Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
G |
T |
11: 109,865,393 (GRCm39) |
P355T |
probably benign |
Het |
Abhd15 |
T |
C |
11: 77,406,764 (GRCm39) |
V247A |
probably benign |
Het |
Adamts1 |
C |
T |
16: 85,592,507 (GRCm39) |
V634M |
possibly damaging |
Het |
BC049715 |
T |
C |
6: 136,817,453 (GRCm39) |
I231T |
possibly damaging |
Het |
Chpf |
A |
T |
1: 75,454,184 (GRCm39) |
V198E |
probably damaging |
Het |
Cp |
C |
T |
3: 20,025,198 (GRCm39) |
P386S |
probably damaging |
Het |
Cth |
A |
G |
3: 157,625,677 (GRCm39) |
I107T |
possibly damaging |
Het |
Ctrc |
T |
C |
4: 141,567,632 (GRCm39) |
D157G |
probably damaging |
Het |
D630003M21Rik |
A |
G |
2: 158,042,280 (GRCm39) |
Y889H |
probably damaging |
Het |
Elavl3 |
A |
G |
9: 21,930,040 (GRCm39) |
V288A |
probably damaging |
Het |
Esyt3 |
A |
T |
9: 99,218,245 (GRCm39) |
I130K |
probably benign |
Het |
F13a1 |
A |
T |
13: 37,100,875 (GRCm39) |
V423D |
probably damaging |
Het |
Faf1 |
T |
C |
4: 109,614,889 (GRCm39) |
|
probably benign |
Het |
Fam227b |
A |
T |
2: 125,968,980 (GRCm39) |
D31E |
probably benign |
Het |
Fastkd2 |
A |
G |
1: 63,776,995 (GRCm39) |
D377G |
possibly damaging |
Het |
Fbxl6 |
G |
A |
15: 76,420,824 (GRCm39) |
R384* |
probably null |
Het |
Fcamr |
A |
T |
1: 130,732,313 (GRCm39) |
H44L |
probably damaging |
Het |
Fhod3 |
A |
G |
18: 25,223,818 (GRCm39) |
N1055D |
probably benign |
Het |
Garem1 |
A |
T |
18: 21,281,863 (GRCm39) |
Y164* |
probably null |
Het |
Gemin4 |
C |
T |
11: 76,103,714 (GRCm39) |
C349Y |
probably damaging |
Het |
Gnal |
A |
G |
18: 67,268,441 (GRCm39) |
|
probably null |
Het |
Hacl1 |
T |
C |
14: 31,356,148 (GRCm39) |
|
probably benign |
Het |
Hectd3 |
T |
C |
4: 116,855,727 (GRCm39) |
V409A |
probably benign |
Het |
Hps6 |
A |
G |
19: 45,992,492 (GRCm39) |
E143G |
probably damaging |
Het |
Hspa4 |
T |
A |
11: 53,161,776 (GRCm39) |
I459L |
probably benign |
Het |
Ighv3-6 |
G |
A |
12: 114,252,061 (GRCm39) |
Q21* |
probably null |
Het |
Ints3 |
G |
A |
3: 90,311,294 (GRCm39) |
R438* |
probably null |
Het |
Jmjd6 |
T |
C |
11: 116,731,991 (GRCm39) |
N237D |
probably benign |
Het |
Lrrk2 |
C |
A |
15: 91,662,707 (GRCm39) |
T1912K |
probably damaging |
Het |
Mdga2 |
C |
A |
12: 67,267,980 (GRCm39) |
|
probably benign |
Het |
Mroh2a |
A |
G |
1: 88,186,386 (GRCm39) |
S64G |
probably benign |
Het |
Myh6 |
T |
C |
14: 55,200,512 (GRCm39) |
D203G |
probably benign |
Het |
Myo5b |
T |
C |
18: 74,849,108 (GRCm39) |
S1116P |
probably damaging |
Het |
Nalcn |
T |
A |
14: 123,607,357 (GRCm39) |
D704V |
probably benign |
Het |
Nes |
A |
T |
3: 87,878,543 (GRCm39) |
M12L |
probably benign |
Het |
Or10ak7 |
T |
C |
4: 118,791,880 (GRCm39) |
D53G |
probably damaging |
Het |
Or10al2 |
A |
G |
17: 37,983,858 (GRCm39) |
T315A |
probably benign |
Het |
Or2f1 |
T |
A |
6: 42,721,010 (GRCm39) |
I13N |
probably damaging |
Het |
Or5j3 |
T |
A |
2: 86,128,360 (GRCm39) |
S67T |
probably damaging |
Het |
Pcdha2 |
T |
C |
18: 37,074,376 (GRCm39) |
V669A |
probably benign |
Het |
Pdhx |
T |
C |
2: 102,852,564 (GRCm39) |
N433S |
probably damaging |
Het |
Pip5kl1 |
A |
G |
2: 32,469,124 (GRCm39) |
R261G |
probably damaging |
Het |
Plekhj1 |
A |
G |
10: 80,633,609 (GRCm39) |
I76T |
probably damaging |
Het |
Ppp1r3a |
A |
T |
6: 14,719,073 (GRCm39) |
S614T |
probably damaging |
Het |
Ptpru |
T |
C |
4: 131,501,615 (GRCm39) |
N1207S |
probably damaging |
Het |
Ranbp2 |
T |
C |
10: 58,312,294 (GRCm39) |
F1005L |
probably benign |
Het |
Rims2 |
A |
G |
15: 39,301,241 (GRCm39) |
E324G |
probably damaging |
Het |
Sema6d |
A |
T |
2: 124,498,770 (GRCm39) |
I227L |
probably benign |
Het |
Smarcad1 |
T |
G |
6: 65,091,320 (GRCm39) |
L1014V |
probably damaging |
Het |
Spag9 |
T |
G |
11: 93,935,305 (GRCm39) |
S39A |
possibly damaging |
Het |
Spag9 |
T |
C |
11: 93,935,243 (GRCm39) |
V18A |
possibly damaging |
Het |
Sun2 |
T |
C |
15: 79,618,356 (GRCm39) |
K268E |
probably benign |
Het |
Tbpl2 |
C |
T |
2: 23,977,151 (GRCm39) |
R289Q |
probably benign |
Het |
Tcea3 |
T |
A |
4: 135,982,454 (GRCm39) |
|
probably benign |
Het |
Tmem185a |
C |
T |
X: 69,505,792 (GRCm39) |
|
probably null |
Het |
Tnrc6c |
C |
T |
11: 117,614,355 (GRCm39) |
R838W |
probably damaging |
Het |
Vmn1r212 |
A |
T |
13: 23,067,358 (GRCm39) |
V325E |
unknown |
Het |
Vmn1r35 |
T |
A |
6: 66,656,057 (GRCm39) |
R204S |
probably damaging |
Het |
Vmn2r57 |
A |
G |
7: 41,077,554 (GRCm39) |
M204T |
probably damaging |
Het |
Wdfy3 |
A |
T |
5: 102,092,105 (GRCm39) |
Y411* |
probably null |
Het |
Zfp335 |
G |
T |
2: 164,752,620 (GRCm39) |
D41E |
probably damaging |
Het |
|
Other mutations in 2510039O18Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01327:2510039O18Rik
|
APN |
4 |
148,029,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R1135:2510039O18Rik
|
UTSW |
4 |
148,029,115 (GRCm39) |
missense |
probably benign |
0.26 |
R1546:2510039O18Rik
|
UTSW |
4 |
148,026,232 (GRCm39) |
missense |
probably damaging |
0.97 |
R2008:2510039O18Rik
|
UTSW |
4 |
148,026,034 (GRCm39) |
missense |
probably benign |
0.31 |
R2437:2510039O18Rik
|
UTSW |
4 |
148,031,075 (GRCm39) |
makesense |
probably null |
|
R3970:2510039O18Rik
|
UTSW |
4 |
148,029,779 (GRCm39) |
missense |
probably damaging |
0.99 |
R3973:2510039O18Rik
|
UTSW |
4 |
148,029,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R3974:2510039O18Rik
|
UTSW |
4 |
148,029,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R4050:2510039O18Rik
|
UTSW |
4 |
148,029,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R4431:2510039O18Rik
|
UTSW |
4 |
148,026,022 (GRCm39) |
missense |
probably benign |
0.01 |
R4750:2510039O18Rik
|
UTSW |
4 |
148,025,945 (GRCm39) |
missense |
probably damaging |
0.99 |
R4943:2510039O18Rik
|
UTSW |
4 |
148,029,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R5139:2510039O18Rik
|
UTSW |
4 |
148,029,905 (GRCm39) |
missense |
probably damaging |
0.98 |
R6735:2510039O18Rik
|
UTSW |
4 |
148,026,274 (GRCm39) |
missense |
probably benign |
|
R7139:2510039O18Rik
|
UTSW |
4 |
148,026,295 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7689:2510039O18Rik
|
UTSW |
4 |
148,029,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R8307:2510039O18Rik
|
UTSW |
4 |
148,025,837 (GRCm39) |
missense |
probably benign |
0.00 |
R9336:2510039O18Rik
|
UTSW |
4 |
148,029,490 (GRCm39) |
missense |
probably benign |
0.01 |
R9591:2510039O18Rik
|
UTSW |
4 |
148,029,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R9618:2510039O18Rik
|
UTSW |
4 |
148,029,873 (GRCm39) |
nonsense |
probably null |
|
V5088:2510039O18Rik
|
UTSW |
4 |
148,026,233 (GRCm39) |
missense |
probably benign |
0.18 |
V5622:2510039O18Rik
|
UTSW |
4 |
148,026,233 (GRCm39) |
missense |
probably benign |
0.18 |
V5622:2510039O18Rik
|
UTSW |
4 |
148,026,233 (GRCm39) |
missense |
probably benign |
0.18 |
Z1088:2510039O18Rik
|
UTSW |
4 |
148,029,202 (GRCm39) |
missense |
probably benign |
0.03 |
|