Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc1 |
G |
T |
16: 14,214,215 (GRCm39) |
D177Y |
possibly damaging |
Het |
Casc3 |
T |
C |
11: 98,718,390 (GRCm39) |
|
probably benign |
Het |
Catspere2 |
G |
A |
1: 177,842,754 (GRCm39) |
V60I |
possibly damaging |
Het |
Cnga1 |
C |
T |
5: 72,762,615 (GRCm39) |
V300I |
probably benign |
Het |
Dcun1d4 |
A |
G |
5: 73,668,495 (GRCm39) |
D41G |
probably damaging |
Het |
Dnm1l |
T |
C |
16: 16,147,758 (GRCm39) |
S181G |
possibly damaging |
Het |
Dyrk1a |
T |
G |
16: 94,472,221 (GRCm39) |
S242A |
possibly damaging |
Het |
Fcgbp |
T |
A |
7: 27,771,068 (GRCm39) |
|
probably benign |
Het |
Fibcd1 |
T |
C |
2: 31,706,604 (GRCm39) |
Y409C |
probably damaging |
Het |
Fig4 |
A |
T |
10: 41,143,770 (GRCm39) |
W230R |
probably null |
Het |
Flt1 |
T |
C |
5: 147,519,436 (GRCm39) |
S960G |
probably benign |
Het |
Fyb1 |
A |
G |
15: 6,649,143 (GRCm39) |
S390G |
possibly damaging |
Het |
Gbx2 |
T |
C |
1: 89,856,698 (GRCm39) |
T231A |
probably benign |
Het |
Gm5852 |
T |
A |
3: 93,635,055 (GRCm39) |
|
noncoding transcript |
Het |
Lmo7 |
T |
C |
14: 102,124,909 (GRCm39) |
V456A |
probably damaging |
Het |
Mark3 |
A |
G |
12: 111,593,541 (GRCm39) |
N191S |
probably damaging |
Het |
Or7h8 |
C |
A |
9: 20,124,314 (GRCm39) |
S223Y |
possibly damaging |
Het |
Pik3c2a |
C |
T |
7: 116,005,126 (GRCm39) |
E381K |
probably damaging |
Het |
Pik3r5 |
A |
G |
11: 68,383,552 (GRCm39) |
D457G |
probably benign |
Het |
Plcg2 |
T |
C |
8: 118,311,919 (GRCm39) |
S404P |
probably damaging |
Het |
Prr16 |
T |
C |
18: 51,436,301 (GRCm39) |
F260S |
probably damaging |
Het |
Psd4 |
T |
C |
2: 24,291,835 (GRCm39) |
|
probably null |
Het |
Ptgs1 |
A |
G |
2: 36,132,983 (GRCm39) |
D327G |
probably null |
Het |
Rgsl1 |
C |
T |
1: 153,679,755 (GRCm39) |
|
probably null |
Het |
Spart |
T |
A |
3: 55,025,147 (GRCm39) |
|
probably null |
Het |
Sugp1 |
A |
G |
8: 70,495,734 (GRCm39) |
|
probably benign |
Het |
Tubgcp3 |
A |
T |
8: 12,675,056 (GRCm39) |
I713N |
probably damaging |
Het |
Usp19 |
A |
G |
9: 108,371,057 (GRCm39) |
T240A |
probably benign |
Het |
Vash2 |
A |
G |
1: 190,710,412 (GRCm39) |
V81A |
probably benign |
Het |
Vmn2r41 |
T |
G |
7: 8,141,767 (GRCm39) |
N566H |
probably damaging |
Het |
Wdr31 |
A |
G |
4: 62,377,083 (GRCm39) |
I42T |
possibly damaging |
Het |
Zfp292 |
C |
T |
4: 34,809,244 (GRCm39) |
V1272I |
possibly damaging |
Het |
|
Other mutations in Zfp638 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00335:Zfp638
|
APN |
6 |
83,956,700 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00514:Zfp638
|
APN |
6 |
83,933,680 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00705:Zfp638
|
APN |
6 |
83,954,112 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00785:Zfp638
|
APN |
6 |
83,906,146 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01068:Zfp638
|
APN |
6 |
83,911,976 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01084:Zfp638
|
APN |
6 |
83,921,780 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01570:Zfp638
|
APN |
6 |
83,924,829 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01758:Zfp638
|
APN |
6 |
83,956,508 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02939:Zfp638
|
APN |
6 |
83,946,214 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03007:Zfp638
|
APN |
6 |
83,961,866 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03118:Zfp638
|
APN |
6 |
83,912,000 (GRCm39) |
splice site |
probably benign |
|
IGL03135:Zfp638
|
APN |
6 |
83,919,857 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03264:Zfp638
|
APN |
6 |
83,923,229 (GRCm39) |
missense |
probably benign |
0.04 |
R0190:Zfp638
|
UTSW |
6 |
83,905,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R0200:Zfp638
|
UTSW |
6 |
83,944,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R0766:Zfp638
|
UTSW |
6 |
83,906,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R0801:Zfp638
|
UTSW |
6 |
83,949,220 (GRCm39) |
unclassified |
probably benign |
|
R0938:Zfp638
|
UTSW |
6 |
83,961,023 (GRCm39) |
missense |
probably benign |
0.16 |
R1312:Zfp638
|
UTSW |
6 |
83,906,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R1458:Zfp638
|
UTSW |
6 |
83,921,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R1584:Zfp638
|
UTSW |
6 |
83,955,047 (GRCm39) |
splice site |
probably null |
|
R1634:Zfp638
|
UTSW |
6 |
83,956,894 (GRCm39) |
splice site |
probably null |
|
R1651:Zfp638
|
UTSW |
6 |
83,931,719 (GRCm39) |
missense |
probably benign |
0.00 |
R2079:Zfp638
|
UTSW |
6 |
83,930,371 (GRCm39) |
critical splice donor site |
probably null |
|
R2134:Zfp638
|
UTSW |
6 |
83,905,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R2142:Zfp638
|
UTSW |
6 |
83,963,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R2201:Zfp638
|
UTSW |
6 |
83,906,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R2422:Zfp638
|
UTSW |
6 |
83,943,421 (GRCm39) |
splice site |
probably benign |
|
R4353:Zfp638
|
UTSW |
6 |
83,961,041 (GRCm39) |
missense |
probably damaging |
0.97 |
R4681:Zfp638
|
UTSW |
6 |
83,958,719 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4716:Zfp638
|
UTSW |
6 |
83,956,544 (GRCm39) |
nonsense |
probably null |
|
R4807:Zfp638
|
UTSW |
6 |
83,920,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R4850:Zfp638
|
UTSW |
6 |
83,956,457 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5079:Zfp638
|
UTSW |
6 |
83,906,438 (GRCm39) |
missense |
probably benign |
0.03 |
R5236:Zfp638
|
UTSW |
6 |
83,953,557 (GRCm39) |
nonsense |
probably null |
|
R5323:Zfp638
|
UTSW |
6 |
83,939,076 (GRCm39) |
missense |
probably damaging |
0.96 |
R5426:Zfp638
|
UTSW |
6 |
83,953,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R5557:Zfp638
|
UTSW |
6 |
83,944,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R5570:Zfp638
|
UTSW |
6 |
83,956,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R5614:Zfp638
|
UTSW |
6 |
83,906,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R5662:Zfp638
|
UTSW |
6 |
83,920,111 (GRCm39) |
missense |
probably damaging |
0.97 |
R5685:Zfp638
|
UTSW |
6 |
83,906,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R5689:Zfp638
|
UTSW |
6 |
83,906,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R5783:Zfp638
|
UTSW |
6 |
83,921,829 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5856:Zfp638
|
UTSW |
6 |
83,954,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R6310:Zfp638
|
UTSW |
6 |
83,844,212 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6477:Zfp638
|
UTSW |
6 |
83,942,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R6557:Zfp638
|
UTSW |
6 |
83,907,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R7084:Zfp638
|
UTSW |
6 |
83,930,108 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7101:Zfp638
|
UTSW |
6 |
83,931,708 (GRCm39) |
missense |
probably benign |
0.00 |
R7141:Zfp638
|
UTSW |
6 |
83,844,181 (GRCm39) |
missense |
unknown |
|
R7368:Zfp638
|
UTSW |
6 |
83,906,437 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7402:Zfp638
|
UTSW |
6 |
83,905,670 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7455:Zfp638
|
UTSW |
6 |
83,907,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R7762:Zfp638
|
UTSW |
6 |
83,953,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R7773:Zfp638
|
UTSW |
6 |
83,956,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R8090:Zfp638
|
UTSW |
6 |
83,906,801 (GRCm39) |
missense |
probably damaging |
0.99 |
R8154:Zfp638
|
UTSW |
6 |
83,954,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R8161:Zfp638
|
UTSW |
6 |
83,906,713 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8327:Zfp638
|
UTSW |
6 |
83,905,679 (GRCm39) |
missense |
probably damaging |
0.99 |
R8384:Zfp638
|
UTSW |
6 |
83,956,747 (GRCm39) |
missense |
probably benign |
0.28 |
R8703:Zfp638
|
UTSW |
6 |
83,954,143 (GRCm39) |
missense |
probably damaging |
0.96 |
R8738:Zfp638
|
UTSW |
6 |
83,931,745 (GRCm39) |
critical splice donor site |
probably null |
|
R8865:Zfp638
|
UTSW |
6 |
83,954,035 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8874:Zfp638
|
UTSW |
6 |
83,946,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R9080:Zfp638
|
UTSW |
6 |
83,844,155 (GRCm39) |
missense |
unknown |
|
R9113:Zfp638
|
UTSW |
6 |
83,953,894 (GRCm39) |
missense |
probably damaging |
0.96 |
R9574:Zfp638
|
UTSW |
6 |
83,956,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R9661:Zfp638
|
UTSW |
6 |
83,923,320 (GRCm39) |
missense |
probably damaging |
0.99 |
R9722:Zfp638
|
UTSW |
6 |
83,923,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R9745:Zfp638
|
UTSW |
6 |
83,921,795 (GRCm39) |
missense |
probably benign |
0.27 |
Z1088:Zfp638
|
UTSW |
6 |
83,921,793 (GRCm39) |
missense |
probably damaging |
1.00 |
|