Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700048O20Rik |
C |
A |
9: 121,769,833 (GRCm39) |
|
noncoding transcript |
Het |
4930579F01Rik |
C |
A |
3: 137,891,959 (GRCm39) |
|
probably benign |
Het |
Aurkc |
T |
A |
7: 6,999,547 (GRCm39) |
I18N |
probably damaging |
Het |
Bace1 |
T |
C |
9: 45,750,588 (GRCm39) |
|
probably null |
Het |
Chrne |
C |
T |
11: 70,506,588 (GRCm39) |
V311I |
probably benign |
Het |
Cimip2b |
G |
A |
4: 43,428,158 (GRCm39) |
R100W |
possibly damaging |
Het |
Cyp2c70 |
C |
T |
19: 40,156,020 (GRCm39) |
V177M |
probably damaging |
Het |
Dusp10 |
A |
G |
1: 183,801,328 (GRCm39) |
E365G |
probably benign |
Het |
Fcgbp |
C |
A |
7: 27,785,560 (GRCm39) |
N332K |
possibly damaging |
Het |
Irx4 |
T |
C |
13: 73,416,810 (GRCm39) |
V402A |
probably benign |
Het |
Kcnq4 |
G |
A |
4: 120,555,213 (GRCm39) |
Q657* |
probably null |
Het |
Kif14 |
G |
A |
1: 136,396,756 (GRCm39) |
S354N |
probably benign |
Het |
Lama3 |
A |
G |
18: 12,582,645 (GRCm39) |
|
probably benign |
Het |
Lhfpl7 |
A |
G |
5: 113,383,869 (GRCm39) |
R96G |
probably benign |
Het |
Lrrc8b |
T |
C |
5: 105,628,365 (GRCm39) |
I237T |
probably damaging |
Het |
Mepe |
G |
T |
5: 104,485,843 (GRCm39) |
G328C |
probably damaging |
Het |
Numb |
A |
G |
12: 83,854,906 (GRCm39) |
I129T |
probably damaging |
Het |
Or5h25 |
T |
C |
16: 58,930,961 (GRCm39) |
D4G |
probably benign |
Het |
Or6c209 |
T |
C |
10: 129,483,306 (GRCm39) |
I103T |
probably benign |
Het |
Osmr |
T |
C |
15: 6,866,504 (GRCm39) |
D390G |
probably benign |
Het |
Pglyrp3 |
G |
A |
3: 91,929,986 (GRCm39) |
V51I |
probably damaging |
Het |
Phactr2 |
T |
C |
10: 13,121,279 (GRCm39) |
T470A |
probably damaging |
Het |
Psmg1 |
G |
A |
16: 95,781,268 (GRCm39) |
T259I |
possibly damaging |
Het |
Rtl3 |
T |
C |
X: 105,882,543 (GRCm39) |
T240A |
probably benign |
Het |
Ryr1 |
C |
T |
7: 28,824,385 (GRCm39) |
|
probably null |
Het |
Slc10a6 |
A |
G |
5: 103,756,991 (GRCm39) |
S258P |
probably benign |
Het |
Slc1a6 |
T |
C |
10: 78,637,647 (GRCm39) |
L391P |
probably damaging |
Het |
Slc6a7 |
C |
T |
18: 61,134,681 (GRCm39) |
V465M |
possibly damaging |
Het |
Sost |
T |
C |
11: 101,857,705 (GRCm39) |
D32G |
probably damaging |
Het |
Sox4 |
C |
A |
13: 29,136,956 (GRCm39) |
G17W |
probably damaging |
Het |
Tifab |
A |
G |
13: 56,324,282 (GRCm39) |
S54P |
probably damaging |
Het |
Tnrc6a |
T |
A |
7: 122,770,003 (GRCm39) |
S598T |
probably benign |
Het |
Vmn2r1 |
T |
A |
3: 64,012,809 (GRCm39) |
I890N |
probably damaging |
Het |
Wapl |
A |
G |
14: 34,414,593 (GRCm39) |
D485G |
probably benign |
Het |
Wee2 |
A |
T |
6: 40,438,995 (GRCm39) |
I373F |
probably damaging |
Het |
Xkr6 |
A |
G |
14: 64,056,664 (GRCm39) |
T192A |
probably damaging |
Het |
|
Other mutations in Zfp638 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
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 |
IGL02345:Zfp638
|
APN |
6 |
83,961,857 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|