Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932414N04Rik |
T |
C |
2: 68,562,377 (GRCm39) |
S335P |
unknown |
Het |
Adcy2 |
T |
A |
13: 68,886,707 (GRCm39) |
N281Y |
probably damaging |
Het |
Adgra1 |
T |
A |
7: 139,455,196 (GRCm39) |
W275R |
probably damaging |
Het |
Apmap |
T |
C |
2: 150,450,341 (GRCm39) |
D20G |
probably damaging |
Het |
Arap2 |
T |
C |
5: 62,807,116 (GRCm39) |
T1184A |
probably damaging |
Het |
Atp13a2 |
T |
C |
4: 140,722,907 (GRCm39) |
V303A |
possibly damaging |
Het |
BC004004 |
A |
T |
17: 29,501,282 (GRCm39) |
|
probably benign |
Het |
C1s1 |
G |
A |
6: 124,517,912 (GRCm39) |
P23S |
possibly damaging |
Het |
C1s2 |
T |
A |
6: 124,608,123 (GRCm39) |
N197Y |
probably damaging |
Het |
Camsap3 |
A |
G |
8: 3,653,980 (GRCm39) |
H539R |
probably damaging |
Het |
Catsperb |
A |
T |
12: 101,569,025 (GRCm39) |
N899I |
probably damaging |
Het |
Cct4 |
T |
C |
11: 22,951,354 (GRCm39) |
|
probably benign |
Het |
Chrm2 |
A |
T |
6: 36,500,385 (GRCm39) |
T81S |
probably damaging |
Het |
Dnaaf3 |
A |
T |
7: 4,526,686 (GRCm39) |
S464T |
possibly damaging |
Het |
Dnah10 |
T |
A |
5: 124,900,437 (GRCm39) |
I3898N |
possibly damaging |
Het |
Dnah3 |
TTCCTC |
TTC |
7: 119,550,244 (GRCm39) |
|
probably benign |
Het |
Dnajc13 |
T |
C |
9: 104,067,584 (GRCm39) |
K1187E |
probably damaging |
Het |
Dock4 |
A |
T |
12: 40,867,735 (GRCm39) |
D1437V |
probably damaging |
Het |
Dst |
C |
T |
1: 34,234,942 (GRCm39) |
Q3674* |
probably null |
Het |
Eef1a2 |
T |
C |
2: 180,794,776 (GRCm39) |
Y141C |
probably damaging |
Het |
Fads3 |
G |
T |
19: 10,030,397 (GRCm39) |
Q178H |
probably null |
Het |
Fbxw22 |
T |
A |
9: 109,215,829 (GRCm39) |
M140L |
probably benign |
Het |
Fndc7 |
A |
G |
3: 108,788,707 (GRCm39) |
I178T |
probably damaging |
Het |
Foxd1 |
T |
C |
13: 98,491,549 (GRCm39) |
M141T |
probably damaging |
Het |
H4c2 |
T |
C |
13: 23,941,215 (GRCm39) |
V71A |
possibly damaging |
Het |
Havcr2 |
T |
C |
11: 46,360,343 (GRCm39) |
I141T |
probably benign |
Het |
Hectd1 |
A |
C |
12: 51,820,618 (GRCm39) |
N1190K |
probably damaging |
Het |
Hook3 |
T |
A |
8: 26,534,355 (GRCm39) |
|
probably benign |
Het |
Hpgd |
T |
A |
8: 56,760,702 (GRCm39) |
I133N |
possibly damaging |
Het |
Itih2 |
T |
C |
2: 10,102,714 (GRCm39) |
R807G |
probably benign |
Het |
Klhl35 |
G |
A |
7: 99,122,094 (GRCm39) |
G65D |
probably damaging |
Het |
Lrch4 |
C |
G |
5: 137,631,919 (GRCm39) |
C48W |
probably damaging |
Het |
Mafa |
A |
G |
15: 75,619,627 (GRCm39) |
S49P |
probably benign |
Het |
Magi1 |
A |
G |
6: 93,662,584 (GRCm39) |
V1170A |
probably damaging |
Het |
Mprip |
A |
T |
11: 59,649,380 (GRCm39) |
K1028M |
probably damaging |
Het |
Mtpn |
C |
T |
6: 35,489,225 (GRCm39) |
D100N |
probably benign |
Het |
Numb |
G |
T |
12: 83,923,521 (GRCm39) |
|
probably benign |
Het |
Obscn |
A |
G |
11: 58,929,435 (GRCm39) |
L6063P |
probably damaging |
Het |
Or2y6 |
A |
G |
11: 52,103,881 (GRCm39) |
*312Q |
probably null |
Het |
Or6c6c |
A |
T |
10: 129,540,756 (GRCm39) |
N3I |
probably damaging |
Het |
P3h3 |
A |
T |
6: 124,834,157 (GRCm39) |
|
probably null |
Het |
Pi4k2a |
A |
G |
19: 42,103,477 (GRCm39) |
D329G |
probably benign |
Het |
Ptch1 |
T |
C |
13: 63,713,268 (GRCm39) |
|
probably benign |
Het |
Samd9l |
A |
G |
6: 3,376,754 (GRCm39) |
V169A |
probably benign |
Het |
Sdk1 |
T |
C |
5: 142,100,148 (GRCm39) |
Y1393H |
probably damaging |
Het |
Slc18a3 |
T |
A |
14: 32,185,880 (GRCm39) |
M168L |
probably benign |
Het |
Smurf1 |
T |
C |
5: 144,816,190 (GRCm39) |
T722A |
probably damaging |
Het |
Ssr2 |
C |
T |
3: 88,488,379 (GRCm39) |
P85L |
probably damaging |
Het |
Syne2 |
G |
T |
12: 76,074,898 (GRCm39) |
A4614S |
probably benign |
Het |
Tgfbr3 |
C |
A |
5: 107,288,521 (GRCm39) |
G380V |
possibly damaging |
Het |
Tk1 |
G |
T |
11: 117,706,748 (GRCm39) |
|
probably benign |
Het |
Tmem245 |
A |
T |
4: 56,903,241 (GRCm39) |
S610T |
probably benign |
Het |
Tmtc2 |
A |
G |
10: 105,107,302 (GRCm39) |
|
probably benign |
Het |
Trim30b |
A |
G |
7: 104,006,578 (GRCm39) |
Y93H |
possibly damaging |
Het |
Tsks |
A |
G |
7: 44,593,412 (GRCm39) |
D126G |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,733,812 (GRCm39) |
|
probably benign |
Het |
Usp15 |
A |
G |
10: 123,017,647 (GRCm39) |
W50R |
probably damaging |
Het |
Vmn2r55 |
A |
T |
7: 12,404,492 (GRCm39) |
F304I |
probably benign |
Het |
Xirp2 |
T |
A |
2: 67,339,587 (GRCm39) |
D609E |
probably damaging |
Het |
Zan |
C |
T |
5: 137,392,638 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Ace3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1932:Ace3
|
UTSW |
11 |
105,895,436 (GRCm39) |
critical splice donor site |
probably null |
|
R4074:Ace3
|
UTSW |
11 |
105,888,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R4415:Ace3
|
UTSW |
11 |
105,895,947 (GRCm39) |
missense |
probably benign |
0.11 |
R5315:Ace3
|
UTSW |
11 |
105,885,747 (GRCm39) |
missense |
probably benign |
0.00 |
R5325:Ace3
|
UTSW |
11 |
105,896,079 (GRCm39) |
missense |
probably benign |
|
R5866:Ace3
|
UTSW |
11 |
105,888,330 (GRCm39) |
missense |
probably damaging |
0.99 |
R6122:Ace3
|
UTSW |
11 |
105,885,764 (GRCm39) |
missense |
probably benign |
0.08 |
R6160:Ace3
|
UTSW |
11 |
105,885,558 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6815:Ace3
|
UTSW |
11 |
105,888,084 (GRCm39) |
nonsense |
probably null |
|
R8031:Ace3
|
UTSW |
11 |
105,888,924 (GRCm39) |
critical splice donor site |
probably null |
|
R8179:Ace3
|
UTSW |
11 |
105,895,383 (GRCm39) |
missense |
probably benign |
0.15 |
R8349:Ace3
|
UTSW |
11 |
105,885,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R8449:Ace3
|
UTSW |
11 |
105,885,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R8679:Ace3
|
UTSW |
11 |
105,886,701 (GRCm39) |
missense |
probably benign |
0.00 |
R8780:Ace3
|
UTSW |
11 |
105,888,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R8839:Ace3
|
UTSW |
11 |
105,889,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R8965:Ace3
|
UTSW |
11 |
105,896,175 (GRCm39) |
missense |
probably benign |
|
R9287:Ace3
|
UTSW |
11 |
105,888,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R9457:Ace3
|
UTSW |
11 |
105,885,687 (GRCm39) |
missense |
probably benign |
0.02 |
R9486:Ace3
|
UTSW |
11 |
105,896,219 (GRCm39) |
missense |
probably benign |
0.30 |
|