Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc12 |
G |
T |
8: 87,244,077 (GRCm39) |
F1025L |
probably damaging |
Het |
Acss2 |
C |
T |
2: 155,399,130 (GRCm39) |
T477I |
probably damaging |
Het |
Aplp2 |
G |
A |
9: 31,069,026 (GRCm39) |
P601L |
probably benign |
Het |
Arl2bp |
T |
C |
8: 95,394,281 (GRCm39) |
I32T |
probably damaging |
Het |
Avpi1 |
C |
A |
19: 42,113,180 (GRCm39) |
|
probably benign |
Het |
C030005K15Rik |
T |
C |
10: 97,561,404 (GRCm39) |
Y109C |
unknown |
Het |
Ccdc150 |
T |
A |
1: 54,317,970 (GRCm39) |
M303K |
probably benign |
Het |
Chrna5 |
T |
C |
9: 54,905,370 (GRCm39) |
W61R |
probably damaging |
Het |
Copa |
T |
C |
1: 171,935,942 (GRCm39) |
V428A |
probably damaging |
Het |
Crybb3 |
A |
G |
5: 113,227,735 (GRCm39) |
Y29H |
probably damaging |
Het |
Dcun1d4 |
A |
G |
5: 73,691,980 (GRCm39) |
D89G |
probably damaging |
Het |
Disp2 |
T |
C |
2: 118,622,361 (GRCm39) |
I1031T |
probably benign |
Het |
Elf1 |
A |
C |
14: 79,806,723 (GRCm39) |
K161Q |
probably damaging |
Het |
Fndc1 |
A |
T |
17: 7,988,584 (GRCm39) |
Y1159* |
probably null |
Het |
Hspa12a |
T |
C |
19: 58,789,289 (GRCm39) |
N449S |
probably benign |
Het |
Hyal4 |
A |
G |
6: 24,756,223 (GRCm39) |
E147G |
probably damaging |
Het |
Hydin |
T |
C |
8: 111,336,679 (GRCm39) |
I5152T |
probably benign |
Het |
Ighv9-1 |
C |
T |
12: 114,057,844 (GRCm39) |
A19T |
probably benign |
Het |
Kcnt1 |
T |
G |
2: 25,806,060 (GRCm39) |
S1216R |
possibly damaging |
Het |
Kdm5d |
T |
A |
Y: 916,910 (GRCm39) |
V435E |
probably damaging |
Het |
Klhl30 |
G |
A |
1: 91,288,879 (GRCm39) |
R546H |
probably benign |
Het |
Lrp1b |
C |
T |
2: 40,592,860 (GRCm39) |
G3753D |
probably benign |
Het |
Ltbp3 |
G |
A |
19: 5,804,050 (GRCm39) |
R854Q |
probably benign |
Het |
Macf1 |
A |
G |
4: 123,275,105 (GRCm39) |
L6303P |
probably damaging |
Het |
Mblac2 |
T |
C |
13: 81,898,208 (GRCm39) |
S195P |
possibly damaging |
Het |
Mindy3 |
A |
C |
2: 12,405,894 (GRCm39) |
|
probably null |
Het |
Neurod1 |
C |
T |
2: 79,284,370 (GRCm39) |
D338N |
probably benign |
Het |
Polr1e |
A |
T |
4: 45,018,685 (GRCm39) |
E5V |
probably benign |
Het |
Polr2b |
G |
A |
5: 77,496,252 (GRCm39) |
R1141H |
possibly damaging |
Het |
Ppp2r2a |
T |
C |
14: 67,266,425 (GRCm39) |
S79G |
probably damaging |
Het |
Psmd2 |
G |
A |
16: 20,481,955 (GRCm39) |
G896D |
probably damaging |
Het |
Rap1gds1 |
T |
C |
3: 138,756,353 (GRCm39) |
|
probably benign |
Het |
Rsph10b |
A |
G |
5: 143,922,486 (GRCm39) |
|
probably null |
Het |
Slc26a10 |
A |
G |
10: 127,013,871 (GRCm39) |
V297A |
possibly damaging |
Het |
Slc26a5 |
T |
C |
5: 22,052,189 (GRCm39) |
K47E |
probably damaging |
Het |
Slurp1 |
T |
C |
15: 74,599,336 (GRCm39) |
E58G |
probably damaging |
Het |
Spo11 |
T |
A |
2: 172,828,625 (GRCm39) |
|
probably benign |
Het |
Tm9sf4 |
T |
C |
2: 153,040,264 (GRCm39) |
|
probably benign |
Het |
Trak1 |
T |
C |
9: 121,280,736 (GRCm39) |
I272T |
probably damaging |
Het |
Tshz1 |
T |
C |
18: 84,032,954 (GRCm39) |
K485E |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,585,168 (GRCm39) |
I22042F |
probably damaging |
Het |
Unc79 |
T |
A |
12: 103,039,018 (GRCm39) |
S671T |
possibly damaging |
Het |
Usp43 |
G |
T |
11: 67,804,659 (GRCm39) |
A186D |
probably damaging |
Het |
Vmn2r107 |
G |
A |
17: 20,595,483 (GRCm39) |
V679I |
probably benign |
Het |
Vsig10l |
C |
T |
7: 43,114,798 (GRCm39) |
A333V |
probably damaging |
Het |
Vwa3a |
G |
A |
7: 120,367,455 (GRCm39) |
|
probably null |
Het |
Wdr49 |
C |
A |
3: 75,230,972 (GRCm39) |
L563F |
probably benign |
Het |
Wnk1 |
T |
C |
6: 119,928,029 (GRCm39) |
T1141A |
probably damaging |
Het |
Zfp236 |
T |
A |
18: 82,642,590 (GRCm39) |
E1052V |
probably damaging |
Het |
Zfp317 |
A |
T |
9: 19,558,008 (GRCm39) |
H163L |
possibly damaging |
Het |
|
Other mutations in Zfp975 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02008:Zfp975
|
APN |
7 |
42,312,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R0194:Zfp975
|
UTSW |
7 |
42,311,916 (GRCm39) |
missense |
probably benign |
0.02 |
R0662:Zfp975
|
UTSW |
7 |
42,311,950 (GRCm39) |
missense |
probably benign |
0.02 |
R1491:Zfp975
|
UTSW |
7 |
42,312,236 (GRCm39) |
missense |
probably benign |
0.19 |
R1573:Zfp975
|
UTSW |
7 |
42,311,507 (GRCm39) |
missense |
probably benign |
0.03 |
R1738:Zfp975
|
UTSW |
7 |
42,312,373 (GRCm39) |
missense |
probably benign |
0.05 |
R1833:Zfp975
|
UTSW |
7 |
42,311,263 (GRCm39) |
missense |
probably benign |
0.01 |
R2185:Zfp975
|
UTSW |
7 |
42,311,105 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4090:Zfp975
|
UTSW |
7 |
42,312,298 (GRCm39) |
missense |
probably benign |
0.10 |
R4356:Zfp975
|
UTSW |
7 |
42,311,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R4631:Zfp975
|
UTSW |
7 |
42,312,369 (GRCm39) |
missense |
probably benign |
0.09 |
R4795:Zfp975
|
UTSW |
7 |
42,314,570 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4896:Zfp975
|
UTSW |
7 |
42,311,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R5266:Zfp975
|
UTSW |
7 |
42,311,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R5267:Zfp975
|
UTSW |
7 |
42,311,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R5580:Zfp975
|
UTSW |
7 |
42,314,513 (GRCm39) |
nonsense |
probably null |
|
R5874:Zfp975
|
UTSW |
7 |
42,312,312 (GRCm39) |
missense |
probably benign |
0.00 |
R5898:Zfp975
|
UTSW |
7 |
42,311,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R6529:Zfp975
|
UTSW |
7 |
42,311,325 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6782:Zfp975
|
UTSW |
7 |
42,311,454 (GRCm39) |
missense |
probably benign |
0.41 |
R6937:Zfp975
|
UTSW |
7 |
42,314,480 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7088:Zfp975
|
UTSW |
7 |
42,312,096 (GRCm39) |
missense |
probably benign |
0.02 |
R7233:Zfp975
|
UTSW |
7 |
42,311,918 (GRCm39) |
missense |
probably benign |
0.38 |
R7253:Zfp975
|
UTSW |
7 |
42,311,036 (GRCm39) |
makesense |
probably null |
|
R7358:Zfp975
|
UTSW |
7 |
42,312,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R7659:Zfp975
|
UTSW |
7 |
42,311,848 (GRCm39) |
missense |
probably benign |
0.00 |
R7999:Zfp975
|
UTSW |
7 |
42,312,356 (GRCm39) |
missense |
probably benign |
0.02 |
R8676:Zfp975
|
UTSW |
7 |
42,312,264 (GRCm39) |
missense |
probably benign |
0.44 |
R8957:Zfp975
|
UTSW |
7 |
42,311,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R9274:Zfp975
|
UTSW |
7 |
42,312,299 (GRCm39) |
missense |
probably benign |
0.02 |
R9326:Zfp975
|
UTSW |
7 |
42,311,837 (GRCm39) |
nonsense |
probably null |
|
R9536:Zfp975
|
UTSW |
7 |
42,312,345 (GRCm39) |
missense |
probably benign |
0.11 |
R9569:Zfp975
|
UTSW |
7 |
42,311,413 (GRCm39) |
missense |
probably benign |
0.00 |
R9717:Zfp975
|
UTSW |
7 |
42,312,332 (GRCm39) |
missense |
possibly damaging |
0.50 |
|