Other mutations in this stock |
Total: 115 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
A |
T |
3: 124,210,482 (GRCm39) |
H143Q |
probably benign |
Het |
Abca3 |
C |
T |
17: 24,593,274 (GRCm39) |
R224C |
probably damaging |
Het |
Adcy8 |
A |
T |
15: 64,659,207 (GRCm39) |
W528R |
probably damaging |
Het |
Agbl1 |
A |
G |
7: 76,071,665 (GRCm39) |
E329G |
probably damaging |
Het |
Agbl5 |
G |
A |
5: 31,060,403 (GRCm39) |
R141Q |
probably damaging |
Het |
Ampd2 |
A |
T |
3: 107,986,549 (GRCm39) |
M245K |
probably damaging |
Het |
Apob |
G |
A |
12: 8,055,219 (GRCm39) |
|
probably null |
Het |
Apool |
C |
T |
X: 111,259,540 (GRCm39) |
Q60* |
probably null |
Het |
Aqp1 |
A |
T |
6: 55,322,520 (GRCm39) |
I172F |
probably damaging |
Het |
Atp7a |
A |
G |
X: 105,153,374 (GRCm39) |
D1092G |
probably benign |
Het |
Ccdc83 |
A |
T |
7: 89,899,737 (GRCm39) |
F45Y |
probably damaging |
Het |
Cct8l1 |
G |
A |
5: 25,721,881 (GRCm39) |
V199I |
probably benign |
Het |
Cdc23 |
C |
A |
18: 34,784,742 (GRCm39) |
V7L |
unknown |
Het |
Cdc25a |
T |
A |
9: 109,713,208 (GRCm39) |
C227S |
possibly damaging |
Het |
Ces1a |
A |
G |
8: 93,759,303 (GRCm39) |
S278P |
possibly damaging |
Het |
Cfap65 |
A |
T |
1: 74,962,137 (GRCm39) |
S695T |
probably benign |
Het |
Col13a1 |
A |
G |
10: 61,709,797 (GRCm39) |
|
silent |
Het |
Ctps1 |
A |
T |
4: 120,411,170 (GRCm39) |
L282Q |
probably damaging |
Het |
Cyp2a22 |
A |
T |
7: 26,631,906 (GRCm39) |
F450Y |
probably benign |
Het |
Cyp2d10 |
C |
T |
15: 82,287,954 (GRCm39) |
R383H |
probably benign |
Het |
Dennd3 |
G |
A |
15: 73,419,144 (GRCm39) |
R645H |
probably damaging |
Het |
Dnaaf5 |
G |
T |
5: 139,159,962 (GRCm39) |
R620L |
probably damaging |
Het |
Dnah11 |
A |
T |
12: 118,046,188 (GRCm39) |
L1750* |
probably null |
Het |
Dnah9 |
A |
G |
11: 65,740,866 (GRCm39) |
F4107L |
probably damaging |
Het |
Dnaja3 |
A |
T |
16: 4,514,289 (GRCm39) |
T274S |
probably damaging |
Het |
Dot1l |
A |
G |
10: 80,620,480 (GRCm39) |
D514G |
possibly damaging |
Het |
Dst |
A |
C |
1: 34,334,344 (GRCm39) |
K4857N |
probably damaging |
Het |
Dysf |
A |
T |
6: 84,114,254 (GRCm39) |
K1226M |
probably damaging |
Het |
Enpep |
T |
A |
3: 129,097,404 (GRCm39) |
Q409L |
probably damaging |
Het |
Fign |
A |
T |
2: 63,810,037 (GRCm39) |
L411* |
probably null |
Het |
Flt1 |
C |
A |
5: 147,620,749 (GRCm39) |
A132S |
probably benign |
Het |
Fryl |
G |
A |
5: 73,232,110 (GRCm39) |
P1550L |
probably damaging |
Het |
Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,266,820 (GRCm39) |
|
probably benign |
Het |
H2ab3 |
T |
C |
X: 119,222,543 (GRCm39) |
T84A |
probably damaging |
Het |
Hal |
A |
T |
10: 93,349,904 (GRCm39) |
I555F |
probably damaging |
Het |
Hibadh |
C |
T |
6: 52,597,079 (GRCm39) |
V122M |
possibly damaging |
Het |
Ifi44 |
T |
C |
3: 151,455,269 (GRCm39) |
|
probably benign |
Het |
Ifi47 |
A |
G |
11: 48,986,361 (GRCm39) |
T43A |
probably benign |
Het |
Inf2 |
A |
T |
12: 112,578,473 (GRCm39) |
|
probably null |
Het |
Itga10 |
C |
T |
3: 96,559,527 (GRCm39) |
Q475* |
probably null |
Het |
Itga6 |
T |
A |
2: 71,656,779 (GRCm39) |
D344E |
probably benign |
Het |
Kcnmb4 |
T |
C |
10: 116,309,102 (GRCm39) |
T109A |
probably benign |
Het |
Kif19a |
G |
A |
11: 114,658,053 (GRCm39) |
M37I |
probably benign |
Het |
Kiss1r |
C |
A |
10: 79,754,596 (GRCm39) |
S30* |
probably null |
Het |
Lrrc66 |
G |
A |
5: 73,765,354 (GRCm39) |
P563L |
probably damaging |
Het |
Mamdc2 |
T |
C |
19: 23,356,160 (GRCm39) |
D96G |
probably benign |
Het |
Map3k12 |
A |
T |
15: 102,410,267 (GRCm39) |
|
probably null |
Het |
Mc3r |
A |
T |
2: 172,091,533 (GRCm39) |
I252F |
possibly damaging |
Het |
Metrn |
C |
T |
17: 26,015,613 (GRCm39) |
G34D |
probably damaging |
Het |
Mipep |
A |
G |
14: 61,046,462 (GRCm39) |
E328G |
probably benign |
Het |
Mrtfa |
A |
G |
15: 80,906,627 (GRCm39) |
V91A |
probably damaging |
Het |
Muc5b |
A |
T |
7: 141,412,999 (GRCm39) |
T1982S |
unknown |
Het |
Myh8 |
A |
T |
11: 67,196,742 (GRCm39) |
T1792S |
possibly damaging |
Het |
Myo1a |
T |
C |
10: 127,543,288 (GRCm39) |
|
probably null |
Het |
Myo5a |
T |
A |
9: 75,081,438 (GRCm39) |
S1008T |
probably benign |
Het |
Ncald |
A |
T |
15: 37,397,478 (GRCm39) |
H67Q |
probably damaging |
Het |
Nudt5 |
T |
A |
2: 5,869,198 (GRCm39) |
H141Q |
probably benign |
Het |
Numbl |
G |
A |
7: 26,980,415 (GRCm39) |
D466N |
probably damaging |
Het |
Nup210 |
T |
A |
6: 91,032,309 (GRCm39) |
I20F |
probably benign |
Het |
Odad1 |
T |
A |
7: 45,578,514 (GRCm39) |
M29K |
probably benign |
Het |
Or10ak12 |
A |
C |
4: 118,666,057 (GRCm39) |
W319G |
possibly damaging |
Het |
Or10p21 |
T |
C |
10: 128,847,213 (GRCm39) |
Y20H |
possibly damaging |
Het |
Or14c46 |
A |
G |
7: 85,918,799 (GRCm39) |
I66T |
probably damaging |
Het |
Or51l14 |
A |
T |
7: 103,100,617 (GRCm39) |
E24D |
probably benign |
Het |
Or52e8b |
A |
T |
7: 104,673,260 (GRCm39) |
M309K |
probably benign |
Het |
Or52n2c |
A |
C |
7: 104,574,700 (GRCm39) |
N90K |
probably benign |
Het |
Or7h8 |
A |
T |
9: 20,123,878 (GRCm39) |
I78F |
possibly damaging |
Het |
Or8h10 |
A |
T |
2: 86,808,666 (GRCm39) |
V158D |
possibly damaging |
Het |
Papolg |
G |
A |
11: 23,817,331 (GRCm39) |
T153I |
possibly damaging |
Het |
Pappa |
A |
G |
4: 65,123,365 (GRCm39) |
H900R |
probably benign |
Het |
Pcdh17 |
T |
C |
14: 84,770,782 (GRCm39) |
S1087P |
probably benign |
Het |
Phf11a |
T |
G |
14: 59,521,849 (GRCm39) |
L107F |
possibly damaging |
Het |
Phlpp2 |
A |
T |
8: 110,652,461 (GRCm39) |
I602F |
probably damaging |
Het |
Pik3c2g |
T |
A |
6: 139,665,873 (GRCm39) |
C65S |
probably null |
Het |
Pilra |
A |
G |
5: 137,833,674 (GRCm39) |
F131L |
probably damaging |
Het |
Pomt2 |
A |
C |
12: 87,180,234 (GRCm39) |
C256G |
probably damaging |
Het |
Ppl |
A |
T |
16: 4,906,742 (GRCm39) |
S1184R |
probably benign |
Het |
Prkaa1 |
G |
T |
15: 5,206,392 (GRCm39) |
R416L |
possibly damaging |
Het |
Prkdc |
C |
A |
16: 15,589,912 (GRCm39) |
R2592S |
probably damaging |
Het |
Prmt2 |
C |
T |
10: 76,058,390 (GRCm39) |
V140I |
probably damaging |
Het |
Prodh |
A |
T |
16: 17,895,653 (GRCm39) |
|
probably null |
Het |
Psg29 |
T |
A |
7: 16,945,763 (GRCm39) |
D444E |
probably damaging |
Het |
Ptgs1 |
A |
T |
2: 36,141,272 (GRCm39) |
N573I |
probably damaging |
Het |
Rbm38 |
C |
T |
2: 172,863,875 (GRCm39) |
P15S |
probably benign |
Het |
Riox2 |
T |
C |
16: 59,312,236 (GRCm39) |
S458P |
possibly damaging |
Het |
Rnase4 |
T |
C |
14: 51,342,702 (GRCm39) |
V142A |
possibly damaging |
Het |
Rnf138 |
A |
G |
18: 21,159,204 (GRCm39) |
N244S |
probably benign |
Het |
Rnf40 |
T |
C |
7: 127,196,458 (GRCm39) |
L802P |
probably damaging |
Het |
Sfxn4 |
C |
T |
19: 60,839,450 (GRCm39) |
V203M |
probably damaging |
Het |
Skor2 |
G |
T |
18: 76,946,649 (GRCm39) |
E124* |
probably null |
Het |
Slc4a2 |
G |
A |
5: 24,643,760 (GRCm39) |
S855N |
probably benign |
Het |
Slc8a2 |
T |
C |
7: 15,884,508 (GRCm39) |
L626P |
possibly damaging |
Het |
Slco4c1 |
G |
A |
1: 96,768,953 (GRCm39) |
P303L |
probably damaging |
Het |
Slirp |
A |
G |
12: 87,490,784 (GRCm39) |
T29A |
probably damaging |
Het |
Snrpd3 |
G |
T |
10: 75,355,227 (GRCm39) |
C20F |
possibly damaging |
Het |
Spag17 |
T |
A |
3: 99,987,434 (GRCm39) |
Y1575N |
possibly damaging |
Het |
St8sia4 |
G |
A |
1: 95,594,910 (GRCm39) |
A26V |
probably benign |
Het |
Stab2 |
A |
T |
10: 86,699,422 (GRCm39) |
I481N |
probably benign |
Het |
Tenm2 |
T |
A |
11: 35,959,208 (GRCm39) |
T1114S |
probably damaging |
Het |
Tgm1 |
A |
G |
14: 55,947,392 (GRCm39) |
V323A |
probably damaging |
Het |
Tmco4 |
A |
G |
4: 138,785,433 (GRCm39) |
H501R |
probably damaging |
Het |
Tob1 |
A |
T |
11: 94,104,567 (GRCm39) |
R34S |
possibly damaging |
Het |
Trhr2 |
C |
T |
8: 123,084,110 (GRCm39) |
V297I |
probably benign |
Het |
Trim30d |
A |
C |
7: 104,137,165 (GRCm39) |
V13G |
probably damaging |
Het |
Trpm3 |
T |
C |
19: 22,862,713 (GRCm39) |
V485A |
possibly damaging |
Het |
Trrap |
T |
C |
5: 144,787,989 (GRCm39) |
I3518T |
probably damaging |
Het |
Ttc27 |
T |
C |
17: 75,054,750 (GRCm39) |
L352P |
probably damaging |
Het |
Ush1g |
A |
G |
11: 115,209,123 (GRCm39) |
L357P |
possibly damaging |
Het |
Usp24 |
A |
G |
4: 106,277,644 (GRCm39) |
H2258R |
probably benign |
Het |
Vcam1 |
A |
G |
3: 115,918,037 (GRCm39) |
V308A |
probably damaging |
Het |
Vdr |
A |
G |
15: 97,755,459 (GRCm39) |
S355P |
probably benign |
Het |
Vldlr |
T |
C |
19: 27,215,677 (GRCm39) |
S184P |
probably damaging |
Het |
Xpo4 |
C |
A |
14: 57,822,098 (GRCm39) |
A1073S |
probably benign |
Het |
Zfand2b |
A |
G |
1: 75,147,634 (GRCm39) |
D224G |
probably benign |
Het |
Zfp263 |
A |
G |
16: 3,564,704 (GRCm39) |
R240G |
possibly damaging |
Het |
|
Other mutations in Hsd3b3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01551:Hsd3b3
|
APN |
3 |
98,649,216 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01776:Hsd3b3
|
APN |
3 |
98,651,163 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02189:Hsd3b3
|
APN |
3 |
98,649,454 (GRCm39) |
missense |
probably benign |
|
R0689:Hsd3b3
|
UTSW |
3 |
98,649,295 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0893:Hsd3b3
|
UTSW |
3 |
98,649,757 (GRCm39) |
splice site |
probably null |
|
R1759:Hsd3b3
|
UTSW |
3 |
98,649,399 (GRCm39) |
missense |
probably damaging |
0.96 |
R2008:Hsd3b3
|
UTSW |
3 |
98,649,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R3931:Hsd3b3
|
UTSW |
3 |
98,649,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R4614:Hsd3b3
|
UTSW |
3 |
98,649,396 (GRCm39) |
missense |
probably benign |
0.03 |
R4664:Hsd3b3
|
UTSW |
3 |
98,649,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R4749:Hsd3b3
|
UTSW |
3 |
98,649,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R4766:Hsd3b3
|
UTSW |
3 |
98,649,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R4876:Hsd3b3
|
UTSW |
3 |
98,649,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R5622:Hsd3b3
|
UTSW |
3 |
98,649,524 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6280:Hsd3b3
|
UTSW |
3 |
98,660,621 (GRCm39) |
splice site |
probably null |
|
R6348:Hsd3b3
|
UTSW |
3 |
98,663,265 (GRCm39) |
splice site |
probably null |
|
R7070:Hsd3b3
|
UTSW |
3 |
98,649,787 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7283:Hsd3b3
|
UTSW |
3 |
98,649,673 (GRCm39) |
nonsense |
probably null |
|
R7747:Hsd3b3
|
UTSW |
3 |
98,651,214 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8054:Hsd3b3
|
UTSW |
3 |
98,649,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R8553:Hsd3b3
|
UTSW |
3 |
98,651,205 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9130:Hsd3b3
|
UTSW |
3 |
98,651,211 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9164:Hsd3b3
|
UTSW |
3 |
98,660,689 (GRCm39) |
missense |
probably benign |
0.00 |
R9333:Hsd3b3
|
UTSW |
3 |
98,649,216 (GRCm39) |
missense |
probably benign |
0.09 |
Z1176:Hsd3b3
|
UTSW |
3 |
98,651,276 (GRCm39) |
missense |
probably benign |
0.01 |
|