Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acox3 |
A |
G |
5: 35,588,625 (GRCm38) |
I51V |
probably benign |
Het |
Agbl2 |
A |
G |
2: 90,803,197 (GRCm38) |
K559R |
probably benign |
Het |
Arhgap30 |
A |
G |
1: 171,408,050 (GRCm38) |
D664G |
probably benign |
Het |
BC034090 |
A |
G |
1: 155,213,650 (GRCm38) |
V798A |
probably damaging |
Het |
Bdp1 |
A |
T |
13: 100,030,794 (GRCm38) |
C2237* |
probably null |
Het |
C3 |
C |
T |
17: 57,223,938 (GRCm38) |
V388M |
probably damaging |
Het |
Ccdc170 |
G |
A |
10: 4,514,200 (GRCm38) |
E60K |
probably damaging |
Het |
Cdh8 |
G |
A |
8: 99,279,550 (GRCm38) |
T135M |
probably damaging |
Het |
Cep131 |
G |
T |
11: 120,070,609 (GRCm38) |
A572E |
probably damaging |
Het |
Clec16a |
A |
G |
16: 10,741,791 (GRCm38) |
Y976C |
probably benign |
Het |
Dmpk |
C |
G |
7: 19,088,019 (GRCm38) |
L301V |
probably benign |
Het |
Eno3 |
A |
G |
11: 70,662,214 (GRCm38) |
I393V |
probably benign |
Het |
Fbxo47 |
A |
G |
11: 97,857,694 (GRCm38) |
V305A |
probably benign |
Het |
Fry |
G |
A |
5: 150,429,854 (GRCm38) |
V1779M |
probably benign |
Het |
Gm15293 |
A |
T |
8: 21,201,680 (GRCm38) |
D26V |
probably damaging |
Het |
Gtse1 |
T |
C |
15: 85,864,264 (GRCm38) |
|
probably null |
Het |
Gucy2e |
A |
T |
11: 69,235,570 (GRCm38) |
L328Q |
probably damaging |
Het |
Ifi207 |
T |
C |
1: 173,730,498 (GRCm38) |
T225A |
unknown |
Het |
Igkv4-80 |
A |
C |
6: 69,016,665 (GRCm38) |
S81A |
probably benign |
Het |
Lamc3 |
A |
T |
2: 31,887,344 (GRCm38) |
M1L |
probably benign |
Het |
Lman1l |
G |
A |
9: 57,615,619 (GRCm38) |
R153* |
probably null |
Het |
Myo16 |
A |
G |
8: 10,569,745 (GRCm38) |
D1432G |
probably benign |
Het |
Nwd2 |
A |
T |
5: 63,806,037 (GRCm38) |
N988I |
probably damaging |
Het |
Otx1 |
C |
A |
11: 21,997,037 (GRCm38) |
A91S |
probably damaging |
Het |
Parp14 |
T |
C |
16: 35,857,279 (GRCm38) |
E773G |
probably benign |
Het |
Psen1 |
T |
A |
12: 83,714,862 (GRCm38) |
M146K |
probably damaging |
Het |
Ptx4 |
G |
A |
17: 25,123,178 (GRCm38) |
R209Q |
probably benign |
Het |
Slc13a2 |
T |
C |
11: 78,400,808 (GRCm38) |
T340A |
probably damaging |
Het |
St8sia1 |
T |
C |
6: 142,963,708 (GRCm38) |
K21E |
probably damaging |
Het |
Stxbp1 |
T |
C |
2: 32,794,674 (GRCm38) |
D581G |
probably benign |
Het |
Sumo2 |
G |
A |
11: 115,534,660 (GRCm38) |
|
probably benign |
Het |
Supt5 |
G |
A |
7: 28,316,083 (GRCm38) |
P910S |
probably benign |
Het |
Tbc1d30 |
T |
C |
10: 121,306,838 (GRCm38) |
Q158R |
possibly damaging |
Het |
Tenm2 |
T |
A |
11: 36,024,806 (GRCm38) |
H1968L |
probably damaging |
Het |
Trmt1 |
T |
C |
8: 84,695,232 (GRCm38) |
Y220H |
probably damaging |
Het |
Trp73 |
C |
T |
4: 154,104,838 (GRCm38) |
E60K |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,787,069 (GRCm38) |
Y8026H |
probably damaging |
Het |
Zar1l |
A |
G |
5: 150,517,585 (GRCm38) |
|
probably null |
Het |
Zfp740 |
T |
C |
15: 102,209,205 (GRCm38) |
Y117H |
probably damaging |
Het |
Zp1 |
C |
A |
19: 10,920,554 (GRCm38) |
V8F |
possibly damaging |
Het |
|
Other mutations in Zfp941 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01393:Zfp941
|
APN |
7 |
140,811,928 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02399:Zfp941
|
APN |
7 |
140,812,699 (GRCm38) |
missense |
probably benign |
0.37 |
IGL03202:Zfp941
|
APN |
7 |
140,813,053 (GRCm38) |
missense |
probably benign |
0.02 |
R0025:Zfp941
|
UTSW |
7 |
140,813,272 (GRCm38) |
missense |
probably benign |
0.01 |
R0025:Zfp941
|
UTSW |
7 |
140,813,272 (GRCm38) |
missense |
probably benign |
0.01 |
R0226:Zfp941
|
UTSW |
7 |
140,813,275 (GRCm38) |
missense |
probably damaging |
1.00 |
R0945:Zfp941
|
UTSW |
7 |
140,811,664 (GRCm38) |
missense |
probably damaging |
0.99 |
R1455:Zfp941
|
UTSW |
7 |
140,812,774 (GRCm38) |
missense |
probably benign |
0.29 |
R1581:Zfp941
|
UTSW |
7 |
140,812,120 (GRCm38) |
missense |
probably benign |
0.03 |
R2474:Zfp941
|
UTSW |
7 |
140,811,471 (GRCm38) |
missense |
probably damaging |
1.00 |
R4052:Zfp941
|
UTSW |
7 |
140,812,427 (GRCm38) |
missense |
possibly damaging |
0.81 |
R4576:Zfp941
|
UTSW |
7 |
140,811,590 (GRCm38) |
nonsense |
probably null |
|
R4604:Zfp941
|
UTSW |
7 |
140,812,211 (GRCm38) |
missense |
probably damaging |
1.00 |
R5311:Zfp941
|
UTSW |
7 |
140,811,959 (GRCm38) |
nonsense |
probably null |
|
R5505:Zfp941
|
UTSW |
7 |
140,811,917 (GRCm38) |
missense |
probably benign |
0.03 |
R5549:Zfp941
|
UTSW |
7 |
140,808,108 (GRCm38) |
missense |
possibly damaging |
0.46 |
R5566:Zfp941
|
UTSW |
7 |
140,812,766 (GRCm38) |
missense |
probably benign |
0.01 |
R5723:Zfp941
|
UTSW |
7 |
140,812,850 (GRCm38) |
unclassified |
probably benign |
|
R5736:Zfp941
|
UTSW |
7 |
140,813,060 (GRCm38) |
missense |
probably benign |
0.01 |
R5861:Zfp941
|
UTSW |
7 |
140,812,139 (GRCm38) |
missense |
probably damaging |
1.00 |
R6041:Zfp941
|
UTSW |
7 |
140,812,245 (GRCm38) |
nonsense |
probably null |
|
R6058:Zfp941
|
UTSW |
7 |
140,812,097 (GRCm38) |
missense |
probably damaging |
1.00 |
R6226:Zfp941
|
UTSW |
7 |
140,812,485 (GRCm38) |
missense |
probably benign |
0.01 |
R6488:Zfp941
|
UTSW |
7 |
140,812,750 (GRCm38) |
missense |
probably benign |
0.37 |
R6824:Zfp941
|
UTSW |
7 |
140,812,699 (GRCm38) |
missense |
probably benign |
0.37 |
R7356:Zfp941
|
UTSW |
7 |
140,812,115 (GRCm38) |
missense |
possibly damaging |
0.66 |
R7554:Zfp941
|
UTSW |
7 |
140,812,057 (GRCm38) |
missense |
possibly damaging |
0.69 |
Z1177:Zfp941
|
UTSW |
7 |
140,812,186 (GRCm38) |
missense |
possibly damaging |
0.53 |
|