Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
C |
A |
5: 77,036,501 (GRCm39) |
E347* |
probably null |
Het |
Adam12 |
T |
C |
7: 133,774,594 (GRCm39) |
D5G |
probably damaging |
Het |
Adam26b |
A |
C |
8: 43,974,234 (GRCm39) |
V256G |
probably benign |
Het |
Ago1 |
A |
G |
4: 126,354,837 (GRCm39) |
I125T |
probably benign |
Het |
Bckdk |
C |
A |
7: 127,504,590 (GRCm39) |
R105S |
probably damaging |
Het |
Bub1b |
T |
A |
2: 118,445,936 (GRCm39) |
N319K |
possibly damaging |
Het |
Clcn6 |
G |
T |
4: 148,108,644 (GRCm39) |
C128* |
probably null |
Het |
Col6a4 |
C |
A |
9: 105,897,864 (GRCm39) |
|
probably null |
Het |
Cyp4v3 |
G |
A |
8: 45,768,745 (GRCm39) |
R272* |
probably null |
Het |
Dlg5 |
G |
A |
14: 24,215,328 (GRCm39) |
A665V |
probably damaging |
Het |
Foxd1 |
G |
C |
13: 98,492,424 (GRCm39) |
A433P |
unknown |
Het |
Hsd17b3 |
A |
T |
13: 64,210,993 (GRCm39) |
|
probably null |
Het |
Kcnc4 |
A |
G |
3: 107,355,506 (GRCm39) |
V314A |
probably benign |
Het |
Lrba |
T |
G |
3: 86,283,260 (GRCm39) |
L1858R |
probably damaging |
Het |
Marcks |
G |
A |
10: 37,016,866 (GRCm39) |
|
probably benign |
Het |
Mroh2b |
G |
A |
15: 4,981,728 (GRCm39) |
W1513* |
probably null |
Het |
Nefh |
A |
G |
11: 4,889,937 (GRCm39) |
V894A |
probably benign |
Het |
Pdzph1 |
A |
T |
17: 59,280,331 (GRCm39) |
Y650* |
probably null |
Het |
Plce1 |
A |
C |
19: 38,766,343 (GRCm39) |
I2109L |
probably benign |
Het |
Primpol |
A |
T |
8: 47,052,848 (GRCm39) |
D154E |
probably benign |
Het |
Relch |
C |
T |
1: 105,681,302 (GRCm39) |
T1178I |
probably damaging |
Het |
Rtca |
A |
T |
3: 116,286,650 (GRCm39) |
F327L |
probably benign |
Het |
Scn2a |
T |
G |
2: 65,544,115 (GRCm39) |
V832G |
probably damaging |
Het |
Secisbp2l |
C |
T |
2: 125,582,657 (GRCm39) |
G933D |
possibly damaging |
Het |
Skil |
A |
G |
3: 31,170,983 (GRCm39) |
N354S |
probably benign |
Het |
Slk |
T |
G |
19: 47,608,248 (GRCm39) |
D400E |
possibly damaging |
Het |
Spata31 |
G |
T |
13: 65,069,557 (GRCm39) |
L568F |
probably benign |
Het |
Spon1 |
T |
C |
7: 113,365,621 (GRCm39) |
L19P |
probably damaging |
Het |
Spon1 |
T |
A |
7: 113,616,024 (GRCm39) |
V297E |
possibly damaging |
Het |
Tas2r136 |
A |
T |
6: 132,754,200 (GRCm39) |
F309Y |
probably damaging |
Het |
Tcp11l1 |
A |
G |
2: 104,528,887 (GRCm39) |
I137T |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,584,350 (GRCm39) |
H22253Y |
probably damaging |
Het |
Upf1 |
G |
T |
8: 70,786,000 (GRCm39) |
N975K |
possibly damaging |
Het |
Usp1 |
C |
T |
4: 98,822,357 (GRCm39) |
|
probably null |
Het |
Zfhx4 |
G |
A |
3: 5,308,225 (GRCm39) |
E484K |
possibly damaging |
Het |
Zswim4 |
G |
A |
8: 84,938,676 (GRCm39) |
P1069S |
possibly damaging |
Het |
|
Other mutations in Pramel18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02430:Pramel18
|
APN |
4 |
101,767,477 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02683:Pramel18
|
APN |
4 |
101,767,551 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03403:Pramel18
|
APN |
4 |
101,767,125 (GRCm39) |
missense |
probably benign |
0.40 |
R0833:Pramel18
|
UTSW |
4 |
101,767,294 (GRCm39) |
missense |
probably damaging |
0.97 |
R1054:Pramel18
|
UTSW |
4 |
101,766,361 (GRCm39) |
missense |
probably benign |
0.00 |
R1953:Pramel18
|
UTSW |
4 |
101,767,312 (GRCm39) |
missense |
probably benign |
|
R2216:Pramel18
|
UTSW |
4 |
101,767,257 (GRCm39) |
missense |
probably damaging |
0.99 |
R3746:Pramel18
|
UTSW |
4 |
101,767,073 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3747:Pramel18
|
UTSW |
4 |
101,767,073 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4931:Pramel18
|
UTSW |
4 |
101,766,367 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5102:Pramel18
|
UTSW |
4 |
101,766,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R5586:Pramel18
|
UTSW |
4 |
101,767,317 (GRCm39) |
missense |
probably benign |
0.00 |
R5822:Pramel18
|
UTSW |
4 |
101,767,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R6395:Pramel18
|
UTSW |
4 |
101,767,189 (GRCm39) |
missense |
probably benign |
|
R6904:Pramel18
|
UTSW |
4 |
101,767,291 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7544:Pramel18
|
UTSW |
4 |
101,768,599 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7768:Pramel18
|
UTSW |
4 |
101,769,010 (GRCm39) |
missense |
probably benign |
|
R8342:Pramel18
|
UTSW |
4 |
101,767,581 (GRCm39) |
missense |
probably benign |
0.01 |
R8917:Pramel18
|
UTSW |
4 |
101,768,935 (GRCm39) |
missense |
probably benign |
0.09 |
Z1088:Pramel18
|
UTSW |
4 |
101,766,315 (GRCm39) |
splice site |
probably null |
|
Z1088:Pramel18
|
UTSW |
4 |
101,767,383 (GRCm39) |
missense |
probably benign |
0.00 |
|