |
probably benign |
0.10 |
R6573:Cstf2t
|
UTSW |
19 |
31,061,180 (GRCm39) |
missense |
probably benign |
0.00 |
R7408:Cstf2t
|
UTSW |
19 |
31,060,593 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7648:Cstf2t
|
UTSW |
19 |
31,060,992 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8317:Cstf2t
|
UTSW |
19 |
31,061,648 (GRCm39) |
missense |
probably benign |
0.09 |
|