Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr8 |
A |
T |
14: 29,712,847 (GRCm39) |
R497W |
probably damaging |
Het |
Atp2a3 |
C |
A |
11: 72,866,165 (GRCm39) |
H262N |
probably benign |
Het |
Bmx |
T |
C |
X: 162,988,231 (GRCm39) |
E495G |
probably damaging |
Het |
Cbx5 |
T |
C |
15: 103,109,330 (GRCm39) |
|
probably null |
Het |
Cenpj |
C |
T |
14: 56,767,536 (GRCm39) |
V1203M |
probably damaging |
Het |
Ces1b |
T |
C |
8: 93,783,672 (GRCm39) |
H516R |
probably benign |
Het |
D430041D05Rik |
T |
C |
2: 104,078,611 (GRCm39) |
N1235S |
probably damaging |
Het |
Depdc1a |
A |
T |
3: 159,228,503 (GRCm39) |
K418N |
probably damaging |
Het |
Dysf |
G |
A |
6: 84,114,355 (GRCm39) |
V1215M |
probably damaging |
Het |
Flacc1 |
T |
C |
1: 58,709,613 (GRCm39) |
T181A |
probably benign |
Het |
Foxf2 |
A |
T |
13: 31,811,218 (GRCm39) |
N386Y |
probably damaging |
Het |
Frem1 |
A |
T |
4: 82,919,991 (GRCm39) |
V455E |
probably damaging |
Het |
Fzd7 |
C |
A |
1: 59,523,554 (GRCm39) |
P479Q |
probably damaging |
Het |
Hnmt |
G |
A |
2: 23,904,319 (GRCm39) |
S114F |
possibly damaging |
Het |
Irf3 |
A |
G |
7: 44,649,800 (GRCm39) |
N6S |
probably benign |
Het |
Krt26 |
C |
T |
11: 99,224,471 (GRCm39) |
R349Q |
probably benign |
Het |
Lrba |
A |
G |
3: 86,267,038 (GRCm39) |
D1576G |
probably benign |
Het |
Lsg1 |
A |
T |
16: 30,404,370 (GRCm39) |
|
probably null |
Het |
Mal2 |
T |
C |
15: 54,451,833 (GRCm39) |
F85L |
probably damaging |
Het |
Me2 |
A |
C |
18: 73,930,974 (GRCm39) |
S106R |
probably benign |
Het |
Med21 |
T |
C |
6: 146,550,731 (GRCm39) |
S81P |
probably benign |
Het |
Mos |
T |
C |
4: 3,870,961 (GRCm39) |
Y285C |
probably damaging |
Het |
Mtmr1 |
A |
G |
X: 70,436,939 (GRCm39) |
N256S |
probably damaging |
Het |
Or7e174 |
T |
A |
9: 20,012,505 (GRCm39) |
M150K |
probably benign |
Het |
R3hdm2 |
C |
T |
10: 127,295,353 (GRCm39) |
S240L |
probably damaging |
Het |
Semp2l2a |
T |
C |
8: 13,886,979 (GRCm39) |
T371A |
probably damaging |
Het |
Skint6 |
A |
T |
4: 112,985,088 (GRCm39) |
|
probably benign |
Het |
Ubr5 |
A |
G |
15: 37,992,326 (GRCm39) |
S1933P |
probably damaging |
Het |
Veph1 |
A |
T |
3: 66,066,869 (GRCm39) |
|
probably benign |
Het |
Xpo7 |
A |
G |
14: 70,922,905 (GRCm39) |
F557S |
probably damaging |
Het |
Zfp647 |
T |
C |
15: 76,801,915 (GRCm39) |
E30G |
probably damaging |
Het |
Zfp655 |
A |
T |
5: 145,179,816 (GRCm39) |
I75L |
probably benign |
Het |
Zfp981 |
C |
A |
4: 146,621,709 (GRCm39) |
Y211* |
probably null |
Het |
|
Other mutations in Prl3d2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00899:Prl3d2
|
APN |
13 |
27,306,332 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01362:Prl3d2
|
APN |
13 |
27,306,438 (GRCm39) |
nonsense |
probably null |
|
IGL02751:Prl3d2
|
APN |
13 |
27,310,014 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02992:Prl3d2
|
APN |
13 |
27,311,266 (GRCm39) |
missense |
probably benign |
0.00 |
R1116:Prl3d2
|
UTSW |
13 |
27,309,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R1500:Prl3d2
|
UTSW |
13 |
27,305,689 (GRCm39) |
unclassified |
probably benign |
|
R4713:Prl3d2
|
UTSW |
13 |
27,306,379 (GRCm39) |
missense |
probably benign |
|
R5193:Prl3d2
|
UTSW |
13 |
27,306,312 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6386:Prl3d2
|
UTSW |
13 |
27,311,286 (GRCm39) |
missense |
probably damaging |
0.97 |
R7830:Prl3d2
|
UTSW |
13 |
27,310,000 (GRCm39) |
missense |
probably benign |
0.00 |
R7999:Prl3d2
|
UTSW |
13 |
27,307,949 (GRCm39) |
missense |
probably benign |
0.00 |
R8446:Prl3d2
|
UTSW |
13 |
27,307,976 (GRCm39) |
missense |
probably benign |
0.25 |
R8837:Prl3d2
|
UTSW |
13 |
27,307,926 (GRCm39) |
missense |
probably benign |
0.01 |
|