Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
C |
G |
3: 124,199,999 (GRCm39) |
G531A |
probably damaging |
Het |
4921504E06Rik |
T |
C |
2: 19,528,892 (GRCm39) |
D163G |
probably damaging |
Het |
Abcd4 |
C |
T |
12: 84,650,067 (GRCm39) |
|
probably null |
Het |
Alg9 |
T |
C |
9: 50,734,011 (GRCm39) |
S570P |
possibly damaging |
Het |
Angptl3 |
C |
A |
4: 98,922,723 (GRCm39) |
H255N |
probably benign |
Het |
Ank3 |
G |
A |
10: 69,838,395 (GRCm39) |
R1566K |
possibly damaging |
Het |
Cdc37 |
A |
T |
9: 21,052,060 (GRCm39) |
D326E |
probably benign |
Het |
Cdk13 |
T |
C |
13: 17,946,898 (GRCm39) |
K6R |
probably damaging |
Het |
Ces1b |
T |
C |
8: 93,793,645 (GRCm39) |
K315E |
probably benign |
Het |
Cfap61 |
G |
A |
2: 145,951,908 (GRCm39) |
G190S |
probably damaging |
Het |
Cimap3 |
T |
C |
3: 105,908,419 (GRCm39) |
T107A |
probably benign |
Het |
Ckap4 |
T |
C |
10: 84,364,238 (GRCm39) |
E275G |
probably benign |
Het |
Cplane1 |
G |
A |
15: 8,290,174 (GRCm39) |
|
probably null |
Het |
Csf3r |
A |
G |
4: 125,929,137 (GRCm39) |
D349G |
probably benign |
Het |
Cyp2d37-ps |
T |
C |
15: 82,574,012 (GRCm39) |
|
noncoding transcript |
Het |
Dmbt1 |
T |
A |
7: 130,642,751 (GRCm39) |
C190S |
probably damaging |
Het |
Dnah11 |
A |
G |
12: 118,049,415 (GRCm39) |
F1670L |
possibly damaging |
Het |
Dnah5 |
A |
T |
15: 28,229,797 (GRCm39) |
I144F |
possibly damaging |
Het |
Eno2 |
C |
A |
6: 124,744,056 (GRCm39) |
V84L |
probably damaging |
Het |
Ercc4 |
G |
T |
16: 12,948,028 (GRCm39) |
R325L |
probably damaging |
Het |
Fcgr2b |
T |
G |
1: 170,793,279 (GRCm39) |
Q250P |
probably benign |
Het |
Garin5a |
T |
C |
7: 44,149,606 (GRCm39) |
V109A |
probably damaging |
Het |
Garre1 |
T |
A |
7: 33,945,180 (GRCm39) |
K355* |
probably null |
Het |
Gcfc2 |
T |
C |
6: 81,920,524 (GRCm39) |
|
probably null |
Het |
Glb1l2 |
C |
T |
9: 26,676,055 (GRCm39) |
G509D |
probably damaging |
Het |
Gm11595 |
G |
A |
11: 99,663,381 (GRCm39) |
R100C |
unknown |
Het |
Grn |
A |
G |
11: 102,327,018 (GRCm39) |
N160D |
possibly damaging |
Het |
Hexd |
T |
A |
11: 121,113,095 (GRCm39) |
V510D |
probably damaging |
Het |
Igfbp1 |
G |
A |
11: 7,149,919 (GRCm39) |
|
probably null |
Het |
Itga11 |
T |
A |
9: 62,663,051 (GRCm39) |
M589K |
probably benign |
Het |
Itpr1 |
A |
T |
6: 108,333,472 (GRCm39) |
S51C |
probably damaging |
Het |
Klra3 |
T |
C |
6: 130,311,270 (GRCm39) |
|
probably null |
Het |
Mad2l1 |
T |
C |
6: 66,514,675 (GRCm39) |
|
probably null |
Het |
Matn3 |
CGGGGCTCGGGGGC |
CGGGGC |
12: 9,002,308 (GRCm39) |
|
probably null |
Het |
Myo9a |
T |
A |
9: 59,771,244 (GRCm39) |
Y939N |
probably damaging |
Het |
Nxpe3 |
C |
T |
16: 55,686,834 (GRCm39) |
S58N |
probably benign |
Het |
Or1j16 |
T |
A |
2: 36,530,706 (GRCm39) |
Y218* |
probably null |
Het |
Or3a1c |
T |
A |
11: 74,046,397 (GRCm39) |
M139K |
probably damaging |
Het |
Or4c103 |
T |
C |
2: 88,513,749 (GRCm39) |
E109G |
probably benign |
Het |
Or4k45 |
C |
T |
2: 111,394,899 (GRCm39) |
A297T |
probably damaging |
Het |
Paics |
T |
C |
5: 77,104,479 (GRCm39) |
S35P |
probably damaging |
Het |
Pcnt |
A |
C |
10: 76,192,159 (GRCm39) |
Y2717* |
probably null |
Het |
Plekho2 |
T |
A |
9: 65,465,957 (GRCm39) |
N144Y |
probably damaging |
Het |
Plscr5 |
T |
C |
9: 92,080,565 (GRCm39) |
F17S |
possibly damaging |
Het |
Prrc2a |
C |
T |
17: 35,380,023 (GRCm39) |
R192H |
unknown |
Het |
Rbm27 |
T |
A |
18: 42,460,275 (GRCm39) |
M735K |
probably damaging |
Het |
Rfc1 |
T |
A |
5: 65,436,804 (GRCm39) |
K625N |
probably damaging |
Het |
Ric8b |
T |
A |
10: 84,783,611 (GRCm39) |
F156L |
probably benign |
Het |
Romo1 |
C |
A |
2: 155,986,473 (GRCm39) |
A32E |
possibly damaging |
Het |
Rpl26 |
T |
A |
11: 68,795,284 (GRCm39) |
Y135N |
probably damaging |
Het |
Sacs |
T |
C |
14: 61,429,849 (GRCm39) |
V636A |
probably benign |
Het |
Scyl2 |
A |
T |
10: 89,477,869 (GRCm39) |
I710N |
probably benign |
Het |
Sh3bp5 |
C |
A |
14: 31,099,452 (GRCm39) |
R265L |
probably benign |
Het |
Slc4a1 |
T |
A |
11: 102,249,903 (GRCm39) |
I154F |
probably damaging |
Het |
Snx11 |
A |
G |
11: 96,661,535 (GRCm39) |
S157P |
probably damaging |
Het |
Snx18 |
G |
A |
13: 113,753,383 (GRCm39) |
Q517* |
probably null |
Het |
Stard4 |
G |
T |
18: 33,336,678 (GRCm39) |
N212K |
probably damaging |
Het |
Strn3 |
A |
G |
12: 51,676,168 (GRCm39) |
Y454H |
probably damaging |
Het |
Stx17 |
A |
T |
4: 48,182,851 (GRCm39) |
|
probably benign |
Het |
Tas2r121 |
G |
A |
6: 132,677,480 (GRCm39) |
T164I |
possibly damaging |
Het |
Tbc1d8 |
T |
C |
1: 39,428,490 (GRCm39) |
Y485C |
probably damaging |
Het |
Tmem45b |
T |
C |
9: 31,340,380 (GRCm39) |
M8V |
probably damaging |
Het |
Usp28 |
T |
C |
9: 48,948,501 (GRCm39) |
F844L |
probably damaging |
Het |
Usp32 |
T |
A |
11: 84,908,544 (GRCm39) |
N1054I |
probably benign |
Het |
Xpa |
T |
A |
4: 46,185,659 (GRCm39) |
E106D |
probably benign |
Het |
|
Other mutations in Zfp85 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0383:Zfp85
|
UTSW |
13 |
67,896,791 (GRCm39) |
missense |
probably benign |
0.05 |
R1187:Zfp85
|
UTSW |
13 |
67,897,835 (GRCm39) |
missense |
probably damaging |
0.99 |
R1510:Zfp85
|
UTSW |
13 |
67,903,084 (GRCm39) |
intron |
probably benign |
|
R1775:Zfp85
|
UTSW |
13 |
67,897,823 (GRCm39) |
missense |
probably damaging |
0.99 |
R1803:Zfp85
|
UTSW |
13 |
67,899,747 (GRCm39) |
missense |
probably benign |
0.15 |
R2108:Zfp85
|
UTSW |
13 |
67,897,003 (GRCm39) |
missense |
probably benign |
0.08 |
R2412:Zfp85
|
UTSW |
13 |
67,897,765 (GRCm39) |
missense |
probably damaging |
0.99 |
R3147:Zfp85
|
UTSW |
13 |
67,900,612 (GRCm39) |
missense |
probably damaging |
0.96 |
R4811:Zfp85
|
UTSW |
13 |
67,897,745 (GRCm39) |
missense |
probably damaging |
0.97 |
R5334:Zfp85
|
UTSW |
13 |
67,899,803 (GRCm39) |
missense |
probably damaging |
0.99 |
R5373:Zfp85
|
UTSW |
13 |
67,897,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R7045:Zfp85
|
UTSW |
13 |
67,897,712 (GRCm39) |
missense |
probably benign |
0.00 |
R7391:Zfp85
|
UTSW |
13 |
67,897,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R7438:Zfp85
|
UTSW |
13 |
67,897,064 (GRCm39) |
missense |
probably benign |
0.09 |
R7544:Zfp85
|
UTSW |
13 |
67,897,184 (GRCm39) |
missense |
probably benign |
0.02 |
R8046:Zfp85
|
UTSW |
13 |
67,897,098 (GRCm39) |
nonsense |
probably null |
|
R8112:Zfp85
|
UTSW |
13 |
67,896,893 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9533:Zfp85
|
UTSW |
13 |
67,897,722 (GRCm39) |
missense |
probably benign |
0.08 |
R9615:Zfp85
|
UTSW |
13 |
67,897,326 (GRCm39) |
missense |
probably damaging |
0.98 |
|