Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
T |
C |
14: 32,382,414 (GRCm39) |
T1184A |
possibly damaging |
Het |
A2ml1 |
A |
G |
6: 128,557,375 (GRCm39) |
I106T |
probably damaging |
Het |
Asic4 |
C |
T |
1: 75,427,510 (GRCm39) |
A12V |
probably damaging |
Het |
Cacna1d |
A |
T |
14: 29,821,099 (GRCm39) |
V1139D |
probably damaging |
Het |
Edc4 |
T |
C |
8: 106,616,613 (GRCm39) |
|
probably benign |
Het |
Eif4h |
A |
T |
5: 134,654,393 (GRCm39) |
|
probably null |
Het |
Exog |
C |
A |
9: 119,291,592 (GRCm39) |
Q290K |
probably damaging |
Het |
Fam83c |
A |
T |
2: 155,676,728 (GRCm39) |
I14K |
possibly damaging |
Het |
Fes |
A |
T |
7: 80,033,021 (GRCm39) |
Y268N |
probably benign |
Het |
Fhod1 |
A |
G |
8: 106,056,281 (GRCm39) |
L1144P |
probably damaging |
Het |
Frem3 |
C |
T |
8: 81,340,944 (GRCm39) |
T1079I |
probably damaging |
Het |
Gbp10 |
A |
G |
5: 105,368,980 (GRCm39) |
|
probably benign |
Het |
Herc1 |
T |
C |
9: 66,404,918 (GRCm39) |
V4496A |
possibly damaging |
Het |
Lamb1 |
A |
G |
12: 31,350,261 (GRCm39) |
R729G |
possibly damaging |
Het |
Lifr |
T |
A |
15: 7,205,147 (GRCm39) |
C461* |
probably null |
Het |
Lypd6 |
T |
C |
2: 50,078,795 (GRCm39) |
V97A |
probably benign |
Het |
Map3k5 |
A |
G |
10: 19,993,933 (GRCm39) |
E973G |
possibly damaging |
Het |
Mep1b |
A |
T |
18: 21,230,524 (GRCm39) |
N692I |
probably benign |
Het |
Mrpl15 |
A |
G |
1: 4,846,754 (GRCm39) |
V274A |
probably damaging |
Het |
Naaa |
A |
G |
5: 92,411,507 (GRCm39) |
I264T |
probably damaging |
Het |
Nlrp4c |
T |
C |
7: 6,103,783 (GRCm39) |
C906R |
possibly damaging |
Het |
Or1j15 |
T |
A |
2: 36,458,754 (GRCm39) |
L48H |
probably damaging |
Het |
Or4x11 |
T |
C |
2: 89,868,162 (GRCm39) |
W300R |
possibly damaging |
Het |
Or5b95 |
T |
C |
19: 12,658,035 (GRCm39) |
S188P |
possibly damaging |
Het |
Or8b38 |
A |
T |
9: 37,973,300 (GRCm39) |
H228L |
possibly damaging |
Het |
Or8k3 |
T |
C |
2: 86,058,628 (GRCm39) |
N229S |
probably benign |
Het |
Phc2 |
C |
T |
4: 128,616,903 (GRCm39) |
T392I |
probably benign |
Het |
Ptprg |
G |
A |
14: 12,213,702 (GRCm38) |
W248* |
probably null |
Het |
Pzp |
T |
A |
6: 128,498,087 (GRCm39) |
E243D |
probably benign |
Het |
Rbm33 |
T |
A |
5: 28,592,846 (GRCm39) |
L542Q |
probably damaging |
Het |
Recql4 |
G |
A |
15: 76,593,144 (GRCm39) |
T229I |
probably benign |
Het |
Ssbp3 |
T |
C |
4: 106,894,855 (GRCm39) |
|
probably benign |
Het |
Tfap2d |
A |
T |
1: 19,218,620 (GRCm39) |
Q373L |
probably damaging |
Het |
Timmdc1 |
A |
G |
16: 38,338,902 (GRCm39) |
|
probably benign |
Het |
Tiparp |
G |
T |
3: 65,460,030 (GRCm39) |
G442* |
probably null |
Het |
Vmn2r4 |
A |
T |
3: 64,313,816 (GRCm39) |
N388K |
probably damaging |
Het |
Vps13c |
T |
C |
9: 67,820,209 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Zfp551 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01990:Zfp551
|
APN |
7 |
12,156,343 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02511:Zfp551
|
APN |
7 |
12,150,602 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2001:Zfp551
|
UTSW |
7 |
12,150,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R3120:Zfp551
|
UTSW |
7 |
12,149,943 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4256:Zfp551
|
UTSW |
7 |
12,150,318 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4387:Zfp551
|
UTSW |
7 |
12,152,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R5314:Zfp551
|
UTSW |
7 |
12,150,087 (GRCm39) |
nonsense |
probably null |
|
R5536:Zfp551
|
UTSW |
7 |
12,149,488 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5874:Zfp551
|
UTSW |
7 |
12,150,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R6265:Zfp551
|
UTSW |
7 |
12,149,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R6765:Zfp551
|
UTSW |
7 |
12,150,767 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6803:Zfp551
|
UTSW |
7 |
12,151,108 (GRCm39) |
nonsense |
probably null |
|
R6953:Zfp551
|
UTSW |
7 |
12,150,715 (GRCm39) |
nonsense |
probably null |
|
R7334:Zfp551
|
UTSW |
7 |
12,150,681 (GRCm39) |
missense |
probably damaging |
0.97 |
R7345:Zfp551
|
UTSW |
7 |
12,150,522 (GRCm39) |
missense |
probably benign |
|
R7502:Zfp551
|
UTSW |
7 |
12,149,725 (GRCm39) |
nonsense |
probably null |
|
R7772:Zfp551
|
UTSW |
7 |
12,152,535 (GRCm39) |
missense |
probably damaging |
0.98 |
R7776:Zfp551
|
UTSW |
7 |
12,152,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R7999:Zfp551
|
UTSW |
7 |
12,151,138 (GRCm39) |
nonsense |
probably null |
|
R8032:Zfp551
|
UTSW |
7 |
12,152,487 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8984:Zfp551
|
UTSW |
7 |
12,156,559 (GRCm39) |
unclassified |
probably benign |
|
R9082:Zfp551
|
UTSW |
7 |
12,151,004 (GRCm39) |
missense |
probably damaging |
1.00 |
|