Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2410002F23Rik |
T |
A |
7: 43,900,677 (GRCm39) |
V194E |
possibly damaging |
Het |
Adgrv1 |
T |
C |
13: 81,561,296 (GRCm39) |
N5406S |
probably damaging |
Het |
Arhgef38 |
T |
A |
3: 132,843,323 (GRCm39) |
R416* |
probably null |
Het |
Asb7 |
T |
A |
7: 66,328,932 (GRCm39) |
Q36L |
probably benign |
Het |
Bbof1 |
G |
A |
12: 84,457,991 (GRCm39) |
M85I |
probably benign |
Het |
Bin1 |
T |
G |
18: 32,539,198 (GRCm39) |
F44V |
probably damaging |
Het |
Bnc2 |
C |
A |
4: 84,210,573 (GRCm39) |
V599L |
probably benign |
Het |
Bnip3l |
A |
G |
14: 67,226,651 (GRCm39) |
S181P |
probably damaging |
Het |
Btnl9 |
A |
G |
11: 49,066,442 (GRCm39) |
L374P |
probably benign |
Het |
Cd109 |
T |
C |
9: 78,571,633 (GRCm39) |
I424T |
probably benign |
Het |
Cdhr2 |
G |
A |
13: 54,882,035 (GRCm39) |
V1162M |
probably damaging |
Het |
Dgkb |
G |
A |
12: 38,174,216 (GRCm39) |
E181K |
probably benign |
Het |
Dnase1 |
A |
T |
16: 3,855,861 (GRCm39) |
D64V |
probably damaging |
Het |
E130308A19Rik |
T |
C |
4: 59,719,767 (GRCm39) |
I433T |
probably damaging |
Het |
Ecsit |
C |
T |
9: 21,987,592 (GRCm39) |
R149H |
probably benign |
Het |
Eif1ad8 |
G |
A |
12: 87,563,911 (GRCm39) |
R82Q |
possibly damaging |
Het |
Enpep |
A |
T |
3: 129,099,165 (GRCm39) |
V437E |
probably damaging |
Het |
Esrp1 |
A |
T |
4: 11,338,767 (GRCm39) |
V679D |
probably damaging |
Het |
Fa2h |
T |
A |
8: 112,074,817 (GRCm39) |
|
probably null |
Het |
Fabp1 |
G |
A |
6: 71,176,956 (GRCm39) |
E16K |
probably damaging |
Het |
Fstl5 |
T |
A |
3: 76,614,810 (GRCm39) |
S624T |
probably benign |
Het |
Gemin5 |
G |
A |
11: 58,019,686 (GRCm39) |
R1128W |
probably benign |
Het |
H2bc8 |
T |
C |
13: 23,755,841 (GRCm39) |
S79P |
probably damaging |
Het |
Hps3 |
T |
C |
3: 20,057,492 (GRCm39) |
H896R |
probably benign |
Het |
Hsf1 |
T |
A |
15: 76,382,481 (GRCm39) |
I284K |
probably benign |
Het |
Igkv3-2 |
T |
A |
6: 70,675,988 (GRCm39) |
I99N |
probably damaging |
Het |
Iqub |
T |
A |
6: 24,503,784 (GRCm39) |
I163F |
possibly damaging |
Het |
Jak2 |
T |
C |
19: 29,275,732 (GRCm39) |
I724T |
probably damaging |
Het |
Kbtbd3 |
A |
T |
9: 4,330,408 (GRCm39) |
T261S |
probably benign |
Het |
Kctd20 |
G |
T |
17: 29,171,732 (GRCm39) |
|
probably null |
Het |
Kif28 |
C |
T |
1: 179,537,014 (GRCm39) |
V490M |
probably benign |
Het |
Kif9 |
T |
C |
9: 110,348,208 (GRCm39) |
L677P |
probably damaging |
Het |
Klhl18 |
T |
C |
9: 110,257,829 (GRCm39) |
Y537C |
probably damaging |
Het |
Mmut |
T |
A |
17: 41,254,784 (GRCm39) |
I331K |
probably benign |
Het |
Myo5a |
T |
A |
9: 75,089,228 (GRCm39) |
S1119R |
probably damaging |
Het |
Napepld |
C |
A |
5: 21,870,319 (GRCm39) |
E366D |
probably benign |
Het |
Nbea |
A |
G |
3: 55,895,402 (GRCm39) |
V1540A |
probably damaging |
Het |
Neb |
T |
A |
2: 52,111,738 (GRCm39) |
I130L |
probably benign |
Het |
Opcml |
T |
C |
9: 28,724,640 (GRCm39) |
V146A |
probably damaging |
Het |
Or2g7 |
T |
C |
17: 38,378,370 (GRCm39) |
S103P |
probably damaging |
Het |
Or2r11 |
A |
T |
6: 42,437,764 (GRCm39) |
L63H |
probably damaging |
Het |
Or7e178 |
C |
T |
9: 20,225,941 (GRCm39) |
D92N |
probably damaging |
Het |
Pappa2 |
A |
C |
1: 158,675,970 (GRCm39) |
C925W |
probably damaging |
Het |
Parp12 |
T |
A |
6: 39,066,038 (GRCm39) |
N562Y |
probably damaging |
Het |
Patj |
C |
A |
4: 98,427,201 (GRCm39) |
H1198Q |
probably benign |
Het |
Pcyox1 |
T |
A |
6: 86,366,128 (GRCm39) |
K362M |
possibly damaging |
Het |
Pcyt2 |
T |
C |
11: 120,501,765 (GRCm39) |
Y350C |
probably benign |
Het |
Pkd1 |
A |
T |
17: 24,784,617 (GRCm39) |
T388S |
probably benign |
Het |
Prl3d1 |
T |
A |
13: 27,284,011 (GRCm39) |
Y193* |
probably null |
Het |
Psme1 |
A |
T |
14: 55,817,056 (GRCm39) |
D15V |
possibly damaging |
Het |
Ranbp2 |
A |
G |
10: 58,315,441 (GRCm39) |
N2054D |
probably damaging |
Het |
Serpinb1c |
T |
A |
13: 33,066,052 (GRCm39) |
K298* |
probably null |
Het |
Slc22a27 |
A |
T |
19: 7,857,532 (GRCm39) |
M355K |
probably benign |
Het |
Spp1 |
T |
A |
5: 104,588,280 (GRCm39) |
H227Q |
probably benign |
Het |
Stam2 |
T |
A |
2: 52,609,785 (GRCm39) |
N75I |
probably damaging |
Het |
Tacc1 |
T |
C |
8: 25,659,230 (GRCm39) |
T579A |
probably benign |
Het |
Tbx3 |
A |
G |
5: 119,821,132 (GRCm39) |
D734G |
probably benign |
Het |
Tmem233 |
G |
T |
5: 116,221,141 (GRCm39) |
S35* |
probably null |
Het |
Trim43c |
A |
T |
9: 88,722,390 (GRCm39) |
E12V |
probably damaging |
Het |
Trio |
A |
G |
15: 27,891,540 (GRCm39) |
S463P |
unknown |
Het |
Uggt2 |
A |
T |
14: 119,263,834 (GRCm39) |
D1065E |
probably damaging |
Het |
Usp1 |
A |
G |
4: 98,817,150 (GRCm39) |
N114S |
probably benign |
Het |
Usp34 |
A |
G |
11: 23,396,787 (GRCm39) |
E2377G |
|
Het |
Virma |
T |
A |
4: 11,528,643 (GRCm39) |
H1243Q |
probably benign |
Het |
Vmn2r3 |
A |
T |
3: 64,178,714 (GRCm39) |
V517D |
probably damaging |
Het |
Zfp931 |
T |
C |
2: 177,709,889 (GRCm39) |
K166E |
probably damaging |
Het |
Zp3 |
T |
A |
5: 136,011,604 (GRCm39) |
Y141N |
probably damaging |
Het |
|
Other mutations in Qrsl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00477:Qrsl1
|
APN |
10 |
43,752,488 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01724:Qrsl1
|
APN |
10 |
43,750,604 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01896:Qrsl1
|
APN |
10 |
43,752,500 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02192:Qrsl1
|
APN |
10 |
43,761,010 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02239:Qrsl1
|
APN |
10 |
43,770,596 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02478:Qrsl1
|
APN |
10 |
43,758,158 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02756:Qrsl1
|
APN |
10 |
43,758,110 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03386:Qrsl1
|
APN |
10 |
43,752,546 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0277:Qrsl1
|
UTSW |
10 |
43,772,003 (GRCm39) |
critical splice donor site |
probably null |
|
R0323:Qrsl1
|
UTSW |
10 |
43,772,003 (GRCm39) |
critical splice donor site |
probably null |
|
R0674:Qrsl1
|
UTSW |
10 |
43,771,997 (GRCm39) |
splice site |
probably benign |
|
R1054:Qrsl1
|
UTSW |
10 |
43,758,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R1719:Qrsl1
|
UTSW |
10 |
43,772,026 (GRCm39) |
missense |
probably damaging |
0.97 |
R1743:Qrsl1
|
UTSW |
10 |
43,757,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R1854:Qrsl1
|
UTSW |
10 |
43,770,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R2233:Qrsl1
|
UTSW |
10 |
43,772,092 (GRCm39) |
missense |
probably benign |
0.00 |
R4176:Qrsl1
|
UTSW |
10 |
43,760,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R4452:Qrsl1
|
UTSW |
10 |
43,758,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R4732:Qrsl1
|
UTSW |
10 |
43,752,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:Qrsl1
|
UTSW |
10 |
43,752,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R5626:Qrsl1
|
UTSW |
10 |
43,757,516 (GRCm39) |
missense |
probably benign |
0.00 |
R6159:Qrsl1
|
UTSW |
10 |
43,758,189 (GRCm39) |
missense |
probably benign |
0.00 |
R7563:Qrsl1
|
UTSW |
10 |
43,752,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R8092:Qrsl1
|
UTSW |
10 |
43,760,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R8221:Qrsl1
|
UTSW |
10 |
43,758,080 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8331:Qrsl1
|
UTSW |
10 |
43,752,521 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Qrsl1
|
UTSW |
10 |
43,760,944 (GRCm39) |
missense |
probably damaging |
0.98 |
|