Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadat |
A |
T |
8: 60,969,106 (GRCm39) |
D117V |
probably damaging |
Het |
Abca14 |
T |
C |
7: 119,852,644 (GRCm39) |
Y870H |
possibly damaging |
Het |
Ankrd36 |
T |
C |
11: 5,585,092 (GRCm39) |
I301T |
probably benign |
Het |
Atp10b |
T |
A |
11: 43,150,672 (GRCm39) |
S1457T |
probably benign |
Het |
Bltp1 |
A |
G |
3: 36,996,531 (GRCm39) |
D1081G |
possibly damaging |
Het |
Ccdc175 |
G |
A |
12: 72,177,916 (GRCm39) |
|
probably benign |
Het |
Ccdc93 |
A |
G |
1: 121,389,628 (GRCm39) |
K224E |
probably benign |
Het |
Cep131 |
C |
T |
11: 119,956,786 (GRCm39) |
A886T |
probably damaging |
Het |
Clip1 |
A |
C |
5: 123,717,442 (GRCm39) |
H1282Q |
probably damaging |
Het |
Ctcfl |
T |
G |
2: 172,959,177 (GRCm39) |
D183A |
probably benign |
Het |
Cyp17a1 |
C |
T |
19: 46,659,495 (GRCm39) |
V112I |
probably benign |
Het |
Fhod3 |
T |
C |
18: 25,263,659 (GRCm39) |
I1521T |
probably damaging |
Het |
Gipc2 |
A |
G |
3: 151,843,214 (GRCm39) |
I141T |
probably damaging |
Het |
Glo1 |
T |
C |
17: 30,815,393 (GRCm39) |
R141G |
possibly damaging |
Het |
Ipmk |
C |
A |
10: 71,208,631 (GRCm39) |
A140E |
probably damaging |
Het |
Kynu |
A |
G |
2: 43,561,394 (GRCm39) |
D310G |
possibly damaging |
Het |
Myo1f |
T |
A |
17: 33,798,857 (GRCm39) |
I174N |
probably damaging |
Het |
Nat10 |
T |
A |
2: 103,588,102 (GRCm39) |
N8Y |
probably damaging |
Het |
Nhlrc2 |
A |
G |
19: 56,564,587 (GRCm39) |
I304V |
probably benign |
Het |
Pdk4 |
T |
C |
6: 5,491,979 (GRCm39) |
H31R |
probably damaging |
Het |
Sema6d |
T |
C |
2: 124,505,995 (GRCm39) |
V644A |
possibly damaging |
Het |
Slc30a4 |
T |
A |
2: 122,544,308 (GRCm39) |
K11N |
possibly damaging |
Het |
Slc6a3 |
T |
C |
13: 73,686,668 (GRCm39) |
S12P |
probably benign |
Het |
Spats2 |
C |
T |
15: 99,110,127 (GRCm39) |
A508V |
probably benign |
Het |
Tinag |
A |
G |
9: 76,952,820 (GRCm39) |
Y55H |
probably damaging |
Het |
Topbp1 |
T |
C |
9: 103,188,844 (GRCm39) |
I172T |
possibly damaging |
Het |
Trim17 |
A |
G |
11: 58,861,423 (GRCm39) |
T279A |
probably damaging |
Het |
Vmn1r216 |
C |
A |
13: 23,283,519 (GRCm39) |
N67K |
probably benign |
Het |
Washc4 |
T |
C |
10: 83,411,996 (GRCm39) |
L709P |
probably benign |
Het |
Xdh |
T |
C |
17: 74,230,132 (GRCm39) |
|
probably null |
Het |
Zfhx4 |
C |
T |
3: 5,309,036 (GRCm39) |
P754L |
probably damaging |
Het |
Zfp267 |
T |
C |
3: 36,218,729 (GRCm39) |
Y251H |
possibly damaging |
Het |
Zmat3 |
G |
A |
3: 32,395,827 (GRCm39) |
R227C |
possibly damaging |
Het |
|
Other mutations in Zfp623 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00226:Zfp623
|
APN |
15 |
75,820,052 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01927:Zfp623
|
APN |
15 |
75,819,354 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL03199:Zfp623
|
APN |
15 |
75,819,119 (GRCm39) |
missense |
probably benign |
0.40 |
R0076:Zfp623
|
UTSW |
15 |
75,819,058 (GRCm39) |
missense |
probably benign |
|
R0352:Zfp623
|
UTSW |
15 |
75,820,433 (GRCm39) |
missense |
probably benign |
0.00 |
R0360:Zfp623
|
UTSW |
15 |
75,820,510 (GRCm39) |
missense |
probably benign |
|
R0364:Zfp623
|
UTSW |
15 |
75,820,510 (GRCm39) |
missense |
probably benign |
|
R1783:Zfp623
|
UTSW |
15 |
75,819,760 (GRCm39) |
missense |
probably damaging |
0.99 |
R2219:Zfp623
|
UTSW |
15 |
75,819,379 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5975:Zfp623
|
UTSW |
15 |
75,820,012 (GRCm39) |
missense |
probably benign |
0.43 |
R6161:Zfp623
|
UTSW |
15 |
75,820,470 (GRCm39) |
missense |
probably benign |
0.22 |
R6342:Zfp623
|
UTSW |
15 |
75,819,837 (GRCm39) |
nonsense |
probably null |
|
R6490:Zfp623
|
UTSW |
15 |
75,820,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R6513:Zfp623
|
UTSW |
15 |
75,819,317 (GRCm39) |
missense |
probably benign |
|
R7028:Zfp623
|
UTSW |
15 |
75,820,154 (GRCm39) |
missense |
probably damaging |
0.99 |
R7399:Zfp623
|
UTSW |
15 |
75,819,247 (GRCm39) |
missense |
probably damaging |
0.98 |
R7716:Zfp623
|
UTSW |
15 |
75,820,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R8362:Zfp623
|
UTSW |
15 |
75,819,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R8445:Zfp623
|
UTSW |
15 |
75,819,402 (GRCm39) |
nonsense |
probably null |
|
R9028:Zfp623
|
UTSW |
15 |
75,819,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R9035:Zfp623
|
UTSW |
15 |
75,820,162 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9310:Zfp623
|
UTSW |
15 |
75,819,949 (GRCm39) |
missense |
probably damaging |
1.00 |
|