Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
A |
T |
16: 4,668,228 (GRCm39) |
T540S |
probably benign |
Het |
Acp7 |
G |
T |
7: 28,314,001 (GRCm39) |
H369Q |
probably benign |
Het |
Adgrg3 |
A |
G |
8: 95,747,702 (GRCm39) |
N65S |
probably benign |
Het |
Anln |
A |
G |
9: 22,272,259 (GRCm39) |
V620A |
probably benign |
Het |
Atp10a |
T |
A |
7: 58,463,366 (GRCm39) |
S966R |
probably benign |
Het |
Atp8b3 |
T |
A |
10: 80,370,017 (GRCm39) |
Q132L |
possibly damaging |
Het |
Col4a1 |
T |
A |
8: 11,285,092 (GRCm39) |
|
probably null |
Het |
Ddx21 |
T |
C |
10: 62,429,871 (GRCm39) |
H291R |
possibly damaging |
Het |
Dlgap3 |
A |
G |
4: 127,088,416 (GRCm39) |
Y4C |
probably damaging |
Het |
Dnah5 |
A |
G |
15: 28,278,722 (GRCm39) |
N1106D |
probably benign |
Het |
Esyt1 |
T |
C |
10: 128,352,914 (GRCm39) |
D662G |
probably damaging |
Het |
F830016B08Rik |
T |
A |
18: 60,433,808 (GRCm39) |
V297E |
possibly damaging |
Het |
Faf1 |
T |
A |
4: 109,698,525 (GRCm39) |
N328K |
possibly damaging |
Het |
Gdf3 |
A |
C |
6: 122,583,859 (GRCm39) |
F169L |
probably benign |
Het |
Ifi213 |
G |
A |
1: 173,417,590 (GRCm39) |
T274I |
probably benign |
Het |
Igf2r |
T |
C |
17: 12,914,231 (GRCm39) |
D1746G |
possibly damaging |
Het |
Ighv1-75 |
T |
C |
12: 115,797,826 (GRCm39) |
K32R |
probably benign |
Het |
Ipo8 |
T |
A |
6: 148,698,239 (GRCm39) |
Q594L |
probably benign |
Het |
Krt87 |
A |
T |
15: 101,384,890 (GRCm39) |
I402N |
probably benign |
Het |
Med18 |
G |
A |
4: 132,187,281 (GRCm39) |
R118W |
probably damaging |
Het |
Mmrn2 |
A |
G |
14: 34,120,372 (GRCm39) |
E414G |
probably damaging |
Het |
Myo6 |
A |
G |
9: 80,168,176 (GRCm39) |
T447A |
probably benign |
Het |
Ncoa6 |
T |
C |
2: 155,279,935 (GRCm39) |
E27G |
probably benign |
Het |
Ngly1 |
T |
C |
14: 16,283,439 (GRCm38) |
L406S |
possibly damaging |
Het |
Or14j1 |
T |
C |
17: 38,145,998 (GRCm39) |
I36T |
probably benign |
Het |
Or51l4 |
A |
G |
7: 103,404,735 (GRCm39) |
I19T |
probably damaging |
Het |
Phldb1 |
T |
C |
9: 44,629,585 (GRCm39) |
Y156C |
probably damaging |
Het |
Pkd2l1 |
T |
A |
19: 44,145,708 (GRCm39) |
T172S |
probably benign |
Het |
Pknox2 |
G |
A |
9: 36,820,987 (GRCm39) |
R292* |
probably null |
Het |
Plod3 |
G |
C |
5: 137,017,000 (GRCm39) |
A50P |
probably benign |
Het |
Polr3e |
T |
C |
7: 120,532,600 (GRCm39) |
L212P |
probably damaging |
Het |
Ppp4r4 |
A |
G |
12: 103,547,653 (GRCm39) |
I215M |
possibly damaging |
Het |
Psmg2 |
T |
C |
18: 67,781,288 (GRCm39) |
Y127H |
possibly damaging |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Ptp4a1 |
A |
T |
1: 30,985,213 (GRCm39) |
M4K |
probably benign |
Het |
R3hcc1l |
A |
T |
19: 42,552,427 (GRCm39) |
I475L |
possibly damaging |
Het |
Rbp3 |
C |
T |
14: 33,677,975 (GRCm39) |
T641M |
probably damaging |
Het |
Rsf1 |
GGC |
GGCGGCGGCGGC |
7: 97,229,140 (GRCm39) |
|
probably benign |
Het |
Sec63 |
T |
A |
10: 42,659,522 (GRCm39) |
I70N |
probably benign |
Het |
Slc2a5 |
A |
C |
4: 150,205,203 (GRCm39) |
K4T |
probably benign |
Het |
Slc4a3 |
A |
G |
1: 75,532,119 (GRCm39) |
Y939C |
possibly damaging |
Het |
Slc7a15 |
T |
C |
12: 8,579,345 (GRCm39) |
*229W |
probably null |
Het |
Slco1a6 |
C |
A |
6: 142,058,662 (GRCm39) |
G206C |
probably damaging |
Het |
Spata9 |
A |
G |
13: 76,125,895 (GRCm39) |
Q126R |
probably benign |
Het |
Speg |
A |
T |
1: 75,383,570 (GRCm39) |
D1186V |
probably benign |
Het |
Spink5 |
T |
G |
18: 44,115,359 (GRCm39) |
M197R |
probably damaging |
Het |
Stab2 |
T |
C |
10: 86,697,363 (GRCm39) |
D1975G |
probably benign |
Het |
Syngap1 |
T |
A |
17: 27,176,385 (GRCm39) |
C224* |
probably null |
Het |
Ttn |
T |
C |
2: 76,698,807 (GRCm39) |
|
probably benign |
Het |
Txnrd1 |
G |
A |
10: 82,721,116 (GRCm39) |
E397K |
probably benign |
Het |
Ugt2b36 |
A |
T |
5: 87,237,344 (GRCm39) |
M313K |
probably damaging |
Het |
Ulk3 |
A |
G |
9: 57,497,724 (GRCm39) |
I74V |
possibly damaging |
Het |
Zcchc4 |
T |
C |
5: 52,953,573 (GRCm39) |
V194A |
probably damaging |
Het |
Zfp27 |
C |
T |
7: 29,595,792 (GRCm39) |
A58T |
possibly damaging |
Het |
|
Other mutations in Zfp398 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01420:Zfp398
|
APN |
6 |
47,842,868 (GRCm39) |
missense |
probably benign |
|
IGL01543:Zfp398
|
APN |
6 |
47,842,997 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01822:Zfp398
|
APN |
6 |
47,843,205 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02118:Zfp398
|
APN |
6 |
47,835,879 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02454:Zfp398
|
APN |
6 |
47,817,301 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02725:Zfp398
|
APN |
6 |
47,842,737 (GRCm39) |
missense |
probably benign |
0.00 |
R0453:Zfp398
|
UTSW |
6 |
47,842,782 (GRCm39) |
missense |
probably benign |
0.01 |
R0635:Zfp398
|
UTSW |
6 |
47,840,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R1759:Zfp398
|
UTSW |
6 |
47,836,412 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2366:Zfp398
|
UTSW |
6 |
47,840,143 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4090:Zfp398
|
UTSW |
6 |
47,843,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R4157:Zfp398
|
UTSW |
6 |
47,812,843 (GRCm39) |
missense |
probably benign |
|
R4610:Zfp398
|
UTSW |
6 |
47,817,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R4784:Zfp398
|
UTSW |
6 |
47,817,186 (GRCm39) |
missense |
probably benign |
|
R4849:Zfp398
|
UTSW |
6 |
47,836,446 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5166:Zfp398
|
UTSW |
6 |
47,842,838 (GRCm39) |
missense |
probably benign |
|
R5289:Zfp398
|
UTSW |
6 |
47,840,115 (GRCm39) |
missense |
probably benign |
|
R5877:Zfp398
|
UTSW |
6 |
47,817,638 (GRCm39) |
intron |
probably benign |
|
R6326:Zfp398
|
UTSW |
6 |
47,843,355 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6383:Zfp398
|
UTSW |
6 |
47,843,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R6825:Zfp398
|
UTSW |
6 |
47,843,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R6882:Zfp398
|
UTSW |
6 |
47,843,016 (GRCm39) |
missense |
probably damaging |
0.99 |
R7038:Zfp398
|
UTSW |
6 |
47,843,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R7114:Zfp398
|
UTSW |
6 |
47,842,910 (GRCm39) |
missense |
probably benign |
0.00 |
R7386:Zfp398
|
UTSW |
6 |
47,835,884 (GRCm39) |
missense |
probably benign |
0.05 |
R7519:Zfp398
|
UTSW |
6 |
47,836,407 (GRCm39) |
missense |
probably benign |
0.00 |
R7525:Zfp398
|
UTSW |
6 |
47,842,752 (GRCm39) |
missense |
probably benign |
|
R7571:Zfp398
|
UTSW |
6 |
47,843,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R8374:Zfp398
|
UTSW |
6 |
47,836,468 (GRCm39) |
critical splice donor site |
probably null |
|
R9055:Zfp398
|
UTSW |
6 |
47,843,319 (GRCm39) |
missense |
possibly damaging |
0.73 |
Z1176:Zfp398
|
UTSW |
6 |
47,843,789 (GRCm39) |
missense |
probably benign |
|
|