Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aire |
T |
C |
10: 77,879,309 (GRCm39) |
T17A |
|
Het |
Ankrd31 |
T |
C |
13: 96,940,773 (GRCm39) |
|
probably null |
Het |
Brwd1 |
C |
T |
16: 95,848,314 (GRCm39) |
R569K |
probably damaging |
Het |
Capns1 |
A |
T |
7: 29,889,978 (GRCm39) |
I177K |
probably benign |
Het |
Ccdc182 |
A |
G |
11: 88,185,343 (GRCm39) |
N141S |
probably benign |
Het |
Celsr1 |
A |
G |
15: 85,803,217 (GRCm39) |
W2441R |
probably damaging |
Het |
Cftr |
A |
T |
6: 18,235,310 (GRCm39) |
R516S |
probably damaging |
Het |
Ckap4 |
C |
T |
10: 84,363,507 (GRCm39) |
V519M |
probably damaging |
Het |
Col27a1 |
C |
T |
4: 63,231,974 (GRCm39) |
P1277L |
unknown |
Het |
Cspg4 |
T |
C |
9: 56,797,736 (GRCm39) |
L1400P |
probably damaging |
Het |
Cyp4f39 |
T |
A |
17: 32,711,296 (GRCm39) |
F481Y |
probably damaging |
Het |
Dmxl2 |
T |
C |
9: 54,309,011 (GRCm39) |
I1913M |
probably benign |
Het |
Dock10 |
T |
C |
1: 80,490,156 (GRCm39) |
T1989A |
probably damaging |
Het |
Eef2 |
CC |
CCC |
10: 81,014,603 (GRCm39) |
|
probably null |
Het |
Fcgbpl1 |
G |
A |
7: 27,853,754 (GRCm39) |
V1573I |
possibly damaging |
Het |
Fshr |
T |
A |
17: 89,292,948 (GRCm39) |
I577F |
probably damaging |
Het |
Gfm2 |
T |
C |
13: 97,301,707 (GRCm39) |
|
probably null |
Het |
Gm12695 |
T |
C |
4: 96,657,846 (GRCm39) |
N108D |
possibly damaging |
Het |
Gm3285 |
T |
A |
10: 77,698,007 (GRCm39) |
L52H |
unknown |
Het |
Gm5930 |
A |
T |
14: 44,575,006 (GRCm39) |
L95* |
probably null |
Het |
Hjurp |
CTCTGGGAGGGCTTGCTCCGGGGGCAGTGTGTCCTGTTCTTGTGCAGCCCCT |
C |
1: 88,193,999 (GRCm39) |
|
probably benign |
Het |
Klhl26 |
A |
G |
8: 70,904,896 (GRCm39) |
M338T |
possibly damaging |
Het |
Lrrc4c |
T |
C |
2: 97,459,686 (GRCm39) |
I104T |
probably benign |
Het |
Mapk10 |
A |
T |
5: 103,186,532 (GRCm39) |
V60E |
|
Het |
Mfsd4b3-ps |
T |
A |
10: 39,824,012 (GRCm39) |
K83* |
probably null |
Het |
Muc15 |
C |
T |
2: 110,562,089 (GRCm39) |
T175I |
probably damaging |
Het |
Nmu |
G |
A |
5: 76,511,572 (GRCm39) |
|
probably benign |
Het |
Nol4l |
G |
T |
2: 153,253,638 (GRCm39) |
T645K |
probably damaging |
Het |
Nr2f1 |
A |
G |
13: 78,337,869 (GRCm39) |
S416P |
probably benign |
Het |
Ntn4 |
A |
C |
10: 93,569,675 (GRCm39) |
I463L |
probably benign |
Het |
Nxt2 |
C |
T |
X: 141,020,747 (GRCm39) |
A118V |
possibly damaging |
Het |
Or12k7 |
T |
C |
2: 36,959,052 (GRCm39) |
L245P |
probably damaging |
Het |
Or52h2 |
C |
A |
7: 103,838,931 (GRCm39) |
C161F |
possibly damaging |
Het |
Or8h8 |
T |
A |
2: 86,752,998 (GRCm39) |
R293W |
probably damaging |
Het |
Pccb |
T |
A |
9: 100,869,908 (GRCm39) |
N341I |
probably damaging |
Het |
Pgm3 |
G |
A |
9: 86,447,662 (GRCm39) |
L194F |
probably damaging |
Het |
Prkra |
T |
A |
2: 76,478,193 (GRCm39) |
H3L |
probably benign |
Het |
Rbm12 |
TATTGCGGGACCGGGCATTGCGGGACCGGGCATTGCGGGACCGGGCATTGCGGGACCGGGCATTGCGGGACCGGGCATTGCGGGACCAGGCATTGCGGGACC |
TATTGCGGGACCGGGCATTGCGGGACCGGGCATTGCGGGACCGGGCATTGCGGGACCAGGCATTGCGGGACC |
2: 155,938,030 (GRCm39) |
|
probably benign |
Het |
Ryr1 |
T |
A |
7: 28,803,989 (GRCm39) |
K600* |
probably null |
Het |
Sema4d |
A |
T |
13: 51,877,596 (GRCm39) |
S79T |
probably benign |
Het |
Slc37a1 |
T |
C |
17: 31,534,486 (GRCm39) |
C53R |
probably damaging |
Het |
Sptbn1 |
A |
G |
11: 30,087,526 (GRCm39) |
I971T |
probably damaging |
Het |
Tcstv1a |
T |
A |
13: 120,355,453 (GRCm39) |
I60F |
possibly damaging |
Het |
Tdrkh |
G |
T |
3: 94,335,598 (GRCm39) |
C397F |
possibly damaging |
Het |
Tecrl |
A |
T |
5: 83,427,906 (GRCm39) |
M314K |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,780,496 (GRCm39) |
K1131R |
unknown |
Het |
Uimc1 |
A |
T |
13: 55,198,584 (GRCm39) |
Y531N |
possibly damaging |
Het |
Usp5 |
A |
G |
6: 124,803,384 (GRCm39) |
S39P |
probably damaging |
Het |
Virma |
A |
G |
4: 11,498,744 (GRCm39) |
T62A |
probably benign |
Het |
Vmn2r85 |
A |
G |
10: 130,254,153 (GRCm39) |
Y844H |
probably benign |
Het |
Yars1 |
T |
C |
4: 129,109,143 (GRCm39) |
V458A |
probably benign |
Het |
Zfp712 |
A |
T |
13: 67,189,241 (GRCm39) |
S429T |
probably damaging |
Het |
Zmynd11 |
A |
T |
13: 9,743,495 (GRCm39) |
D307E |
probably damaging |
Het |
|
Other mutations in Zfp235 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00951:Zfp235
|
APN |
7 |
23,836,505 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02326:Zfp235
|
APN |
7 |
23,834,727 (GRCm39) |
start codon destroyed |
probably null |
0.98 |
R0107:Zfp235
|
UTSW |
7 |
23,836,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R0271:Zfp235
|
UTSW |
7 |
23,836,556 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0513:Zfp235
|
UTSW |
7 |
23,841,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R1004:Zfp235
|
UTSW |
7 |
23,840,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R1928:Zfp235
|
UTSW |
7 |
23,840,563 (GRCm39) |
nonsense |
probably null |
|
R1958:Zfp235
|
UTSW |
7 |
23,839,771 (GRCm39) |
missense |
probably damaging |
0.98 |
R2167:Zfp235
|
UTSW |
7 |
23,840,387 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2511:Zfp235
|
UTSW |
7 |
23,841,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R3013:Zfp235
|
UTSW |
7 |
23,840,157 (GRCm39) |
missense |
probably damaging |
0.98 |
R3806:Zfp235
|
UTSW |
7 |
23,840,046 (GRCm39) |
missense |
probably benign |
0.01 |
R4613:Zfp235
|
UTSW |
7 |
23,841,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R4876:Zfp235
|
UTSW |
7 |
23,840,384 (GRCm39) |
missense |
probably benign |
0.01 |
R4977:Zfp235
|
UTSW |
7 |
23,841,609 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5085:Zfp235
|
UTSW |
7 |
23,836,546 (GRCm39) |
missense |
probably damaging |
0.96 |
R5664:Zfp235
|
UTSW |
7 |
23,841,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R6440:Zfp235
|
UTSW |
7 |
23,840,040 (GRCm39) |
missense |
probably damaging |
0.96 |
R6650:Zfp235
|
UTSW |
7 |
23,836,463 (GRCm39) |
splice site |
probably null |
|
R7694:Zfp235
|
UTSW |
7 |
23,841,525 (GRCm39) |
missense |
probably benign |
0.37 |
R8031:Zfp235
|
UTSW |
7 |
23,841,114 (GRCm39) |
missense |
probably benign |
0.19 |
R8188:Zfp235
|
UTSW |
7 |
23,841,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R8744:Zfp235
|
UTSW |
7 |
23,839,924 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9244:Zfp235
|
UTSW |
7 |
23,839,919 (GRCm39) |
missense |
probably benign |
0.00 |
R9401:Zfp235
|
UTSW |
7 |
23,841,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R9404:Zfp235
|
UTSW |
7 |
23,839,862 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9523:Zfp235
|
UTSW |
7 |
23,840,381 (GRCm39) |
missense |
probably benign |
0.00 |
R9563:Zfp235
|
UTSW |
7 |
23,841,669 (GRCm39) |
missense |
possibly damaging |
0.91 |
|