Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700012B07Rik |
G |
T |
11: 109,794,154 |
C172* |
probably null |
Het |
Actl9 |
A |
G |
17: 33,434,088 |
N374S |
probably benign |
Het |
Ahcyl2 |
T |
A |
6: 29,768,556 |
|
probably benign |
Het |
Arfgef2 |
T |
C |
2: 166,878,544 |
M1501T |
probably benign |
Het |
Asb17 |
A |
T |
3: 153,844,538 |
D69V |
probably damaging |
Het |
Atp13a5 |
T |
C |
16: 29,263,450 |
Y877C |
probably damaging |
Het |
Atrip |
T |
C |
9: 109,065,203 |
Q64R |
probably benign |
Het |
Auts2 |
A |
G |
5: 131,476,891 |
|
probably benign |
Het |
Cacna2d1 |
G |
T |
5: 16,359,070 |
R893L |
probably damaging |
Het |
Ccdc138 |
C |
T |
10: 58,573,636 |
R596C |
probably damaging |
Het |
Cd163 |
A |
G |
6: 124,311,669 |
Y353C |
probably damaging |
Het |
Cdon |
T |
C |
9: 35,489,034 |
Y1015H |
probably damaging |
Het |
Chsy3 |
T |
C |
18: 59,179,471 |
Y339H |
probably damaging |
Het |
Cspp1 |
T |
C |
1: 10,066,519 |
W190R |
probably benign |
Het |
Ddx1 |
A |
T |
12: 13,223,992 |
I570N |
probably damaging |
Het |
Duox1 |
G |
A |
2: 122,337,317 |
R1027H |
probably benign |
Het |
Dync1h1 |
C |
T |
12: 110,626,892 |
Q1198* |
probably null |
Het |
Ecel1 |
G |
A |
1: 87,154,253 |
S246L |
probably damaging |
Het |
Fam228b |
T |
G |
12: 4,763,042 |
R109S |
probably damaging |
Het |
Fut9 |
T |
A |
4: 25,799,245 |
|
probably benign |
Het |
Gm5346 |
T |
C |
8: 43,626,471 |
N239D |
probably damaging |
Het |
Gm5592 |
A |
G |
7: 41,289,735 |
R814G |
probably damaging |
Het |
Gmps |
A |
G |
3: 63,990,325 |
K233E |
probably benign |
Het |
Gramd1c |
A |
G |
16: 43,990,663 |
Y438H |
probably damaging |
Het |
Gsdmc |
A |
T |
15: 63,802,033 |
D134E |
possibly damaging |
Het |
Gxylt2 |
A |
G |
6: 100,783,181 |
I226V |
probably benign |
Het |
Hc |
T |
C |
2: 35,013,532 |
I1037V |
probably benign |
Het |
Hspa4 |
T |
G |
11: 53,289,123 |
R69S |
possibly damaging |
Het |
Hspg2 |
C |
T |
4: 137,518,940 |
R1010C |
probably damaging |
Het |
Kifc3 |
A |
G |
8: 95,102,726 |
S508P |
probably damaging |
Het |
Krt7 |
G |
A |
15: 101,412,547 |
R25H |
probably benign |
Het |
Lhfp |
T |
A |
3: 53,043,433 |
S43T |
possibly damaging |
Het |
Lrrc7 |
T |
A |
3: 158,181,580 |
K394N |
possibly damaging |
Het |
Lypd4 |
A |
T |
7: 24,866,815 |
L28Q |
probably damaging |
Het |
Mdc1 |
A |
G |
17: 35,850,589 |
E798G |
probably benign |
Het |
Mta1 |
T |
A |
12: 113,133,525 |
|
probably null |
Het |
Mtg2 |
A |
T |
2: 180,083,390 |
Q132L |
possibly damaging |
Het |
Myh1 |
G |
T |
11: 67,206,048 |
E382* |
probably null |
Het |
Myo3a |
T |
C |
2: 22,282,602 |
L175P |
probably damaging |
Het |
Nckap5 |
A |
T |
1: 125,977,049 |
F144L |
possibly damaging |
Het |
Nfrkb |
T |
A |
9: 31,389,055 |
|
probably null |
Het |
Nmt2 |
C |
T |
2: 3,284,392 |
P5L |
probably benign |
Het |
Nsmf |
T |
C |
2: 25,055,061 |
|
probably null |
Het |
Olfr635 |
A |
T |
7: 103,979,374 |
M61L |
probably damaging |
Het |
Olfr76 |
T |
A |
19: 12,120,056 |
I219F |
probably benign |
Het |
Oprl1 |
C |
T |
2: 181,719,002 |
R257C |
probably damaging |
Het |
Pcdhgc3 |
T |
A |
18: 37,807,585 |
N346K |
probably damaging |
Het |
Pcnt |
G |
A |
10: 76,355,077 |
P2791S |
probably benign |
Het |
Pdia3 |
A |
G |
2: 121,414,139 |
N11S |
probably benign |
Het |
Pik3c2g |
A |
T |
6: 139,896,202 |
T778S |
probably benign |
Het |
Pik3ip1 |
T |
A |
11: 3,333,520 |
I75N |
probably damaging |
Het |
Ppargc1b |
A |
G |
18: 61,307,265 |
S845P |
probably damaging |
Het |
Prdm2 |
A |
T |
4: 143,179,367 |
L50* |
probably null |
Het |
Ptpro |
T |
A |
6: 137,443,594 |
V1007D |
probably damaging |
Het |
Pxdn |
G |
A |
12: 30,003,141 |
V926I |
probably benign |
Het |
Rab11fip2 |
A |
T |
19: 59,937,367 |
N139K |
probably damaging |
Het |
Rcn2 |
T |
A |
9: 56,053,016 |
M189K |
probably damaging |
Het |
Rev1 |
A |
T |
1: 38,074,489 |
|
probably benign |
Het |
Rhbg |
C |
A |
3: 88,245,134 |
G368C |
probably damaging |
Het |
Rnf214 |
A |
G |
9: 45,899,744 |
|
probably null |
Het |
Sf3a3 |
T |
C |
4: 124,725,166 |
S307P |
probably benign |
Het |
Slc6a18 |
T |
A |
13: 73,666,323 |
Y494F |
probably damaging |
Het |
Son |
T |
C |
16: 91,657,664 |
S1100P |
probably damaging |
Het |
Spag16 |
T |
G |
1: 69,853,352 |
N97K |
probably benign |
Het |
Tmem192 |
T |
C |
8: 64,959,511 |
V114A |
possibly damaging |
Het |
Urb1 |
G |
T |
16: 90,756,171 |
P1901T |
probably benign |
Het |
Vwa5b2 |
A |
G |
16: 20,600,709 |
T601A |
probably damaging |
Het |
Wdtc1 |
G |
T |
4: 133,308,851 |
T126K |
possibly damaging |
Het |
Xirp2 |
T |
C |
2: 67,525,670 |
Y3592H |
possibly damaging |
Het |
Xylt2 |
A |
T |
11: 94,670,016 |
V232E |
probably damaging |
Het |
|