Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933430I17Rik |
T |
A |
4: 62,457,164 (GRCm39) |
V161E |
possibly damaging |
Het |
Arhgap40 |
T |
C |
2: 158,388,629 (GRCm39) |
V521A |
possibly damaging |
Het |
Atrn |
T |
C |
2: 130,841,050 (GRCm39) |
|
probably benign |
Het |
Casp12 |
T |
C |
9: 5,352,923 (GRCm39) |
|
probably benign |
Het |
Cenpf |
G |
A |
1: 189,411,230 (GRCm39) |
T318M |
probably damaging |
Het |
Cfap119 |
C |
T |
7: 127,184,663 (GRCm39) |
R172H |
probably benign |
Het |
Clcn2 |
T |
C |
16: 20,527,892 (GRCm39) |
K525E |
probably damaging |
Het |
Cntln |
A |
G |
4: 84,889,419 (GRCm39) |
T301A |
probably benign |
Het |
Crat |
T |
C |
2: 30,305,378 (GRCm39) |
|
probably benign |
Het |
Cul5 |
A |
G |
9: 53,545,027 (GRCm39) |
|
probably benign |
Het |
Cxcl14 |
A |
T |
13: 56,443,708 (GRCm39) |
I34N |
probably damaging |
Het |
Cyp2b19 |
A |
G |
7: 26,470,819 (GRCm39) |
I487V |
probably benign |
Het |
Cyp4a10 |
T |
A |
4: 115,386,690 (GRCm39) |
F446I |
probably damaging |
Het |
Dclk3 |
T |
C |
9: 111,296,963 (GRCm39) |
F169S |
probably damaging |
Het |
Ddx52 |
T |
C |
11: 83,848,306 (GRCm39) |
I532T |
probably damaging |
Het |
Dnm1 |
T |
C |
2: 32,226,023 (GRCm39) |
D352G |
probably damaging |
Het |
Eif4g2 |
T |
C |
7: 110,677,509 (GRCm39) |
E174G |
probably damaging |
Het |
Enpp6 |
G |
T |
8: 47,546,067 (GRCm39) |
V386L |
probably damaging |
Het |
Entr1 |
C |
A |
2: 26,278,909 (GRCm39) |
|
probably benign |
Het |
Eps15l1 |
T |
C |
8: 73,095,238 (GRCm39) |
D904G |
probably damaging |
Het |
Esrrb |
A |
G |
12: 86,565,604 (GRCm39) |
Y356C |
probably damaging |
Het |
Flt3 |
A |
T |
5: 147,291,509 (GRCm39) |
S619T |
possibly damaging |
Het |
Fndc7 |
A |
T |
3: 108,766,218 (GRCm39) |
C716S |
probably damaging |
Het |
Gm26996 |
T |
A |
6: 130,556,448 (GRCm39) |
|
noncoding transcript |
Het |
Grik2 |
A |
T |
10: 49,298,711 (GRCm39) |
F50I |
possibly damaging |
Het |
Guf1 |
T |
C |
5: 69,723,786 (GRCm39) |
V367A |
possibly damaging |
Het |
Hspg2 |
C |
T |
4: 137,246,251 (GRCm39) |
R1010C |
probably damaging |
Het |
Ifnar2 |
T |
C |
16: 91,188,684 (GRCm39) |
V55A |
probably benign |
Het |
Impg1 |
T |
A |
9: 80,322,907 (GRCm39) |
I33F |
probably benign |
Het |
Ltbp4 |
A |
C |
7: 27,024,608 (GRCm39) |
V674G |
probably damaging |
Het |
Mroh2b |
T |
A |
15: 4,947,772 (GRCm39) |
L529H |
probably damaging |
Het |
Negr1 |
T |
C |
3: 156,914,023 (GRCm39) |
|
probably benign |
Het |
Neurog3 |
A |
G |
10: 61,969,599 (GRCm39) |
T25A |
probably damaging |
Het |
Or10v1 |
T |
C |
19: 11,874,126 (GRCm39) |
V247A |
probably benign |
Het |
Or4a69 |
T |
A |
2: 89,313,100 (GRCm39) |
K126N |
probably damaging |
Het |
Or51h1 |
A |
C |
7: 102,308,685 (GRCm39) |
Y219S |
probably damaging |
Het |
Or5k17 |
T |
C |
16: 58,746,455 (GRCm39) |
T160A |
probably benign |
Het |
Pax8 |
T |
A |
2: 24,333,201 (GRCm39) |
|
probably benign |
Het |
Pcsk6 |
A |
C |
7: 65,581,480 (GRCm39) |
I254L |
possibly damaging |
Het |
Pde3a |
A |
G |
6: 141,404,942 (GRCm39) |
K389R |
probably benign |
Het |
Rab3gap1 |
C |
A |
1: 127,852,996 (GRCm39) |
|
probably benign |
Het |
Rbck1 |
G |
A |
2: 152,160,653 (GRCm39) |
Q428* |
probably null |
Het |
Rptor |
A |
G |
11: 119,689,666 (GRCm39) |
D321G |
probably null |
Het |
Sall2 |
C |
A |
14: 52,551,260 (GRCm39) |
R643L |
probably damaging |
Het |
Skp1 |
T |
C |
11: 52,134,446 (GRCm39) |
I59T |
possibly damaging |
Het |
Slc23a3 |
T |
G |
1: 75,105,200 (GRCm39) |
N456T |
probably damaging |
Het |
Slc4a7 |
G |
A |
14: 14,778,850 (GRCm38) |
G920S |
probably damaging |
Het |
Smarcd3 |
T |
C |
5: 24,797,802 (GRCm39) |
I467V |
probably benign |
Het |
Spata31d1c |
C |
T |
13: 65,183,874 (GRCm39) |
A472V |
probably damaging |
Het |
Spmap1 |
A |
G |
11: 97,662,441 (GRCm39) |
S144P |
probably damaging |
Het |
Srsf6 |
T |
C |
2: 162,773,643 (GRCm39) |
I18T |
probably damaging |
Het |
Stom |
C |
T |
2: 35,213,758 (GRCm39) |
G80D |
probably damaging |
Het |
Svep1 |
A |
T |
4: 58,084,028 (GRCm39) |
Y1915N |
possibly damaging |
Het |
Tmf1 |
C |
T |
6: 97,150,361 (GRCm39) |
V449I |
probably benign |
Het |
Triobp |
C |
T |
15: 78,851,295 (GRCm39) |
A483V |
probably benign |
Het |
Vdac1 |
G |
A |
11: 52,265,799 (GRCm39) |
|
probably null |
Het |
Vmn2r75 |
T |
G |
7: 85,815,494 (GRCm39) |
E123D |
probably benign |
Het |
Vmn2r79 |
T |
A |
7: 86,653,319 (GRCm39) |
V528D |
possibly damaging |
Het |
Zdbf2 |
T |
G |
1: 63,345,750 (GRCm39) |
N1376K |
possibly damaging |
Het |
Zeb1os1 |
T |
C |
18: 5,525,375 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in D430041D05Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00838:D430041D05Rik
|
APN |
2 |
104,031,648 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01114:D430041D05Rik
|
APN |
2 |
104,088,511 (GRCm39) |
nonsense |
probably null |
|
IGL01669:D430041D05Rik
|
APN |
2 |
104,085,306 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02015:D430041D05Rik
|
APN |
2 |
104,060,749 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02037:D430041D05Rik
|
APN |
2 |
104,038,559 (GRCm39) |
splice site |
probably benign |
|
IGL02268:D430041D05Rik
|
APN |
2 |
104,071,500 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02294:D430041D05Rik
|
APN |
2 |
104,085,351 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02457:D430041D05Rik
|
APN |
2 |
104,079,690 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02601:D430041D05Rik
|
APN |
2 |
104,060,631 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02647:D430041D05Rik
|
APN |
2 |
104,078,611 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02679:D430041D05Rik
|
APN |
2 |
104,060,650 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02926:D430041D05Rik
|
APN |
2 |
104,044,604 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03171:D430041D05Rik
|
APN |
2 |
104,071,508 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03178:D430041D05Rik
|
APN |
2 |
104,051,556 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03371:D430041D05Rik
|
APN |
2 |
104,078,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R0027:D430041D05Rik
|
UTSW |
2 |
104,085,389 (GRCm39) |
missense |
probably benign |
|
R0064:D430041D05Rik
|
UTSW |
2 |
104,079,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R0135:D430041D05Rik
|
UTSW |
2 |
104,085,379 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0227:D430041D05Rik
|
UTSW |
2 |
104,035,545 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0265:D430041D05Rik
|
UTSW |
2 |
103,998,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R0268:D430041D05Rik
|
UTSW |
2 |
103,998,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R0282:D430041D05Rik
|
UTSW |
2 |
104,031,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R0366:D430041D05Rik
|
UTSW |
2 |
104,085,685 (GRCm39) |
missense |
probably damaging |
0.99 |
R0402:D430041D05Rik
|
UTSW |
2 |
103,998,509 (GRCm39) |
missense |
probably damaging |
0.99 |
R0436:D430041D05Rik
|
UTSW |
2 |
103,998,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R0441:D430041D05Rik
|
UTSW |
2 |
103,998,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R0540:D430041D05Rik
|
UTSW |
2 |
104,063,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R0607:D430041D05Rik
|
UTSW |
2 |
104,063,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R0613:D430041D05Rik
|
UTSW |
2 |
103,998,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R0626:D430041D05Rik
|
UTSW |
2 |
103,998,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R0747:D430041D05Rik
|
UTSW |
2 |
104,060,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R0864:D430041D05Rik
|
UTSW |
2 |
104,060,773 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0980:D430041D05Rik
|
UTSW |
2 |
104,079,690 (GRCm39) |
missense |
probably damaging |
0.99 |
R1014:D430041D05Rik
|
UTSW |
2 |
104,088,674 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1254:D430041D05Rik
|
UTSW |
2 |
104,031,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R1364:D430041D05Rik
|
UTSW |
2 |
103,985,363 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1456:D430041D05Rik
|
UTSW |
2 |
104,038,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R1574:D430041D05Rik
|
UTSW |
2 |
104,051,553 (GRCm39) |
small deletion |
probably benign |
|
R1604:D430041D05Rik
|
UTSW |
2 |
104,035,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R1605:D430041D05Rik
|
UTSW |
2 |
104,085,915 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1623:D430041D05Rik
|
UTSW |
2 |
103,983,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R1634:D430041D05Rik
|
UTSW |
2 |
104,051,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R1834:D430041D05Rik
|
UTSW |
2 |
103,998,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R1885:D430041D05Rik
|
UTSW |
2 |
104,060,800 (GRCm39) |
missense |
probably benign |
0.39 |
R2080:D430041D05Rik
|
UTSW |
2 |
103,987,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R2101:D430041D05Rik
|
UTSW |
2 |
103,979,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R2240:D430041D05Rik
|
UTSW |
2 |
103,987,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R2923:D430041D05Rik
|
UTSW |
2 |
104,085,660 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3751:D430041D05Rik
|
UTSW |
2 |
104,085,403 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3862:D430041D05Rik
|
UTSW |
2 |
104,044,522 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3863:D430041D05Rik
|
UTSW |
2 |
104,044,522 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3864:D430041D05Rik
|
UTSW |
2 |
104,044,522 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3949:D430041D05Rik
|
UTSW |
2 |
104,087,713 (GRCm39) |
missense |
probably benign |
0.02 |
R4493:D430041D05Rik
|
UTSW |
2 |
104,086,684 (GRCm39) |
missense |
probably benign |
0.02 |
R4526:D430041D05Rik
|
UTSW |
2 |
104,022,778 (GRCm39) |
critical splice donor site |
probably null |
|
R4598:D430041D05Rik
|
UTSW |
2 |
104,038,528 (GRCm39) |
missense |
probably damaging |
0.99 |
R4599:D430041D05Rik
|
UTSW |
2 |
104,038,528 (GRCm39) |
missense |
probably damaging |
0.99 |
R4647:D430041D05Rik
|
UTSW |
2 |
104,088,788 (GRCm39) |
missense |
probably damaging |
0.99 |
R4765:D430041D05Rik
|
UTSW |
2 |
104,044,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R4808:D430041D05Rik
|
UTSW |
2 |
104,031,455 (GRCm39) |
critical splice donor site |
probably null |
|
R4868:D430041D05Rik
|
UTSW |
2 |
104,085,754 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4982:D430041D05Rik
|
UTSW |
2 |
104,085,732 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5144:D430041D05Rik
|
UTSW |
2 |
104,088,847 (GRCm39) |
missense |
probably damaging |
0.99 |
R5255:D430041D05Rik
|
UTSW |
2 |
104,086,945 (GRCm39) |
missense |
probably benign |
0.26 |
R5356:D430041D05Rik
|
UTSW |
2 |
104,085,754 (GRCm39) |
missense |
probably damaging |
0.99 |
R5368:D430041D05Rik
|
UTSW |
2 |
104,078,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R5963:D430041D05Rik
|
UTSW |
2 |
104,078,630 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5993:D430041D05Rik
|
UTSW |
2 |
103,998,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R6122:D430041D05Rik
|
UTSW |
2 |
104,086,637 (GRCm39) |
missense |
probably benign |
0.01 |
R6410:D430041D05Rik
|
UTSW |
2 |
103,998,548 (GRCm39) |
splice site |
probably null |
|
R6804:D430041D05Rik
|
UTSW |
2 |
103,979,371 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6850:D430041D05Rik
|
UTSW |
2 |
104,031,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R6853:D430041D05Rik
|
UTSW |
2 |
104,071,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R7034:D430041D05Rik
|
UTSW |
2 |
104,022,883 (GRCm39) |
missense |
probably damaging |
0.99 |
R7146:D430041D05Rik
|
UTSW |
2 |
104,088,698 (GRCm39) |
missense |
probably benign |
0.06 |
R7250:D430041D05Rik
|
UTSW |
2 |
104,086,961 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7251:D430041D05Rik
|
UTSW |
2 |
104,051,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R7313:D430041D05Rik
|
UTSW |
2 |
104,085,910 (GRCm39) |
missense |
probably benign |
|
R7359:D430041D05Rik
|
UTSW |
2 |
104,044,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R7361:D430041D05Rik
|
UTSW |
2 |
104,085,363 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7436:D430041D05Rik
|
UTSW |
2 |
104,087,447 (GRCm39) |
missense |
probably benign |
0.02 |
R7472:D430041D05Rik
|
UTSW |
2 |
104,240,484 (GRCm39) |
missense |
unknown |
|
R7492:D430041D05Rik
|
UTSW |
2 |
104,031,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R7631:D430041D05Rik
|
UTSW |
2 |
103,979,363 (GRCm39) |
nonsense |
probably null |
|
R7672:D430041D05Rik
|
UTSW |
2 |
104,071,581 (GRCm39) |
missense |
probably benign |
0.01 |
R7721:D430041D05Rik
|
UTSW |
2 |
104,088,874 (GRCm39) |
missense |
probably benign |
0.00 |
R7754:D430041D05Rik
|
UTSW |
2 |
104,087,504 (GRCm39) |
missense |
probably benign |
0.01 |
R7882:D430041D05Rik
|
UTSW |
2 |
104,087,974 (GRCm39) |
nonsense |
probably null |
|
R7896:D430041D05Rik
|
UTSW |
2 |
104,088,385 (GRCm39) |
missense |
probably benign |
0.05 |
R7986:D430041D05Rik
|
UTSW |
2 |
104,087,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R8005:D430041D05Rik
|
UTSW |
2 |
104,088,599 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8016:D430041D05Rik
|
UTSW |
2 |
104,022,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R8054:D430041D05Rik
|
UTSW |
2 |
103,985,390 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8058:D430041D05Rik
|
UTSW |
2 |
103,979,128 (GRCm39) |
makesense |
probably null |
|
R8100:D430041D05Rik
|
UTSW |
2 |
104,087,287 (GRCm39) |
missense |
probably benign |
0.00 |
R8461:D430041D05Rik
|
UTSW |
2 |
103,998,280 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8695:D430041D05Rik
|
UTSW |
2 |
104,085,299 (GRCm39) |
critical splice donor site |
probably null |
|
R8885:D430041D05Rik
|
UTSW |
2 |
104,071,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R9007:D430041D05Rik
|
UTSW |
2 |
104,087,930 (GRCm39) |
missense |
probably benign |
0.08 |
R9009:D430041D05Rik
|
UTSW |
2 |
104,240,521 (GRCm39) |
start gained |
probably benign |
|
R9335:D430041D05Rik
|
UTSW |
2 |
104,078,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R9348:D430041D05Rik
|
UTSW |
2 |
104,088,337 (GRCm39) |
missense |
probably benign |
0.05 |
R9384:D430041D05Rik
|
UTSW |
2 |
104,087,920 (GRCm39) |
missense |
probably benign |
|
R9483:D430041D05Rik
|
UTSW |
2 |
104,087,563 (GRCm39) |
missense |
probably benign |
0.44 |
R9489:D430041D05Rik
|
UTSW |
2 |
104,087,189 (GRCm39) |
missense |
probably benign |
0.20 |
R9605:D430041D05Rik
|
UTSW |
2 |
104,087,189 (GRCm39) |
missense |
probably benign |
0.20 |
R9613:D430041D05Rik
|
UTSW |
2 |
104,060,737 (GRCm39) |
missense |
probably benign |
0.09 |
R9698:D430041D05Rik
|
UTSW |
2 |
103,985,396 (GRCm39) |
missense |
probably damaging |
1.00 |
X0024:D430041D05Rik
|
UTSW |
2 |
104,022,911 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1176:D430041D05Rik
|
UTSW |
2 |
104,087,201 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:D430041D05Rik
|
UTSW |
2 |
103,985,280 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:D430041D05Rik
|
UTSW |
2 |
104,071,536 (GRCm39) |
missense |
possibly damaging |
0.82 |
|