Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930563M21Rik |
T |
C |
9: 55,890,653 (GRCm39) |
D352G |
probably benign |
Het |
Abi1 |
A |
T |
2: 22,831,989 (GRCm39) |
Y447* |
probably null |
Het |
Acot1 |
A |
G |
12: 84,064,189 (GRCm39) |
Y124C |
|
Het |
Adgrf4 |
T |
C |
17: 42,978,704 (GRCm39) |
N213S |
possibly damaging |
Het |
Alg9 |
T |
A |
9: 50,717,545 (GRCm39) |
Y443N |
probably damaging |
Het |
Bhlhe22 |
A |
G |
3: 18,109,024 (GRCm39) |
T25A |
probably benign |
Het |
Bpifa1 |
C |
A |
2: 153,985,789 (GRCm39) |
P35T |
unknown |
Het |
Btbd16 |
T |
C |
7: 130,381,437 (GRCm39) |
|
probably null |
Het |
Ccdc187 |
G |
T |
2: 26,183,409 (GRCm39) |
T197K |
probably benign |
Het |
Cd209b |
A |
G |
8: 3,968,771 (GRCm39) |
V295A |
probably benign |
Het |
Cdcp3 |
C |
T |
7: 130,824,481 (GRCm39) |
S192L |
possibly damaging |
Het |
Clrn2 |
G |
T |
5: 45,617,518 (GRCm39) |
A130S |
probably benign |
Het |
Cnrip1 |
A |
G |
11: 17,004,740 (GRCm39) |
T97A |
probably damaging |
Het |
Col15a1 |
G |
C |
4: 47,288,200 (GRCm39) |
|
probably benign |
Het |
Col6a5 |
T |
C |
9: 105,758,940 (GRCm39) |
T2089A |
possibly damaging |
Het |
Cyfip1 |
T |
A |
7: 55,523,273 (GRCm39) |
|
probably null |
Het |
Ddx1 |
A |
G |
12: 13,286,119 (GRCm39) |
S278P |
probably benign |
Het |
Dnah12 |
A |
C |
14: 26,445,060 (GRCm39) |
E654D |
probably benign |
Het |
Efcab7 |
T |
C |
4: 99,735,437 (GRCm39) |
S154P |
probably damaging |
Het |
Emcn |
T |
C |
3: 137,047,029 (GRCm39) |
F10S |
probably damaging |
Het |
Fhip2a |
A |
G |
19: 57,373,756 (GRCm39) |
H672R |
probably damaging |
Het |
Flg2 |
G |
T |
3: 93,110,884 (GRCm39) |
A971S |
unknown |
Het |
Gli2 |
A |
T |
1: 118,795,791 (GRCm39) |
H121Q |
probably damaging |
Het |
Gm3633 |
A |
G |
14: 42,460,359 (GRCm39) |
|
probably benign |
Het |
Golga2 |
T |
C |
2: 32,195,822 (GRCm39) |
L846P |
probably damaging |
Het |
Golga7b |
A |
T |
19: 42,255,440 (GRCm39) |
I106F |
probably damaging |
Het |
Hltf |
T |
C |
3: 20,140,280 (GRCm39) |
S460P |
probably benign |
Het |
Hyal5 |
A |
G |
6: 24,876,403 (GRCm39) |
Y92C |
probably damaging |
Het |
Kif19b |
G |
A |
5: 140,468,257 (GRCm39) |
R649Q |
probably benign |
Het |
Mapk1 |
T |
A |
16: 16,853,549 (GRCm39) |
C84S |
probably benign |
Het |
Marchf10 |
A |
G |
11: 105,281,100 (GRCm39) |
V395A |
probably benign |
Het |
Meltf |
A |
G |
16: 31,697,763 (GRCm39) |
T7A |
probably benign |
Het |
Mfhas1 |
T |
A |
8: 36,057,730 (GRCm39) |
V735D |
probably damaging |
Het |
Mia2 |
G |
T |
12: 59,223,150 (GRCm39) |
R486L |
possibly damaging |
Het |
Mmp20 |
T |
C |
9: 7,628,327 (GRCm39) |
L25P |
probably benign |
Het |
Mprip |
C |
T |
11: 59,650,901 (GRCm39) |
T1535I |
possibly damaging |
Het |
Mrpl9 |
T |
A |
3: 94,355,126 (GRCm39) |
S233T |
possibly damaging |
Het |
Muc21 |
T |
A |
17: 35,931,838 (GRCm39) |
S783C |
unknown |
Het |
Nckap5 |
A |
C |
1: 125,942,376 (GRCm39) |
V1576G |
probably benign |
Het |
Ntng1 |
T |
C |
3: 109,841,921 (GRCm39) |
Y284C |
probably damaging |
Het |
Numa1 |
T |
A |
7: 101,650,139 (GRCm39) |
V1290D |
probably damaging |
Het |
Or52l1 |
T |
G |
7: 104,829,587 (GRCm39) |
Y326S |
probably benign |
Het |
Pcdhgc4 |
A |
T |
18: 37,950,264 (GRCm39) |
D560V |
probably damaging |
Het |
Pla2g1b |
A |
G |
5: 115,610,107 (GRCm39) |
K84E |
possibly damaging |
Het |
Pramel16 |
T |
C |
4: 143,675,750 (GRCm39) |
I359V |
probably benign |
Het |
Prrt4 |
C |
T |
6: 29,170,767 (GRCm39) |
A562T |
possibly damaging |
Het |
Rab6a |
T |
C |
7: 100,275,786 (GRCm39) |
F33S |
probably damaging |
Het |
Rgs11 |
A |
G |
17: 26,427,260 (GRCm39) |
Y397C |
probably damaging |
Het |
Ryr1 |
A |
G |
7: 28,785,187 (GRCm39) |
S1842P |
possibly damaging |
Het |
Slc25a34 |
C |
T |
4: 141,350,641 (GRCm39) |
A123T |
probably damaging |
Het |
Smoc2 |
A |
G |
17: 14,556,839 (GRCm39) |
Y96C |
probably damaging |
Het |
Sqle |
A |
G |
15: 59,194,765 (GRCm39) |
E267G |
probably benign |
Het |
Sspo |
G |
A |
6: 48,440,869 (GRCm39) |
R1777H |
possibly damaging |
Het |
Stx6 |
T |
A |
1: 155,067,210 (GRCm39) |
N133K |
probably benign |
Het |
Taf7l2 |
T |
C |
10: 115,948,903 (GRCm39) |
T208A |
probably benign |
Het |
Thoc5 |
A |
T |
11: 4,864,303 (GRCm39) |
Q320L |
probably benign |
Het |
Tmc4 |
G |
C |
7: 3,670,497 (GRCm39) |
C531W |
probably damaging |
Het |
Tmigd1 |
A |
G |
11: 76,801,031 (GRCm39) |
T173A |
probably damaging |
Het |
Tpp2 |
A |
C |
1: 44,031,514 (GRCm39) |
M1111L |
probably benign |
Het |
Ttc21a |
T |
C |
9: 119,772,941 (GRCm39) |
V206A |
probably benign |
Het |
Ulk1 |
A |
T |
5: 110,936,663 (GRCm39) |
V758E |
possibly damaging |
Het |
Vdr |
T |
A |
15: 97,767,600 (GRCm39) |
H130L |
probably benign |
Het |
Vps13b |
A |
G |
15: 35,623,892 (GRCm39) |
T1270A |
probably damaging |
Het |
Zc3h13 |
A |
G |
14: 75,560,991 (GRCm39) |
D527G |
unknown |
Het |
Zfp512 |
C |
T |
5: 31,637,434 (GRCm39) |
R508W |
probably damaging |
Het |
Zfp606 |
A |
G |
7: 12,215,026 (GRCm39) |
T85A |
unknown |
Het |
|
Other mutations in Rnf43 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01077:Rnf43
|
APN |
11 |
87,622,718 (GRCm39) |
missense |
probably benign |
0.15 |
IGL01520:Rnf43
|
APN |
11 |
87,555,542 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01541:Rnf43
|
APN |
11 |
87,621,046 (GRCm39) |
missense |
probably null |
1.00 |
IGL01784:Rnf43
|
APN |
11 |
87,622,632 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL02037:Rnf43
|
APN |
11 |
87,622,479 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02725:Rnf43
|
APN |
11 |
87,622,411 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03062:Rnf43
|
APN |
11 |
87,623,130 (GRCm39) |
nonsense |
probably null |
|
R0226:Rnf43
|
UTSW |
11 |
87,622,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R0391:Rnf43
|
UTSW |
11 |
87,622,108 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0834:Rnf43
|
UTSW |
11 |
87,622,077 (GRCm39) |
missense |
probably benign |
|
R1163:Rnf43
|
UTSW |
11 |
87,620,339 (GRCm39) |
missense |
probably damaging |
0.98 |
R1203:Rnf43
|
UTSW |
11 |
87,618,301 (GRCm39) |
splice site |
probably benign |
|
R1314:Rnf43
|
UTSW |
11 |
87,623,145 (GRCm39) |
missense |
probably benign |
|
R1404:Rnf43
|
UTSW |
11 |
87,625,003 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1404:Rnf43
|
UTSW |
11 |
87,625,003 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1469:Rnf43
|
UTSW |
11 |
87,622,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Rnf43
|
UTSW |
11 |
87,622,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R1511:Rnf43
|
UTSW |
11 |
87,622,173 (GRCm39) |
missense |
probably benign |
0.00 |
R1513:Rnf43
|
UTSW |
11 |
87,620,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R1614:Rnf43
|
UTSW |
11 |
87,622,485 (GRCm39) |
nonsense |
probably null |
|
R1615:Rnf43
|
UTSW |
11 |
87,622,485 (GRCm39) |
nonsense |
probably null |
|
R2341:Rnf43
|
UTSW |
11 |
87,622,851 (GRCm39) |
missense |
probably damaging |
0.96 |
R2410:Rnf43
|
UTSW |
11 |
87,623,085 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2847:Rnf43
|
UTSW |
11 |
87,623,093 (GRCm39) |
missense |
probably benign |
0.04 |
R2849:Rnf43
|
UTSW |
11 |
87,623,093 (GRCm39) |
missense |
probably benign |
0.04 |
R5567:Rnf43
|
UTSW |
11 |
87,618,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R5943:Rnf43
|
UTSW |
11 |
87,622,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R6135:Rnf43
|
UTSW |
11 |
87,622,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R6452:Rnf43
|
UTSW |
11 |
87,623,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R6511:Rnf43
|
UTSW |
11 |
87,622,989 (GRCm39) |
missense |
probably benign |
0.01 |
R7426:Rnf43
|
UTSW |
11 |
87,622,678 (GRCm39) |
missense |
probably benign |
0.03 |
R7528:Rnf43
|
UTSW |
11 |
87,622,954 (GRCm39) |
missense |
probably benign |
0.00 |
R8029:Rnf43
|
UTSW |
11 |
87,622,720 (GRCm39) |
missense |
probably benign |
0.06 |
R8167:Rnf43
|
UTSW |
11 |
87,618,232 (GRCm39) |
missense |
probably benign |
0.03 |
R8174:Rnf43
|
UTSW |
11 |
87,622,057 (GRCm39) |
missense |
probably benign |
0.39 |
R8498:Rnf43
|
UTSW |
11 |
87,618,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R8905:Rnf43
|
UTSW |
11 |
87,621,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R9562:Rnf43
|
UTSW |
11 |
87,618,891 (GRCm39) |
missense |
probably benign |
0.03 |
X0064:Rnf43
|
UTSW |
11 |
87,618,168 (GRCm39) |
missense |
probably benign |
0.11 |
|