Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
A |
3: 138,068,225 (GRCm38) |
D1058E |
probably damaging |
Het |
4933405L10Rik |
A |
T |
8: 105,708,931 (GRCm38) |
|
probably null |
Het |
Adamtsl3 |
T |
A |
7: 82,465,699 (GRCm38) |
|
probably benign |
Het |
Afdn |
C |
T |
17: 13,852,436 (GRCm38) |
P874S |
probably damaging |
Het |
Ankrd6 |
G |
A |
4: 32,815,326 (GRCm38) |
A391V |
probably damaging |
Het |
Arhgef28 |
T |
G |
13: 97,931,254 (GRCm38) |
T1388P |
probably damaging |
Het |
Asxl3 |
G |
T |
18: 22,524,451 (GRCm38) |
M1839I |
probably benign |
Het |
BC005537 |
T |
C |
13: 24,805,940 (GRCm38) |
F129L |
probably damaging |
Het |
Celf2 |
A |
G |
2: 6,721,415 (GRCm38) |
|
probably null |
Het |
Chid1 |
C |
T |
7: 141,496,677 (GRCm38) |
V325I |
probably benign |
Het |
Cnn3 |
T |
A |
3: 121,449,984 (GRCm38) |
D31E |
probably benign |
Het |
Col12a1 |
G |
A |
9: 79,652,035 (GRCm38) |
P1857L |
probably damaging |
Het |
Cpeb1 |
T |
A |
7: 81,351,870 (GRCm38) |
R430W |
probably benign |
Het |
Daw1 |
T |
C |
1: 83,191,338 (GRCm38) |
|
probably benign |
Het |
Dcaf13 |
A |
G |
15: 39,138,089 (GRCm38) |
Y264C |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,087,602 (GRCm38) |
I2666V |
probably damaging |
Het |
Dnai2 |
A |
C |
11: 114,754,332 (GRCm38) |
D531A |
probably benign |
Het |
Dock10 |
A |
T |
1: 80,523,975 (GRCm38) |
F1833I |
probably damaging |
Het |
Efhd2 |
C |
T |
4: 141,859,872 (GRCm38) |
A200T |
probably damaging |
Het |
Epb41l5 |
T |
A |
1: 119,623,911 (GRCm38) |
|
probably benign |
Het |
Ermp1 |
A |
G |
19: 29,631,388 (GRCm38) |
Y164H |
possibly damaging |
Het |
Gkn2 |
T |
C |
6: 87,373,419 (GRCm38) |
|
probably benign |
Het |
Golgb1 |
A |
T |
16: 36,918,790 (GRCm38) |
Q2497L |
probably damaging |
Het |
Gzme |
A |
T |
14: 56,117,739 (GRCm38) |
M245K |
probably damaging |
Het |
Iars2 |
A |
T |
1: 185,322,388 (GRCm38) |
|
probably benign |
Het |
Icosl |
T |
A |
10: 78,073,941 (GRCm38) |
V240D |
probably damaging |
Het |
Igsf3 |
T |
C |
3: 101,427,393 (GRCm38) |
M262T |
probably benign |
Het |
Ing3 |
G |
T |
6: 21,971,237 (GRCm38) |
E336* |
probably null |
Het |
Kat2a |
A |
T |
11: 100,706,471 (GRCm38) |
V625E |
probably damaging |
Het |
Ksr1 |
A |
G |
11: 79,038,247 (GRCm38) |
|
probably benign |
Het |
Lypd8 |
A |
T |
11: 58,386,757 (GRCm38) |
M122L |
probably benign |
Het |
Mdfi |
A |
T |
17: 47,832,930 (GRCm38) |
|
probably benign |
Het |
Med13 |
A |
G |
11: 86,301,353 (GRCm38) |
|
probably benign |
Het |
Msh6 |
C |
T |
17: 87,986,684 (GRCm38) |
R956C |
probably damaging |
Het |
Myo15b |
A |
G |
11: 115,883,838 (GRCm38) |
E670G |
probably damaging |
Het |
Myo1d |
A |
G |
11: 80,484,332 (GRCm38) |
L972P |
probably damaging |
Het |
Or4s2b |
A |
G |
2: 88,678,674 (GRCm38) |
D266G |
probably damaging |
Het |
Or51ai2 |
G |
A |
7: 103,937,817 (GRCm38) |
A146T |
probably benign |
Het |
Or7g12 |
T |
A |
9: 18,988,151 (GRCm38) |
N54K |
probably benign |
Het |
Pde8b |
C |
G |
13: 95,107,817 (GRCm38) |
S143T |
possibly damaging |
Het |
Pias4 |
G |
T |
10: 81,157,530 (GRCm38) |
|
probably benign |
Het |
Prkca |
A |
G |
11: 107,981,654 (GRCm38) |
Y427H |
probably benign |
Het |
Psg25 |
G |
A |
7: 18,529,560 (GRCm38) |
Q113* |
probably null |
Het |
Rab3gap2 |
T |
A |
1: 185,249,926 (GRCm38) |
S392T |
probably damaging |
Het |
Scrib |
A |
G |
15: 76,066,907 (GRCm38) |
|
probably benign |
Het |
Sdk2 |
A |
G |
11: 113,903,144 (GRCm38) |
|
probably benign |
Het |
Serpinb1c |
T |
A |
13: 32,886,283 (GRCm38) |
|
probably benign |
Het |
Serpinb9f |
T |
A |
13: 33,327,921 (GRCm38) |
W136R |
probably damaging |
Het |
Skic3 |
C |
T |
13: 76,182,891 (GRCm38) |
P1480L |
probably damaging |
Het |
Skint10 |
C |
A |
4: 112,715,905 (GRCm38) |
|
probably benign |
Het |
Slc25a13 |
T |
C |
6: 6,117,128 (GRCm38) |
T196A |
probably damaging |
Het |
Slc26a5 |
T |
C |
5: 21,847,232 (GRCm38) |
H33R |
probably damaging |
Het |
Slc27a6 |
T |
C |
18: 58,598,757 (GRCm38) |
|
probably benign |
Het |
Slitrk6 |
A |
T |
14: 110,749,819 (GRCm38) |
Y819N |
probably damaging |
Het |
Spata46 |
C |
T |
1: 170,312,034 (GRCm38) |
Q201* |
probably null |
Het |
Sptbn1 |
A |
T |
11: 30,114,739 (GRCm38) |
V1920E |
probably damaging |
Het |
Taf6l |
A |
G |
19: 8,778,517 (GRCm38) |
F256L |
probably benign |
Het |
Tmco3 |
T |
A |
8: 13,292,039 (GRCm38) |
N104K |
probably damaging |
Het |
Tmem200c |
A |
G |
17: 68,842,254 (GRCm38) |
T611A |
probably damaging |
Het |
Tmem202 |
T |
G |
9: 59,525,372 (GRCm38) |
Y24S |
probably damaging |
Het |
Tpp1 |
A |
G |
7: 105,749,419 (GRCm38) |
L230P |
probably damaging |
Het |
Trim56 |
C |
T |
5: 137,112,992 (GRCm38) |
E557K |
probably benign |
Het |
Trrap |
C |
T |
5: 144,853,499 (GRCm38) |
L3590F |
probably damaging |
Het |
Tulp4 |
A |
G |
17: 6,139,112 (GRCm38) |
T70A |
possibly damaging |
Het |
Vcp |
G |
C |
4: 42,986,201 (GRCm38) |
A297G |
probably benign |
Het |
Vwf |
T |
A |
6: 125,626,271 (GRCm38) |
H861Q |
probably benign |
Het |
Wdr64 |
T |
C |
1: 175,772,185 (GRCm38) |
I536T |
probably benign |
Het |
Zfp72 |
G |
A |
13: 74,376,425 (GRCm38) |
|
probably benign |
Het |
|
Other mutations in Zfp850 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02278:Zfp850
|
APN |
7 |
28,008,397 (GRCm38) |
missense |
probably damaging |
0.96 |
R0610:Zfp850
|
UTSW |
7 |
27,989,394 (GRCm38) |
missense |
probably damaging |
0.99 |
R0690:Zfp850
|
UTSW |
7 |
27,985,217 (GRCm38) |
missense |
possibly damaging |
0.67 |
R1310:Zfp850
|
UTSW |
7 |
27,989,459 (GRCm38) |
missense |
probably benign |
0.40 |
R1594:Zfp850
|
UTSW |
7 |
27,989,391 (GRCm38) |
missense |
probably benign |
0.00 |
R1771:Zfp850
|
UTSW |
7 |
27,985,275 (GRCm38) |
nonsense |
probably null |
|
R2189:Zfp850
|
UTSW |
7 |
27,989,055 (GRCm38) |
missense |
probably benign |
0.02 |
R2192:Zfp850
|
UTSW |
7 |
27,985,195 (GRCm38) |
missense |
probably damaging |
1.00 |
R2417:Zfp850
|
UTSW |
7 |
27,989,183 (GRCm38) |
missense |
possibly damaging |
0.54 |
R4321:Zfp850
|
UTSW |
7 |
27,989,400 (GRCm38) |
missense |
probably damaging |
0.99 |
R4770:Zfp850
|
UTSW |
7 |
27,984,986 (GRCm38) |
splice site |
probably null |
|
R4970:Zfp850
|
UTSW |
7 |
27,990,233 (GRCm38) |
nonsense |
probably null |
|
R5112:Zfp850
|
UTSW |
7 |
27,990,233 (GRCm38) |
nonsense |
probably null |
|
R5166:Zfp850
|
UTSW |
7 |
27,990,356 (GRCm38) |
nonsense |
probably null |
|
R5303:Zfp850
|
UTSW |
7 |
28,008,413 (GRCm38) |
missense |
probably damaging |
1.00 |
R5315:Zfp850
|
UTSW |
7 |
27,990,318 (GRCm38) |
missense |
probably benign |
0.02 |
R5496:Zfp850
|
UTSW |
7 |
28,007,346 (GRCm38) |
missense |
probably damaging |
0.98 |
R5547:Zfp850
|
UTSW |
7 |
27,989,419 (GRCm38) |
missense |
probably damaging |
1.00 |
R5677:Zfp850
|
UTSW |
7 |
27,989,088 (GRCm38) |
missense |
probably damaging |
1.00 |
R5927:Zfp850
|
UTSW |
7 |
27,990,195 (GRCm38) |
missense |
probably benign |
0.17 |
R6654:Zfp850
|
UTSW |
7 |
27,985,215 (GRCm38) |
nonsense |
probably null |
|
R6950:Zfp850
|
UTSW |
7 |
27,990,514 (GRCm38) |
missense |
possibly damaging |
0.86 |
R6987:Zfp850
|
UTSW |
7 |
27,990,001 (GRCm38) |
missense |
probably damaging |
1.00 |
R6990:Zfp850
|
UTSW |
7 |
27,990,376 (GRCm38) |
missense |
probably benign |
0.09 |
R7640:Zfp850
|
UTSW |
7 |
27,989,209 (GRCm38) |
missense |
probably benign |
0.05 |
R7856:Zfp850
|
UTSW |
7 |
27,990,474 (GRCm38) |
missense |
probably benign |
0.02 |
R9498:Zfp850
|
UTSW |
7 |
27,989,850 (GRCm38) |
missense |
possibly damaging |
0.88 |
R9506:Zfp850
|
UTSW |
7 |
27,989,562 (GRCm38) |
missense |
possibly damaging |
0.82 |
Z1186:Zfp850
|
UTSW |
7 |
27,990,279 (GRCm38) |
missense |
probably benign |
0.00 |
Z1186:Zfp850
|
UTSW |
7 |
27,989,124 (GRCm38) |
missense |
probably benign |
0.00 |
|