Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1a |
G |
A |
5: 8,752,216 (GRCm39) |
G426S |
probably damaging |
Het |
Casp4 |
A |
T |
9: 5,328,573 (GRCm39) |
|
probably benign |
Het |
Ccdc40 |
T |
A |
11: 119,144,229 (GRCm39) |
F988Y |
probably damaging |
Het |
Ccdc9b |
T |
C |
2: 118,590,098 (GRCm39) |
T249A |
probably benign |
Het |
Chd5 |
T |
A |
4: 152,464,389 (GRCm39) |
V1516E |
probably benign |
Het |
Chrnd |
T |
A |
1: 87,123,389 (GRCm39) |
|
probably null |
Het |
Col5a3 |
C |
A |
9: 20,683,738 (GRCm39) |
G1506V |
unknown |
Het |
Csgalnact2 |
A |
T |
6: 118,106,215 (GRCm39) |
C34* |
probably null |
Het |
Ddx23 |
T |
C |
15: 98,549,832 (GRCm39) |
K195E |
probably benign |
Het |
Dhps |
T |
G |
8: 85,800,880 (GRCm39) |
S240A |
probably benign |
Het |
Dnah5 |
T |
A |
15: 28,234,599 (GRCm39) |
|
probably null |
Het |
Dock10 |
T |
C |
1: 80,514,676 (GRCm39) |
T1414A |
probably benign |
Het |
Dock4 |
A |
G |
12: 40,805,812 (GRCm39) |
D928G |
probably damaging |
Het |
Dolpp1 |
T |
C |
2: 30,285,658 (GRCm39) |
|
probably benign |
Het |
Dse |
T |
A |
10: 34,028,601 (GRCm39) |
I830F |
probably damaging |
Het |
Elmod1 |
C |
T |
9: 53,843,091 (GRCm39) |
R29Q |
probably damaging |
Het |
Ephx4 |
T |
A |
5: 107,577,518 (GRCm39) |
|
probably null |
Het |
Evi5 |
A |
T |
5: 107,968,302 (GRCm39) |
M215K |
probably damaging |
Het |
Fbxl4 |
T |
C |
4: 22,390,678 (GRCm39) |
L287P |
probably damaging |
Het |
Gbp9 |
G |
A |
5: 105,230,724 (GRCm39) |
S400L |
probably damaging |
Het |
Gm6291 |
T |
C |
18: 6,371,365 (GRCm39) |
|
noncoding transcript |
Het |
Gmcl1 |
A |
T |
6: 86,688,596 (GRCm39) |
D301E |
probably benign |
Het |
Gna14 |
C |
T |
19: 16,580,692 (GRCm39) |
R177C |
possibly damaging |
Het |
Golph3 |
C |
T |
15: 12,339,756 (GRCm39) |
R90C |
probably damaging |
Het |
Gpr142 |
T |
A |
11: 114,689,785 (GRCm39) |
C12* |
probably null |
Het |
Hat1 |
T |
A |
2: 71,239,357 (GRCm39) |
N43K |
possibly damaging |
Het |
Hivep1 |
A |
T |
13: 42,310,694 (GRCm39) |
E978V |
possibly damaging |
Het |
Hormad1 |
G |
A |
3: 95,467,044 (GRCm39) |
|
probably null |
Het |
Kalrn |
C |
T |
16: 33,795,805 (GRCm39) |
|
probably benign |
Het |
Mars1 |
T |
C |
10: 127,132,418 (GRCm39) |
T860A |
probably benign |
Het |
Mdn1 |
A |
T |
4: 32,695,400 (GRCm39) |
L1146F |
probably damaging |
Het |
Met |
A |
G |
6: 17,531,581 (GRCm39) |
T620A |
probably benign |
Het |
Mppe1 |
T |
C |
18: 67,358,834 (GRCm39) |
E378G |
probably benign |
Het |
Mybpc3 |
T |
A |
2: 90,955,010 (GRCm39) |
V481D |
probably damaging |
Het |
Myh14 |
A |
T |
7: 44,256,133 (GRCm39) |
L1924Q |
probably damaging |
Het |
Mylip |
G |
T |
13: 45,562,178 (GRCm39) |
E327* |
probably null |
Het |
Naip1 |
C |
T |
13: 100,559,636 (GRCm39) |
G1123R |
probably benign |
Het |
Naip6 |
A |
G |
13: 100,452,500 (GRCm39) |
V187A |
possibly damaging |
Het |
Ncam1 |
T |
A |
9: 49,418,343 (GRCm39) |
T986S |
probably benign |
Het |
Or13p4 |
T |
C |
4: 118,547,314 (GRCm39) |
I112V |
probably damaging |
Het |
Or4x13 |
T |
C |
2: 90,231,800 (GRCm39) |
I265T |
probably benign |
Het |
Phactr2 |
C |
T |
10: 13,121,261 (GRCm39) |
G480S |
probably damaging |
Het |
Por |
A |
G |
5: 135,744,838 (GRCm39) |
I34V |
probably benign |
Het |
Ppp2r5b |
C |
T |
19: 6,284,764 (GRCm39) |
R33H |
probably damaging |
Het |
Prkdc |
C |
A |
16: 15,570,693 (GRCm39) |
Y2325* |
probably null |
Het |
Prx |
A |
G |
7: 27,214,709 (GRCm39) |
E73G |
probably damaging |
Het |
Rbms2 |
C |
A |
10: 127,981,556 (GRCm39) |
A126S |
possibly damaging |
Het |
Rhoq |
C |
T |
17: 87,302,117 (GRCm39) |
A111V |
probably damaging |
Het |
Rpl14 |
T |
A |
9: 120,403,240 (GRCm39) |
|
probably benign |
Het |
Serbp1 |
A |
G |
6: 67,249,870 (GRCm39) |
*75W |
probably null |
Het |
Sptbn1 |
C |
A |
11: 30,073,978 (GRCm39) |
V1351F |
probably damaging |
Het |
Supt16 |
A |
G |
14: 52,401,979 (GRCm39) |
V897A |
probably benign |
Het |
Tfdp1 |
T |
A |
8: 13,407,038 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
A |
2: 76,780,487 (GRCm39) |
Y1088F |
probably damaging |
Het |
Vmn2r105 |
G |
T |
17: 20,448,929 (GRCm39) |
Q83K |
probably benign |
Het |
Wdr76 |
A |
T |
2: 121,359,323 (GRCm39) |
S221C |
probably damaging |
Het |
Zfhx2 |
G |
T |
14: 55,303,348 (GRCm39) |
F1545L |
probably benign |
Het |
|
Other mutations in Zfp318 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00705:Zfp318
|
APN |
17 |
46,723,398 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00978:Zfp318
|
APN |
17 |
46,724,652 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01016:Zfp318
|
APN |
17 |
46,711,003 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01310:Zfp318
|
APN |
17 |
46,724,153 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01453:Zfp318
|
APN |
17 |
46,719,942 (GRCm39) |
splice site |
probably null |
|
IGL01887:Zfp318
|
APN |
17 |
46,710,094 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02025:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02026:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02070:Zfp318
|
APN |
17 |
46,707,644 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02182:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02187:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02188:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02189:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02190:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02191:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02192:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02203:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02224:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02230:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02231:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02232:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02233:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02234:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02412:Zfp318
|
APN |
17 |
46,720,043 (GRCm39) |
nonsense |
probably null |
|
IGL02792:Zfp318
|
APN |
17 |
46,720,104 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02826:Zfp318
|
APN |
17 |
46,709,680 (GRCm39) |
missense |
probably damaging |
1.00 |
Wonton
|
UTSW |
17 |
46,720,618 (GRCm39) |
missense |
possibly damaging |
0.89 |
I0000:Zfp318
|
UTSW |
17 |
46,710,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R0206:Zfp318
|
UTSW |
17 |
46,709,945 (GRCm39) |
missense |
probably benign |
0.07 |
R0240:Zfp318
|
UTSW |
17 |
46,707,739 (GRCm39) |
missense |
probably benign |
0.00 |
R0240:Zfp318
|
UTSW |
17 |
46,707,739 (GRCm39) |
missense |
probably benign |
0.00 |
R0281:Zfp318
|
UTSW |
17 |
46,723,540 (GRCm39) |
missense |
probably benign |
0.05 |
R0350:Zfp318
|
UTSW |
17 |
46,724,124 (GRCm39) |
missense |
probably benign |
0.00 |
R0383:Zfp318
|
UTSW |
17 |
46,724,222 (GRCm39) |
missense |
probably damaging |
0.99 |
R0453:Zfp318
|
UTSW |
17 |
46,707,634 (GRCm39) |
missense |
probably damaging |
0.96 |
R1014:Zfp318
|
UTSW |
17 |
46,723,462 (GRCm39) |
nonsense |
probably null |
|
R1166:Zfp318
|
UTSW |
17 |
46,720,618 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1208:Zfp318
|
UTSW |
17 |
46,723,446 (GRCm39) |
unclassified |
probably benign |
|
R1208:Zfp318
|
UTSW |
17 |
46,723,446 (GRCm39) |
unclassified |
probably benign |
|
R1327:Zfp318
|
UTSW |
17 |
46,724,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R1330:Zfp318
|
UTSW |
17 |
46,724,684 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1737:Zfp318
|
UTSW |
17 |
46,710,403 (GRCm39) |
missense |
probably benign |
0.35 |
R1800:Zfp318
|
UTSW |
17 |
46,722,980 (GRCm39) |
missense |
probably benign |
0.00 |
R1846:Zfp318
|
UTSW |
17 |
46,724,592 (GRCm39) |
missense |
probably benign |
0.00 |
R1848:Zfp318
|
UTSW |
17 |
46,716,981 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1861:Zfp318
|
UTSW |
17 |
46,722,366 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1913:Zfp318
|
UTSW |
17 |
46,723,450 (GRCm39) |
unclassified |
probably benign |
|
R1913:Zfp318
|
UTSW |
17 |
46,723,440 (GRCm39) |
unclassified |
probably benign |
|
R2059:Zfp318
|
UTSW |
17 |
46,707,950 (GRCm39) |
missense |
probably damaging |
0.99 |
R2085:Zfp318
|
UTSW |
17 |
46,720,590 (GRCm39) |
splice site |
probably null |
|
R2122:Zfp318
|
UTSW |
17 |
46,724,297 (GRCm39) |
missense |
probably benign |
0.01 |
R2339:Zfp318
|
UTSW |
17 |
46,710,389 (GRCm39) |
missense |
probably benign |
0.01 |
R4526:Zfp318
|
UTSW |
17 |
46,723,284 (GRCm39) |
missense |
probably benign |
0.00 |
R4564:Zfp318
|
UTSW |
17 |
46,723,741 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4689:Zfp318
|
UTSW |
17 |
46,710,560 (GRCm39) |
missense |
probably damaging |
0.99 |
R4795:Zfp318
|
UTSW |
17 |
46,722,988 (GRCm39) |
missense |
probably benign |
0.07 |
R5256:Zfp318
|
UTSW |
17 |
46,722,995 (GRCm39) |
missense |
probably benign |
0.19 |
R5317:Zfp318
|
UTSW |
17 |
46,723,463 (GRCm39) |
unclassified |
probably benign |
|
R5323:Zfp318
|
UTSW |
17 |
46,697,662 (GRCm39) |
missense |
probably damaging |
0.99 |
R5436:Zfp318
|
UTSW |
17 |
46,723,975 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5485:Zfp318
|
UTSW |
17 |
46,723,180 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5627:Zfp318
|
UTSW |
17 |
46,724,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R5643:Zfp318
|
UTSW |
17 |
46,720,170 (GRCm39) |
intron |
probably benign |
|
R5782:Zfp318
|
UTSW |
17 |
46,723,440 (GRCm39) |
unclassified |
probably benign |
|
R5783:Zfp318
|
UTSW |
17 |
46,723,440 (GRCm39) |
unclassified |
probably benign |
|
R5820:Zfp318
|
UTSW |
17 |
46,723,699 (GRCm39) |
missense |
probably benign |
|
R6189:Zfp318
|
UTSW |
17 |
46,723,440 (GRCm39) |
unclassified |
probably benign |
|
R6385:Zfp318
|
UTSW |
17 |
46,721,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R6428:Zfp318
|
UTSW |
17 |
46,710,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R6471:Zfp318
|
UTSW |
17 |
46,710,431 (GRCm39) |
missense |
probably benign |
0.05 |
R6666:Zfp318
|
UTSW |
17 |
46,720,140 (GRCm39) |
missense |
probably benign |
0.01 |
R6812:Zfp318
|
UTSW |
17 |
46,723,468 (GRCm39) |
unclassified |
probably benign |
|
R6852:Zfp318
|
UTSW |
17 |
46,723,464 (GRCm39) |
unclassified |
probably benign |
|
R6852:Zfp318
|
UTSW |
17 |
46,723,459 (GRCm39) |
unclassified |
probably benign |
|
R6852:Zfp318
|
UTSW |
17 |
46,723,460 (GRCm39) |
unclassified |
probably benign |
|
R6854:Zfp318
|
UTSW |
17 |
46,723,468 (GRCm39) |
unclassified |
probably benign |
|
R6980:Zfp318
|
UTSW |
17 |
46,708,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R6999:Zfp318
|
UTSW |
17 |
46,710,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R7164:Zfp318
|
UTSW |
17 |
46,716,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R7164:Zfp318
|
UTSW |
17 |
46,708,232 (GRCm39) |
critical splice donor site |
probably null |
|
R7175:Zfp318
|
UTSW |
17 |
46,697,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R7233:Zfp318
|
UTSW |
17 |
46,716,978 (GRCm39) |
missense |
probably damaging |
0.99 |
R7339:Zfp318
|
UTSW |
17 |
46,722,173 (GRCm39) |
missense |
probably damaging |
0.99 |
R7426:Zfp318
|
UTSW |
17 |
46,710,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R7600:Zfp318
|
UTSW |
17 |
46,695,210 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7608:Zfp318
|
UTSW |
17 |
46,710,935 (GRCm39) |
missense |
probably damaging |
0.96 |
R7779:Zfp318
|
UTSW |
17 |
46,710,820 (GRCm39) |
missense |
probably benign |
0.16 |
R8057:Zfp318
|
UTSW |
17 |
46,710,692 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8273:Zfp318
|
UTSW |
17 |
46,723,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R8274:Zfp318
|
UTSW |
17 |
46,723,915 (GRCm39) |
missense |
probably benign |
|
R8695:Zfp318
|
UTSW |
17 |
46,723,576 (GRCm39) |
missense |
probably benign |
0.01 |
R8822:Zfp318
|
UTSW |
17 |
46,723,831 (GRCm39) |
missense |
probably benign |
0.00 |
R8851:Zfp318
|
UTSW |
17 |
46,710,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R8913:Zfp318
|
UTSW |
17 |
46,722,699 (GRCm39) |
missense |
probably benign |
0.07 |
R8953:Zfp318
|
UTSW |
17 |
46,731,356 (GRCm39) |
missense |
probably benign |
0.38 |
R9031:Zfp318
|
UTSW |
17 |
46,723,433 (GRCm39) |
missense |
probably benign |
0.15 |
R9327:Zfp318
|
UTSW |
17 |
46,721,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R9329:Zfp318
|
UTSW |
17 |
46,722,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R9352:Zfp318
|
UTSW |
17 |
46,721,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R9633:Zfp318
|
UTSW |
17 |
46,710,421 (GRCm39) |
missense |
probably damaging |
0.99 |
R9662:Zfp318
|
UTSW |
17 |
46,724,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R9728:Zfp318
|
UTSW |
17 |
46,707,713 (GRCm39) |
missense |
probably benign |
0.10 |
R9755:Zfp318
|
UTSW |
17 |
46,722,055 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Zfp318
|
UTSW |
17 |
46,721,564 (GRCm39) |
missense |
possibly damaging |
0.89 |
X0054:Zfp318
|
UTSW |
17 |
46,723,535 (GRCm39) |
missense |
possibly damaging |
0.79 |
X0065:Zfp318
|
UTSW |
17 |
46,721,915 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Zfp318
|
UTSW |
17 |
46,716,904 (GRCm39) |
missense |
probably benign |
0.03 |
|