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 |
Zfp975 |
G |
A |
7: 42,312,377 (GRCm39) |
Q79* |
probably null |
Het |
|
Other mutations in Zfp317 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02425:Zfp317
|
APN |
9 |
19,554,909 (GRCm39) |
nonsense |
probably null |
|
R1520:Zfp317
|
UTSW |
9 |
19,559,144 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1646:Zfp317
|
UTSW |
9 |
19,558,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R1860:Zfp317
|
UTSW |
9 |
19,553,280 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2029:Zfp317
|
UTSW |
9 |
19,556,532 (GRCm39) |
missense |
probably benign |
0.13 |
R2364:Zfp317
|
UTSW |
9 |
19,559,031 (GRCm39) |
missense |
probably benign |
0.01 |
R4006:Zfp317
|
UTSW |
9 |
19,559,333 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4293:Zfp317
|
UTSW |
9 |
19,557,990 (GRCm39) |
splice site |
probably null |
|
R4897:Zfp317
|
UTSW |
9 |
19,558,143 (GRCm39) |
missense |
probably benign |
0.28 |
R5593:Zfp317
|
UTSW |
9 |
19,558,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R6077:Zfp317
|
UTSW |
9 |
19,558,184 (GRCm39) |
missense |
probably benign |
0.00 |
R6573:Zfp317
|
UTSW |
9 |
19,556,550 (GRCm39) |
missense |
probably damaging |
0.99 |
R6652:Zfp317
|
UTSW |
9 |
19,558,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R6750:Zfp317
|
UTSW |
9 |
19,559,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R6875:Zfp317
|
UTSW |
9 |
19,554,961 (GRCm39) |
missense |
probably damaging |
0.98 |
R7688:Zfp317
|
UTSW |
9 |
19,559,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R8054:Zfp317
|
UTSW |
9 |
19,553,265 (GRCm39) |
missense |
probably benign |
0.00 |
R8900:Zfp317
|
UTSW |
9 |
19,558,708 (GRCm39) |
nonsense |
probably null |
|
R8927:Zfp317
|
UTSW |
9 |
19,552,521 (GRCm39) |
start codon destroyed |
probably null |
|
R8928:Zfp317
|
UTSW |
9 |
19,552,521 (GRCm39) |
start codon destroyed |
probably null |
|
R9052:Zfp317
|
UTSW |
9 |
19,556,568 (GRCm39) |
missense |
probably benign |
0.03 |
R9176:Zfp317
|
UTSW |
9 |
19,559,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R9210:Zfp317
|
UTSW |
9 |
19,558,442 (GRCm39) |
nonsense |
probably null |
|
R9212:Zfp317
|
UTSW |
9 |
19,558,442 (GRCm39) |
nonsense |
probably null |
|
Z1177:Zfp317
|
UTSW |
9 |
19,558,326 (GRCm39) |
missense |
probably damaging |
1.00 |
|