Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
C |
A |
6: 121,631,571 (GRCm39) |
L623M |
probably benign |
Het |
Adrm1b |
T |
A |
3: 92,335,538 (GRCm39) |
D388V |
probably damaging |
Het |
Akap13 |
T |
G |
7: 75,260,783 (GRCm39) |
C333G |
probably benign |
Het |
Akap6 |
T |
C |
12: 53,115,908 (GRCm39) |
S1004P |
probably damaging |
Het |
Akap7 |
T |
C |
10: 25,115,583 (GRCm39) |
T181A |
probably benign |
Het |
Ap3b1 |
A |
G |
13: 94,545,305 (GRCm39) |
E186G |
possibly damaging |
Het |
Arhgap17 |
T |
C |
7: 122,885,925 (GRCm39) |
T736A |
probably benign |
Het |
Bltp3a |
T |
A |
17: 28,113,720 (GRCm39) |
D1297E |
probably damaging |
Het |
Bmp8a |
G |
T |
4: 123,218,378 (GRCm39) |
R214S |
possibly damaging |
Het |
Cacna1f |
T |
C |
X: 7,486,678 (GRCm39) |
S890P |
probably damaging |
Het |
Cd96 |
A |
T |
16: 45,938,362 (GRCm39) |
Y34* |
probably null |
Het |
Cdc42ep4 |
A |
G |
11: 113,620,163 (GRCm39) |
L76P |
probably damaging |
Het |
Cdh23 |
A |
G |
10: 60,227,505 (GRCm39) |
V1195A |
possibly damaging |
Het |
Cfap57 |
G |
A |
4: 118,428,921 (GRCm39) |
T1015M |
possibly damaging |
Het |
Chrm3 |
C |
A |
13: 9,927,452 (GRCm39) |
G528V |
probably damaging |
Het |
Cimap1c |
A |
T |
9: 56,759,027 (GRCm39) |
F43I |
possibly damaging |
Het |
Clip4 |
T |
C |
17: 72,108,937 (GRCm39) |
|
probably benign |
Het |
Col9a1 |
A |
T |
1: 24,224,386 (GRCm39) |
R189S |
unknown |
Het |
Cul4b |
A |
T |
X: 37,636,728 (GRCm39) |
I481N |
probably damaging |
Het |
Cyp26b1 |
A |
G |
6: 84,561,441 (GRCm39) |
S74P |
probably benign |
Het |
Cyp3a57 |
A |
G |
5: 145,307,820 (GRCm39) |
N192S |
probably benign |
Het |
Dcbld1 |
A |
G |
10: 52,195,572 (GRCm39) |
D260G |
probably damaging |
Het |
Dhrs7 |
T |
C |
12: 72,699,939 (GRCm39) |
N231S |
probably benign |
Het |
Disp3 |
G |
A |
4: 148,325,975 (GRCm39) |
P1261L |
probably damaging |
Het |
Dnaaf4 |
T |
C |
9: 72,867,966 (GRCm39) |
Y76H |
possibly damaging |
Het |
Eml5 |
C |
A |
12: 98,853,315 (GRCm39) |
V95F |
probably benign |
Het |
Emsy |
A |
G |
7: 98,297,087 (GRCm39) |
I32T |
probably damaging |
Het |
Esr1 |
A |
G |
10: 4,733,913 (GRCm39) |
R238G |
probably damaging |
Het |
Exosc1 |
T |
C |
19: 41,916,524 (GRCm39) |
K84R |
probably benign |
Het |
F830016B08Rik |
T |
A |
18: 60,433,589 (GRCm39) |
V224E |
probably benign |
Het |
Fam228a |
T |
A |
12: 4,782,748 (GRCm39) |
N115I |
probably damaging |
Het |
Farp1 |
T |
C |
14: 121,494,157 (GRCm39) |
I546T |
probably damaging |
Het |
Fbxo30 |
T |
A |
10: 11,165,531 (GRCm39) |
C84* |
probably null |
Het |
Fbxw17 |
A |
G |
13: 50,579,810 (GRCm39) |
|
probably benign |
Het |
Foxo4 |
G |
C |
X: 100,302,069 (GRCm39) |
R192P |
probably benign |
Het |
Galnt7 |
G |
T |
8: 57,995,564 (GRCm39) |
T377K |
probably benign |
Het |
Glod4 |
A |
G |
11: 76,128,534 (GRCm39) |
Y104H |
probably damaging |
Het |
Glrb |
T |
C |
3: 80,767,482 (GRCm39) |
Y246C |
probably damaging |
Het |
Gm5292 |
A |
G |
5: 44,101,752 (GRCm39) |
|
noncoding transcript |
Het |
Gm5424 |
C |
A |
10: 61,908,086 (GRCm39) |
|
noncoding transcript |
Het |
Gm7276 |
C |
T |
18: 77,273,431 (GRCm39) |
|
probably benign |
Het |
Golga5 |
A |
G |
12: 102,458,390 (GRCm39) |
N611S |
possibly damaging |
Het |
Gucy2c |
A |
C |
6: 136,721,025 (GRCm39) |
Y391D |
probably damaging |
Het |
H6pd |
A |
G |
4: 150,066,130 (GRCm39) |
I760T |
probably damaging |
Het |
Hapln2 |
T |
A |
3: 87,931,712 (GRCm39) |
I5F |
possibly damaging |
Het |
Hdac11 |
G |
T |
6: 91,145,806 (GRCm39) |
V169L |
probably benign |
Het |
Hectd2 |
T |
C |
19: 36,586,816 (GRCm39) |
V557A |
possibly damaging |
Het |
Huwe1 |
T |
A |
X: 150,647,749 (GRCm39) |
N747K |
probably benign |
Het |
Ints1 |
A |
G |
5: 139,760,277 (GRCm39) |
S66P |
probably benign |
Het |
Ipo7 |
A |
G |
7: 109,626,339 (GRCm39) |
D49G |
probably damaging |
Het |
Itgb4 |
G |
A |
11: 115,879,346 (GRCm39) |
C575Y |
probably damaging |
Het |
Klhl3 |
A |
G |
13: 58,181,044 (GRCm39) |
V250A |
possibly damaging |
Het |
Klk1b24 |
A |
G |
7: 43,839,852 (GRCm39) |
|
probably null |
Het |
Map3k11 |
T |
A |
19: 5,745,600 (GRCm39) |
Y333* |
probably null |
Het |
Mbp |
A |
G |
18: 82,572,474 (GRCm39) |
T57A |
probably benign |
Het |
Myh9 |
A |
G |
15: 77,657,464 (GRCm39) |
|
probably benign |
Het |
Mypn |
C |
T |
10: 62,961,472 (GRCm39) |
R1040Q |
probably damaging |
Het |
Ncdn |
A |
G |
4: 126,645,732 (GRCm39) |
|
probably null |
Het |
Ndn |
C |
T |
7: 61,998,256 (GRCm39) |
P34L |
probably benign |
Het |
Or10ab5 |
T |
A |
7: 108,245,571 (GRCm39) |
T71S |
probably benign |
Het |
Or11h4 |
AGGGATTGGG |
AGGGATTGGGATTGGG |
14: 50,974,144 (GRCm39) |
|
probably benign |
Het |
Or4k15c |
A |
G |
14: 50,321,499 (GRCm39) |
F213S |
probably benign |
Het |
Or51b6b |
T |
C |
7: 103,310,005 (GRCm39) |
|
probably null |
Het |
Or51f1 |
G |
A |
7: 102,505,569 (GRCm39) |
Q307* |
probably null |
Het |
Or8d2 |
T |
A |
9: 38,759,901 (GRCm39) |
S164T |
possibly damaging |
Het |
Pbx3 |
T |
C |
2: 34,114,464 (GRCm39) |
T82A |
possibly damaging |
Het |
Pi15 |
T |
C |
1: 17,672,945 (GRCm39) |
F48S |
probably benign |
Het |
Pkhd1 |
A |
G |
1: 20,655,376 (GRCm39) |
|
probably benign |
Het |
Ppard |
C |
G |
17: 28,505,348 (GRCm39) |
R12G |
unknown |
Het |
Prrc2c |
G |
T |
1: 162,532,551 (GRCm39) |
|
probably benign |
Het |
Prune1 |
A |
G |
3: 95,175,553 (GRCm39) |
Y41H |
possibly damaging |
Het |
Rcsd1 |
T |
C |
1: 165,483,541 (GRCm39) |
D150G |
probably damaging |
Het |
Rgs12 |
A |
T |
5: 35,123,456 (GRCm39) |
Q413L |
possibly damaging |
Het |
Rhox2h |
A |
G |
X: 36,850,848 (GRCm39) |
Y185H |
probably damaging |
Het |
Rnf17 |
T |
A |
14: 56,741,464 (GRCm39) |
C1306* |
probably null |
Het |
Ros1 |
T |
A |
10: 51,976,183 (GRCm39) |
M1499L |
probably benign |
Het |
Rubcnl |
T |
C |
14: 75,284,989 (GRCm39) |
S503P |
probably damaging |
Het |
Sap18b |
A |
T |
8: 96,552,342 (GRCm39) |
R117S |
probably benign |
Het |
Shank2 |
A |
G |
7: 143,964,336 (GRCm39) |
E858G |
probably damaging |
Het |
Shtn1 |
T |
C |
19: 59,020,632 (GRCm39) |
R197G |
probably damaging |
Het |
Slamf8 |
G |
A |
1: 172,412,087 (GRCm39) |
R163* |
probably null |
Het |
Slc6a3 |
T |
C |
13: 73,714,411 (GRCm39) |
I392T |
possibly damaging |
Het |
Sp140 |
C |
T |
1: 85,547,772 (GRCm39) |
|
probably benign |
Het |
Sp8 |
T |
C |
12: 118,812,751 (GRCm39) |
V202A |
possibly damaging |
Het |
Spata13 |
T |
C |
14: 60,946,908 (GRCm39) |
V652A |
probably damaging |
Het |
Stpg2 |
A |
T |
3: 139,023,162 (GRCm39) |
T393S |
probably benign |
Het |
Tagap |
T |
C |
17: 8,150,299 (GRCm39) |
M228T |
probably damaging |
Het |
Tagap |
A |
G |
17: 8,152,377 (GRCm39) |
T521A |
probably benign |
Het |
Tas2r123 |
T |
G |
6: 132,824,528 (GRCm39) |
S142A |
probably damaging |
Het |
Tat |
T |
A |
8: 110,718,261 (GRCm39) |
S49T |
probably benign |
Het |
Tfap4 |
G |
T |
16: 4,369,933 (GRCm39) |
Q41K |
possibly damaging |
Het |
Thbs2 |
T |
C |
17: 14,906,075 (GRCm39) |
N275S |
probably benign |
Het |
Tnfsf14 |
T |
A |
17: 57,497,867 (GRCm39) |
R122W |
probably damaging |
Het |
Tnrc6a |
T |
C |
7: 122,792,140 (GRCm39) |
V1886A |
possibly damaging |
Het |
Trim56 |
G |
A |
5: 137,143,252 (GRCm39) |
A88V |
probably damaging |
Het |
Trio |
A |
G |
15: 27,841,842 (GRCm39) |
Y1081H |
probably damaging |
Het |
Tspear |
T |
A |
10: 77,706,253 (GRCm39) |
L341H |
possibly damaging |
Het |
Ube2o |
G |
A |
11: 116,432,320 (GRCm39) |
T882I |
probably benign |
Het |
Upk3a |
A |
G |
15: 84,904,815 (GRCm39) |
T188A |
possibly damaging |
Het |
Vmn1r79 |
A |
C |
7: 11,910,358 (GRCm39) |
D80A |
probably damaging |
Het |
Wls |
C |
A |
3: 159,617,450 (GRCm39) |
T375K |
probably benign |
Het |
Wnt5a |
T |
C |
14: 28,233,835 (GRCm39) |
M1T |
probably null |
Het |
Zcchc4 |
A |
G |
5: 52,953,932 (GRCm39) |
E204G |
probably damaging |
Het |
Zfp513 |
G |
A |
5: 31,357,678 (GRCm39) |
P232S |
possibly damaging |
Het |
|
Other mutations in Garnl3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01102:Garnl3
|
APN |
2 |
32,896,828 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01601:Garnl3
|
APN |
2 |
32,887,701 (GRCm39) |
nonsense |
probably null |
|
IGL01981:Garnl3
|
APN |
2 |
32,887,741 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02209:Garnl3
|
APN |
2 |
32,975,942 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02434:Garnl3
|
APN |
2 |
32,944,217 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02512:Garnl3
|
APN |
2 |
32,921,150 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02947:Garnl3
|
APN |
2 |
32,936,606 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4403001:Garnl3
|
UTSW |
2 |
32,880,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R0123:Garnl3
|
UTSW |
2 |
32,896,816 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0134:Garnl3
|
UTSW |
2 |
32,896,816 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0225:Garnl3
|
UTSW |
2 |
32,896,816 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0551:Garnl3
|
UTSW |
2 |
32,906,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R0691:Garnl3
|
UTSW |
2 |
32,975,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R0693:Garnl3
|
UTSW |
2 |
32,975,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R0737:Garnl3
|
UTSW |
2 |
32,880,654 (GRCm39) |
missense |
probably damaging |
0.98 |
R1350:Garnl3
|
UTSW |
2 |
32,942,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R1691:Garnl3
|
UTSW |
2 |
32,887,675 (GRCm39) |
nonsense |
probably null |
|
R1938:Garnl3
|
UTSW |
2 |
32,895,212 (GRCm39) |
missense |
probably damaging |
0.99 |
R2100:Garnl3
|
UTSW |
2 |
32,936,657 (GRCm39) |
missense |
probably benign |
0.35 |
R2316:Garnl3
|
UTSW |
2 |
32,895,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R2353:Garnl3
|
UTSW |
2 |
32,954,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R3161:Garnl3
|
UTSW |
2 |
32,924,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R3839:Garnl3
|
UTSW |
2 |
32,879,558 (GRCm39) |
missense |
probably benign |
0.00 |
R3847:Garnl3
|
UTSW |
2 |
32,882,240 (GRCm39) |
missense |
probably benign |
|
R4871:Garnl3
|
UTSW |
2 |
32,977,100 (GRCm39) |
start codon destroyed |
probably null |
0.77 |
R5682:Garnl3
|
UTSW |
2 |
32,944,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R5811:Garnl3
|
UTSW |
2 |
32,896,911 (GRCm39) |
missense |
probably damaging |
0.99 |
R6267:Garnl3
|
UTSW |
2 |
32,994,892 (GRCm39) |
missense |
probably benign |
0.20 |
R6502:Garnl3
|
UTSW |
2 |
32,896,833 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6532:Garnl3
|
UTSW |
2 |
32,921,131 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6639:Garnl3
|
UTSW |
2 |
32,879,537 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6763:Garnl3
|
UTSW |
2 |
32,944,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R6866:Garnl3
|
UTSW |
2 |
32,892,785 (GRCm39) |
splice site |
probably null |
|
R6913:Garnl3
|
UTSW |
2 |
32,876,841 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7002:Garnl3
|
UTSW |
2 |
32,944,205 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7168:Garnl3
|
UTSW |
2 |
32,885,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R7341:Garnl3
|
UTSW |
2 |
32,924,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R7746:Garnl3
|
UTSW |
2 |
32,882,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R7919:Garnl3
|
UTSW |
2 |
32,936,611 (GRCm39) |
missense |
probably benign |
0.38 |
R8079:Garnl3
|
UTSW |
2 |
32,908,511 (GRCm39) |
critical splice donor site |
probably null |
|
R8087:Garnl3
|
UTSW |
2 |
32,935,548 (GRCm39) |
missense |
probably benign |
0.01 |
R8123:Garnl3
|
UTSW |
2 |
32,994,950 (GRCm39) |
missense |
probably damaging |
0.97 |
R8170:Garnl3
|
UTSW |
2 |
32,905,235 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8347:Garnl3
|
UTSW |
2 |
32,975,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R8418:Garnl3
|
UTSW |
2 |
32,942,158 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8679:Garnl3
|
UTSW |
2 |
32,916,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R8940:Garnl3
|
UTSW |
2 |
32,895,241 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9081:Garnl3
|
UTSW |
2 |
32,896,920 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9183:Garnl3
|
UTSW |
2 |
32,895,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R9213:Garnl3
|
UTSW |
2 |
32,895,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R9219:Garnl3
|
UTSW |
2 |
32,975,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R9453:Garnl3
|
UTSW |
2 |
32,893,881 (GRCm39) |
missense |
probably damaging |
1.00 |
X0022:Garnl3
|
UTSW |
2 |
32,912,680 (GRCm39) |
missense |
probably damaging |
1.00 |
X0023:Garnl3
|
UTSW |
2 |
32,916,161 (GRCm39) |
missense |
probably damaging |
1.00 |
X0024:Garnl3
|
UTSW |
2 |
32,895,191 (GRCm39) |
missense |
probably damaging |
0.98 |
|