Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
C |
12: 71,197,018 (GRCm39) |
V197A |
possibly damaging |
Het |
9230109A22Rik |
T |
C |
15: 25,139,176 (GRCm39) |
|
noncoding transcript |
Het |
Actr3b |
T |
C |
5: 26,054,156 (GRCm39) |
|
probably null |
Het |
Aldh5a1 |
T |
C |
13: 25,111,555 (GRCm39) |
D124G |
probably benign |
Het |
Arhgap35 |
G |
A |
7: 16,295,874 (GRCm39) |
R1064W |
possibly damaging |
Het |
Arhgef9 |
T |
A |
X: 94,125,142 (GRCm39) |
I225F |
probably damaging |
Het |
Arl16 |
T |
C |
11: 120,357,587 (GRCm39) |
T43A |
probably damaging |
Het |
Camsap3 |
T |
C |
8: 3,653,485 (GRCm39) |
W409R |
probably damaging |
Het |
Cfap43 |
T |
A |
19: 47,885,655 (GRCm39) |
H320L |
probably damaging |
Het |
Chac2 |
T |
A |
11: 30,927,496 (GRCm39) |
N141I |
probably damaging |
Het |
Chtf18 |
C |
A |
17: 25,944,913 (GRCm39) |
G211C |
probably damaging |
Het |
Cplane1 |
A |
G |
15: 8,299,129 (GRCm39) |
K3106E |
unknown |
Het |
Cwf19l1 |
T |
A |
19: 44,115,826 (GRCm39) |
Y201F |
probably benign |
Het |
Dcun1d1 |
A |
T |
3: 35,973,153 (GRCm39) |
L114* |
probably null |
Het |
Fdps |
A |
T |
3: 89,002,350 (GRCm39) |
H249Q |
probably benign |
Het |
Fhip1a |
T |
A |
3: 85,573,136 (GRCm39) |
T938S |
probably damaging |
Het |
Gabrg1 |
T |
A |
5: 70,931,756 (GRCm39) |
Y329F |
probably damaging |
Het |
Kctd8 |
T |
A |
5: 69,497,684 (GRCm39) |
I321F |
probably damaging |
Het |
Kdm5b |
G |
T |
1: 134,525,408 (GRCm39) |
R299L |
possibly damaging |
Het |
Kif23 |
T |
C |
9: 61,833,720 (GRCm39) |
T494A |
possibly damaging |
Het |
Kmt2e |
A |
G |
5: 23,678,545 (GRCm39) |
H208R |
probably damaging |
Het |
Lipo5 |
A |
T |
19: 33,441,995 (GRCm39) |
|
probably null |
Het |
Lrrc28 |
G |
T |
7: 67,290,859 (GRCm39) |
T54K |
probably damaging |
Het |
Luc7l2 |
G |
A |
6: 38,575,754 (GRCm39) |
|
probably null |
Het |
Man2a2 |
A |
G |
7: 80,008,681 (GRCm39) |
F899L |
probably benign |
Het |
Myo9b |
T |
C |
8: 71,786,002 (GRCm39) |
I633T |
probably damaging |
Het |
Nynrin |
A |
T |
14: 56,107,835 (GRCm39) |
I981F |
possibly damaging |
Het |
Or5an1c |
A |
T |
19: 12,218,612 (GRCm39) |
S138T |
probably damaging |
Het |
Or8g28 |
A |
G |
9: 39,169,695 (GRCm39) |
I91T |
possibly damaging |
Het |
Pank1 |
A |
G |
19: 34,855,084 (GRCm39) |
|
probably null |
Het |
Phc2 |
C |
T |
4: 128,637,336 (GRCm39) |
A47V |
probably damaging |
Het |
Plekhs1 |
A |
G |
19: 56,466,954 (GRCm39) |
R262G |
possibly damaging |
Het |
Pnp2 |
C |
A |
14: 51,201,914 (GRCm39) |
P300Q |
possibly damaging |
Het |
Polq |
T |
A |
16: 36,849,780 (GRCm39) |
S345T |
possibly damaging |
Het |
Prag1 |
A |
G |
8: 36,570,958 (GRCm39) |
T514A |
probably benign |
Het |
Psmd5 |
T |
C |
2: 34,760,758 (GRCm39) |
|
probably null |
Het |
Rfx6 |
T |
G |
10: 51,599,221 (GRCm39) |
|
probably null |
Het |
Rhbdd2 |
G |
A |
5: 135,664,903 (GRCm39) |
C78Y |
probably damaging |
Het |
Rnf157 |
G |
T |
11: 116,245,477 (GRCm39) |
P313T |
probably damaging |
Het |
Ryr2 |
A |
G |
13: 11,602,202 (GRCm39) |
L4560P |
probably damaging |
Het |
Scai |
A |
T |
2: 38,996,990 (GRCm39) |
M268K |
possibly damaging |
Het |
Scd3 |
A |
T |
19: 44,230,245 (GRCm39) |
T343S |
probably benign |
Het |
Scimp |
A |
T |
11: 70,682,423 (GRCm39) |
S98T |
probably benign |
Het |
Sfrp2 |
A |
G |
3: 83,680,461 (GRCm39) |
N207S |
probably benign |
Het |
Shf |
G |
A |
2: 122,199,163 (GRCm39) |
P51S |
probably damaging |
Het |
Sis |
T |
C |
3: 72,828,475 (GRCm39) |
Y1200C |
probably damaging |
Het |
Sp1 |
T |
A |
15: 102,317,511 (GRCm39) |
S343R |
possibly damaging |
Het |
Spata31d1a |
A |
T |
13: 59,849,069 (GRCm39) |
C1020S |
possibly damaging |
Het |
Spink5 |
A |
G |
18: 44,122,486 (GRCm39) |
N317S |
possibly damaging |
Het |
Sptbn2 |
A |
G |
19: 4,776,624 (GRCm39) |
D224G |
probably damaging |
Het |
St8sia3 |
T |
C |
18: 64,402,703 (GRCm39) |
I114T |
probably damaging |
Het |
Zscan5b |
C |
A |
7: 6,242,162 (GRCm39) |
H460Q |
probably damaging |
Het |
|
Other mutations in Acbd3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03215:Acbd3
|
APN |
1 |
180,572,670 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0321:Acbd3
|
UTSW |
1 |
180,579,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R0365:Acbd3
|
UTSW |
1 |
180,566,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R0524:Acbd3
|
UTSW |
1 |
180,574,624 (GRCm39) |
small deletion |
probably benign |
|
R0733:Acbd3
|
UTSW |
1 |
180,579,783 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0884:Acbd3
|
UTSW |
1 |
180,574,624 (GRCm39) |
small deletion |
probably benign |
|
R1074:Acbd3
|
UTSW |
1 |
180,566,113 (GRCm39) |
nonsense |
probably null |
|
R1327:Acbd3
|
UTSW |
1 |
180,560,748 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1352:Acbd3
|
UTSW |
1 |
180,566,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R4697:Acbd3
|
UTSW |
1 |
180,549,509 (GRCm39) |
unclassified |
probably benign |
|
R5187:Acbd3
|
UTSW |
1 |
180,564,297 (GRCm39) |
nonsense |
probably null |
|
R5217:Acbd3
|
UTSW |
1 |
180,553,938 (GRCm39) |
missense |
probably benign |
0.18 |
R5368:Acbd3
|
UTSW |
1 |
180,549,660 (GRCm39) |
unclassified |
probably benign |
|
R6018:Acbd3
|
UTSW |
1 |
180,579,903 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7072:Acbd3
|
UTSW |
1 |
180,553,934 (GRCm39) |
missense |
probably benign |
|
R7366:Acbd3
|
UTSW |
1 |
180,562,064 (GRCm39) |
missense |
probably benign |
0.41 |
R7952:Acbd3
|
UTSW |
1 |
180,579,903 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8260:Acbd3
|
UTSW |
1 |
180,566,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R8267:Acbd3
|
UTSW |
1 |
180,574,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R8327:Acbd3
|
UTSW |
1 |
180,566,158 (GRCm39) |
missense |
probably damaging |
0.98 |
R8356:Acbd3
|
UTSW |
1 |
180,553,881 (GRCm39) |
missense |
probably benign |
|
R8848:Acbd3
|
UTSW |
1 |
180,562,084 (GRCm39) |
critical splice donor site |
probably null |
|
R9483:Acbd3
|
UTSW |
1 |
180,572,721 (GRCm39) |
missense |
probably benign |
0.41 |
R9681:Acbd3
|
UTSW |
1 |
180,566,082 (GRCm39) |
nonsense |
probably null |
|
X0027:Acbd3
|
UTSW |
1 |
180,574,595 (GRCm39) |
missense |
possibly damaging |
0.80 |
|