Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930402F06Rik |
A |
T |
2: 35,270,410 (GRCm39) |
V97E |
probably damaging |
Het |
Abhd16a |
C |
T |
17: 35,320,221 (GRCm39) |
T362M |
probably damaging |
Het |
Adam23 |
T |
G |
1: 63,607,136 (GRCm39) |
|
probably benign |
Het |
Apeh |
C |
A |
9: 107,970,908 (GRCm39) |
R87L |
possibly damaging |
Het |
Arid3a |
T |
A |
10: 79,786,717 (GRCm39) |
M490K |
probably damaging |
Het |
Atp6v1b1 |
T |
A |
6: 83,732,433 (GRCm39) |
V251D |
probably benign |
Het |
Cog8 |
C |
T |
8: 107,783,055 (GRCm39) |
R78Q |
possibly damaging |
Het |
Cyld |
T |
C |
8: 89,462,522 (GRCm39) |
I701T |
probably damaging |
Het |
Dmgdh |
A |
G |
13: 93,811,047 (GRCm39) |
|
probably benign |
Het |
Dnm1 |
T |
C |
2: 32,205,931 (GRCm39) |
|
probably null |
Het |
Dop1b |
T |
A |
16: 93,574,293 (GRCm39) |
V2D |
probably damaging |
Het |
Dusp22 |
A |
T |
13: 30,889,628 (GRCm39) |
S70C |
possibly damaging |
Het |
Dync2h1 |
T |
C |
9: 7,035,700 (GRCm39) |
Q3415R |
possibly damaging |
Het |
Dysf |
T |
C |
6: 84,163,498 (GRCm39) |
|
probably benign |
Het |
Fam114a1 |
G |
A |
5: 65,163,491 (GRCm39) |
|
probably null |
Het |
Fam20a |
T |
A |
11: 109,568,620 (GRCm39) |
Q302L |
possibly damaging |
Het |
Fancm |
T |
A |
12: 65,139,236 (GRCm39) |
L374H |
probably damaging |
Het |
Fcgbpl1 |
G |
A |
7: 27,857,317 (GRCm39) |
E2222K |
probably benign |
Het |
Fgf17 |
G |
A |
14: 70,874,178 (GRCm39) |
Q204* |
probably null |
Het |
Gap43 |
T |
C |
16: 42,112,495 (GRCm39) |
T89A |
probably benign |
Het |
Gm5069 |
A |
G |
1: 180,155,464 (GRCm39) |
|
probably benign |
Het |
Gm9913 |
C |
T |
2: 125,348,254 (GRCm39) |
|
probably benign |
Het |
Gpr174 |
T |
C |
X: 106,336,854 (GRCm39) |
L222P |
probably benign |
Het |
Grid2 |
A |
T |
6: 64,322,857 (GRCm39) |
Q619L |
possibly damaging |
Het |
Hoxc13 |
A |
G |
15: 102,830,233 (GRCm39) |
D204G |
possibly damaging |
Het |
Itgav |
T |
C |
2: 83,601,580 (GRCm39) |
V317A |
probably benign |
Het |
Keg1 |
A |
T |
19: 12,696,521 (GRCm39) |
N288I |
probably damaging |
Het |
Ksr1 |
C |
T |
11: 78,935,684 (GRCm39) |
V234I |
possibly damaging |
Het |
Lrp1 |
T |
A |
10: 127,387,555 (GRCm39) |
D3365V |
probably damaging |
Het |
Luc7l3 |
A |
T |
11: 94,190,894 (GRCm39) |
|
probably null |
Het |
Mta2 |
T |
C |
19: 8,925,415 (GRCm39) |
I348T |
probably benign |
Het |
Nphp4 |
A |
G |
4: 152,640,677 (GRCm39) |
I1015V |
probably benign |
Het |
Nup214 |
C |
T |
2: 31,867,872 (GRCm39) |
S113F |
probably damaging |
Het |
Or4f7 |
T |
C |
2: 111,644,162 (GRCm39) |
K303R |
probably benign |
Het |
Pabpn1l |
T |
A |
8: 123,347,122 (GRCm39) |
T228S |
probably damaging |
Het |
Paxx |
T |
C |
2: 25,349,674 (GRCm39) |
*206W |
probably null |
Het |
Pcdhb10 |
A |
G |
18: 37,546,126 (GRCm39) |
T401A |
probably benign |
Het |
Ppp1r3a |
A |
C |
6: 14,719,761 (GRCm39) |
D384E |
probably benign |
Het |
Rif1 |
T |
C |
2: 51,967,077 (GRCm39) |
V122A |
probably damaging |
Het |
Scn4b |
T |
C |
9: 45,057,980 (GRCm39) |
L24P |
probably damaging |
Het |
Sec22c |
T |
C |
9: 121,513,716 (GRCm39) |
|
probably benign |
Het |
Sh3rf2 |
A |
G |
18: 42,289,207 (GRCm39) |
D676G |
probably damaging |
Het |
Slc20a1 |
A |
G |
2: 129,049,604 (GRCm39) |
T289A |
probably benign |
Het |
Tekt2 |
T |
C |
4: 126,218,418 (GRCm39) |
D84G |
possibly damaging |
Het |
Tgfbr2 |
T |
A |
9: 115,959,066 (GRCm39) |
N116I |
probably benign |
Het |
Tmem196 |
A |
G |
12: 119,910,209 (GRCm39) |
M1V |
probably null |
Het |
Tnn |
A |
G |
1: 159,942,123 (GRCm39) |
V1125A |
probably damaging |
Het |
Vmn2r51 |
A |
T |
7: 9,834,243 (GRCm39) |
M265K |
probably benign |
Het |
Zfp65 |
A |
T |
13: 67,856,184 (GRCm39) |
V365E |
possibly damaging |
Het |
Zp3 |
T |
A |
5: 136,016,464 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Zfp319 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01611:Zfp319
|
APN |
8 |
96,055,540 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02478:Zfp319
|
APN |
8 |
96,055,721 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02622:Zfp319
|
APN |
8 |
96,055,589 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02945:Zfp319
|
APN |
8 |
96,050,446 (GRCm39) |
unclassified |
probably benign |
|
Lanky
|
UTSW |
8 |
96,054,733 (GRCm39) |
frame shift |
probably null |
|
R0894:Zfp319
|
UTSW |
8 |
96,056,250 (GRCm39) |
unclassified |
probably benign |
|
R1898:Zfp319
|
UTSW |
8 |
96,055,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R1937:Zfp319
|
UTSW |
8 |
96,055,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R2127:Zfp319
|
UTSW |
8 |
96,050,391 (GRCm39) |
unclassified |
probably benign |
|
R2157:Zfp319
|
UTSW |
8 |
96,054,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R2256:Zfp319
|
UTSW |
8 |
96,055,129 (GRCm39) |
missense |
possibly damaging |
0.47 |
R3547:Zfp319
|
UTSW |
8 |
96,055,445 (GRCm39) |
missense |
probably damaging |
0.96 |
R4665:Zfp319
|
UTSW |
8 |
96,052,201 (GRCm39) |
unclassified |
probably benign |
|
R5174:Zfp319
|
UTSW |
8 |
96,054,797 (GRCm39) |
splice site |
probably null |
|
R5249:Zfp319
|
UTSW |
8 |
96,055,099 (GRCm39) |
missense |
probably benign |
0.00 |
R5478:Zfp319
|
UTSW |
8 |
96,052,193 (GRCm39) |
unclassified |
probably benign |
|
R5623:Zfp319
|
UTSW |
8 |
96,052,199 (GRCm39) |
unclassified |
probably benign |
|
R6165:Zfp319
|
UTSW |
8 |
96,054,733 (GRCm39) |
frame shift |
probably null |
|
R7175:Zfp319
|
UTSW |
8 |
96,055,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R7271:Zfp319
|
UTSW |
8 |
96,058,471 (GRCm39) |
unclassified |
probably benign |
|
R8303:Zfp319
|
UTSW |
8 |
96,055,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R8734:Zfp319
|
UTSW |
8 |
96,054,938 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9443:Zfp319
|
UTSW |
8 |
96,054,922 (GRCm39) |
missense |
probably benign |
0.00 |
R9550:Zfp319
|
UTSW |
8 |
96,055,025 (GRCm39) |
missense |
probably benign |
0.06 |
|