Other mutations in this stock |
Total: 25 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abtb2 |
C |
A |
2: 103,397,577 (GRCm39) |
A169E |
probably benign |
Het |
Agmo |
C |
T |
12: 37,293,799 (GRCm39) |
T74I |
probably damaging |
Het |
Ano6 |
T |
C |
15: 95,865,602 (GRCm39) |
V862A |
probably damaging |
Het |
Bltp1 |
C |
T |
3: 37,096,061 (GRCm39) |
Q4614* |
probably null |
Het |
Cavin2 |
T |
A |
1: 51,340,565 (GRCm39) |
V414E |
probably damaging |
Het |
Clrn3 |
A |
C |
7: 135,115,854 (GRCm39) |
Y165* |
probably null |
Het |
Cp |
A |
T |
3: 20,029,121 (GRCm39) |
M533L |
probably benign |
Het |
Dhrs3 |
T |
A |
4: 144,646,628 (GRCm39) |
M226K |
probably damaging |
Het |
Fignl2 |
A |
G |
15: 100,951,004 (GRCm39) |
F426S |
unknown |
Het |
Fpr1 |
C |
T |
17: 18,097,420 (GRCm39) |
D190N |
probably benign |
Het |
Grik3 |
C |
A |
4: 125,587,763 (GRCm39) |
L628M |
probably damaging |
Het |
Grik3 |
T |
A |
4: 125,587,764 (GRCm39) |
L628Q |
probably damaging |
Het |
Grin2c |
T |
A |
11: 115,141,469 (GRCm39) |
D883V |
probably damaging |
Het |
Gtf3c6 |
T |
A |
10: 40,127,169 (GRCm39) |
E123V |
probably null |
Het |
H2-Eb1 |
A |
G |
17: 34,528,655 (GRCm39) |
E62G |
probably damaging |
Het |
Kif1a |
C |
T |
1: 92,964,575 (GRCm39) |
D1334N |
possibly damaging |
Het |
Lef1 |
A |
G |
3: 130,978,407 (GRCm39) |
D175G |
probably damaging |
Het |
Myom1 |
A |
G |
17: 71,352,658 (GRCm39) |
|
probably null |
Het |
Or6k2 |
A |
T |
1: 173,986,746 (GRCm39) |
M136L |
probably benign |
Het |
Pgr |
A |
T |
9: 8,922,630 (GRCm39) |
N600I |
probably damaging |
Het |
Rab36 |
G |
A |
10: 74,880,328 (GRCm39) |
V63I |
probably damaging |
Het |
Selp |
T |
C |
1: 163,951,344 (GRCm39) |
F26S |
probably benign |
Het |
Tchh |
A |
T |
3: 93,352,414 (GRCm39) |
D618V |
unknown |
Het |
Tenm4 |
A |
T |
7: 96,202,723 (GRCm39) |
M88L |
probably benign |
Het |
Zfat |
A |
T |
15: 67,956,402 (GRCm39) |
D1143E |
probably benign |
Het |
|
Other mutations in Adam3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00429:Adam3
|
APN |
8 |
25,184,294 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01792:Adam3
|
APN |
8 |
25,187,219 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01894:Adam3
|
APN |
8 |
25,177,954 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01941:Adam3
|
APN |
8 |
25,171,462 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02355:Adam3
|
APN |
8 |
25,187,207 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02362:Adam3
|
APN |
8 |
25,187,207 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02511:Adam3
|
APN |
8 |
25,185,192 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03070:Adam3
|
APN |
8 |
25,193,800 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03106:Adam3
|
APN |
8 |
25,205,135 (GRCm39) |
splice site |
probably benign |
|
IGL03238:Adam3
|
APN |
8 |
25,177,981 (GRCm39) |
splice site |
probably null |
|
I2288:Adam3
|
UTSW |
8 |
25,174,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R0511:Adam3
|
UTSW |
8 |
25,185,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R1103:Adam3
|
UTSW |
8 |
25,204,287 (GRCm39) |
splice site |
probably benign |
|
R1104:Adam3
|
UTSW |
8 |
25,171,545 (GRCm39) |
missense |
probably benign |
0.10 |
R1430:Adam3
|
UTSW |
8 |
25,204,287 (GRCm39) |
splice site |
probably benign |
|
R1599:Adam3
|
UTSW |
8 |
25,215,377 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1663:Adam3
|
UTSW |
8 |
25,177,949 (GRCm39) |
missense |
probably benign |
0.03 |
R2023:Adam3
|
UTSW |
8 |
25,179,479 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2278:Adam3
|
UTSW |
8 |
25,201,400 (GRCm39) |
missense |
probably damaging |
0.99 |
R3033:Adam3
|
UTSW |
8 |
25,184,227 (GRCm39) |
missense |
probably benign |
0.00 |
R3441:Adam3
|
UTSW |
8 |
25,170,759 (GRCm39) |
utr 3 prime |
probably benign |
|
R3688:Adam3
|
UTSW |
8 |
25,193,864 (GRCm39) |
missense |
probably benign |
0.02 |
R4478:Adam3
|
UTSW |
8 |
25,185,171 (GRCm39) |
missense |
probably benign |
0.04 |
R4654:Adam3
|
UTSW |
8 |
25,193,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R4811:Adam3
|
UTSW |
8 |
25,201,740 (GRCm39) |
missense |
probably benign |
0.10 |
R4910:Adam3
|
UTSW |
8 |
25,184,321 (GRCm39) |
missense |
probably benign |
0.03 |
R4921:Adam3
|
UTSW |
8 |
25,174,630 (GRCm39) |
missense |
probably benign |
0.01 |
R4941:Adam3
|
UTSW |
8 |
25,167,332 (GRCm39) |
unclassified |
probably benign |
|
R5239:Adam3
|
UTSW |
8 |
25,184,207 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5771:Adam3
|
UTSW |
8 |
25,197,427 (GRCm39) |
missense |
probably benign |
0.00 |
R5897:Adam3
|
UTSW |
8 |
25,187,244 (GRCm39) |
missense |
probably benign |
0.00 |
R5916:Adam3
|
UTSW |
8 |
25,174,555 (GRCm39) |
critical splice donor site |
probably null |
|
R5979:Adam3
|
UTSW |
8 |
25,167,383 (GRCm39) |
missense |
probably benign |
0.03 |
R6168:Adam3
|
UTSW |
8 |
25,171,630 (GRCm39) |
splice site |
probably null |
|
R6189:Adam3
|
UTSW |
8 |
25,201,352 (GRCm39) |
missense |
probably benign |
0.01 |
R6801:Adam3
|
UTSW |
8 |
25,174,680 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6997:Adam3
|
UTSW |
8 |
25,171,539 (GRCm39) |
missense |
probably benign |
0.10 |
R7065:Adam3
|
UTSW |
8 |
25,201,691 (GRCm39) |
critical splice donor site |
probably null |
|
R7074:Adam3
|
UTSW |
8 |
25,184,363 (GRCm39) |
missense |
probably benign |
0.01 |
R7151:Adam3
|
UTSW |
8 |
25,185,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R7208:Adam3
|
UTSW |
8 |
25,201,417 (GRCm39) |
missense |
probably damaging |
0.98 |
R7341:Adam3
|
UTSW |
8 |
25,177,996 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7528:Adam3
|
UTSW |
8 |
25,167,279 (GRCm39) |
missense |
unknown |
|
R7797:Adam3
|
UTSW |
8 |
25,184,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R7891:Adam3
|
UTSW |
8 |
25,197,513 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8064:Adam3
|
UTSW |
8 |
25,171,566 (GRCm39) |
missense |
probably benign |
0.10 |
R8157:Adam3
|
UTSW |
8 |
25,197,453 (GRCm39) |
missense |
probably benign |
0.27 |
R8229:Adam3
|
UTSW |
8 |
25,201,754 (GRCm39) |
missense |
probably damaging |
0.98 |
R9007:Adam3
|
UTSW |
8 |
25,205,127 (GRCm39) |
missense |
probably benign |
0.02 |
R9018:Adam3
|
UTSW |
8 |
25,184,292 (GRCm39) |
nonsense |
probably null |
|
R9098:Adam3
|
UTSW |
8 |
25,179,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R9110:Adam3
|
UTSW |
8 |
25,193,821 (GRCm39) |
missense |
probably benign |
0.00 |
R9125:Adam3
|
UTSW |
8 |
25,213,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R9211:Adam3
|
UTSW |
8 |
25,177,910 (GRCm39) |
missense |
probably benign |
0.08 |
R9267:Adam3
|
UTSW |
8 |
25,171,605 (GRCm39) |
missense |
probably benign |
|
R9331:Adam3
|
UTSW |
8 |
25,177,951 (GRCm39) |
missense |
probably benign |
0.01 |
R9432:Adam3
|
UTSW |
8 |
25,193,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R9716:Adam3
|
UTSW |
8 |
25,204,274 (GRCm39) |
missense |
possibly damaging |
0.65 |
X0063:Adam3
|
UTSW |
8 |
25,201,722 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1088:Adam3
|
UTSW |
8 |
25,171,447 (GRCm39) |
utr 3 prime |
probably benign |
|
|