Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam3 |
A |
T |
8: 25,193,819 (GRCm39) |
C398S |
probably damaging |
Het |
Adamts10 |
A |
G |
17: 33,756,304 (GRCm39) |
K316E |
possibly damaging |
Het |
Ap1m1 |
T |
C |
8: 73,006,717 (GRCm39) |
F238L |
possibly damaging |
Het |
Aph1a |
T |
A |
3: 95,803,088 (GRCm39) |
D180E |
probably benign |
Het |
Atp9b |
A |
G |
18: 80,935,093 (GRCm39) |
F201L |
probably benign |
Het |
Btbd9 |
A |
C |
17: 30,704,561 (GRCm39) |
|
probably benign |
Het |
C2cd5 |
T |
C |
6: 142,975,910 (GRCm39) |
T768A |
probably benign |
Het |
Casq1 |
C |
T |
1: 172,037,965 (GRCm39) |
|
probably benign |
Het |
Cimap2 |
C |
A |
4: 106,467,612 (GRCm39) |
M341I |
probably benign |
Het |
Cltc |
A |
T |
11: 86,617,196 (GRCm39) |
M351K |
probably benign |
Het |
Cnp |
A |
G |
11: 100,469,877 (GRCm39) |
E271G |
possibly damaging |
Het |
Col22a1 |
T |
C |
15: 71,845,544 (GRCm39) |
D406G |
possibly damaging |
Het |
Cylc2 |
T |
C |
4: 51,228,279 (GRCm39) |
S117P |
probably benign |
Het |
Cyp2b13 |
T |
C |
7: 25,761,072 (GRCm39) |
L43P |
probably damaging |
Het |
Cyp3a16 |
A |
G |
5: 145,373,267 (GRCm39) |
V500A |
probably benign |
Het |
Dclk2 |
T |
C |
3: 86,743,683 (GRCm39) |
D262G |
probably damaging |
Het |
Dcun1d3 |
A |
C |
7: 119,458,742 (GRCm39) |
Y98D |
probably damaging |
Het |
Ddx39b |
A |
G |
17: 35,472,464 (GRCm39) |
*429W |
probably null |
Het |
Dennd5b |
T |
C |
6: 148,908,335 (GRCm39) |
N986S |
probably damaging |
Het |
Dipk1a |
T |
C |
5: 108,057,982 (GRCm39) |
|
probably null |
Het |
Dusp9 |
G |
A |
X: 72,684,378 (GRCm39) |
R182Q |
probably benign |
Het |
Ecpas |
A |
T |
4: 58,834,523 (GRCm39) |
I785N |
possibly damaging |
Het |
Edil3 |
A |
G |
13: 89,437,589 (GRCm39) |
K397E |
probably damaging |
Het |
Ehd1 |
T |
C |
19: 6,326,994 (GRCm39) |
|
probably benign |
Het |
Fam13a |
A |
T |
6: 58,964,152 (GRCm39) |
H93Q |
probably benign |
Het |
Farp1 |
T |
C |
14: 121,513,716 (GRCm39) |
I837T |
possibly damaging |
Het |
Fbxl5 |
T |
A |
5: 43,922,771 (GRCm39) |
I216F |
probably damaging |
Het |
Gadl1 |
G |
A |
9: 115,770,408 (GRCm39) |
E74K |
probably damaging |
Het |
Gnpnat1 |
A |
G |
14: 45,618,436 (GRCm39) |
V122A |
probably damaging |
Het |
Hdac10 |
C |
T |
15: 89,011,036 (GRCm39) |
|
probably benign |
Het |
Heatr5b |
T |
C |
17: 79,128,130 (GRCm39) |
S502G |
possibly damaging |
Het |
Hr |
C |
A |
14: 70,801,013 (GRCm39) |
A695E |
probably damaging |
Het |
Ift80 |
A |
T |
3: 68,825,870 (GRCm39) |
I490N |
possibly damaging |
Het |
Ipo11 |
A |
G |
13: 106,970,692 (GRCm39) |
|
probably benign |
Het |
Iqch |
T |
G |
9: 63,432,195 (GRCm39) |
Y400S |
probably damaging |
Het |
Jag2 |
C |
T |
12: 112,877,266 (GRCm39) |
D702N |
probably benign |
Het |
Kiss1r |
T |
A |
10: 79,757,624 (GRCm39) |
L326Q |
probably damaging |
Het |
Lrrc42 |
A |
T |
4: 107,104,746 (GRCm39) |
I73N |
probably damaging |
Het |
Lrrc55 |
C |
T |
2: 85,026,880 (GRCm39) |
G48D |
possibly damaging |
Het |
Lrrk2 |
T |
C |
15: 91,649,884 (GRCm39) |
S1674P |
probably damaging |
Het |
Mctp2 |
A |
G |
7: 71,739,942 (GRCm39) |
L816P |
probably damaging |
Het |
Mkrn3 |
C |
T |
7: 62,069,452 (GRCm39) |
R113H |
probably damaging |
Het |
Mmp1b |
A |
G |
9: 7,370,849 (GRCm39) |
V302A |
probably benign |
Het |
Msc |
A |
T |
1: 14,826,053 (GRCm39) |
|
probably null |
Het |
Msmo1 |
C |
A |
8: 65,180,888 (GRCm39) |
V9L |
probably benign |
Het |
Nbeal2 |
G |
A |
9: 110,461,072 (GRCm39) |
R1630C |
probably damaging |
Het |
Nlgn1 |
C |
T |
3: 26,187,850 (GRCm39) |
V12I |
possibly damaging |
Het |
Npas3 |
T |
C |
12: 54,108,915 (GRCm39) |
|
probably null |
Het |
Nr2e3 |
A |
G |
9: 59,856,355 (GRCm39) |
|
probably benign |
Het |
Oca2 |
C |
T |
7: 55,978,560 (GRCm39) |
A576V |
probably benign |
Het |
Or5b21 |
T |
A |
19: 12,839,596 (GRCm39) |
C152* |
probably null |
Het |
Or6d12 |
T |
C |
6: 116,493,409 (GRCm39) |
Y224H |
probably damaging |
Het |
Or6z7 |
T |
C |
7: 6,484,045 (GRCm39) |
T37A |
probably benign |
Het |
Parp6 |
A |
G |
9: 59,548,383 (GRCm39) |
|
probably null |
Het |
Pate13 |
T |
A |
9: 35,820,287 (GRCm39) |
C4S |
probably damaging |
Het |
Phlpp1 |
A |
T |
1: 106,267,231 (GRCm39) |
M715L |
probably benign |
Het |
Pi4k2a |
G |
A |
19: 42,101,544 (GRCm39) |
|
probably null |
Het |
Pik3ap1 |
A |
G |
19: 41,316,348 (GRCm39) |
S305P |
probably damaging |
Het |
Plcg2 |
G |
A |
8: 118,231,054 (GRCm39) |
M45I |
probably benign |
Het |
Ppm1m |
A |
T |
9: 106,073,601 (GRCm39) |
L317H |
probably damaging |
Het |
Ppp1r21 |
T |
G |
17: 88,866,227 (GRCm39) |
M341R |
probably benign |
Het |
Prdx3 |
A |
G |
19: 60,853,674 (GRCm39) |
V217A |
possibly damaging |
Het |
Ptk2b |
A |
G |
14: 66,400,496 (GRCm39) |
V773A |
possibly damaging |
Het |
Raly |
T |
C |
2: 154,699,376 (GRCm39) |
V60A |
probably damaging |
Het |
Reps1 |
A |
G |
10: 17,990,148 (GRCm39) |
D420G |
probably damaging |
Het |
Rev1 |
A |
T |
1: 38,118,337 (GRCm39) |
|
probably benign |
Het |
Rgs2 |
T |
G |
1: 143,878,650 (GRCm39) |
|
probably benign |
Het |
Rlf |
G |
T |
4: 121,007,798 (GRCm39) |
T394K |
probably benign |
Het |
Rptn |
A |
T |
3: 93,304,792 (GRCm39) |
R708S |
possibly damaging |
Het |
Sec23b |
T |
A |
2: 144,414,494 (GRCm39) |
M402K |
probably benign |
Het |
Skic2 |
A |
G |
17: 35,068,922 (GRCm39) |
C26R |
probably damaging |
Het |
Slx9 |
T |
C |
10: 77,325,860 (GRCm39) |
M170V |
possibly damaging |
Het |
Smpd4 |
A |
G |
16: 17,459,992 (GRCm39) |
|
probably benign |
Het |
Synj2 |
A |
G |
17: 6,063,813 (GRCm39) |
E434G |
probably damaging |
Het |
Tatdn2 |
T |
A |
6: 113,684,326 (GRCm39) |
F64I |
probably benign |
Het |
Tex21 |
A |
C |
12: 76,263,860 (GRCm39) |
H177Q |
probably benign |
Het |
Tln1 |
T |
A |
4: 43,535,954 (GRCm39) |
Q2077L |
probably null |
Het |
Tnrc6c |
T |
C |
11: 117,611,797 (GRCm39) |
V145A |
probably benign |
Het |
Ttn |
C |
T |
2: 76,616,936 (GRCm39) |
|
probably benign |
Het |
Uggt2 |
A |
G |
14: 119,269,670 (GRCm39) |
F954S |
possibly damaging |
Het |
Ugt2a1 |
A |
G |
5: 87,634,083 (GRCm39) |
S175P |
probably damaging |
Het |
Vcl |
A |
G |
14: 21,035,820 (GRCm39) |
|
probably null |
Het |
Vegfa |
A |
T |
17: 46,336,176 (GRCm39) |
|
probably benign |
Het |
Vmn2r68 |
G |
A |
7: 84,882,769 (GRCm39) |
Q328* |
probably null |
Het |
Vmn2r7 |
A |
G |
3: 64,626,864 (GRCm39) |
Y142H |
probably benign |
Het |
Wdr17 |
C |
T |
8: 55,134,434 (GRCm39) |
G349R |
probably damaging |
Het |
Ybx3 |
G |
T |
6: 131,347,290 (GRCm39) |
R282S |
probably damaging |
Het |
Zfp566 |
T |
C |
7: 29,777,194 (GRCm39) |
H329R |
probably damaging |
Het |
Zfp786 |
T |
C |
6: 47,797,868 (GRCm39) |
I357V |
probably benign |
Het |
Zfr2 |
C |
A |
10: 81,087,083 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Mipol1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00719:Mipol1
|
APN |
12 |
57,354,139 (GRCm39) |
splice site |
probably benign |
|
IGL01139:Mipol1
|
APN |
12 |
57,352,821 (GRCm39) |
nonsense |
probably null |
|
IGL02679:Mipol1
|
APN |
12 |
57,352,829 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03109:Mipol1
|
APN |
12 |
57,411,010 (GRCm39) |
missense |
probably benign |
0.20 |
R0001:Mipol1
|
UTSW |
12 |
57,507,625 (GRCm39) |
splice site |
probably benign |
|
R0220:Mipol1
|
UTSW |
12 |
57,503,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R0271:Mipol1
|
UTSW |
12 |
57,507,740 (GRCm39) |
unclassified |
probably benign |
|
R0284:Mipol1
|
UTSW |
12 |
57,503,855 (GRCm39) |
missense |
probably damaging |
0.98 |
R0496:Mipol1
|
UTSW |
12 |
57,503,963 (GRCm39) |
missense |
probably damaging |
0.99 |
R0538:Mipol1
|
UTSW |
12 |
57,461,197 (GRCm39) |
critical splice donor site |
probably null |
|
R1082:Mipol1
|
UTSW |
12 |
57,372,402 (GRCm39) |
missense |
probably damaging |
0.98 |
R1552:Mipol1
|
UTSW |
12 |
57,352,874 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1558:Mipol1
|
UTSW |
12 |
57,379,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R1928:Mipol1
|
UTSW |
12 |
57,379,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R2104:Mipol1
|
UTSW |
12 |
57,352,842 (GRCm39) |
splice site |
probably null |
|
R2495:Mipol1
|
UTSW |
12 |
57,507,776 (GRCm39) |
splice site |
probably benign |
|
R3723:Mipol1
|
UTSW |
12 |
57,503,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R4431:Mipol1
|
UTSW |
12 |
57,350,310 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4447:Mipol1
|
UTSW |
12 |
57,399,534 (GRCm39) |
intron |
probably benign |
|
R4847:Mipol1
|
UTSW |
12 |
57,350,282 (GRCm39) |
missense |
probably damaging |
0.99 |
R4851:Mipol1
|
UTSW |
12 |
57,379,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R5113:Mipol1
|
UTSW |
12 |
57,543,285 (GRCm39) |
missense |
probably benign |
0.36 |
R5668:Mipol1
|
UTSW |
12 |
57,372,346 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6535:Mipol1
|
UTSW |
12 |
57,352,886 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7172:Mipol1
|
UTSW |
12 |
57,372,321 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7191:Mipol1
|
UTSW |
12 |
57,503,852 (GRCm39) |
missense |
probably benign |
0.01 |
R7560:Mipol1
|
UTSW |
12 |
57,352,859 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8508:Mipol1
|
UTSW |
12 |
57,352,874 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8752:Mipol1
|
UTSW |
12 |
57,372,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R8772:Mipol1
|
UTSW |
12 |
57,372,418 (GRCm39) |
missense |
probably benign |
0.23 |
R8861:Mipol1
|
UTSW |
12 |
57,352,802 (GRCm39) |
missense |
probably benign |
0.00 |
R8928:Mipol1
|
UTSW |
12 |
57,507,651 (GRCm39) |
missense |
probably benign |
0.00 |
R9011:Mipol1
|
UTSW |
12 |
57,503,865 (GRCm39) |
missense |
probably benign |
0.03 |
R9250:Mipol1
|
UTSW |
12 |
57,461,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R9383:Mipol1
|
UTSW |
12 |
57,352,820 (GRCm39) |
missense |
probably benign |
0.00 |
|