Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6030445D17Rik |
T |
C |
4: 136,190,059 (GRCm39) |
S147P |
unknown |
Het |
Ano2 |
A |
G |
6: 125,792,553 (GRCm39) |
D349G |
probably damaging |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Ccnf |
C |
A |
17: 24,445,678 (GRCm39) |
E523* |
probably null |
Het |
Ccr10 |
C |
T |
11: 101,065,375 (GRCm39) |
A52T |
possibly damaging |
Het |
Cdc14b |
C |
T |
13: 64,353,338 (GRCm39) |
|
probably benign |
Het |
Cirop |
G |
T |
14: 54,933,116 (GRCm39) |
Q356K |
noncoding transcript |
Het |
Cmya5 |
T |
C |
13: 93,230,951 (GRCm39) |
E1379G |
probably damaging |
Het |
Cyfip1 |
A |
G |
7: 55,558,189 (GRCm39) |
D822G |
possibly damaging |
Het |
Cyp4a29 |
A |
C |
4: 115,106,927 (GRCm39) |
T195P |
probably damaging |
Het |
Dmxl1 |
A |
T |
18: 50,035,434 (GRCm39) |
T2283S |
probably damaging |
Het |
Dnah7b |
A |
G |
1: 46,272,745 (GRCm39) |
D2291G |
probably benign |
Het |
Dock3 |
T |
A |
9: 106,872,080 (GRCm39) |
L493F |
probably damaging |
Het |
Fbxw7 |
G |
A |
3: 84,876,520 (GRCm39) |
G227D |
probably damaging |
Het |
Fmo2 |
A |
T |
1: 162,708,085 (GRCm39) |
V350D |
probably damaging |
Het |
Glis1 |
C |
T |
4: 107,489,102 (GRCm39) |
P487S |
probably benign |
Het |
Gm10549 |
C |
A |
18: 33,597,358 (GRCm39) |
|
probably benign |
Het |
Gm35315 |
G |
T |
5: 110,226,410 (GRCm39) |
T343K |
probably benign |
Het |
Gpr141 |
A |
G |
13: 19,936,697 (GRCm39) |
I26T |
probably benign |
Het |
Hectd4 |
T |
G |
5: 121,446,941 (GRCm39) |
V311G |
possibly damaging |
Het |
Ino80d |
C |
T |
1: 63,118,206 (GRCm39) |
E322K |
possibly damaging |
Het |
Irs2 |
A |
G |
8: 11,055,121 (GRCm39) |
S1104P |
probably damaging |
Het |
Lama1 |
T |
C |
17: 68,097,851 (GRCm39) |
F1744L |
probably benign |
Het |
Lcn10 |
A |
T |
2: 25,573,587 (GRCm39) |
R55* |
probably null |
Het |
Lrp2 |
A |
T |
2: 69,299,822 (GRCm39) |
C3077S |
probably damaging |
Het |
Mdc1 |
T |
A |
17: 36,161,566 (GRCm39) |
S826R |
probably benign |
Het |
Nr2c1 |
G |
T |
10: 93,999,648 (GRCm39) |
V103L |
probably benign |
Het |
Nup133 |
A |
T |
8: 124,663,612 (GRCm39) |
D310E |
possibly damaging |
Het |
Or7c70 |
A |
G |
10: 78,683,093 (GRCm39) |
S219P |
possibly damaging |
Het |
Pip5k1b |
T |
A |
19: 24,359,187 (GRCm39) |
E112D |
probably damaging |
Het |
Pira12 |
A |
T |
7: 3,897,640 (GRCm39) |
V485E |
probably damaging |
Het |
Reln |
T |
C |
5: 22,153,594 (GRCm39) |
K2237E |
probably damaging |
Het |
Sirt2 |
A |
G |
7: 28,466,940 (GRCm39) |
|
probably benign |
Het |
Slit2 |
A |
T |
5: 48,459,770 (GRCm39) |
H1350L |
possibly damaging |
Het |
Snx15 |
A |
G |
19: 6,171,538 (GRCm39) |
S179P |
probably damaging |
Het |
Sp8 |
T |
G |
12: 118,812,402 (GRCm39) |
S86A |
probably benign |
Het |
Sptbn5 |
T |
C |
2: 119,907,803 (GRCm39) |
|
probably benign |
Het |
Tfap4 |
A |
G |
16: 4,365,175 (GRCm39) |
S196P |
probably damaging |
Het |
Tgm3 |
T |
C |
2: 129,880,530 (GRCm39) |
|
probably null |
Het |
Tnks2 |
T |
C |
19: 36,843,604 (GRCm39) |
|
probably benign |
Het |
Ttll11 |
A |
T |
2: 35,642,511 (GRCm39) |
|
probably null |
Het |
Vwa3b |
C |
A |
1: 37,139,779 (GRCm39) |
Q367K |
possibly damaging |
Het |
Zdhhc20 |
A |
T |
14: 58,078,340 (GRCm39) |
V312E |
probably damaging |
Het |
|
Other mutations in Acat2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01920:Acat2
|
APN |
17 |
13,162,912 (GRCm39) |
missense |
probably benign |
0.00 |
R0243:Acat2
|
UTSW |
17 |
13,162,908 (GRCm39) |
missense |
probably benign |
|
R4153:Acat2
|
UTSW |
17 |
13,171,153 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4224:Acat2
|
UTSW |
17 |
13,181,772 (GRCm39) |
unclassified |
probably benign |
|
R4332:Acat2
|
UTSW |
17 |
13,181,782 (GRCm39) |
unclassified |
probably benign |
|
R6605:Acat2
|
UTSW |
17 |
13,162,774 (GRCm39) |
missense |
probably benign |
0.07 |
R6683:Acat2
|
UTSW |
17 |
13,162,814 (GRCm39) |
missense |
probably benign |
0.00 |
R7313:Acat2
|
UTSW |
17 |
13,178,893 (GRCm39) |
missense |
probably benign |
0.18 |
R7566:Acat2
|
UTSW |
17 |
13,166,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R8294:Acat2
|
UTSW |
17 |
13,175,243 (GRCm39) |
missense |
probably benign |
0.03 |
R9098:Acat2
|
UTSW |
17 |
13,178,979 (GRCm39) |
start gained |
probably benign |
|
R9341:Acat2
|
UTSW |
17 |
13,167,538 (GRCm39) |
missense |
probably damaging |
0.99 |
R9343:Acat2
|
UTSW |
17 |
13,167,538 (GRCm39) |
missense |
probably damaging |
0.99 |
|