Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700029H14Rik |
T |
A |
8: 13,604,695 (GRCm39) |
T203S |
possibly damaging |
Het |
2700049A03Rik |
G |
A |
12: 71,235,457 (GRCm39) |
E1136K |
possibly damaging |
Het |
Abca6 |
C |
A |
11: 110,103,059 (GRCm39) |
R844L |
probably damaging |
Het |
Abcb9 |
C |
T |
5: 124,221,753 (GRCm39) |
R207Q |
probably benign |
Het |
Abcd4 |
T |
C |
12: 84,655,581 (GRCm39) |
R343G |
probably damaging |
Het |
Arhgap45 |
T |
A |
10: 79,855,564 (GRCm39) |
M1K |
probably null |
Het |
Art3 |
A |
G |
5: 92,541,013 (GRCm39) |
Y252C |
probably damaging |
Het |
Ascc3 |
T |
C |
10: 50,525,230 (GRCm39) |
M475T |
probably benign |
Het |
Atxn2 |
C |
T |
5: 121,940,201 (GRCm39) |
P992L |
possibly damaging |
Het |
Dclk3 |
G |
A |
9: 111,311,819 (GRCm39) |
|
probably null |
Het |
Ddx21 |
T |
C |
10: 62,429,881 (GRCm39) |
T288A |
possibly damaging |
Het |
Fat3 |
T |
C |
9: 15,908,703 (GRCm39) |
D2433G |
probably damaging |
Het |
Flnc |
G |
A |
6: 29,441,484 (GRCm39) |
R422Q |
probably benign |
Het |
Fmnl2 |
G |
T |
2: 53,007,016 (GRCm39) |
R776L |
unknown |
Het |
Fndc1 |
T |
A |
17: 7,991,198 (GRCm39) |
T833S |
unknown |
Het |
Igf1r |
T |
A |
7: 67,857,001 (GRCm39) |
Y988N |
probably damaging |
Het |
Ints2 |
T |
C |
11: 86,117,589 (GRCm39) |
Y711C |
probably damaging |
Het |
Irx5 |
A |
G |
8: 93,086,351 (GRCm39) |
K145E |
probably damaging |
Het |
Kdm5a |
A |
G |
6: 120,365,991 (GRCm39) |
Y377C |
probably damaging |
Het |
Lrp1 |
T |
A |
10: 127,409,287 (GRCm39) |
T1611S |
probably damaging |
Het |
Lrrc28 |
T |
A |
7: 67,181,512 (GRCm39) |
E241V |
probably damaging |
Het |
Med23 |
T |
C |
10: 24,778,019 (GRCm39) |
F789S |
probably damaging |
Het |
Ncapd3 |
C |
T |
9: 26,967,451 (GRCm39) |
Q596* |
probably null |
Het |
Nrde2 |
C |
A |
12: 100,096,681 (GRCm39) |
E1040* |
probably null |
Het |
Or2n1d |
A |
T |
17: 38,646,320 (GRCm39) |
T91S |
possibly damaging |
Het |
Pcdh15 |
CAGAGA |
CAGA |
10: 74,481,663 (GRCm39) |
|
probably null |
Het |
Pcm1 |
T |
G |
8: 41,740,788 (GRCm39) |
N972K |
probably damaging |
Het |
Peg10 |
C |
CTCT |
6: 4,756,453 (GRCm39) |
|
probably benign |
Het |
Pla2g4a |
T |
C |
1: 149,755,772 (GRCm39) |
T222A |
probably damaging |
Het |
Ptchd3 |
A |
T |
11: 121,732,779 (GRCm39) |
K556N |
possibly damaging |
Het |
Relch |
A |
G |
1: 105,662,288 (GRCm39) |
T936A |
probably benign |
Het |
Scap |
T |
C |
9: 110,207,673 (GRCm39) |
C461R |
possibly damaging |
Het |
Scgb1b10 |
T |
A |
7: 31,800,627 (GRCm39) |
L72* |
probably null |
Het |
Serpinb6c |
C |
A |
13: 34,081,371 (GRCm39) |
A93S |
probably benign |
Het |
Serpinb9c |
C |
A |
13: 33,334,231 (GRCm39) |
L298F |
probably damaging |
Het |
Slf2 |
A |
T |
19: 44,930,460 (GRCm39) |
E512D |
probably benign |
Het |
Snapc3 |
C |
T |
4: 83,354,570 (GRCm39) |
H194Y |
probably benign |
Het |
Suox |
T |
A |
10: 128,507,758 (GRCm39) |
D90V |
possibly damaging |
Het |
Supt20 |
TCAGCAGCAGCAGCAGCAGCAGCA |
TCAGCAGCAGCAGCAGCAGCA |
3: 54,635,069 (GRCm39) |
|
probably benign |
Het |
Tert |
C |
T |
13: 73,797,046 (GRCm39) |
R1095W |
probably benign |
Het |
Tut4 |
A |
T |
4: 108,414,561 (GRCm39) |
H46L |
|
Het |
Unc13c |
T |
C |
9: 73,839,772 (GRCm39) |
I360V |
probably benign |
Het |
Uqcc1 |
A |
G |
2: 155,693,329 (GRCm39) |
C235R |
probably benign |
Het |
Vmn2r9 |
T |
A |
5: 108,991,484 (GRCm39) |
I626F |
probably damaging |
Het |
Vmn2r90 |
T |
G |
17: 17,954,213 (GRCm39) |
C792W |
probably damaging |
Het |
Zfp57 |
C |
T |
17: 37,320,814 (GRCm39) |
P223S |
probably benign |
Het |
|
Other mutations in Zfp787 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02546:Zfp787
|
APN |
7 |
6,135,297 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02721:Zfp787
|
APN |
7 |
6,135,463 (GRCm39) |
splice site |
probably null |
|
cheater
|
UTSW |
7 |
6,136,039 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0063:Zfp787
|
UTSW |
7 |
6,135,322 (GRCm39) |
splice site |
probably null |
|
R1415:Zfp787
|
UTSW |
7 |
6,135,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R1434:Zfp787
|
UTSW |
7 |
6,135,234 (GRCm39) |
missense |
probably damaging |
0.98 |
R2042:Zfp787
|
UTSW |
7 |
6,135,763 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5657:Zfp787
|
UTSW |
7 |
6,136,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R5919:Zfp787
|
UTSW |
7 |
6,135,834 (GRCm39) |
missense |
probably damaging |
0.98 |
R6306:Zfp787
|
UTSW |
7 |
6,135,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R7273:Zfp787
|
UTSW |
7 |
6,136,039 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7316:Zfp787
|
UTSW |
7 |
6,158,523 (GRCm39) |
unclassified |
probably benign |
|
R7396:Zfp787
|
UTSW |
7 |
6,135,106 (GRCm39) |
makesense |
probably null |
|
R7880:Zfp787
|
UTSW |
7 |
6,135,190 (GRCm39) |
missense |
probably benign |
0.00 |
R7979:Zfp787
|
UTSW |
7 |
6,146,094 (GRCm39) |
missense |
probably damaging |
0.97 |
R9527:Zfp787
|
UTSW |
7 |
6,136,027 (GRCm39) |
missense |
probably damaging |
0.99 |
R9713:Zfp787
|
UTSW |
7 |
6,146,059 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Zfp787
|
UTSW |
7 |
6,135,123 (GRCm39) |
missense |
probably damaging |
0.98 |
|