Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610507B11Rik |
T |
A |
11: 78,286,491 (GRCm38) |
|
probably null |
Het |
Adamdec1 |
A |
T |
14: 68,568,723 (GRCm38) |
C434* |
probably null |
Het |
Adprhl1 |
A |
G |
8: 13,242,391 (GRCm38) |
|
probably benign |
Het |
Ago1 |
T |
A |
4: 126,463,706 (GRCm38) |
I59F |
possibly damaging |
Het |
Arel1 |
T |
C |
12: 84,920,693 (GRCm38) |
T786A |
probably damaging |
Het |
Arhgap26 |
A |
G |
18: 39,363,131 (GRCm38) |
K117R |
probably benign |
Het |
Atp6v0b |
C |
T |
4: 117,884,622 (GRCm38) |
G204D |
probably damaging |
Het |
Bace2 |
T |
A |
16: 97,436,773 (GRCm38) |
|
probably null |
Het |
Camk4 |
G |
A |
18: 33,179,625 (GRCm38) |
|
probably null |
Het |
Cdh26 |
C |
T |
2: 178,481,632 (GRCm38) |
R675C |
possibly damaging |
Het |
Cep152 |
T |
C |
2: 125,564,214 (GRCm38) |
E1466G |
probably benign |
Het |
Ces3b |
T |
C |
8: 105,092,635 (GRCm38) |
F441S |
probably damaging |
Het |
Cfap52 |
T |
C |
11: 67,926,382 (GRCm38) |
T562A |
possibly damaging |
Het |
Clca3a2 |
C |
A |
3: 144,813,898 (GRCm38) |
M238I |
possibly damaging |
Het |
Cntnap5c |
A |
T |
17: 58,102,168 (GRCm38) |
D467V |
probably damaging |
Het |
Col7a1 |
T |
A |
9: 108,972,184 (GRCm38) |
|
probably null |
Het |
Cstf1 |
A |
G |
2: 172,377,710 (GRCm38) |
N247S |
possibly damaging |
Het |
Dffb |
G |
T |
4: 153,974,615 (GRCm38) |
N68K |
probably benign |
Het |
Duox2 |
C |
T |
2: 122,291,860 (GRCm38) |
G595S |
probably benign |
Het |
Eftud2 |
T |
A |
11: 102,864,725 (GRCm38) |
I228F |
probably damaging |
Het |
Elmo3 |
T |
C |
8: 105,309,171 (GRCm38) |
V578A |
probably benign |
Het |
Elp2 |
A |
G |
18: 24,631,471 (GRCm38) |
D625G |
possibly damaging |
Het |
Ep300 |
C |
T |
15: 81,640,128 (GRCm38) |
P1386S |
unknown |
Het |
Fam120b |
A |
G |
17: 15,417,637 (GRCm38) |
D610G |
probably damaging |
Het |
Fastk |
A |
T |
5: 24,442,178 (GRCm38) |
|
probably benign |
Het |
Fbxl6 |
A |
G |
15: 76,537,191 (GRCm38) |
S252P |
probably damaging |
Het |
Fbxo43 |
T |
C |
15: 36,161,793 (GRCm38) |
K423E |
probably damaging |
Het |
Filip1 |
T |
A |
9: 79,819,462 (GRCm38) |
E625V |
possibly damaging |
Het |
Fkbp9 |
T |
A |
6: 56,856,378 (GRCm38) |
Y283* |
probably null |
Het |
Gigyf2 |
T |
A |
1: 87,379,015 (GRCm38) |
D142E |
possibly damaging |
Het |
Gm10142 |
T |
C |
10: 77,716,014 (GRCm38) |
|
probably null |
Het |
Golga5 |
T |
C |
12: 102,476,188 (GRCm38) |
V262A |
probably benign |
Het |
Hectd4 |
T |
C |
5: 121,329,605 (GRCm38) |
V2539A |
probably benign |
Het |
Ica1 |
G |
T |
6: 8,653,632 (GRCm38) |
S335* |
probably null |
Het |
Itga1 |
A |
T |
13: 115,006,897 (GRCm38) |
|
probably benign |
Het |
Itgb1 |
T |
C |
8: 128,717,685 (GRCm38) |
|
probably benign |
Het |
Itpr1 |
G |
A |
6: 108,473,589 (GRCm38) |
V1960I |
probably benign |
Het |
Kcnh4 |
C |
T |
11: 100,746,932 (GRCm38) |
G633E |
probably benign |
Het |
Kprp |
C |
T |
3: 92,825,411 (GRCm38) |
V111I |
probably benign |
Het |
Lamc3 |
T |
C |
2: 31,940,721 (GRCm38) |
I1490T |
probably damaging |
Het |
Lcp1 |
A |
T |
14: 75,227,001 (GRCm38) |
D554V |
possibly damaging |
Het |
Lgi3 |
A |
G |
14: 70,534,698 (GRCm38) |
T228A |
probably benign |
Het |
Lipa |
A |
T |
19: 34,501,541 (GRCm38) |
F260I |
probably damaging |
Het |
Lrriq1 |
C |
T |
10: 103,215,773 (GRCm38) |
E373K |
probably damaging |
Het |
Map6 |
G |
A |
7: 99,336,836 (GRCm38) |
G649D |
probably benign |
Het |
Mccc1 |
A |
G |
3: 35,990,047 (GRCm38) |
|
probably null |
Het |
Mical3 |
A |
T |
6: 120,957,722 (GRCm38) |
S1799T |
probably benign |
Het |
Mmp23 |
T |
A |
4: 155,652,132 (GRCm38) |
T151S |
probably damaging |
Het |
Myo1d |
T |
A |
11: 80,674,708 (GRCm38) |
N401I |
probably damaging |
Het |
Myo9b |
T |
A |
8: 71,321,813 (GRCm38) |
S323T |
probably damaging |
Het |
Nbn |
G |
T |
4: 15,979,353 (GRCm38) |
W446L |
probably benign |
Het |
Nedd1 |
A |
T |
10: 92,716,265 (GRCm38) |
|
probably benign |
Het |
Ngef |
C |
A |
1: 87,487,962 (GRCm38) |
|
probably benign |
Het |
Nup153 |
A |
T |
13: 46,693,936 (GRCm38) |
N672K |
probably benign |
Het |
Olfr1308 |
T |
C |
2: 111,961,016 (GRCm38) |
N19S |
probably benign |
Het |
Olfr149 |
T |
A |
9: 39,702,173 (GRCm38) |
I199F |
probably damaging |
Het |
Olfr1509 |
T |
C |
14: 52,450,512 (GRCm38) |
V33A |
probably benign |
Het |
Olfr372 |
C |
T |
8: 72,058,400 (GRCm38) |
T240M |
probably damaging |
Het |
Palm2 |
T |
G |
4: 57,710,177 (GRCm38) |
V374G |
possibly damaging |
Het |
Pdlim3 |
C |
A |
8: 45,908,460 (GRCm38) |
|
probably benign |
Het |
Pmfbp1 |
G |
A |
8: 109,541,673 (GRCm38) |
E951K |
probably damaging |
Het |
Pop1 |
T |
A |
15: 34,515,891 (GRCm38) |
C548* |
probably null |
Het |
Ppp1r16a |
C |
T |
15: 76,690,799 (GRCm38) |
|
probably benign |
Het |
Ptpdc1 |
A |
T |
13: 48,585,980 (GRCm38) |
N658K |
probably benign |
Het |
Ptprk |
A |
C |
10: 28,206,225 (GRCm38) |
E63D |
possibly damaging |
Het |
Rtf1 |
C |
T |
2: 119,732,877 (GRCm38) |
R712W |
probably damaging |
Het |
Samd7 |
A |
C |
3: 30,751,073 (GRCm38) |
T2P |
probably benign |
Het |
Sft2d1 |
A |
G |
17: 8,319,422 (GRCm38) |
T52A |
probably benign |
Het |
Slc25a26 |
A |
G |
6: 94,510,833 (GRCm38) |
H91R |
probably damaging |
Het |
Slc5a4a |
A |
G |
10: 76,189,152 (GRCm38) |
E621G |
possibly damaging |
Het |
Slf1 |
A |
T |
13: 77,126,632 (GRCm38) |
L28* |
probably null |
Het |
Snapc1 |
C |
T |
12: 73,975,032 (GRCm38) |
R81C |
probably damaging |
Het |
Sorcs2 |
G |
A |
5: 36,397,553 (GRCm38) |
|
probably benign |
Het |
Tacc2 |
T |
C |
7: 130,751,825 (GRCm38) |
|
probably benign |
Het |
Tas2r140 |
A |
G |
6: 133,055,327 (GRCm38) |
V156A |
possibly damaging |
Het |
Terf2ip |
C |
A |
8: 112,018,164 (GRCm38) |
T371K |
possibly damaging |
Het |
Tifa |
C |
T |
3: 127,796,888 (GRCm38) |
L103F |
probably damaging |
Het |
Tmco3 |
A |
G |
8: 13,292,037 (GRCm38) |
N104D |
probably damaging |
Het |
Tmem259 |
T |
A |
10: 79,978,963 (GRCm38) |
D240V |
probably damaging |
Het |
Trim60 |
C |
T |
8: 65,001,048 (GRCm38) |
R183H |
probably benign |
Het |
Trps1 |
T |
C |
15: 50,664,743 (GRCm38) |
N725D |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,814,806 (GRCm38) |
V12902M |
probably damaging |
Het |
Ubxn4 |
G |
A |
1: 128,262,904 (GRCm38) |
E256K |
probably benign |
Het |
Unc79 |
A |
G |
12: 103,112,891 (GRCm38) |
K1772E |
probably damaging |
Het |
Vwde |
C |
T |
6: 13,193,126 (GRCm38) |
V405I |
probably benign |
Het |
Wdr18 |
T |
A |
10: 79,966,408 (GRCm38) |
D290E |
probably damaging |
Het |
Wdr92 |
T |
C |
11: 17,229,851 (GRCm38) |
L284P |
probably damaging |
Het |
Wwc2 |
G |
A |
8: 47,900,721 (GRCm38) |
A126V |
probably benign |
Het |
Zfp942 |
A |
T |
17: 21,928,572 (GRCm38) |
C359S |
probably benign |
Het |
|
Other mutations in Zfp882 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00676:Zfp882
|
APN |
8 |
71,913,827 (GRCm38) |
missense |
probably benign |
|
R0270:Zfp882
|
UTSW |
8 |
71,914,615 (GRCm38) |
missense |
probably benign |
0.05 |
R0636:Zfp882
|
UTSW |
8 |
71,914,337 (GRCm38) |
missense |
probably benign |
0.01 |
R0840:Zfp882
|
UTSW |
8 |
71,914,686 (GRCm38) |
nonsense |
probably null |
|
R1299:Zfp882
|
UTSW |
8 |
71,913,473 (GRCm38) |
missense |
probably damaging |
1.00 |
R4439:Zfp882
|
UTSW |
8 |
71,913,609 (GRCm38) |
missense |
probably damaging |
0.97 |
R4829:Zfp882
|
UTSW |
8 |
71,914,389 (GRCm38) |
missense |
probably damaging |
1.00 |
R5028:Zfp882
|
UTSW |
8 |
71,914,654 (GRCm38) |
missense |
possibly damaging |
0.70 |
R5296:Zfp882
|
UTSW |
8 |
71,914,360 (GRCm38) |
missense |
probably damaging |
1.00 |
R5882:Zfp882
|
UTSW |
8 |
71,913,459 (GRCm38) |
critical splice acceptor site |
probably null |
|
R5974:Zfp882
|
UTSW |
8 |
71,913,155 (GRCm38) |
missense |
probably damaging |
1.00 |
R6052:Zfp882
|
UTSW |
8 |
71,914,505 (GRCm38) |
missense |
probably benign |
0.01 |
R6383:Zfp882
|
UTSW |
8 |
71,914,640 (GRCm38) |
missense |
probably damaging |
1.00 |
R6888:Zfp882
|
UTSW |
8 |
71,914,286 (GRCm38) |
missense |
probably benign |
0.01 |
R6987:Zfp882
|
UTSW |
8 |
71,914,673 (GRCm38) |
missense |
probably benign |
0.01 |
R7045:Zfp882
|
UTSW |
8 |
71,913,249 (GRCm38) |
critical splice donor site |
probably null |
|
R7780:Zfp882
|
UTSW |
8 |
71,914,229 (GRCm38) |
missense |
possibly damaging |
0.89 |
R7793:Zfp882
|
UTSW |
8 |
71,913,141 (GRCm38) |
missense |
probably damaging |
1.00 |
R8386:Zfp882
|
UTSW |
8 |
71,914,118 (GRCm38) |
missense |
probably benign |
0.00 |
R9452:Zfp882
|
UTSW |
8 |
71,914,987 (GRCm38) |
missense |
probably damaging |
1.00 |
R9694:Zfp882
|
UTSW |
8 |
71,914,071 (GRCm38) |
missense |
probably benign |
0.01 |
|