Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
A |
G |
7: 119,924,295 (GRCm39) |
Y1649C |
probably damaging |
Het |
Abcc10 |
A |
C |
17: 46,614,880 (GRCm39) |
C1459W |
possibly damaging |
Het |
Amfr |
A |
T |
8: 94,712,097 (GRCm39) |
F278I |
probably benign |
Het |
Anks1b |
G |
T |
10: 90,757,291 (GRCm39) |
|
probably null |
Het |
Bak1 |
A |
G |
17: 27,240,247 (GRCm39) |
S147P |
possibly damaging |
Het |
Bltp1 |
C |
A |
3: 37,037,602 (GRCm39) |
H2469N |
possibly damaging |
Het |
Bltp1 |
T |
A |
3: 37,098,829 (GRCm39) |
M1152K |
probably benign |
Het |
C7 |
T |
C |
15: 5,075,260 (GRCm39) |
N144S |
possibly damaging |
Het |
Casd1 |
T |
C |
6: 4,641,967 (GRCm39) |
V748A |
probably benign |
Het |
Ccdc168 |
C |
T |
1: 44,100,087 (GRCm39) |
G337D |
probably damaging |
Het |
Ccdc180 |
T |
C |
4: 45,916,375 (GRCm39) |
S859P |
probably benign |
Het |
Ccne2 |
T |
C |
4: 11,192,707 (GRCm39) |
S2P |
probably damaging |
Het |
Cdc42bpg |
T |
A |
19: 6,364,051 (GRCm39) |
I541N |
probably benign |
Het |
Cgnl1 |
T |
A |
9: 71,633,177 (GRCm39) |
N58I |
probably damaging |
Het |
Chd7 |
T |
C |
4: 8,822,402 (GRCm39) |
S832P |
possibly damaging |
Het |
Chl1 |
A |
T |
6: 103,652,038 (GRCm39) |
Y318F |
possibly damaging |
Het |
Coq2 |
G |
T |
5: 100,805,813 (GRCm39) |
N274K |
probably benign |
Het |
Crhr2 |
A |
T |
6: 55,077,720 (GRCm39) |
V214E |
probably damaging |
Het |
Dgkg |
G |
C |
16: 22,419,291 (GRCm39) |
P70A |
probably damaging |
Het |
Dync2h1 |
T |
C |
9: 7,147,731 (GRCm39) |
I966M |
probably benign |
Het |
Eif5b |
C |
G |
1: 38,061,248 (GRCm39) |
R380G |
unknown |
Het |
Fat4 |
T |
A |
3: 38,945,541 (GRCm39) |
I1478N |
probably damaging |
Het |
Impact |
A |
T |
18: 13,109,581 (GRCm39) |
I92L |
probably benign |
Het |
Ly6c2 |
A |
G |
15: 74,983,445 (GRCm39) |
|
probably null |
Het |
Lypd6b |
G |
A |
2: 49,837,468 (GRCm39) |
V147I |
possibly damaging |
Het |
Mdga2 |
T |
C |
12: 66,769,894 (GRCm39) |
D192G |
probably damaging |
Het |
Mms22l |
T |
C |
4: 24,586,344 (GRCm39) |
|
probably null |
Het |
Myo9a |
C |
T |
9: 59,739,484 (GRCm39) |
T732I |
possibly damaging |
Het |
Myrf |
C |
T |
19: 10,200,850 (GRCm39) |
M274I |
probably benign |
Het |
Nfx1 |
G |
A |
4: 41,003,057 (GRCm39) |
R686Q |
probably damaging |
Het |
Ofcc1 |
C |
T |
13: 40,362,305 (GRCm39) |
G206R |
probably benign |
Het |
Oog4 |
T |
C |
4: 143,164,581 (GRCm39) |
T245A |
possibly damaging |
Het |
Or1a1b |
C |
T |
11: 74,097,608 (GRCm39) |
V145I |
probably benign |
Het |
Or52e3 |
A |
T |
7: 102,869,625 (GRCm39) |
E233D |
probably benign |
Het |
Pclo |
A |
T |
5: 14,590,069 (GRCm39) |
K790* |
probably null |
Het |
Pcm1 |
A |
G |
8: 41,774,937 (GRCm39) |
E1668G |
probably damaging |
Het |
Pkhd1l1 |
T |
A |
15: 44,455,360 (GRCm39) |
N4040K |
probably damaging |
Het |
Podnl1 |
T |
A |
8: 84,855,905 (GRCm39) |
S222T |
probably benign |
Het |
Ppil4 |
A |
G |
10: 7,675,396 (GRCm39) |
T182A |
possibly damaging |
Het |
Prdm13 |
T |
C |
4: 21,678,544 (GRCm39) |
K649E |
probably damaging |
Het |
Prob1 |
A |
T |
18: 35,786,663 (GRCm39) |
H530Q |
probably benign |
Het |
Rbbp4 |
A |
T |
4: 129,211,442 (GRCm39) |
M404K |
probably damaging |
Het |
Rilpl1 |
A |
T |
5: 124,631,900 (GRCm39) |
F149I |
probably damaging |
Het |
Sema6c |
T |
A |
3: 95,078,527 (GRCm39) |
S543T |
probably benign |
Het |
Sh3rf3 |
G |
T |
10: 58,842,904 (GRCm39) |
W290L |
probably damaging |
Het |
Slc2a12 |
T |
G |
10: 22,541,350 (GRCm39) |
S402A |
probably benign |
Het |
Tas2r131 |
T |
A |
6: 132,934,030 (GRCm39) |
I260F |
possibly damaging |
Het |
Tasp1 |
A |
G |
2: 139,850,684 (GRCm39) |
I113T |
possibly damaging |
Het |
Tnrc18 |
G |
A |
5: 142,759,614 (GRCm39) |
R741* |
probably null |
Het |
Ube2o |
G |
T |
11: 116,437,290 (GRCm39) |
D244E |
probably damaging |
Het |
Vmn1r206 |
A |
T |
13: 22,804,784 (GRCm39) |
M141K |
probably benign |
Het |
Zbtb14 |
C |
A |
17: 69,695,497 (GRCm39) |
F398L |
probably damaging |
Het |
Zfp951 |
A |
T |
5: 104,963,151 (GRCm39) |
H138Q |
possibly damaging |
Het |
|
Other mutations in Zfp747 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02964:Zfp747
|
APN |
7 |
126,973,666 (GRCm39) |
missense |
probably benign |
0.21 |
IGL03201:Zfp747
|
APN |
7 |
126,973,180 (GRCm39) |
missense |
probably damaging |
0.99 |
R0066:Zfp747
|
UTSW |
7 |
126,973,772 (GRCm39) |
missense |
probably benign |
0.00 |
R1190:Zfp747
|
UTSW |
7 |
126,973,726 (GRCm39) |
missense |
probably damaging |
0.99 |
R1457:Zfp747
|
UTSW |
7 |
126,973,676 (GRCm39) |
missense |
probably benign |
0.37 |
R1727:Zfp747
|
UTSW |
7 |
126,973,249 (GRCm39) |
missense |
probably damaging |
0.99 |
R2072:Zfp747
|
UTSW |
7 |
126,973,142 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2157:Zfp747
|
UTSW |
7 |
126,974,929 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3724:Zfp747
|
UTSW |
7 |
126,973,762 (GRCm39) |
missense |
probably benign |
0.06 |
R4762:Zfp747
|
UTSW |
7 |
126,973,498 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4770:Zfp747
|
UTSW |
7 |
126,974,971 (GRCm39) |
missense |
probably damaging |
0.99 |
R5135:Zfp747
|
UTSW |
7 |
126,973,566 (GRCm39) |
missense |
probably damaging |
0.98 |
R5355:Zfp747
|
UTSW |
7 |
126,973,769 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6232:Zfp747
|
UTSW |
7 |
126,973,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R6263:Zfp747
|
UTSW |
7 |
126,975,138 (GRCm39) |
start gained |
probably benign |
|
R6835:Zfp747
|
UTSW |
7 |
126,973,219 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7638:Zfp747
|
UTSW |
7 |
126,973,819 (GRCm39) |
missense |
probably benign |
0.09 |
R7735:Zfp747
|
UTSW |
7 |
126,973,672 (GRCm39) |
missense |
probably damaging |
0.99 |
R8043:Zfp747
|
UTSW |
7 |
126,973,225 (GRCm39) |
missense |
probably benign |
0.00 |
R8543:Zfp747
|
UTSW |
7 |
126,973,655 (GRCm39) |
missense |
probably damaging |
0.99 |
R9132:Zfp747
|
UTSW |
7 |
126,974,922 (GRCm39) |
missense |
probably damaging |
0.99 |
R9329:Zfp747
|
UTSW |
7 |
126,973,655 (GRCm39) |
missense |
probably damaging |
0.99 |
R9415:Zfp747
|
UTSW |
7 |
126,973,198 (GRCm39) |
missense |
possibly damaging |
0.71 |
Z1176:Zfp747
|
UTSW |
7 |
126,974,631 (GRCm39) |
nonsense |
probably null |
|
|