Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3930402G23Rik |
T |
A |
8: 10,976,129 (GRCm39) |
|
noncoding transcript |
Het |
Acsl6 |
A |
G |
11: 54,219,229 (GRCm39) |
D278G |
probably damaging |
Het |
Adamdec1 |
C |
T |
14: 68,810,568 (GRCm39) |
R196Q |
probably benign |
Het |
Akap13 |
T |
A |
7: 75,392,508 (GRCm39) |
F2450L |
probably damaging |
Het |
Alg11 |
C |
A |
8: 22,558,095 (GRCm39) |
A469E |
probably benign |
Het |
Arhgef18 |
A |
G |
8: 3,487,097 (GRCm39) |
E272G |
probably damaging |
Het |
Bpifb6 |
A |
G |
2: 153,748,688 (GRCm39) |
E228G |
possibly damaging |
Het |
Brca2 |
T |
G |
5: 150,459,518 (GRCm39) |
D264E |
probably damaging |
Het |
Cdca4 |
T |
C |
12: 112,785,278 (GRCm39) |
N150S |
probably benign |
Het |
Cep162 |
T |
C |
9: 87,107,861 (GRCm39) |
S510G |
probably damaging |
Het |
Cldn12 |
T |
C |
5: 5,558,398 (GRCm39) |
T10A |
probably damaging |
Het |
Clip2 |
C |
T |
5: 134,531,807 (GRCm39) |
G631D |
possibly damaging |
Het |
Col19a1 |
T |
A |
1: 24,361,116 (GRCm39) |
T625S |
probably damaging |
Het |
Col6a5 |
C |
T |
9: 105,781,720 (GRCm39) |
G1635D |
unknown |
Het |
Dcp1b |
A |
G |
6: 119,183,437 (GRCm39) |
T175A |
probably benign |
Het |
Eln |
C |
T |
5: 134,754,635 (GRCm39) |
|
probably benign |
Het |
Galnt2 |
A |
G |
8: 125,022,116 (GRCm39) |
D14G |
probably benign |
Het |
Gm9894 |
T |
A |
13: 67,913,199 (GRCm39) |
|
noncoding transcript |
Het |
Herc2 |
T |
C |
7: 55,877,640 (GRCm39) |
L4569P |
probably damaging |
Het |
Iqcm |
T |
C |
8: 76,356,394 (GRCm39) |
S176P |
probably damaging |
Het |
Klhl42 |
G |
A |
6: 146,993,169 (GRCm39) |
G47D |
probably benign |
Het |
Lmo2 |
T |
C |
2: 103,811,407 (GRCm39) |
Y147H |
probably damaging |
Het |
Lzts2 |
A |
T |
19: 45,012,032 (GRCm39) |
K154* |
probably null |
Het |
Map4k3 |
C |
T |
17: 80,911,411 (GRCm39) |
|
probably null |
Het |
Mlc1 |
A |
G |
15: 88,847,693 (GRCm39) |
F285S |
probably benign |
Het |
Myo5a |
T |
A |
9: 75,074,458 (GRCm39) |
M789K |
probably benign |
Het |
Nbeal1 |
T |
A |
1: 60,306,933 (GRCm39) |
S319T |
probably damaging |
Het |
Nsun4 |
A |
T |
4: 115,908,453 (GRCm39) |
Y702* |
probably null |
Het |
Or8b52 |
A |
T |
9: 38,577,050 (GRCm39) |
V30E |
probably benign |
Het |
Or8g34 |
G |
A |
9: 39,373,328 (GRCm39) |
M200I |
probably benign |
Het |
Osbpl5 |
T |
A |
7: 143,248,643 (GRCm39) |
T640S |
probably benign |
Het |
Plaat1 |
C |
T |
16: 29,046,976 (GRCm39) |
T165M |
possibly damaging |
Het |
Rangrf |
A |
T |
11: 68,866,010 (GRCm39) |
|
probably benign |
Het |
Rnpc3 |
T |
C |
3: 113,404,786 (GRCm39) |
|
probably benign |
Het |
Ros1 |
C |
T |
10: 51,954,038 (GRCm39) |
G1867D |
probably damaging |
Het |
Slc11a1 |
C |
A |
1: 74,424,694 (GRCm39) |
|
probably benign |
Het |
Slc15a4 |
A |
G |
5: 127,681,600 (GRCm39) |
|
probably null |
Het |
Speer3 |
C |
G |
5: 13,846,394 (GRCm39) |
A238G |
possibly damaging |
Het |
Syt6 |
A |
G |
3: 103,492,961 (GRCm39) |
H156R |
probably benign |
Het |
Tln2 |
C |
T |
9: 67,251,347 (GRCm39) |
|
probably null |
Het |
Trim58 |
T |
C |
11: 58,542,191 (GRCm39) |
W384R |
probably benign |
Het |
Wwc2 |
A |
G |
8: 48,321,702 (GRCm39) |
Y471H |
unknown |
Het |
|
Other mutations in Angel1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01678:Angel1
|
APN |
12 |
86,763,800 (GRCm39) |
missense |
probably benign |
|
IGL02712:Angel1
|
APN |
12 |
86,769,613 (GRCm39) |
splice site |
probably benign |
|
IGL02738:Angel1
|
APN |
12 |
86,752,060 (GRCm39) |
missense |
probably benign |
0.10 |
R0521:Angel1
|
UTSW |
12 |
86,769,681 (GRCm39) |
missense |
probably benign |
0.01 |
R0626:Angel1
|
UTSW |
12 |
86,764,487 (GRCm39) |
critical splice donor site |
probably null |
|
R1929:Angel1
|
UTSW |
12 |
86,749,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R4291:Angel1
|
UTSW |
12 |
86,767,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R4292:Angel1
|
UTSW |
12 |
86,767,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R4295:Angel1
|
UTSW |
12 |
86,767,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R4726:Angel1
|
UTSW |
12 |
86,768,649 (GRCm39) |
missense |
probably damaging |
0.99 |
R7097:Angel1
|
UTSW |
12 |
86,773,158 (GRCm39) |
missense |
probably damaging |
0.98 |
R7284:Angel1
|
UTSW |
12 |
86,767,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R7616:Angel1
|
UTSW |
12 |
86,764,510 (GRCm39) |
missense |
probably benign |
0.00 |
R7984:Angel1
|
UTSW |
12 |
86,767,068 (GRCm39) |
missense |
probably benign |
0.33 |
R9010:Angel1
|
UTSW |
12 |
86,770,153 (GRCm39) |
missense |
possibly damaging |
0.78 |
|