Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
A |
G |
3: 124,200,119 (GRCm39) |
L491P |
probably damaging |
Het |
Abcc6 |
T |
A |
7: 45,635,894 (GRCm39) |
D1051V |
probably damaging |
Het |
Actmap |
T |
C |
7: 26,900,561 (GRCm39) |
M180T |
probably damaging |
Het |
Aqr |
T |
A |
2: 113,989,424 (GRCm39) |
E133V |
probably benign |
Het |
Bag6 |
A |
G |
17: 35,364,603 (GRCm39) |
N911D |
probably damaging |
Het |
Cdcp3 |
G |
T |
7: 130,803,527 (GRCm39) |
|
probably null |
Het |
Ces4a |
C |
T |
8: 105,874,836 (GRCm39) |
|
probably benign |
Het |
Clec3b |
A |
T |
9: 122,980,100 (GRCm39) |
|
probably benign |
Het |
Cnot1 |
T |
C |
8: 96,496,243 (GRCm39) |
|
probably benign |
Het |
Ctsg |
T |
A |
14: 56,337,417 (GRCm39) |
*262L |
probably null |
Het |
Cyp17a1 |
T |
A |
19: 46,661,050 (GRCm39) |
H78L |
possibly damaging |
Het |
Dcaf13 |
C |
A |
15: 38,991,371 (GRCm39) |
|
probably benign |
Het |
Dcun1d1 |
G |
T |
3: 35,975,141 (GRCm39) |
Q52K |
possibly damaging |
Het |
Ddb1 |
C |
T |
19: 10,590,309 (GRCm39) |
R279W |
probably damaging |
Het |
Dock1 |
A |
G |
7: 134,366,945 (GRCm39) |
|
probably benign |
Het |
Dsel |
A |
G |
1: 111,787,793 (GRCm39) |
L914P |
probably damaging |
Het |
Fbxo31 |
A |
G |
8: 122,286,757 (GRCm39) |
F174L |
probably benign |
Het |
Gm9116 |
A |
G |
3: 93,817,513 (GRCm39) |
|
noncoding transcript |
Het |
Gspt1 |
C |
T |
16: 11,056,763 (GRCm39) |
V211I |
probably benign |
Het |
Hmgb1 |
A |
T |
5: 148,987,508 (GRCm39) |
S14T |
probably benign |
Het |
Igsf8 |
A |
G |
1: 172,140,096 (GRCm39) |
|
probably benign |
Het |
Klf13 |
A |
G |
7: 63,541,417 (GRCm39) |
F237L |
probably damaging |
Het |
Mon2 |
A |
T |
10: 122,854,005 (GRCm39) |
I962N |
probably damaging |
Het |
Nfx1 |
A |
G |
4: 41,024,851 (GRCm39) |
D1108G |
probably damaging |
Het |
Nr2e1 |
T |
C |
10: 42,447,478 (GRCm39) |
Y178C |
probably damaging |
Het |
Or4d10c |
C |
A |
19: 12,065,230 (GRCm39) |
E309* |
probably null |
Het |
Or52d1 |
A |
T |
7: 103,755,854 (GRCm39) |
I123F |
probably damaging |
Het |
Pde3b |
A |
T |
7: 114,122,583 (GRCm39) |
H717L |
probably damaging |
Het |
Polr1b |
T |
C |
2: 128,965,049 (GRCm39) |
Y712H |
probably damaging |
Het |
Pramel16 |
C |
A |
4: 143,676,767 (GRCm39) |
K112N |
probably damaging |
Het |
Rnf157 |
T |
A |
11: 116,238,795 (GRCm39) |
|
probably null |
Het |
Ros1 |
T |
C |
10: 51,974,902 (GRCm39) |
E1561G |
probably damaging |
Het |
Serpina6 |
A |
G |
12: 103,620,154 (GRCm39) |
|
probably null |
Het |
St18 |
A |
G |
1: 6,839,118 (GRCm39) |
|
probably benign |
Het |
Ugp2 |
A |
G |
11: 21,279,722 (GRCm39) |
|
probably benign |
Het |
Vmn1r70 |
T |
C |
7: 10,368,186 (GRCm39) |
S225P |
probably benign |
Het |
|
Other mutations in Zfp641 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01639:Zfp641
|
APN |
15 |
98,189,066 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03191:Zfp641
|
APN |
15 |
98,186,568 (GRCm39) |
missense |
probably damaging |
0.98 |
R0079:Zfp641
|
UTSW |
15 |
98,186,970 (GRCm39) |
missense |
probably benign |
0.28 |
R0243:Zfp641
|
UTSW |
15 |
98,187,008 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0487:Zfp641
|
UTSW |
15 |
98,187,060 (GRCm39) |
missense |
probably benign |
|
R2092:Zfp641
|
UTSW |
15 |
98,191,593 (GRCm39) |
missense |
probably benign |
|
R3415:Zfp641
|
UTSW |
15 |
98,188,421 (GRCm39) |
missense |
probably benign |
0.28 |
R4834:Zfp641
|
UTSW |
15 |
98,191,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R4851:Zfp641
|
UTSW |
15 |
98,186,598 (GRCm39) |
missense |
probably damaging |
0.99 |
R5776:Zfp641
|
UTSW |
15 |
98,186,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R6057:Zfp641
|
UTSW |
15 |
98,190,816 (GRCm39) |
missense |
probably benign |
0.00 |
R6896:Zfp641
|
UTSW |
15 |
98,191,684 (GRCm39) |
start codon destroyed |
probably benign |
0.06 |
R6958:Zfp641
|
UTSW |
15 |
98,190,832 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6969:Zfp641
|
UTSW |
15 |
98,188,448 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8117:Zfp641
|
UTSW |
15 |
98,186,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R8314:Zfp641
|
UTSW |
15 |
98,188,464 (GRCm39) |
missense |
probably damaging |
0.97 |
R9130:Zfp641
|
UTSW |
15 |
98,186,732 (GRCm39) |
missense |
probably benign |
0.12 |
Z1177:Zfp641
|
UTSW |
15 |
98,186,416 (GRCm39) |
missense |
probably damaging |
1.00 |
|