Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc1 |
C |
G |
16: 14,263,283 (GRCm39) |
P748A |
probably damaging |
Het |
Abcc12 |
A |
G |
8: 87,293,182 (GRCm39) |
V2A |
probably damaging |
Het |
Anxa3 |
T |
C |
5: 96,978,263 (GRCm39) |
Y216H |
probably damaging |
Het |
Arpc1a |
C |
A |
5: 145,041,668 (GRCm39) |
T317K |
probably benign |
Het |
C330018D20Rik |
A |
G |
18: 57,095,483 (GRCm39) |
L34S |
probably damaging |
Het |
C5ar1 |
A |
G |
7: 15,982,504 (GRCm39) |
F172S |
probably damaging |
Het |
Ccl27a |
G |
A |
4: 41,774,166 (GRCm39) |
|
probably benign |
Het |
Clip1 |
T |
C |
5: 123,752,342 (GRCm39) |
N480D |
|
Het |
Cttnbp2nl |
A |
G |
3: 104,912,076 (GRCm39) |
S603P |
possibly damaging |
Het |
Dmc1 |
A |
T |
15: 79,480,443 (GRCm39) |
|
probably null |
Het |
Dnhd1 |
A |
G |
7: 105,323,475 (GRCm39) |
I626V |
probably benign |
Het |
Dnm2 |
A |
G |
9: 21,416,930 (GRCm39) |
N821S |
probably benign |
Het |
Dst |
T |
C |
1: 34,238,509 (GRCm39) |
L1723S |
probably benign |
Het |
Ep300 |
T |
A |
15: 81,492,399 (GRCm39) |
M245K |
unknown |
Het |
Fam227a |
T |
C |
15: 79,501,967 (GRCm39) |
T536A |
probably benign |
Het |
Fbn2 |
G |
T |
18: 58,213,299 (GRCm39) |
R963S |
possibly damaging |
Het |
Fbxo42 |
T |
G |
4: 140,927,673 (GRCm39) |
I651S |
possibly damaging |
Het |
Ggnbp1 |
T |
A |
17: 27,237,105 (GRCm39) |
M1K |
probably null |
Het |
Gm10800 |
AAAGAAAACTGAA |
ACAAGAAAACTGAA |
2: 98,497,378 (GRCm39) |
|
probably null |
Het |
Grid2 |
T |
C |
6: 63,908,085 (GRCm39) |
F242L |
possibly damaging |
Het |
Igf2r |
A |
G |
17: 12,917,160 (GRCm39) |
V1580A |
possibly damaging |
Het |
Marchf4 |
A |
G |
1: 72,574,148 (GRCm39) |
V50A |
possibly damaging |
Het |
Mettl15 |
T |
A |
2: 108,923,220 (GRCm39) |
R401* |
probably null |
Het |
Mki67 |
A |
T |
7: 135,301,106 (GRCm39) |
H1309Q |
probably benign |
Het |
Mtor |
T |
C |
4: 148,547,252 (GRCm39) |
Y412H |
probably damaging |
Het |
Myef2 |
C |
T |
2: 124,965,396 (GRCm39) |
G15S |
probably benign |
Het |
Napepld |
A |
T |
5: 21,880,846 (GRCm39) |
I183N |
probably damaging |
Het |
Nbeal2 |
T |
C |
9: 110,454,886 (GRCm39) |
E2644G |
probably benign |
Het |
Neb |
C |
T |
2: 52,186,438 (GRCm39) |
R878Q |
possibly damaging |
Het |
Or52l1 |
A |
G |
7: 104,829,956 (GRCm39) |
V203A |
probably damaging |
Het |
Otol1 |
A |
T |
3: 69,935,202 (GRCm39) |
H398L |
probably damaging |
Het |
Pcdhga9 |
A |
G |
18: 37,871,805 (GRCm39) |
S545G |
probably damaging |
Het |
Pramel19 |
T |
G |
4: 101,798,497 (GRCm39) |
F156C |
probably benign |
Het |
Rhbdl1 |
T |
C |
17: 26,055,991 (GRCm39) |
S4G |
possibly damaging |
Het |
Ric1 |
A |
G |
19: 29,557,175 (GRCm39) |
E420G |
probably benign |
Het |
Sap30l |
G |
A |
11: 57,698,887 (GRCm39) |
R120H |
probably damaging |
Het |
Scn2a |
T |
C |
2: 65,546,247 (GRCm39) |
F937L |
probably damaging |
Het |
Sdf2 |
G |
A |
11: 78,141,989 (GRCm39) |
G108D |
probably damaging |
Het |
Skint5 |
T |
C |
4: 113,381,305 (GRCm39) |
S1263G |
unknown |
Het |
Stab1 |
A |
G |
14: 30,867,194 (GRCm39) |
I1722T |
probably benign |
Het |
Syn3 |
A |
G |
10: 85,893,428 (GRCm39) |
S472P |
unknown |
Het |
Tcp11l2 |
T |
C |
10: 84,430,622 (GRCm39) |
F249S |
probably damaging |
Het |
Thoc7 |
T |
A |
14: 13,961,819 (GRCm38) |
|
probably null |
Het |
Tvp23a |
C |
A |
16: 10,246,602 (GRCm39) |
C61F |
probably damaging |
Het |
Ubfd1 |
G |
A |
7: 121,666,606 (GRCm39) |
G34D |
probably benign |
Het |
Vmn1r160 |
A |
T |
7: 22,570,967 (GRCm39) |
T107S |
probably damaging |
Het |
Vmn2r108 |
T |
A |
17: 20,692,457 (GRCm39) |
K133I |
probably benign |
Het |
Vmn2r15 |
A |
T |
5: 109,436,190 (GRCm39) |
|
probably null |
Het |
Wdr25 |
G |
A |
12: 108,958,819 (GRCm39) |
G344S |
possibly damaging |
Het |
Zfp354c |
C |
T |
11: 50,708,635 (GRCm39) |
|
probably null |
Het |
Zfp560 |
G |
T |
9: 20,260,206 (GRCm39) |
Q219K |
probably benign |
Het |
Zfp691 |
C |
T |
4: 119,028,181 (GRCm39) |
G17E |
probably damaging |
Het |
Zkscan14 |
A |
G |
5: 145,132,169 (GRCm39) |
F454S |
probably benign |
Het |
|
Other mutations in Zfp930 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00429:Zfp930
|
APN |
8 |
69,680,634 (GRCm39) |
missense |
probably damaging |
1.00 |
Bodyguard
|
UTSW |
8 |
69,681,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R0389:Zfp930
|
UTSW |
8 |
69,680,948 (GRCm39) |
nonsense |
probably null |
|
R1275:Zfp930
|
UTSW |
8 |
69,680,631 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1322:Zfp930
|
UTSW |
8 |
69,680,820 (GRCm39) |
missense |
probably benign |
0.02 |
R1802:Zfp930
|
UTSW |
8 |
69,679,046 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1917:Zfp930
|
UTSW |
8 |
69,681,357 (GRCm39) |
missense |
probably benign |
0.02 |
R1918:Zfp930
|
UTSW |
8 |
69,681,357 (GRCm39) |
missense |
probably benign |
0.02 |
R1981:Zfp930
|
UTSW |
8 |
69,680,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R4492:Zfp930
|
UTSW |
8 |
69,680,898 (GRCm39) |
nonsense |
probably null |
|
R4530:Zfp930
|
UTSW |
8 |
69,681,483 (GRCm39) |
nonsense |
probably null |
|
R4769:Zfp930
|
UTSW |
8 |
69,679,344 (GRCm39) |
missense |
probably benign |
0.09 |
R4906:Zfp930
|
UTSW |
8 |
69,681,597 (GRCm39) |
missense |
probably benign |
0.11 |
R5314:Zfp930
|
UTSW |
8 |
69,679,373 (GRCm39) |
missense |
probably benign |
0.27 |
R5708:Zfp930
|
UTSW |
8 |
69,679,113 (GRCm39) |
missense |
probably benign |
0.08 |
R6004:Zfp930
|
UTSW |
8 |
69,680,556 (GRCm39) |
missense |
probably benign |
|
R6385:Zfp930
|
UTSW |
8 |
69,681,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R7095:Zfp930
|
UTSW |
8 |
69,681,193 (GRCm39) |
missense |
probably benign |
|
R7641:Zfp930
|
UTSW |
8 |
69,681,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R7674:Zfp930
|
UTSW |
8 |
69,681,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R8300:Zfp930
|
UTSW |
8 |
69,680,998 (GRCm39) |
missense |
probably benign |
0.00 |
R8905:Zfp930
|
UTSW |
8 |
69,681,351 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8960:Zfp930
|
UTSW |
8 |
69,680,541 (GRCm39) |
missense |
probably damaging |
1.00 |
|