Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts18 |
T |
C |
8: 114,571,741 (GRCm39) |
I81V |
probably benign |
Het |
Aoc1l1 |
A |
C |
6: 48,952,618 (GRCm39) |
D181A |
possibly damaging |
Het |
Armc3 |
T |
A |
2: 19,273,957 (GRCm39) |
D330E |
probably damaging |
Het |
Atp6v0b |
A |
G |
4: 117,743,062 (GRCm39) |
F49S |
probably damaging |
Het |
Atp8b3 |
A |
C |
10: 80,366,802 (GRCm39) |
Y265* |
probably null |
Het |
Cby2 |
A |
G |
14: 75,821,551 (GRCm39) |
F16S |
probably damaging |
Het |
Cdh11 |
A |
G |
8: 103,406,276 (GRCm39) |
Y66H |
probably damaging |
Het |
Cntn5 |
T |
A |
9: 9,673,913 (GRCm39) |
M730L |
probably benign |
Het |
Cntrl |
A |
G |
2: 35,063,071 (GRCm39) |
T1556A |
probably benign |
Het |
Dixdc1 |
A |
G |
9: 50,617,434 (GRCm39) |
S128P |
probably damaging |
Het |
Egfr |
T |
C |
11: 16,855,382 (GRCm39) |
L889S |
probably damaging |
Het |
F830045P16Rik |
A |
G |
2: 129,305,640 (GRCm39) |
Y245H |
probably benign |
Het |
Fam124a |
G |
A |
14: 62,825,181 (GRCm39) |
C225Y |
probably damaging |
Het |
Frem2 |
T |
C |
3: 53,442,702 (GRCm39) |
T2612A |
probably benign |
Het |
Gkap1 |
A |
T |
13: 58,411,106 (GRCm39) |
I89N |
probably benign |
Het |
Gm8247 |
A |
T |
14: 44,823,811 (GRCm39) |
K75* |
probably null |
Het |
Gpi-ps |
A |
G |
8: 5,689,833 (GRCm39) |
|
noncoding transcript |
Het |
Hdac11 |
T |
A |
6: 91,150,162 (GRCm39) |
H320Q |
probably benign |
Het |
Iyd |
A |
G |
10: 3,497,091 (GRCm39) |
I149V |
probably benign |
Het |
Krtap4-6 |
T |
A |
11: 99,556,676 (GRCm39) |
Q17L |
unknown |
Het |
Lrrc24 |
T |
A |
15: 76,606,775 (GRCm39) |
D207V |
probably damaging |
Het |
Mfsd12 |
G |
A |
10: 81,198,858 (GRCm39) |
C425Y |
probably damaging |
Het |
Muc5b |
A |
G |
7: 141,416,977 (GRCm39) |
T3308A |
probably benign |
Het |
Myo18b |
A |
G |
5: 112,905,315 (GRCm39) |
|
probably benign |
Het |
Ndufa6 |
C |
T |
15: 82,238,282 (GRCm39) |
V50M |
possibly damaging |
Het |
Nin |
A |
G |
12: 70,089,962 (GRCm39) |
V1151A |
probably benign |
Het |
Nrf1 |
A |
G |
6: 30,126,366 (GRCm39) |
|
probably benign |
Het |
Pcdhb20 |
T |
C |
18: 37,637,852 (GRCm39) |
I126T |
possibly damaging |
Het |
Pdgfra |
G |
T |
5: 75,338,352 (GRCm39) |
L535F |
probably damaging |
Het |
Pkn2 |
A |
T |
3: 142,535,078 (GRCm39) |
I212K |
possibly damaging |
Het |
Slc5a9 |
T |
A |
4: 111,755,833 (GRCm39) |
T22S |
probably benign |
Het |
Slitrk1 |
A |
G |
14: 109,150,450 (GRCm39) |
L87S |
probably damaging |
Het |
Syne2 |
C |
A |
12: 76,134,589 (GRCm39) |
R29S |
probably damaging |
Het |
Zc3h12b |
C |
A |
X: 94,970,721 (GRCm39) |
F551L |
probably damaging |
Het |
|
Other mutations in Zfp664 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02683:Zfp664
|
APN |
5 |
124,963,386 (GRCm39) |
missense |
probably benign |
0.03 |
R0394:Zfp664
|
UTSW |
5 |
124,963,129 (GRCm39) |
nonsense |
probably null |
|
R0629:Zfp664
|
UTSW |
5 |
124,962,659 (GRCm39) |
missense |
probably damaging |
0.99 |
R1400:Zfp664
|
UTSW |
5 |
124,963,217 (GRCm39) |
missense |
unknown |
|
R6052:Zfp664
|
UTSW |
5 |
124,963,250 (GRCm39) |
missense |
unknown |
|
R6058:Zfp664
|
UTSW |
5 |
124,963,042 (GRCm39) |
nonsense |
probably null |
|
R6529:Zfp664
|
UTSW |
5 |
124,963,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R7031:Zfp664
|
UTSW |
5 |
124,963,070 (GRCm39) |
missense |
probably benign |
0.06 |
R7752:Zfp664
|
UTSW |
5 |
124,962,839 (GRCm39) |
nonsense |
probably null |
|
R7901:Zfp664
|
UTSW |
5 |
124,962,839 (GRCm39) |
nonsense |
probably null |
|
R8434:Zfp664
|
UTSW |
5 |
124,962,827 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8686:Zfp664
|
UTSW |
5 |
124,963,133 (GRCm39) |
missense |
possibly damaging |
0.61 |
|