Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abr |
A |
G |
11: 76,342,753 (GRCm39) |
C585R |
possibly damaging |
Het |
Acaca |
T |
C |
11: 84,202,145 (GRCm39) |
L1380S |
probably damaging |
Het |
Aifm2 |
A |
C |
10: 61,563,505 (GRCm39) |
Q125P |
probably null |
Het |
Ak5 |
A |
T |
3: 152,178,569 (GRCm39) |
L482* |
probably null |
Het |
Aldh3a2 |
T |
C |
11: 61,139,758 (GRCm39) |
Q458R |
probably benign |
Het |
Ank2 |
G |
A |
3: 126,810,565 (GRCm39) |
T524I |
|
Het |
Apoc3 |
A |
T |
9: 46,146,481 (GRCm39) |
S25T |
unknown |
Het |
Ash1l |
A |
T |
3: 88,965,848 (GRCm39) |
R2417* |
probably null |
Het |
Bbs12 |
A |
G |
3: 37,373,205 (GRCm39) |
|
probably benign |
Het |
Birc6 |
T |
A |
17: 74,919,146 (GRCm39) |
I1992N |
|
Het |
Brd9 |
G |
A |
13: 74,092,906 (GRCm39) |
V299M |
probably damaging |
Het |
Brwd1 |
A |
T |
16: 95,866,130 (GRCm39) |
N217K |
probably damaging |
Het |
C3 |
T |
C |
17: 57,518,678 (GRCm39) |
Y1235C |
probably damaging |
Het |
Cacna1c |
T |
C |
6: 118,590,907 (GRCm39) |
Y1538C |
|
Het |
Ccdc172 |
T |
A |
19: 58,525,779 (GRCm39) |
H212Q |
possibly damaging |
Het |
Cdc6 |
A |
G |
11: 98,802,999 (GRCm39) |
D313G |
probably damaging |
Het |
Cyp2e1 |
T |
C |
7: 140,353,022 (GRCm39) |
V353A |
probably damaging |
Het |
Dlg2 |
G |
T |
7: 92,080,258 (GRCm39) |
V711F |
probably damaging |
Het |
Dmac2 |
T |
C |
7: 25,320,448 (GRCm39) |
F49S |
probably damaging |
Het |
Dnah7b |
A |
G |
1: 46,173,674 (GRCm39) |
K660E |
probably benign |
Het |
Dusp8 |
A |
T |
7: 141,642,155 (GRCm39) |
S106T |
probably benign |
Het |
Dynll1 |
T |
A |
5: 115,438,604 (GRCm39) |
I34F |
probably benign |
Het |
Epb41l4b |
A |
G |
4: 57,103,447 (GRCm39) |
F130L |
possibly damaging |
Het |
Erc2 |
T |
C |
14: 27,751,418 (GRCm39) |
Y705H |
probably benign |
Het |
Exosc8 |
T |
A |
3: 54,638,503 (GRCm39) |
L160F |
probably damaging |
Het |
F5 |
A |
G |
1: 164,001,830 (GRCm39) |
T178A |
probably benign |
Het |
F7 |
C |
A |
8: 13,085,059 (GRCm39) |
P362T |
probably damaging |
Het |
Fkbp3 |
T |
C |
12: 65,112,567 (GRCm39) |
K156E |
possibly damaging |
Het |
Folh1 |
G |
A |
7: 86,368,913 (GRCm39) |
T738I |
probably benign |
Het |
Gatad2b |
C |
T |
3: 90,255,936 (GRCm39) |
A134V |
probably benign |
Het |
Glud1 |
T |
A |
14: 34,057,349 (GRCm39) |
W338R |
|
Het |
Gm21149 |
T |
C |
5: 15,680,261 (GRCm39) |
K62E |
possibly damaging |
Het |
Gm32742 |
A |
G |
9: 51,050,049 (GRCm39) |
Y1517H |
probably damaging |
Het |
Grik5 |
G |
A |
7: 24,767,429 (GRCm39) |
|
probably benign |
Het |
Gse1 |
A |
T |
8: 121,295,052 (GRCm39) |
E391V |
unknown |
Het |
Gxylt2 |
C |
T |
6: 100,710,329 (GRCm39) |
Q157* |
probably null |
Het |
Hbq1b |
C |
T |
11: 32,237,092 (GRCm39) |
T27I |
probably damaging |
Het |
Hoxd13 |
T |
A |
2: 74,499,382 (GRCm39) |
D243E |
probably benign |
Het |
Hsd3b3 |
T |
A |
3: 98,651,211 (GRCm39) |
I80F |
possibly damaging |
Het |
Hsf2bp |
A |
T |
17: 32,230,082 (GRCm39) |
|
probably benign |
Het |
Itch |
G |
A |
2: 155,052,045 (GRCm39) |
|
probably benign |
Het |
Kat14 |
T |
C |
2: 144,215,742 (GRCm39) |
F76L |
probably benign |
Het |
Kdm6b |
T |
C |
11: 69,295,424 (GRCm39) |
T948A |
unknown |
Het |
Kmt2c |
A |
T |
5: 25,516,102 (GRCm39) |
H2580Q |
probably benign |
Het |
Lrp1 |
T |
C |
10: 127,382,281 (GRCm39) |
T3727A |
probably benign |
Het |
Lrrc8a |
A |
G |
2: 30,147,042 (GRCm39) |
I619V |
possibly damaging |
Het |
Mansc1 |
C |
A |
6: 134,586,951 (GRCm39) |
G409W |
probably damaging |
Het |
Map3k11 |
C |
A |
19: 5,746,038 (GRCm39) |
L418I |
possibly damaging |
Het |
Mettl4 |
T |
A |
17: 95,042,913 (GRCm39) |
I308L |
possibly damaging |
Het |
Myo9a |
A |
G |
9: 59,739,514 (GRCm39) |
D742G |
probably damaging |
Het |
Mypn |
T |
C |
10: 63,028,652 (GRCm39) |
Q137R |
probably benign |
Het |
Neurod4 |
A |
T |
10: 130,106,427 (GRCm39) |
Y282* |
probably null |
Het |
Nup210 |
A |
G |
6: 91,020,799 (GRCm39) |
F965S |
probably benign |
Het |
Oplah |
T |
C |
15: 76,185,098 (GRCm39) |
T872A |
possibly damaging |
Het |
Or1ab2 |
G |
T |
8: 72,863,697 (GRCm39) |
G96C |
probably damaging |
Het |
Or4b12 |
A |
G |
2: 90,096,358 (GRCm39) |
C139R |
probably damaging |
Het |
Or5m8 |
T |
G |
2: 85,822,819 (GRCm39) |
Y219* |
probably null |
Het |
Or6c68 |
A |
G |
10: 129,157,897 (GRCm39) |
N135S |
probably benign |
Het |
Pkn2 |
A |
T |
3: 142,515,245 (GRCm39) |
D696E |
possibly damaging |
Het |
Pla2r1 |
A |
T |
2: 60,325,729 (GRCm39) |
|
probably benign |
Het |
Plpp1 |
A |
T |
13: 112,988,038 (GRCm39) |
I54L |
|
Het |
Ppp4r2 |
T |
G |
6: 100,842,113 (GRCm39) |
N191K |
probably damaging |
Het |
Ptpdc1 |
G |
T |
13: 48,739,655 (GRCm39) |
P592Q |
probably benign |
Het |
Qrich2 |
A |
T |
11: 116,347,692 (GRCm39) |
L1044* |
probably null |
Het |
Rb1cc1 |
A |
G |
1: 6,315,109 (GRCm39) |
I421V |
probably damaging |
Het |
Ripor3 |
A |
T |
2: 167,823,267 (GRCm39) |
C881* |
probably null |
Het |
Rreb1 |
T |
C |
13: 38,114,282 (GRCm39) |
F547S |
probably benign |
Het |
Scel |
T |
C |
14: 103,770,746 (GRCm39) |
V60A |
probably benign |
Het |
Shank3 |
G |
A |
15: 89,442,419 (GRCm39) |
A1771T |
probably benign |
Het |
Slc6a20a |
A |
G |
9: 123,469,631 (GRCm39) |
|
probably null |
Het |
Slfn5 |
C |
T |
11: 82,851,446 (GRCm39) |
T581I |
probably damaging |
Het |
Ssh3 |
A |
C |
19: 4,314,113 (GRCm39) |
V412G |
probably damaging |
Het |
Stx17 |
T |
G |
4: 48,159,071 (GRCm39) |
|
probably benign |
Het |
Sun3 |
T |
G |
11: 8,968,170 (GRCm39) |
T274P |
probably benign |
Het |
Tm9sf1 |
T |
C |
14: 55,875,464 (GRCm39) |
T427A |
probably damaging |
Het |
Tmem114 |
T |
A |
16: 8,229,983 (GRCm39) |
I140F |
|
Het |
Tmem40 |
T |
C |
6: 115,710,980 (GRCm39) |
R167G |
possibly damaging |
Het |
Top3a |
C |
A |
11: 60,641,401 (GRCm39) |
|
probably null |
Het |
Trafd1 |
A |
G |
5: 121,516,573 (GRCm39) |
V210A |
probably benign |
Het |
Ttn |
G |
A |
2: 76,679,172 (GRCm39) |
A10850V |
unknown |
Het |
Unc80 |
G |
A |
1: 66,677,244 (GRCm39) |
A2058T |
possibly damaging |
Het |
Upp2 |
T |
C |
2: 58,668,020 (GRCm39) |
Y238H |
probably damaging |
Het |
Vmn1r224 |
T |
A |
17: 20,640,242 (GRCm39) |
I273N |
probably damaging |
Het |
Vps13c |
T |
C |
9: 67,836,805 (GRCm39) |
S1768P |
probably damaging |
Het |
Zfp26 |
G |
A |
9: 20,348,723 (GRCm39) |
H614Y |
probably damaging |
Het |
Zfp263 |
C |
T |
16: 3,567,701 (GRCm39) |
T672I |
probably benign |
Het |
Zfp641 |
T |
A |
15: 98,186,732 (GRCm39) |
Q297L |
probably benign |
Het |
Zfp944 |
T |
C |
17: 22,560,031 (GRCm39) |
E25G |
probably damaging |
Het |
Zfp994 |
T |
C |
17: 22,418,981 (GRCm39) |
E656G |
unknown |
Het |
Zfyve19 |
A |
G |
2: 119,045,330 (GRCm39) |
D206G |
probably damaging |
Het |
|
Other mutations in Trim66 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01539:Trim66
|
APN |
7 |
109,054,273 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01758:Trim66
|
APN |
7 |
109,085,252 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01982:Trim66
|
APN |
7 |
109,057,970 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01983:Trim66
|
APN |
7 |
109,057,458 (GRCm39) |
nonsense |
probably null |
|
IGL02149:Trim66
|
APN |
7 |
109,060,109 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02392:Trim66
|
APN |
7 |
109,059,481 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02483:Trim66
|
APN |
7 |
109,076,837 (GRCm39) |
splice site |
probably benign |
|
IGL02832:Trim66
|
APN |
7 |
109,059,704 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02945:Trim66
|
APN |
7 |
109,059,383 (GRCm39) |
nonsense |
probably null |
|
IGL03085:Trim66
|
APN |
7 |
109,057,952 (GRCm39) |
missense |
probably benign |
0.17 |
PIT1430001:Trim66
|
UTSW |
7 |
109,074,454 (GRCm39) |
missense |
probably damaging |
0.99 |
R0326:Trim66
|
UTSW |
7 |
109,059,379 (GRCm39) |
missense |
probably benign |
0.00 |
R0358:Trim66
|
UTSW |
7 |
109,059,383 (GRCm39) |
nonsense |
probably null |
|
R0401:Trim66
|
UTSW |
7 |
109,074,471 (GRCm39) |
missense |
probably damaging |
0.98 |
R0470:Trim66
|
UTSW |
7 |
109,056,749 (GRCm39) |
splice site |
probably benign |
|
R0568:Trim66
|
UTSW |
7 |
109,059,902 (GRCm39) |
missense |
probably benign |
0.00 |
R0669:Trim66
|
UTSW |
7 |
109,054,199 (GRCm39) |
intron |
probably benign |
|
R0980:Trim66
|
UTSW |
7 |
109,054,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R1015:Trim66
|
UTSW |
7 |
109,054,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R1078:Trim66
|
UTSW |
7 |
109,071,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R1099:Trim66
|
UTSW |
7 |
109,074,661 (GRCm39) |
missense |
probably benign |
0.34 |
R1181:Trim66
|
UTSW |
7 |
109,083,784 (GRCm39) |
critical splice donor site |
probably null |
|
R1497:Trim66
|
UTSW |
7 |
109,083,826 (GRCm39) |
missense |
probably benign |
0.00 |
R1583:Trim66
|
UTSW |
7 |
109,054,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R1843:Trim66
|
UTSW |
7 |
109,075,046 (GRCm39) |
missense |
probably damaging |
0.99 |
R1998:Trim66
|
UTSW |
7 |
109,083,784 (GRCm39) |
critical splice donor site |
probably null |
|
R2016:Trim66
|
UTSW |
7 |
109,071,439 (GRCm39) |
critical splice donor site |
probably null |
|
R2143:Trim66
|
UTSW |
7 |
109,074,320 (GRCm39) |
missense |
probably damaging |
0.98 |
R2144:Trim66
|
UTSW |
7 |
109,074,320 (GRCm39) |
missense |
probably damaging |
0.98 |
R2145:Trim66
|
UTSW |
7 |
109,074,320 (GRCm39) |
missense |
probably damaging |
0.98 |
R3945:Trim66
|
UTSW |
7 |
109,071,475 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4012:Trim66
|
UTSW |
7 |
109,057,338 (GRCm39) |
missense |
probably damaging |
0.98 |
R4464:Trim66
|
UTSW |
7 |
109,076,897 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4473:Trim66
|
UTSW |
7 |
109,081,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R4729:Trim66
|
UTSW |
7 |
109,055,267 (GRCm39) |
critical splice donor site |
probably null |
|
R4730:Trim66
|
UTSW |
7 |
109,082,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R4775:Trim66
|
UTSW |
7 |
109,056,796 (GRCm39) |
nonsense |
probably null |
|
R4819:Trim66
|
UTSW |
7 |
109,056,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R5269:Trim66
|
UTSW |
7 |
109,056,797 (GRCm39) |
missense |
probably benign |
0.00 |
R5557:Trim66
|
UTSW |
7 |
109,082,944 (GRCm39) |
missense |
probably benign |
0.06 |
R5832:Trim66
|
UTSW |
7 |
109,054,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R6220:Trim66
|
UTSW |
7 |
109,082,300 (GRCm39) |
missense |
probably damaging |
0.97 |
R6243:Trim66
|
UTSW |
7 |
109,059,481 (GRCm39) |
missense |
probably benign |
0.01 |
R6374:Trim66
|
UTSW |
7 |
109,085,269 (GRCm39) |
missense |
probably benign |
|
R6450:Trim66
|
UTSW |
7 |
109,059,945 (GRCm39) |
missense |
probably benign |
0.09 |
R6543:Trim66
|
UTSW |
7 |
109,075,086 (GRCm39) |
missense |
probably benign |
0.01 |
R6788:Trim66
|
UTSW |
7 |
109,076,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R6842:Trim66
|
UTSW |
7 |
109,059,983 (GRCm39) |
missense |
probably benign |
0.00 |
R7169:Trim66
|
UTSW |
7 |
109,054,328 (GRCm39) |
missense |
probably benign |
0.25 |
R7257:Trim66
|
UTSW |
7 |
109,059,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R7328:Trim66
|
UTSW |
7 |
109,056,958 (GRCm39) |
missense |
probably damaging |
0.99 |
R7616:Trim66
|
UTSW |
7 |
109,082,956 (GRCm39) |
missense |
probably damaging |
0.99 |
R8423:Trim66
|
UTSW |
7 |
109,074,599 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8855:Trim66
|
UTSW |
7 |
109,081,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R9137:Trim66
|
UTSW |
7 |
109,074,330 (GRCm39) |
missense |
probably damaging |
0.99 |
R9640:Trim66
|
UTSW |
7 |
109,074,825 (GRCm39) |
missense |
probably damaging |
1.00 |
RF013:Trim66
|
UTSW |
7 |
109,059,960 (GRCm39) |
missense |
probably damaging |
0.99 |
RF024:Trim66
|
UTSW |
7 |
109,059,947 (GRCm39) |
missense |
possibly damaging |
0.62 |
|