Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
T |
G |
7: 119,911,505 (GRCm39) |
I1363R |
probably benign |
Het |
Abcc1 |
T |
C |
16: 14,221,917 (GRCm39) |
|
probably null |
Het |
Adgrf1 |
T |
A |
17: 43,614,638 (GRCm39) |
F241I |
probably damaging |
Het |
Afg3l1 |
T |
C |
8: 124,216,553 (GRCm39) |
M264T |
probably benign |
Het |
Ankle1 |
T |
C |
8: 71,861,623 (GRCm39) |
S434P |
probably damaging |
Het |
Apoe |
C |
T |
7: 19,430,940 (GRCm39) |
A101T |
probably damaging |
Het |
Apol11a |
G |
T |
15: 77,401,153 (GRCm39) |
K213N |
probably damaging |
Het |
Asap2 |
A |
G |
12: 21,254,082 (GRCm39) |
M198V |
probably damaging |
Het |
Atg4b |
C |
T |
1: 93,714,297 (GRCm39) |
A360V |
probably benign |
Het |
B3gnt5 |
T |
A |
16: 19,588,444 (GRCm39) |
V221D |
probably damaging |
Het |
Baz2b |
A |
T |
2: 59,928,988 (GRCm39) |
|
probably benign |
Het |
Cep350 |
C |
A |
1: 155,809,100 (GRCm39) |
W492L |
probably benign |
Het |
Cln6 |
A |
G |
9: 62,754,375 (GRCm39) |
Y139C |
probably damaging |
Het |
Col16a1 |
C |
T |
4: 129,972,988 (GRCm39) |
T643M |
probably benign |
Het |
Cul9 |
C |
T |
17: 46,811,708 (GRCm39) |
E2507K |
probably damaging |
Het |
Dgkz |
A |
T |
2: 91,775,888 (GRCm39) |
V125D |
probably benign |
Het |
Dnah17 |
T |
C |
11: 117,993,365 (GRCm39) |
M1127V |
probably benign |
Het |
Dnajb1 |
C |
A |
8: 84,336,732 (GRCm39) |
D67E |
probably benign |
Het |
Dync1li1 |
A |
G |
9: 114,542,612 (GRCm39) |
D258G |
probably damaging |
Het |
Egflam |
G |
T |
15: 7,283,125 (GRCm39) |
P311T |
probably benign |
Het |
Fbxw11 |
T |
A |
11: 32,602,811 (GRCm39) |
|
probably benign |
Het |
Fn3krp |
T |
G |
11: 121,320,274 (GRCm39) |
D206E |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,819,477 (GRCm39) |
H5070R |
possibly damaging |
Het |
Gm6605 |
T |
C |
7: 38,149,683 (GRCm39) |
|
noncoding transcript |
Het |
Gna14 |
C |
A |
19: 16,580,636 (GRCm39) |
T158K |
probably benign |
Het |
Gstt2 |
A |
T |
10: 75,667,726 (GRCm39) |
I243N |
probably damaging |
Het |
Haus6 |
C |
T |
4: 86,523,933 (GRCm39) |
D50N |
possibly damaging |
Het |
Hcrtr2 |
A |
G |
9: 76,230,578 (GRCm39) |
I70T |
probably benign |
Het |
Herc1 |
G |
A |
9: 66,380,811 (GRCm39) |
V3563I |
probably benign |
Het |
Herc1 |
A |
T |
9: 66,411,900 (GRCm39) |
I4707F |
probably damaging |
Het |
Hic2 |
C |
T |
16: 17,076,611 (GRCm39) |
A480V |
possibly damaging |
Het |
Hsd17b3 |
A |
G |
13: 64,210,720 (GRCm39) |
Y212H |
probably damaging |
Het |
Hspa5 |
A |
G |
2: 34,665,827 (GRCm39) |
K557R |
probably damaging |
Het |
Iqch |
T |
C |
9: 63,432,294 (GRCm39) |
E367G |
possibly damaging |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Lbp |
T |
C |
2: 158,150,646 (GRCm39) |
I57T |
possibly damaging |
Het |
Liat1 |
A |
G |
11: 75,891,047 (GRCm39) |
K54E |
probably damaging |
Het |
Litaf |
T |
C |
16: 10,778,868 (GRCm39) |
Q142R |
possibly damaging |
Het |
Lpar5 |
G |
C |
6: 125,059,110 (GRCm39) |
R277P |
possibly damaging |
Het |
Muc6 |
T |
A |
7: 141,216,349 (GRCm39) |
I2710F |
probably benign |
Het |
Myo7b |
T |
A |
18: 32,108,265 (GRCm39) |
I1199F |
probably benign |
Het |
Naca |
A |
C |
10: 127,883,990 (GRCm39) |
E2140D |
possibly damaging |
Het |
Nup214 |
G |
T |
2: 31,881,329 (GRCm39) |
G396C |
probably damaging |
Het |
Or2v1 |
A |
T |
11: 49,025,451 (GRCm39) |
Q144L |
probably benign |
Het |
Or5aq7 |
T |
A |
2: 86,938,150 (GRCm39) |
I194F |
probably benign |
Het |
Or5j3 |
G |
A |
2: 86,128,540 (GRCm39) |
V127I |
possibly damaging |
Het |
Or7g33 |
A |
G |
9: 19,448,573 (GRCm39) |
Y218H |
probably damaging |
Het |
Or8b57 |
A |
T |
9: 40,003,690 (GRCm39) |
S187T |
probably damaging |
Het |
P4htm |
A |
G |
9: 108,456,492 (GRCm39) |
V436A |
probably benign |
Het |
Pfkm |
A |
G |
15: 98,017,307 (GRCm39) |
I117V |
possibly damaging |
Het |
Phlpp1 |
T |
G |
1: 106,209,201 (GRCm39) |
V518G |
probably damaging |
Het |
Piwil4 |
G |
A |
9: 14,621,240 (GRCm39) |
L598F |
probably damaging |
Het |
Polr1b |
T |
G |
2: 128,965,803 (GRCm39) |
I815R |
possibly damaging |
Het |
Ppef2 |
T |
C |
5: 92,382,150 (GRCm39) |
N515S |
probably damaging |
Het |
Prp2rt |
A |
G |
13: 97,235,648 (GRCm39) |
I33T |
probably benign |
Het |
Prpsap2 |
G |
T |
11: 61,631,830 (GRCm39) |
|
probably null |
Het |
Rab27a |
A |
G |
9: 73,002,695 (GRCm39) |
D208G |
probably benign |
Het |
Ralgds |
A |
G |
2: 28,442,102 (GRCm39) |
|
probably null |
Het |
Raph1 |
C |
A |
1: 60,535,436 (GRCm39) |
C540F |
probably damaging |
Het |
Rbsn |
A |
G |
6: 92,175,231 (GRCm39) |
L281P |
probably damaging |
Het |
Rigi |
T |
A |
4: 40,208,845 (GRCm39) |
M756L |
probably benign |
Het |
Rmdn1 |
G |
T |
4: 19,588,533 (GRCm39) |
G110* |
probably null |
Het |
Rph3a |
T |
A |
5: 121,092,512 (GRCm39) |
E363V |
possibly damaging |
Het |
Serpina16 |
G |
T |
12: 103,641,262 (GRCm39) |
Y154* |
probably null |
Het |
Sh2d3c |
G |
A |
2: 32,634,814 (GRCm39) |
E198K |
possibly damaging |
Het |
Shank2 |
C |
A |
7: 143,812,842 (GRCm39) |
Y663* |
probably null |
Het |
Sharpin |
T |
C |
15: 76,234,225 (GRCm39) |
|
probably benign |
Het |
Slitrk1 |
G |
A |
14: 109,149,740 (GRCm39) |
P324S |
probably benign |
Het |
Sorbs2 |
T |
A |
8: 46,199,571 (GRCm39) |
|
probably null |
Het |
Spag16 |
C |
T |
1: 69,962,963 (GRCm39) |
|
probably benign |
Het |
Sycp2l |
A |
T |
13: 41,283,247 (GRCm39) |
|
probably null |
Het |
Synj1 |
A |
T |
16: 90,737,407 (GRCm39) |
|
probably null |
Het |
Sytl1 |
T |
C |
4: 132,983,530 (GRCm39) |
|
probably benign |
Het |
Tkfc |
A |
T |
19: 10,570,023 (GRCm39) |
|
probably null |
Het |
Tnn |
T |
C |
1: 159,972,781 (GRCm39) |
T274A |
probably damaging |
Het |
Trav14-2 |
T |
A |
14: 53,878,505 (GRCm39) |
W35R |
probably damaging |
Het |
Trim72 |
T |
C |
7: 127,607,137 (GRCm39) |
M222T |
probably damaging |
Het |
Trim9 |
A |
G |
12: 70,393,482 (GRCm39) |
V154A |
probably damaging |
Het |
Ttc7b |
T |
C |
12: 100,268,001 (GRCm39) |
Y266C |
probably damaging |
Het |
Uchl3 |
T |
A |
14: 101,903,982 (GRCm39) |
I43K |
possibly damaging |
Het |
Vdac1 |
T |
A |
11: 52,279,305 (GRCm39) |
N269K |
possibly damaging |
Het |
Wdr72 |
T |
A |
9: 74,053,258 (GRCm39) |
W187R |
probably damaging |
Het |
Zfp30 |
T |
A |
7: 29,492,491 (GRCm39) |
C248* |
probably null |
Het |
Zfp940 |
A |
T |
7: 29,550,381 (GRCm39) |
|
probably benign |
Het |
Zfp980 |
G |
A |
4: 145,428,653 (GRCm39) |
G461S |
probably benign |
Het |
|
Other mutations in Lars2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01743:Lars2
|
APN |
9 |
123,282,313 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01993:Lars2
|
APN |
9 |
123,224,008 (GRCm39) |
splice site |
probably benign |
|
IGL02155:Lars2
|
APN |
9 |
123,284,047 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02941:Lars2
|
APN |
9 |
123,288,650 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03090:Lars2
|
APN |
9 |
123,285,025 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03271:Lars2
|
APN |
9 |
123,288,549 (GRCm39) |
splice site |
probably null |
|
IGL03386:Lars2
|
APN |
9 |
123,282,455 (GRCm39) |
nonsense |
probably null |
|
IGL03410:Lars2
|
APN |
9 |
123,247,841 (GRCm39) |
missense |
possibly damaging |
0.87 |
ulrich
|
UTSW |
9 |
123,247,758 (GRCm39) |
missense |
probably damaging |
0.99 |
K3955:Lars2
|
UTSW |
9 |
123,206,842 (GRCm39) |
missense |
probably damaging |
1.00 |
P0038:Lars2
|
UTSW |
9 |
123,206,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R0276:Lars2
|
UTSW |
9 |
123,267,186 (GRCm39) |
splice site |
probably benign |
|
R1671:Lars2
|
UTSW |
9 |
123,247,344 (GRCm39) |
missense |
probably benign |
0.02 |
R1829:Lars2
|
UTSW |
9 |
123,260,982 (GRCm39) |
missense |
probably benign |
0.00 |
R2219:Lars2
|
UTSW |
9 |
123,247,845 (GRCm39) |
missense |
probably damaging |
0.98 |
R2220:Lars2
|
UTSW |
9 |
123,247,845 (GRCm39) |
missense |
probably damaging |
0.98 |
R4610:Lars2
|
UTSW |
9 |
123,247,758 (GRCm39) |
missense |
probably damaging |
0.99 |
R5195:Lars2
|
UTSW |
9 |
123,282,375 (GRCm39) |
missense |
probably damaging |
0.97 |
R5597:Lars2
|
UTSW |
9 |
123,284,047 (GRCm39) |
missense |
probably damaging |
0.99 |
R5756:Lars2
|
UTSW |
9 |
123,267,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R5783:Lars2
|
UTSW |
9 |
123,290,661 (GRCm39) |
missense |
probably benign |
|
R6045:Lars2
|
UTSW |
9 |
123,201,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R6235:Lars2
|
UTSW |
9 |
123,240,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R6323:Lars2
|
UTSW |
9 |
123,270,659 (GRCm39) |
nonsense |
probably null |
|
R6377:Lars2
|
UTSW |
9 |
123,283,825 (GRCm39) |
missense |
probably benign |
0.00 |
R6395:Lars2
|
UTSW |
9 |
123,200,990 (GRCm39) |
missense |
probably benign |
0.06 |
R7094:Lars2
|
UTSW |
9 |
123,288,650 (GRCm39) |
missense |
probably damaging |
0.99 |
R7144:Lars2
|
UTSW |
9 |
123,261,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R7233:Lars2
|
UTSW |
9 |
123,241,019 (GRCm39) |
nonsense |
probably null |
|
R7254:Lars2
|
UTSW |
9 |
123,284,028 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7350:Lars2
|
UTSW |
9 |
123,256,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R7413:Lars2
|
UTSW |
9 |
123,288,568 (GRCm39) |
missense |
probably benign |
0.30 |
R7614:Lars2
|
UTSW |
9 |
123,224,176 (GRCm39) |
missense |
|
|
R7683:Lars2
|
UTSW |
9 |
123,206,895 (GRCm39) |
critical splice donor site |
probably null |
|
R8000:Lars2
|
UTSW |
9 |
123,265,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R8061:Lars2
|
UTSW |
9 |
123,288,562 (GRCm39) |
missense |
probably benign |
|
R8355:Lars2
|
UTSW |
9 |
123,283,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R8364:Lars2
|
UTSW |
9 |
123,241,019 (GRCm39) |
nonsense |
probably null |
|
R8818:Lars2
|
UTSW |
9 |
123,221,892 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9007:Lars2
|
UTSW |
9 |
123,260,980 (GRCm39) |
nonsense |
probably null |
|
R9351:Lars2
|
UTSW |
9 |
123,265,366 (GRCm39) |
missense |
probably benign |
0.38 |
Z1177:Lars2
|
UTSW |
9 |
123,283,847 (GRCm39) |
missense |
probably damaging |
1.00 |
|