Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
G |
3: 137,771,131 (GRCm39) |
N107D |
probably benign |
Het |
4833413E03Rik |
A |
C |
17: 31,777,738 (GRCm39) |
|
noncoding transcript |
Het |
4931429L15Rik |
G |
T |
9: 46,220,144 (GRCm39) |
H129Q |
possibly damaging |
Het |
A730018C14Rik |
A |
G |
12: 112,382,069 (GRCm39) |
|
noncoding transcript |
Het |
Abcc6 |
T |
A |
7: 45,646,115 (GRCm39) |
K791N |
probably benign |
Het |
Adcy4 |
T |
G |
14: 56,012,493 (GRCm39) |
Q550P |
probably benign |
Het |
Add3 |
C |
A |
19: 53,223,223 (GRCm39) |
A325E |
possibly damaging |
Het |
Agbl4 |
T |
A |
4: 111,514,528 (GRCm39) |
I513N |
possibly damaging |
Het |
Agfg1 |
C |
A |
1: 82,864,108 (GRCm39) |
T392K |
probably damaging |
Het |
Akna |
C |
A |
4: 63,297,491 (GRCm39) |
M854I |
probably benign |
Het |
Ankrd44 |
T |
C |
1: 54,802,916 (GRCm39) |
N194S |
probably benign |
Het |
Anks1b |
A |
G |
10: 89,709,594 (GRCm39) |
K21E |
probably damaging |
Het |
Ap1s3 |
A |
G |
1: 79,586,889 (GRCm39) |
F154L |
probably benign |
Het |
Apbb2 |
T |
A |
5: 66,520,160 (GRCm39) |
N477I |
probably damaging |
Het |
Apobec3 |
T |
C |
15: 79,783,225 (GRCm39) |
C101R |
possibly damaging |
Het |
Arnt |
G |
T |
3: 95,395,696 (GRCm39) |
V410F |
probably damaging |
Het |
Arsg |
G |
A |
11: 109,424,839 (GRCm39) |
R270H |
possibly damaging |
Het |
B3gnt7 |
T |
A |
1: 86,232,992 (GRCm39) |
D79E |
probably damaging |
Het |
Cd44 |
G |
T |
2: 102,691,910 (GRCm39) |
A126D |
probably damaging |
Het |
Cd69 |
A |
G |
6: 129,248,318 (GRCm39) |
I56T |
probably damaging |
Het |
Cep120 |
G |
A |
18: 53,857,608 (GRCm39) |
P286S |
probably benign |
Het |
Ces2a |
T |
C |
8: 105,463,840 (GRCm39) |
F184S |
probably damaging |
Het |
Chrng |
A |
G |
1: 87,135,246 (GRCm39) |
N185S |
probably damaging |
Het |
Cldn6 |
A |
T |
17: 23,900,221 (GRCm39) |
M62L |
probably benign |
Het |
Cntn6 |
T |
A |
6: 104,822,745 (GRCm39) |
N765K |
probably damaging |
Het |
Cspg4b |
A |
G |
13: 113,454,392 (GRCm39) |
Y146C |
probably damaging |
Het |
Ctnnal1 |
T |
C |
4: 56,847,857 (GRCm39) |
D94G |
probably damaging |
Het |
Depdc1a |
A |
G |
3: 159,232,343 (GRCm39) |
N698S |
probably benign |
Het |
Dnah2 |
A |
T |
11: 69,364,697 (GRCm39) |
I1986N |
probably damaging |
Het |
Dnah7b |
A |
G |
1: 46,392,174 (GRCm39) |
E3845G |
probably benign |
Het |
Dpysl3 |
C |
T |
18: 43,487,867 (GRCm39) |
V159I |
probably benign |
Het |
Dync1h1 |
T |
C |
12: 110,627,630 (GRCm39) |
Y4047H |
probably damaging |
Het |
E130308A19Rik |
C |
T |
4: 59,691,057 (GRCm39) |
P297L |
probably benign |
Het |
E2f5 |
A |
G |
3: 14,652,379 (GRCm39) |
T72A |
probably benign |
Het |
Ephb6 |
G |
T |
6: 41,593,073 (GRCm39) |
R437L |
probably damaging |
Het |
Erbb4 |
T |
C |
1: 68,337,473 (GRCm39) |
H615R |
probably damaging |
Het |
Erbin |
T |
C |
13: 104,020,714 (GRCm39) |
T82A |
probably damaging |
Het |
Eri2 |
T |
C |
7: 119,384,903 (GRCm39) |
N533D |
probably benign |
Het |
Fkbp9 |
A |
G |
6: 56,827,701 (GRCm39) |
N174S |
probably damaging |
Het |
Fsbp |
C |
T |
4: 11,583,709 (GRCm39) |
T136I |
possibly damaging |
Het |
Fubp3 |
C |
A |
2: 31,473,223 (GRCm39) |
D47E |
probably damaging |
Het |
Gm21850 |
G |
A |
2: 153,898,419 (GRCm39) |
|
noncoding transcript |
Het |
Gm5141 |
T |
A |
13: 62,922,764 (GRCm39) |
Y135F |
unknown |
Het |
Gm7353 |
T |
A |
7: 3,160,725 (GRCm39) |
|
noncoding transcript |
Het |
Gm9925 |
T |
C |
18: 74,198,344 (GRCm39) |
|
probably benign |
Het |
Greb1l |
T |
C |
18: 10,541,792 (GRCm39) |
S1180P |
probably benign |
Het |
H2ac11 |
G |
A |
13: 22,227,079 (GRCm39) |
Q7* |
probably null |
Het |
Ift70a2 |
A |
C |
2: 75,807,920 (GRCm39) |
C197W |
probably benign |
Het |
Kiz |
A |
G |
2: 146,731,166 (GRCm39) |
T192A |
possibly damaging |
Het |
Klhl24 |
T |
A |
16: 19,925,708 (GRCm39) |
C79S |
probably damaging |
Het |
Map3k11 |
A |
G |
19: 5,740,966 (GRCm39) |
H231R |
probably damaging |
Het |
Mbd4 |
C |
A |
6: 115,826,345 (GRCm39) |
R194S |
probably benign |
Het |
Mettl21e |
A |
C |
1: 44,250,303 (GRCm39) |
S34R |
probably benign |
Het |
Mrps5 |
T |
C |
2: 127,440,161 (GRCm39) |
V245A |
probably benign |
Het |
Mtrf1 |
T |
C |
14: 79,639,128 (GRCm39) |
Y87H |
probably benign |
Het |
Myh15 |
T |
C |
16: 48,940,420 (GRCm39) |
I790T |
probably benign |
Het |
Necab1 |
T |
G |
4: 14,989,248 (GRCm39) |
I176L |
probably benign |
Het |
Nfkb2 |
T |
A |
19: 46,298,361 (GRCm39) |
L555Q |
probably damaging |
Het |
Nhlrc3 |
T |
A |
3: 53,365,988 (GRCm39) |
E168D |
probably benign |
Het |
Nlrp5 |
T |
A |
7: 23,135,203 (GRCm39) |
C949S |
probably damaging |
Het |
Nup155 |
C |
A |
15: 8,187,187 (GRCm39) |
A1372E |
probably benign |
Het |
Nynrin |
G |
T |
14: 56,100,720 (GRCm39) |
R170L |
probably damaging |
Het |
Ogfrl1 |
T |
A |
1: 23,409,402 (GRCm39) |
N275Y |
probably damaging |
Het |
Olr1 |
A |
T |
6: 129,465,839 (GRCm39) |
S56T |
probably damaging |
Het |
Or4k52 |
A |
G |
2: 111,611,190 (GRCm39) |
D175G |
probably damaging |
Het |
Or5aq1 |
C |
T |
2: 86,966,221 (GRCm39) |
S148N |
probably damaging |
Het |
Or5b121 |
A |
G |
19: 13,507,319 (GRCm39) |
N138S |
probably benign |
Het |
Or8b48 |
A |
G |
9: 38,493,265 (GRCm39) |
T231A |
possibly damaging |
Het |
Ovol2 |
A |
T |
2: 144,173,203 (GRCm39) |
|
probably benign |
Het |
Pcdha6 |
A |
T |
18: 37,102,906 (GRCm39) |
I700F |
probably damaging |
Het |
Prkcz |
C |
T |
4: 155,374,159 (GRCm39) |
V86M |
probably damaging |
Het |
Ptpn13 |
A |
G |
5: 103,734,639 (GRCm39) |
T2124A |
probably benign |
Het |
Ranbp3 |
G |
T |
17: 56,980,346 (GRCm39) |
|
probably benign |
Het |
Rapgef2 |
A |
G |
3: 79,077,076 (GRCm39) |
|
probably benign |
Het |
Rbl1 |
A |
G |
2: 157,016,724 (GRCm39) |
V625A |
probably benign |
Het |
Rbm38 |
G |
T |
2: 172,863,944 (GRCm39) |
G38C |
probably damaging |
Het |
Reg1 |
T |
G |
6: 78,403,333 (GRCm39) |
F7C |
possibly damaging |
Het |
Retnlg |
A |
T |
16: 48,694,697 (GRCm39) |
Q115L |
possibly damaging |
Het |
Rhobtb1 |
G |
A |
10: 69,105,983 (GRCm39) |
V183I |
probably benign |
Het |
Rims1 |
T |
C |
1: 22,361,329 (GRCm39) |
Q1186R |
probably damaging |
Het |
Ryr1 |
A |
G |
7: 28,794,522 (GRCm39) |
F1246L |
possibly damaging |
Het |
Samm50 |
A |
G |
15: 84,094,811 (GRCm39) |
N401S |
possibly damaging |
Het |
Scn3a |
T |
A |
2: 65,336,537 (GRCm39) |
I690F |
probably damaging |
Het |
Sdk1 |
A |
G |
5: 141,944,993 (GRCm39) |
D304G |
probably damaging |
Het |
Skint6 |
T |
C |
4: 113,093,594 (GRCm39) |
Y183C |
probably damaging |
Het |
Slamf1 |
A |
T |
1: 171,604,829 (GRCm39) |
T200S |
probably benign |
Het |
Slc34a2 |
C |
T |
5: 53,226,793 (GRCm39) |
R639C |
probably damaging |
Het |
Smap1 |
A |
T |
1: 23,892,517 (GRCm39) |
M149K |
probably benign |
Het |
Sorcs1 |
T |
C |
19: 50,132,419 (GRCm39) |
|
probably benign |
Het |
Sp140 |
T |
A |
1: 85,538,549 (GRCm39) |
D95E |
possibly damaging |
Het |
Spata13 |
G |
A |
14: 60,991,356 (GRCm39) |
W366* |
probably null |
Het |
Spata31e4 |
C |
A |
13: 50,855,116 (GRCm39) |
S251R |
probably damaging |
Het |
Strip1 |
G |
A |
3: 107,534,314 (GRCm39) |
T136I |
probably benign |
Het |
Tacr1 |
A |
T |
6: 82,534,053 (GRCm39) |
T360S |
probably benign |
Het |
Tbc1d14 |
T |
A |
5: 36,728,600 (GRCm39) |
|
probably benign |
Het |
Tcaf2 |
T |
C |
6: 42,604,996 (GRCm39) |
Y596C |
probably damaging |
Het |
Tspoap1 |
C |
T |
11: 87,669,269 (GRCm39) |
T1454I |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,744,927 (GRCm39) |
M5374K |
probably benign |
Het |
Uts2r |
G |
A |
11: 121,051,705 (GRCm39) |
V190I |
possibly damaging |
Het |
Vmn1r181 |
A |
G |
7: 23,684,008 (GRCm39) |
T158A |
possibly damaging |
Het |
Wdr35 |
A |
T |
12: 9,068,150 (GRCm39) |
T778S |
probably benign |
Het |
Xrn1 |
A |
T |
9: 95,856,797 (GRCm39) |
|
probably benign |
Het |
Zfp35 |
A |
T |
18: 24,136,326 (GRCm39) |
K223N |
probably damaging |
Het |
Zfp764 |
T |
C |
7: 127,003,943 (GRCm39) |
Q396R |
probably benign |
Het |
Zfyve1 |
T |
C |
12: 83,605,421 (GRCm39) |
Y11C |
probably damaging |
Het |
|
Other mutations in Cyp2c69 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01873:Cyp2c69
|
APN |
19 |
39,869,693 (GRCm39) |
splice site |
probably benign |
|
IGL02127:Cyp2c69
|
APN |
19 |
39,839,501 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02945:Cyp2c69
|
APN |
19 |
39,875,091 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL03067:Cyp2c69
|
APN |
19 |
39,869,537 (GRCm39) |
missense |
probably benign |
0.29 |
IGL03069:Cyp2c69
|
APN |
19 |
39,869,537 (GRCm39) |
missense |
probably benign |
0.29 |
BB007:Cyp2c69
|
UTSW |
19 |
39,831,434 (GRCm39) |
missense |
possibly damaging |
0.47 |
BB017:Cyp2c69
|
UTSW |
19 |
39,831,434 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0545:Cyp2c69
|
UTSW |
19 |
39,875,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R1276:Cyp2c69
|
UTSW |
19 |
39,864,668 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1468:Cyp2c69
|
UTSW |
19 |
39,837,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Cyp2c69
|
UTSW |
19 |
39,837,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R1534:Cyp2c69
|
UTSW |
19 |
39,839,593 (GRCm39) |
missense |
probably benign |
|
R1549:Cyp2c69
|
UTSW |
19 |
39,831,430 (GRCm39) |
missense |
probably benign |
0.11 |
R1703:Cyp2c69
|
UTSW |
19 |
39,864,810 (GRCm39) |
missense |
probably benign |
0.10 |
R1752:Cyp2c69
|
UTSW |
19 |
39,869,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R1769:Cyp2c69
|
UTSW |
19 |
39,864,815 (GRCm39) |
missense |
probably benign |
0.00 |
R1843:Cyp2c69
|
UTSW |
19 |
39,865,972 (GRCm39) |
missense |
probably benign |
0.27 |
R1938:Cyp2c69
|
UTSW |
19 |
39,837,810 (GRCm39) |
missense |
probably damaging |
0.97 |
R2100:Cyp2c69
|
UTSW |
19 |
39,875,130 (GRCm39) |
missense |
probably benign |
0.11 |
R2366:Cyp2c69
|
UTSW |
19 |
39,866,038 (GRCm39) |
missense |
probably benign |
0.12 |
R2367:Cyp2c69
|
UTSW |
19 |
39,866,038 (GRCm39) |
missense |
probably benign |
0.12 |
R2440:Cyp2c69
|
UTSW |
19 |
39,864,738 (GRCm39) |
missense |
probably benign |
0.17 |
R2931:Cyp2c69
|
UTSW |
19 |
39,837,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R3709:Cyp2c69
|
UTSW |
19 |
39,839,667 (GRCm39) |
splice site |
probably benign |
|
R3793:Cyp2c69
|
UTSW |
19 |
39,869,600 (GRCm39) |
missense |
probably benign |
0.44 |
R3898:Cyp2c69
|
UTSW |
19 |
39,864,834 (GRCm39) |
missense |
probably benign |
0.00 |
R4579:Cyp2c69
|
UTSW |
19 |
39,869,630 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4707:Cyp2c69
|
UTSW |
19 |
39,837,852 (GRCm39) |
missense |
probably benign |
0.39 |
R4778:Cyp2c69
|
UTSW |
19 |
39,866,038 (GRCm39) |
missense |
probably benign |
0.12 |
R4779:Cyp2c69
|
UTSW |
19 |
39,866,038 (GRCm39) |
missense |
probably benign |
0.12 |
R4838:Cyp2c69
|
UTSW |
19 |
39,866,038 (GRCm39) |
missense |
probably benign |
0.12 |
R4877:Cyp2c69
|
UTSW |
19 |
39,866,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R5488:Cyp2c69
|
UTSW |
19 |
39,839,603 (GRCm39) |
missense |
probably null |
0.94 |
R5489:Cyp2c69
|
UTSW |
19 |
39,839,603 (GRCm39) |
missense |
probably null |
0.94 |
R6083:Cyp2c69
|
UTSW |
19 |
39,837,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R6278:Cyp2c69
|
UTSW |
19 |
39,831,507 (GRCm39) |
nonsense |
probably null |
|
R6415:Cyp2c69
|
UTSW |
19 |
39,831,365 (GRCm39) |
missense |
probably benign |
0.44 |
R6732:Cyp2c69
|
UTSW |
19 |
39,869,943 (GRCm39) |
missense |
probably benign |
|
R6858:Cyp2c69
|
UTSW |
19 |
39,866,009 (GRCm39) |
missense |
probably benign |
0.19 |
R7023:Cyp2c69
|
UTSW |
19 |
39,865,986 (GRCm39) |
missense |
probably benign |
0.43 |
R7227:Cyp2c69
|
UTSW |
19 |
39,869,610 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7228:Cyp2c69
|
UTSW |
19 |
39,869,610 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7260:Cyp2c69
|
UTSW |
19 |
39,831,344 (GRCm39) |
missense |
probably benign |
0.00 |
R7262:Cyp2c69
|
UTSW |
19 |
39,875,176 (GRCm39) |
start gained |
probably benign |
|
R7479:Cyp2c69
|
UTSW |
19 |
39,870,001 (GRCm39) |
missense |
probably benign |
0.00 |
R7570:Cyp2c69
|
UTSW |
19 |
39,848,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R7663:Cyp2c69
|
UTSW |
19 |
39,865,953 (GRCm39) |
nonsense |
probably null |
|
R7785:Cyp2c69
|
UTSW |
19 |
39,839,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R7795:Cyp2c69
|
UTSW |
19 |
39,864,663 (GRCm39) |
missense |
probably benign |
|
R7920:Cyp2c69
|
UTSW |
19 |
39,866,247 (GRCm39) |
splice site |
probably null |
|
R7930:Cyp2c69
|
UTSW |
19 |
39,831,434 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8203:Cyp2c69
|
UTSW |
19 |
39,869,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R8888:Cyp2c69
|
UTSW |
19 |
39,869,910 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8895:Cyp2c69
|
UTSW |
19 |
39,869,910 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9530:Cyp2c69
|
UTSW |
19 |
39,848,311 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9645:Cyp2c69
|
UTSW |
19 |
39,869,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R9665:Cyp2c69
|
UTSW |
19 |
39,839,504 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9753:Cyp2c69
|
UTSW |
19 |
39,865,991 (GRCm39) |
missense |
probably benign |
0.44 |
|