Other mutations in this stock |
Total: 113 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
T |
G |
7: 120,278,181 (GRCm38) |
F1017L |
probably damaging |
Het |
Abcb11 |
A |
C |
2: 69,245,923 (GRCm38) |
V1147G |
probably damaging |
Het |
Abcc10 |
T |
A |
17: 46,306,603 (GRCm38) |
S1128C |
probably damaging |
Het |
Adam6a |
G |
A |
12: 113,545,303 (GRCm38) |
C432Y |
probably damaging |
Het |
Adamdec1 |
C |
T |
14: 68,570,948 (GRCm38) |
V318M |
probably damaging |
Het |
Ahnak |
C |
A |
19: 9,002,048 (GRCm38) |
S232Y |
possibly damaging |
Het |
Amt |
A |
C |
9: 108,297,162 (GRCm38) |
H42P |
probably damaging |
Het |
Anapc1 |
A |
T |
2: 128,659,788 (GRCm38) |
L778Q |
probably damaging |
Het |
Ankhd1 |
G |
A |
18: 36,644,527 (GRCm38) |
A1588T |
probably benign |
Het |
Anln |
A |
T |
9: 22,353,331 (GRCm38) |
L881Q |
probably damaging |
Het |
Appl1 |
A |
G |
14: 26,927,749 (GRCm38) |
S607P |
probably damaging |
Het |
Arg2 |
G |
T |
12: 79,147,662 (GRCm38) |
V87L |
probably benign |
Het |
Atp13a2 |
C |
T |
4: 141,004,012 (GRCm38) |
P869L |
probably benign |
Het |
Atxn7l1 |
T |
A |
12: 33,358,770 (GRCm38) |
D310E |
probably damaging |
Het |
Cd6 |
A |
T |
19: 10,798,602 (GRCm38) |
D164E |
probably damaging |
Het |
Cdan1 |
C |
A |
2: 120,724,936 (GRCm38) |
V775L |
probably benign |
Het |
Cep164 |
A |
T |
9: 45,775,758 (GRCm38) |
|
probably null |
Het |
Cep41 |
A |
G |
6: 30,661,006 (GRCm38) |
S61P |
probably damaging |
Het |
Clcn7 |
C |
A |
17: 25,160,471 (GRCm38) |
D764E |
probably damaging |
Het |
Cramp1l |
T |
C |
17: 24,968,978 (GRCm38) |
D1214G |
probably damaging |
Het |
Cst7 |
G |
T |
2: 150,577,708 (GRCm38) |
C98F |
probably damaging |
Het |
Ctc1 |
T |
A |
11: 69,034,658 (GRCm38) |
L1007Q |
probably damaging |
Het |
Cyb5r4 |
G |
A |
9: 87,022,209 (GRCm38) |
A11T |
possibly damaging |
Het |
Dcaf8 |
A |
G |
1: 172,175,553 (GRCm38) |
D306G |
probably damaging |
Het |
Defb38 |
T |
A |
8: 19,023,576 (GRCm38) |
K27I |
probably benign |
Het |
Disp3 |
T |
C |
4: 148,271,632 (GRCm38) |
E257G |
probably damaging |
Het |
Dnajc6 |
T |
C |
4: 101,598,988 (GRCm38) |
S58P |
probably damaging |
Het |
Dock10 |
A |
T |
1: 80,606,568 (GRCm38) |
D140E |
possibly damaging |
Het |
Dopey1 |
T |
C |
9: 86,492,004 (GRCm38) |
V172A |
probably damaging |
Het |
Dync1h1 |
G |
A |
12: 110,636,509 (GRCm38) |
E2195K |
probably benign |
Het |
Eci3 |
C |
T |
13: 34,953,028 (GRCm38) |
A171T |
possibly damaging |
Het |
Eml2 |
A |
G |
7: 19,194,061 (GRCm38) |
D284G |
probably damaging |
Het |
Eml5 |
T |
C |
12: 98,810,584 (GRCm38) |
D1377G |
probably damaging |
Het |
Fam186a |
T |
C |
15: 99,940,302 (GRCm38) |
E2687G |
possibly damaging |
Het |
Fut9 |
A |
C |
4: 25,620,352 (GRCm38) |
L154R |
probably damaging |
Het |
Gabrb2 |
A |
G |
11: 42,626,713 (GRCm38) |
N454S |
probably benign |
Het |
Gm438 |
T |
A |
4: 144,777,883 (GRCm38) |
M233L |
probably benign |
Het |
Gpr183 |
T |
A |
14: 121,954,741 (GRCm38) |
I123L |
probably benign |
Het |
Gucy1b1 |
A |
T |
3: 82,058,352 (GRCm38) |
N62K |
probably benign |
Het |
Hcrtr2 |
T |
C |
9: 76,259,785 (GRCm38) |
N90S |
probably damaging |
Het |
Hectd1 |
A |
T |
12: 51,744,794 (GRCm38) |
L2556Q |
probably damaging |
Het |
Hfm1 |
T |
A |
5: 106,847,676 (GRCm38) |
M1290L |
probably benign |
Het |
Hgsnat |
A |
G |
8: 25,957,256 (GRCm38) |
W337R |
probably benign |
Het |
Hmbox1 |
T |
C |
14: 64,828,648 (GRCm38) |
Y291C |
probably damaging |
Het |
Hmcn1 |
T |
C |
1: 150,721,664 (GRCm38) |
N1749S |
probably benign |
Het |
Igsf10 |
T |
C |
3: 59,331,272 (GRCm38) |
D496G |
possibly damaging |
Het |
Iqch |
C |
T |
9: 63,534,337 (GRCm38) |
|
probably null |
Het |
Irf6 |
A |
G |
1: 193,167,535 (GRCm38) |
D255G |
probably benign |
Het |
Kif9 |
G |
A |
9: 110,517,719 (GRCm38) |
G642R |
probably null |
Het |
Klhl20 |
A |
G |
1: 161,106,742 (GRCm38) |
Y236H |
probably benign |
Het |
Krt39 |
T |
A |
11: 99,519,088 (GRCm38) |
K208* |
probably null |
Het |
Lama3 |
T |
A |
18: 12,537,781 (GRCm38) |
L808* |
probably null |
Het |
Lrp5 |
C |
T |
19: 3,597,346 (GRCm38) |
A1299T |
probably benign |
Het |
Lysmd4 |
A |
G |
7: 67,226,231 (GRCm38) |
Q214R |
probably benign |
Het |
Macf1 |
T |
A |
4: 123,369,848 (GRCm38) |
E6960V |
probably damaging |
Het |
Mcpt2 |
A |
G |
14: 56,043,699 (GRCm38) |
E120G |
probably benign |
Het |
Mpeg1 |
A |
G |
19: 12,462,356 (GRCm38) |
T393A |
probably benign |
Het |
Myh4 |
G |
A |
11: 67,255,682 (GRCm38) |
E1494K |
probably damaging |
Het |
Nbas |
T |
G |
12: 13,474,229 (GRCm38) |
S1695R |
possibly damaging |
Het |
Nlgn1 |
G |
T |
3: 25,440,037 (GRCm38) |
Y249* |
probably null |
Het |
Ntn4 |
C |
T |
10: 93,707,353 (GRCm38) |
R314W |
probably damaging |
Het |
Nup107 |
A |
G |
10: 117,750,906 (GRCm38) |
L910P |
probably damaging |
Het |
Obscn |
T |
A |
11: 59,040,296 (GRCm38) |
D5838V |
probably damaging |
Het |
Olfr1218 |
G |
A |
2: 89,054,859 (GRCm38) |
T189M |
possibly damaging |
Het |
Olfr347 |
T |
C |
2: 36,734,345 (GRCm38) |
I8T |
probably benign |
Het |
Olfr926 |
T |
C |
9: 38,877,596 (GRCm38) |
I140T |
possibly damaging |
Het |
Olfr978 |
T |
C |
9: 39,994,359 (GRCm38) |
I183T |
probably benign |
Het |
Otogl |
G |
T |
10: 107,854,264 (GRCm38) |
S915Y |
possibly damaging |
Het |
P2rx7 |
T |
A |
5: 122,681,032 (GRCm38) |
C506S |
probably damaging |
Het |
P4hb |
T |
C |
11: 120,563,218 (GRCm38) |
E350G |
probably benign |
Het |
Papolg |
A |
T |
11: 23,867,379 (GRCm38) |
V606E |
probably benign |
Het |
Pappa |
A |
T |
4: 65,340,743 (GRCm38) |
D1576V |
probably damaging |
Het |
Pclo |
G |
T |
5: 14,778,552 (GRCm38) |
V1402F |
probably damaging |
Het |
Pdcd11 |
A |
G |
19: 47,098,187 (GRCm38) |
T211A |
probably benign |
Het |
Pdzd2 |
T |
C |
15: 12,373,855 (GRCm38) |
R2065G |
possibly damaging |
Het |
Plcl2 |
T |
C |
17: 50,607,850 (GRCm38) |
V629A |
probably benign |
Het |
Prkcsh |
G |
A |
9: 22,004,575 (GRCm38) |
V92I |
possibly damaging |
Het |
Prpf19 |
G |
T |
19: 10,902,416 (GRCm38) |
V320F |
probably damaging |
Het |
Ptpn3 |
T |
A |
4: 57,239,682 (GRCm38) |
I283F |
probably damaging |
Het |
Rcc2 |
T |
A |
4: 140,720,604 (GRCm38) |
D480E |
probably benign |
Het |
Rnf182 |
G |
A |
13: 43,668,042 (GRCm38) |
C23Y |
probably damaging |
Het |
Rnf186 |
C |
T |
4: 138,967,362 (GRCm38) |
T71I |
probably benign |
Het |
Scyl3 |
A |
G |
1: 163,933,696 (GRCm38) |
|
probably null |
Het |
Slc12a6 |
G |
T |
2: 112,335,927 (GRCm38) |
|
probably null |
Het |
Slc1a2 |
C |
A |
2: 102,777,567 (GRCm38) |
S520Y |
probably damaging |
Het |
Slc35e2 |
T |
A |
4: 155,611,729 (GRCm38) |
L191Q |
probably damaging |
Het |
Snrnp40 |
C |
G |
4: 130,378,043 (GRCm38) |
|
probably null |
Het |
Snx33 |
T |
C |
9: 56,926,011 (GRCm38) |
H258R |
possibly damaging |
Het |
Tecpr2 |
A |
T |
12: 110,933,064 (GRCm38) |
H622L |
probably benign |
Het |
Thbs3 |
A |
T |
3: 89,226,406 (GRCm38) |
E888D |
probably damaging |
Het |
Tlk2 |
T |
C |
11: 105,221,298 (GRCm38) |
L159P |
probably benign |
Het |
Tmem70 |
A |
T |
1: 16,677,273 (GRCm38) |
T205S |
probably damaging |
Het |
Trappc10 |
T |
A |
10: 78,196,451 (GRCm38) |
H1001L |
probably benign |
Het |
Trim12a |
T |
C |
7: 104,300,857 (GRCm38) |
T292A |
probably benign |
Het |
Trip11 |
G |
A |
12: 101,883,333 (GRCm38) |
R92* |
probably null |
Het |
Trpa1 |
G |
A |
1: 14,899,388 (GRCm38) |
Q386* |
probably null |
Het |
Trpc4 |
T |
A |
3: 54,279,989 (GRCm38) |
V454D |
probably damaging |
Het |
Ttc36 |
A |
T |
9: 44,802,754 (GRCm38) |
D22E |
probably benign |
Het |
Ttk |
A |
T |
9: 83,869,263 (GRCm38) |
I798F |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,743,633 (GRCm38) |
I17312V |
probably damaging |
Het |
Txndc15 |
A |
T |
13: 55,718,062 (GRCm38) |
E113V |
possibly damaging |
Het |
Ube2d4 |
T |
A |
15: 58,846,599 (GRCm38) |
|
noncoding transcript |
Het |
Urb1 |
T |
A |
16: 90,761,695 (GRCm38) |
T1723S |
probably benign |
Het |
Vmn1r65 |
A |
T |
7: 6,008,266 (GRCm38) |
V323D |
possibly damaging |
Het |
Vmn2r54 |
A |
G |
7: 12,632,311 (GRCm38) |
M232T |
probably benign |
Het |
Wdr59 |
A |
G |
8: 111,476,181 (GRCm38) |
S577P |
probably damaging |
Het |
Wfikkn2 |
C |
T |
11: 94,238,123 (GRCm38) |
W397* |
probably null |
Het |
Ypel1 |
T |
A |
16: 17,081,647 (GRCm38) |
|
probably null |
Het |
Ythdf1 |
T |
A |
2: 180,910,970 (GRCm38) |
D484V |
probably damaging |
Het |
Zdhhc17 |
A |
G |
10: 110,947,293 (GRCm38) |
|
probably null |
Het |
Zfp472 |
A |
T |
17: 32,965,913 (GRCm38) |
H2L |
possibly damaging |
Het |
Zfp953 |
A |
T |
13: 67,345,358 (GRCm38) |
M74K |
probably benign |
Het |
Zmat4 |
C |
T |
8: 23,929,135 (GRCm38) |
T61M |
probably benign |
Het |
|
Other mutations in Cog2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01089:Cog2
|
APN |
8 |
124,545,243 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01092:Cog2
|
APN |
8 |
124,545,280 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01150:Cog2
|
APN |
8 |
124,542,891 (GRCm38) |
missense |
possibly damaging |
0.62 |
IGL02052:Cog2
|
APN |
8 |
124,542,888 (GRCm38) |
critical splice acceptor site |
probably null |
|
IGL02308:Cog2
|
APN |
8 |
124,533,212 (GRCm38) |
critical splice acceptor site |
probably null |
|
IGL02543:Cog2
|
APN |
8 |
124,529,959 (GRCm38) |
missense |
probably benign |
0.09 |
IGL02978:Cog2
|
APN |
8 |
124,550,336 (GRCm38) |
missense |
probably benign |
|
IGL03008:Cog2
|
APN |
8 |
124,535,392 (GRCm38) |
splice site |
probably benign |
|
IGL03144:Cog2
|
APN |
8 |
124,541,024 (GRCm38) |
missense |
probably damaging |
0.98 |
kugge
|
UTSW |
8 |
124,550,232 (GRCm38) |
missense |
probably damaging |
1.00 |
Pelota
|
UTSW |
8 |
124,550,306 (GRCm38) |
missense |
probably damaging |
1.00 |
PIT4677001:Cog2
|
UTSW |
8 |
124,545,271 (GRCm38) |
missense |
probably benign |
0.22 |
R0071:Cog2
|
UTSW |
8 |
124,548,668 (GRCm38) |
splice site |
probably benign |
|
R0071:Cog2
|
UTSW |
8 |
124,548,668 (GRCm38) |
splice site |
probably benign |
|
R0110:Cog2
|
UTSW |
8 |
124,529,058 (GRCm38) |
critical splice donor site |
probably null |
|
R0436:Cog2
|
UTSW |
8 |
124,548,514 (GRCm38) |
splice site |
probably benign |
|
R0450:Cog2
|
UTSW |
8 |
124,529,058 (GRCm38) |
critical splice donor site |
probably null |
|
R1365:Cog2
|
UTSW |
8 |
124,540,974 (GRCm38) |
missense |
probably damaging |
0.97 |
R1661:Cog2
|
UTSW |
8 |
124,542,890 (GRCm38) |
missense |
probably benign |
0.20 |
R1698:Cog2
|
UTSW |
8 |
124,525,683 (GRCm38) |
missense |
probably damaging |
1.00 |
R2122:Cog2
|
UTSW |
8 |
124,528,985 (GRCm38) |
missense |
possibly damaging |
0.91 |
R2398:Cog2
|
UTSW |
8 |
124,529,926 (GRCm38) |
missense |
probably benign |
0.07 |
R3855:Cog2
|
UTSW |
8 |
124,530,003 (GRCm38) |
critical splice donor site |
probably null |
|
R4580:Cog2
|
UTSW |
8 |
124,545,136 (GRCm38) |
missense |
probably benign |
0.01 |
R4803:Cog2
|
UTSW |
8 |
124,535,451 (GRCm38) |
missense |
probably damaging |
0.96 |
R5316:Cog2
|
UTSW |
8 |
124,529,040 (GRCm38) |
missense |
probably benign |
0.14 |
R5346:Cog2
|
UTSW |
8 |
124,546,631 (GRCm38) |
missense |
possibly damaging |
0.94 |
R5394:Cog2
|
UTSW |
8 |
124,532,529 (GRCm38) |
missense |
probably benign |
0.00 |
R5395:Cog2
|
UTSW |
8 |
124,545,221 (GRCm38) |
missense |
probably benign |
0.00 |
R5738:Cog2
|
UTSW |
8 |
124,546,038 (GRCm38) |
missense |
probably benign |
0.03 |
R5861:Cog2
|
UTSW |
8 |
124,537,878 (GRCm38) |
missense |
probably damaging |
1.00 |
R5894:Cog2
|
UTSW |
8 |
124,545,267 (GRCm38) |
missense |
probably benign |
0.00 |
R5941:Cog2
|
UTSW |
8 |
124,546,086 (GRCm38) |
missense |
probably benign |
|
R6186:Cog2
|
UTSW |
8 |
124,546,686 (GRCm38) |
missense |
probably damaging |
1.00 |
R6400:Cog2
|
UTSW |
8 |
124,550,306 (GRCm38) |
missense |
probably damaging |
1.00 |
R6518:Cog2
|
UTSW |
8 |
124,527,103 (GRCm38) |
nonsense |
probably null |
|
R6558:Cog2
|
UTSW |
8 |
124,550,232 (GRCm38) |
missense |
probably damaging |
1.00 |
R6717:Cog2
|
UTSW |
8 |
124,525,749 (GRCm38) |
missense |
probably damaging |
1.00 |
R6902:Cog2
|
UTSW |
8 |
124,546,691 (GRCm38) |
missense |
probably damaging |
1.00 |
R6914:Cog2
|
UTSW |
8 |
124,545,136 (GRCm38) |
missense |
probably benign |
0.00 |
R6942:Cog2
|
UTSW |
8 |
124,545,136 (GRCm38) |
missense |
probably benign |
0.00 |
R7103:Cog2
|
UTSW |
8 |
124,541,114 (GRCm38) |
critical splice donor site |
probably null |
|
R7274:Cog2
|
UTSW |
8 |
124,535,519 (GRCm38) |
missense |
possibly damaging |
0.71 |
R7641:Cog2
|
UTSW |
8 |
124,537,882 (GRCm38) |
missense |
probably damaging |
0.96 |
R7674:Cog2
|
UTSW |
8 |
124,537,882 (GRCm38) |
missense |
probably damaging |
0.96 |
R8559:Cog2
|
UTSW |
8 |
124,542,908 (GRCm38) |
missense |
probably benign |
0.25 |
R9190:Cog2
|
UTSW |
8 |
124,533,319 (GRCm38) |
missense |
probably damaging |
1.00 |
R9307:Cog2
|
UTSW |
8 |
124,527,098 (GRCm38) |
critical splice acceptor site |
probably null |
|
R9629:Cog2
|
UTSW |
8 |
124,533,386 (GRCm38) |
missense |
possibly damaging |
0.67 |
X0026:Cog2
|
UTSW |
8 |
124,546,020 (GRCm38) |
missense |
possibly damaging |
0.88 |
|