Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankib1 |
A |
G |
5: 3,743,855 (GRCm39) |
S812P |
possibly damaging |
Het |
Atp2c2 |
A |
G |
8: 120,453,093 (GRCm39) |
E159G |
probably benign |
Het |
Atrn |
A |
G |
2: 130,821,889 (GRCm39) |
I861V |
probably damaging |
Het |
Clip1 |
A |
G |
5: 123,741,717 (GRCm39) |
V1053A |
possibly damaging |
Het |
Cngb1 |
C |
A |
8: 95,975,608 (GRCm39) |
G629C |
probably damaging |
Het |
Cntn5 |
A |
T |
9: 9,743,657 (GRCm39) |
F540Y |
probably damaging |
Het |
Cpb1 |
A |
C |
3: 20,329,748 (GRCm39) |
|
probably null |
Het |
Cyp4a14 |
A |
G |
4: 115,353,280 (GRCm39) |
Y11H |
probably benign |
Het |
Dact2 |
A |
G |
17: 14,419,450 (GRCm39) |
S103P |
probably damaging |
Het |
Dcstamp |
A |
T |
15: 39,618,317 (GRCm39) |
Y242F |
probably benign |
Het |
Drd3 |
G |
T |
16: 43,641,670 (GRCm39) |
G329* |
probably null |
Het |
Duxf1 |
T |
C |
10: 58,059,494 (GRCm39) |
|
probably benign |
Het |
Dysf |
T |
A |
6: 83,985,945 (GRCm39) |
S17T |
probably benign |
Het |
Eno1 |
A |
T |
4: 150,333,009 (GRCm39) |
K366N |
possibly damaging |
Het |
Ffar2 |
C |
T |
7: 30,518,971 (GRCm39) |
V190I |
probably benign |
Het |
Fkbp15 |
T |
C |
4: 62,242,429 (GRCm39) |
T508A |
probably damaging |
Het |
Fndc1 |
A |
G |
17: 7,988,567 (GRCm39) |
V1165A |
unknown |
Het |
Foxj3 |
A |
T |
4: 119,430,945 (GRCm39) |
|
probably null |
Het |
Gabarap |
T |
C |
11: 69,882,630 (GRCm39) |
|
probably null |
Het |
Gm19410 |
T |
A |
8: 36,270,736 (GRCm39) |
L1221* |
probably null |
Het |
Gpat2 |
G |
C |
2: 127,273,838 (GRCm39) |
G294R |
possibly damaging |
Het |
Igf1r |
A |
T |
7: 67,850,998 (GRCm39) |
Y931F |
probably benign |
Het |
Il23r |
A |
T |
6: 67,400,636 (GRCm39) |
S565T |
probably damaging |
Het |
Ipo8 |
A |
T |
6: 148,717,995 (GRCm39) |
Y209* |
probably null |
Het |
Jph2 |
C |
T |
2: 163,181,632 (GRCm39) |
G511R |
probably benign |
Het |
Khdrbs1 |
C |
A |
4: 129,635,890 (GRCm39) |
D22Y |
probably damaging |
Het |
Kif5b |
A |
T |
18: 6,212,562 (GRCm39) |
L754Q |
probably damaging |
Het |
Ksr1 |
C |
T |
11: 78,927,320 (GRCm39) |
|
probably null |
Het |
L3mbtl4 |
G |
T |
17: 69,084,918 (GRCm39) |
V610F |
probably benign |
Het |
Lars2 |
A |
G |
9: 123,283,825 (GRCm39) |
T698A |
probably benign |
Het |
Lonp1 |
A |
G |
17: 56,928,961 (GRCm39) |
V267A |
possibly damaging |
Het |
Loxhd1 |
T |
A |
18: 77,468,128 (GRCm39) |
D925E |
probably damaging |
Het |
Lsg1 |
A |
G |
16: 30,393,386 (GRCm39) |
L187P |
possibly damaging |
Het |
Mki67 |
A |
T |
7: 135,298,050 (GRCm39) |
V2328E |
possibly damaging |
Het |
Mlh3 |
A |
G |
12: 85,315,271 (GRCm39) |
I305T |
probably damaging |
Het |
Mtbp |
A |
G |
15: 55,421,016 (GRCm39) |
M1V |
probably null |
Het |
Myadml2 |
C |
A |
11: 120,538,538 (GRCm39) |
C99F |
probably benign |
Het |
Ncbp1 |
A |
G |
4: 46,150,703 (GRCm39) |
Y185C |
probably damaging |
Het |
Ndufaf7 |
A |
T |
17: 79,250,739 (GRCm39) |
Q222L |
probably null |
Het |
Nlrp4b |
A |
T |
7: 10,449,339 (GRCm39) |
Y147F |
probably benign |
Het |
Or4c11c |
C |
T |
2: 88,661,613 (GRCm39) |
R51* |
probably null |
Het |
Pet100 |
T |
C |
8: 3,672,370 (GRCm39) |
V15A |
probably benign |
Het |
Pot1a |
A |
G |
6: 25,778,869 (GRCm39) |
V75A |
probably benign |
Het |
Ptprs |
A |
T |
17: 56,725,935 (GRCm39) |
M1043K |
probably damaging |
Het |
Rnf31 |
A |
G |
14: 55,832,984 (GRCm39) |
T413A |
probably damaging |
Het |
Rsf1 |
ATGGCG |
ATGGCGACGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Homo |
Rsf1 |
CG |
CGACGGCGGTG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Rubcnl |
A |
T |
14: 75,287,635 (GRCm39) |
|
probably null |
Het |
Ryr3 |
A |
T |
2: 112,462,530 (GRCm39) |
C4839S |
probably damaging |
Het |
Scai |
A |
C |
2: 38,992,340 (GRCm39) |
D379E |
probably benign |
Het |
Scd2 |
G |
T |
19: 44,288,198 (GRCm39) |
G197* |
probably null |
Het |
Sdr39u1 |
A |
C |
14: 56,135,166 (GRCm39) |
I259S |
probably benign |
Het |
Slco1a5 |
A |
T |
6: 142,187,906 (GRCm39) |
|
probably null |
Het |
Sp1 |
A |
T |
15: 102,339,318 (GRCm39) |
T733S |
probably benign |
Het |
Tecta |
A |
G |
9: 42,255,051 (GRCm39) |
S1711P |
probably damaging |
Het |
Tedc1 |
G |
T |
12: 113,124,975 (GRCm39) |
W240L |
probably damaging |
Het |
Trarg1 |
T |
C |
11: 76,571,355 (GRCm39) |
S124P |
probably damaging |
Het |
Trim50 |
A |
G |
5: 135,382,454 (GRCm39) |
K102R |
probably benign |
Het |
Utrn |
A |
G |
10: 12,619,827 (GRCm39) |
Y278H |
probably damaging |
Het |
Vinac1 |
T |
A |
2: 128,878,731 (GRCm39) |
D1065V |
unknown |
Het |
Vmn2r109 |
A |
C |
17: 20,784,796 (GRCm39) |
|
probably null |
Het |
Zbed5 |
T |
C |
5: 129,932,210 (GRCm39) |
S720P |
possibly damaging |
Het |
Zscan4-ps1 |
C |
T |
7: 10,802,418 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Zc3h3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00321:Zc3h3
|
APN |
15 |
75,651,162 (GRCm39) |
missense |
probably damaging |
1.00 |
1mM(1):Zc3h3
|
UTSW |
15 |
75,712,414 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0477:Zc3h3
|
UTSW |
15 |
75,648,932 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0843:Zc3h3
|
UTSW |
15 |
75,709,328 (GRCm39) |
missense |
probably benign |
0.00 |
R1891:Zc3h3
|
UTSW |
15 |
75,628,780 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1918:Zc3h3
|
UTSW |
15 |
75,648,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R2009:Zc3h3
|
UTSW |
15 |
75,651,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R2257:Zc3h3
|
UTSW |
15 |
75,711,415 (GRCm39) |
missense |
possibly damaging |
0.77 |
R3853:Zc3h3
|
UTSW |
15 |
75,709,346 (GRCm39) |
missense |
probably benign |
0.03 |
R5130:Zc3h3
|
UTSW |
15 |
75,651,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R5160:Zc3h3
|
UTSW |
15 |
75,681,512 (GRCm39) |
missense |
probably benign |
0.02 |
R5164:Zc3h3
|
UTSW |
15 |
75,648,875 (GRCm39) |
missense |
probably benign |
0.02 |
R5279:Zc3h3
|
UTSW |
15 |
75,711,439 (GRCm39) |
missense |
probably benign |
0.08 |
R5622:Zc3h3
|
UTSW |
15 |
75,648,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R5743:Zc3h3
|
UTSW |
15 |
75,651,380 (GRCm39) |
nonsense |
probably null |
|
R5923:Zc3h3
|
UTSW |
15 |
75,657,413 (GRCm39) |
missense |
probably damaging |
0.99 |
R6294:Zc3h3
|
UTSW |
15 |
75,681,417 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6735:Zc3h3
|
UTSW |
15 |
75,628,483 (GRCm39) |
missense |
probably benign |
0.00 |
R7043:Zc3h3
|
UTSW |
15 |
75,681,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R7231:Zc3h3
|
UTSW |
15 |
75,712,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R8974:Zc3h3
|
UTSW |
15 |
75,657,452 (GRCm39) |
missense |
probably benign |
0.00 |
R9038:Zc3h3
|
UTSW |
15 |
75,711,237 (GRCm39) |
missense |
probably benign |
0.01 |
R9068:Zc3h3
|
UTSW |
15 |
75,711,499 (GRCm39) |
missense |
probably benign |
|
R9557:Zc3h3
|
UTSW |
15 |
75,711,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R9567:Zc3h3
|
UTSW |
15 |
75,651,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R9681:Zc3h3
|
UTSW |
15 |
75,681,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R9765:Zc3h3
|
UTSW |
15 |
75,709,459 (GRCm39) |
missense |
probably benign |
0.04 |
R9782:Zc3h3
|
UTSW |
15 |
75,681,489 (GRCm39) |
missense |
probably damaging |
1.00 |
|