Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A430110L20Rik |
T |
C |
1: 181,055,274 (GRCm39) |
|
noncoding transcript |
Het |
Alox12b |
G |
T |
11: 69,049,211 (GRCm39) |
V87L |
probably benign |
Het |
Arsk |
T |
G |
13: 76,246,533 (GRCm39) |
N32T |
probably benign |
Het |
Baz1b |
T |
A |
5: 135,245,794 (GRCm39) |
N414K |
probably damaging |
Het |
Cacna1e |
A |
T |
1: 154,287,929 (GRCm39) |
|
probably null |
Het |
Cdc73 |
A |
G |
1: 143,484,252 (GRCm39) |
|
probably benign |
Het |
Cdhr2 |
A |
G |
13: 54,865,701 (GRCm39) |
D233G |
probably null |
Het |
Cep250 |
G |
A |
2: 155,834,552 (GRCm39) |
R2159K |
probably damaging |
Het |
Col4a4 |
T |
A |
1: 82,501,643 (GRCm39) |
Y370F |
unknown |
Het |
Cyp2b9 |
T |
C |
7: 25,872,881 (GRCm39) |
L8P |
probably damaging |
Het |
Ddx4 |
A |
G |
13: 112,750,295 (GRCm39) |
V386A |
probably benign |
Het |
Dnajc28 |
G |
A |
16: 91,413,755 (GRCm39) |
T187M |
probably damaging |
Het |
Dnajc6 |
T |
A |
4: 101,496,593 (GRCm39) |
V920E |
probably damaging |
Het |
Eef2kmt |
A |
T |
16: 5,070,899 (GRCm39) |
I50N |
probably damaging |
Het |
Esyt3 |
T |
C |
9: 99,206,290 (GRCm39) |
M40V |
probably benign |
Het |
Gkn3 |
C |
T |
6: 87,360,507 (GRCm39) |
A163T |
probably damaging |
Het |
Gpr26 |
G |
T |
7: 131,568,805 (GRCm39) |
C50F |
probably benign |
Het |
Hmcn1 |
A |
G |
1: 150,578,967 (GRCm39) |
I1993T |
possibly damaging |
Het |
Hsdl2 |
T |
A |
4: 59,610,636 (GRCm39) |
L211Q |
unknown |
Het |
Khdrbs2 |
A |
G |
1: 32,372,605 (GRCm39) |
E93G |
probably damaging |
Het |
Kif13b |
T |
C |
14: 65,004,904 (GRCm39) |
|
probably null |
Het |
Kif15 |
T |
A |
9: 122,815,254 (GRCm39) |
L423I |
probably benign |
Het |
Kmt2c |
A |
G |
5: 25,492,711 (GRCm39) |
V834A |
probably benign |
Het |
Lama3 |
T |
A |
18: 12,637,365 (GRCm39) |
Y28* |
probably null |
Het |
Map4k2 |
A |
T |
19: 6,403,186 (GRCm39) |
H763L |
probably damaging |
Het |
Mrtfb |
T |
C |
16: 13,202,064 (GRCm39) |
F120S |
probably damaging |
Het |
Ndufs3 |
C |
T |
2: 90,728,689 (GRCm39) |
|
probably benign |
Het |
Nfasc |
A |
T |
1: 132,523,329 (GRCm39) |
V887E |
probably damaging |
Het |
Npsr1 |
G |
A |
9: 24,225,065 (GRCm39) |
E358K |
possibly damaging |
Het |
Nrcam |
T |
C |
12: 44,618,985 (GRCm39) |
L828P |
possibly damaging |
Het |
Oprm1 |
T |
C |
10: 6,780,234 (GRCm39) |
Y299H |
probably damaging |
Het |
Or1j15 |
T |
A |
2: 36,459,030 (GRCm39) |
L140H |
probably damaging |
Het |
Osbpl8 |
T |
C |
10: 111,125,651 (GRCm39) |
V777A |
possibly damaging |
Het |
Pcnt |
T |
C |
10: 76,263,848 (GRCm39) |
E372G |
probably damaging |
Het |
Plekhh2 |
T |
C |
17: 84,925,427 (GRCm39) |
V1408A |
probably benign |
Het |
Sbk2 |
T |
C |
7: 4,960,627 (GRCm39) |
Y181C |
probably damaging |
Het |
Sf1 |
G |
A |
19: 6,418,470 (GRCm39) |
|
probably null |
Het |
Slc26a9 |
A |
G |
1: 131,695,587 (GRCm39) |
E765G |
possibly damaging |
Het |
Stab2 |
A |
G |
10: 86,758,049 (GRCm39) |
L1073P |
probably damaging |
Het |
Sypl2 |
A |
G |
3: 108,124,992 (GRCm39) |
I123T |
possibly damaging |
Het |
Taar3 |
A |
G |
10: 23,825,757 (GRCm39) |
D101G |
possibly damaging |
Het |
Thsd4 |
T |
C |
9: 59,904,505 (GRCm39) |
R204G |
probably benign |
Het |
Traf3ip3 |
A |
G |
1: 192,863,628 (GRCm39) |
V414A |
probably damaging |
Het |
Trim14 |
T |
A |
4: 46,523,709 (GRCm39) |
T110S |
probably benign |
Het |
Trim65 |
G |
A |
11: 116,017,305 (GRCm39) |
Q386* |
probably null |
Het |
Ttn |
G |
A |
2: 76,748,114 (GRCm39) |
Q4312* |
probably null |
Het |
Ubtfl1 |
T |
C |
9: 18,321,264 (GRCm39) |
V264A |
probably damaging |
Het |
Vmn1r58 |
C |
A |
7: 5,413,654 (GRCm39) |
W192L |
probably damaging |
Het |
Washc5 |
C |
A |
15: 59,211,711 (GRCm39) |
C969F |
probably damaging |
Het |
Zdhhc14 |
A |
G |
17: 5,777,131 (GRCm39) |
K296R |
probably benign |
Het |
Zfp281 |
T |
A |
1: 136,553,859 (GRCm39) |
I279N |
probably damaging |
Het |
|
Other mutations in Zfp9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Zfp9
|
APN |
6 |
118,441,436 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01093:Zfp9
|
APN |
6 |
118,442,800 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01512:Zfp9
|
APN |
6 |
118,444,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R0491:Zfp9
|
UTSW |
6 |
118,442,163 (GRCm39) |
missense |
probably damaging |
0.96 |
R1716:Zfp9
|
UTSW |
6 |
118,441,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R1858:Zfp9
|
UTSW |
6 |
118,442,021 (GRCm39) |
missense |
probably benign |
0.15 |
R4490:Zfp9
|
UTSW |
6 |
118,442,273 (GRCm39) |
missense |
probably benign |
0.06 |
R4627:Zfp9
|
UTSW |
6 |
118,441,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R4951:Zfp9
|
UTSW |
6 |
118,441,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R5344:Zfp9
|
UTSW |
6 |
118,442,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R5594:Zfp9
|
UTSW |
6 |
118,442,000 (GRCm39) |
missense |
probably damaging |
0.98 |
R6198:Zfp9
|
UTSW |
6 |
118,454,282 (GRCm39) |
start codon destroyed |
probably null |
|
R6682:Zfp9
|
UTSW |
6 |
118,444,202 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6986:Zfp9
|
UTSW |
6 |
118,441,426 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7147:Zfp9
|
UTSW |
6 |
118,441,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R7799:Zfp9
|
UTSW |
6 |
118,441,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R7921:Zfp9
|
UTSW |
6 |
118,442,032 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7934:Zfp9
|
UTSW |
6 |
118,441,847 (GRCm39) |
missense |
probably damaging |
0.99 |
R8111:Zfp9
|
UTSW |
6 |
118,441,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R8369:Zfp9
|
UTSW |
6 |
118,441,353 (GRCm39) |
missense |
probably damaging |
0.99 |
R8916:Zfp9
|
UTSW |
6 |
118,442,223 (GRCm39) |
nonsense |
probably null |
|
R9660:Zfp9
|
UTSW |
6 |
118,443,851 (GRCm39) |
missense |
probably benign |
|
R9728:Zfp9
|
UTSW |
6 |
118,443,851 (GRCm39) |
missense |
probably benign |
|
|