Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acly |
C |
G |
11: 100,403,800 (GRCm39) |
R362P |
possibly damaging |
Het |
Adam24 |
T |
A |
8: 41,134,805 (GRCm39) |
W758R |
probably benign |
Het |
Adam26b |
G |
T |
8: 43,973,307 (GRCm39) |
T565K |
probably damaging |
Het |
Adam7 |
T |
G |
14: 68,765,076 (GRCm39) |
|
probably benign |
Het |
Adamts19 |
A |
G |
18: 59,102,942 (GRCm39) |
|
probably benign |
Het |
Add1 |
A |
G |
5: 34,767,990 (GRCm39) |
|
probably benign |
Het |
Ago1 |
A |
G |
4: 126,357,484 (GRCm39) |
C64R |
probably benign |
Het |
Ankrd12 |
C |
T |
17: 66,356,943 (GRCm39) |
|
probably null |
Het |
Arhgef33 |
A |
G |
17: 80,688,863 (GRCm39) |
K820E |
probably damaging |
Het |
Arl9 |
T |
C |
5: 77,154,341 (GRCm39) |
V8A |
probably damaging |
Het |
Aspm |
T |
C |
1: 139,406,873 (GRCm39) |
L1920P |
probably damaging |
Het |
Atad2 |
A |
G |
15: 57,963,350 (GRCm39) |
|
probably benign |
Het |
Atp2b2 |
A |
T |
6: 113,770,835 (GRCm39) |
V358E |
probably benign |
Het |
C3ar1 |
A |
C |
6: 122,828,114 (GRCm39) |
C34W |
possibly damaging |
Het |
C6 |
G |
A |
15: 4,792,953 (GRCm39) |
V353M |
probably benign |
Het |
Capn7 |
T |
C |
14: 31,087,538 (GRCm39) |
I593T |
probably damaging |
Het |
Casc3 |
T |
A |
11: 98,712,319 (GRCm39) |
D119E |
probably damaging |
Het |
Ccna1 |
T |
A |
3: 54,961,785 (GRCm39) |
E45V |
probably damaging |
Het |
Cdc37 |
A |
G |
9: 21,053,576 (GRCm39) |
V180A |
probably benign |
Het |
Cdh23 |
A |
G |
10: 60,152,838 (GRCm39) |
I2393T |
probably damaging |
Het |
Cnbd1 |
T |
C |
4: 18,906,988 (GRCm39) |
|
probably benign |
Het |
Crygn |
A |
G |
5: 24,961,036 (GRCm39) |
M90T |
possibly damaging |
Het |
Cse1l |
T |
A |
2: 166,782,008 (GRCm39) |
S661R |
probably benign |
Het |
D830013O20Rik |
C |
T |
12: 73,411,095 (GRCm39) |
|
noncoding transcript |
Het |
Ddx24 |
C |
T |
12: 103,385,220 (GRCm39) |
|
probably null |
Het |
Dnah3 |
A |
T |
7: 119,676,998 (GRCm39) |
|
probably null |
Het |
Dnah9 |
C |
T |
11: 65,786,731 (GRCm39) |
G3634E |
probably benign |
Het |
Dnttip2 |
A |
T |
3: 122,069,810 (GRCm39) |
T342S |
probably benign |
Het |
Evx2 |
G |
T |
2: 74,489,388 (GRCm39) |
R125S |
probably damaging |
Het |
Fbxl5 |
A |
T |
5: 43,928,140 (GRCm39) |
L40Q |
probably damaging |
Het |
Git1 |
T |
A |
11: 77,391,899 (GRCm39) |
D240E |
probably benign |
Het |
Glp2r |
T |
A |
11: 67,600,534 (GRCm39) |
K438N |
probably damaging |
Het |
Hivep1 |
T |
A |
13: 42,309,629 (GRCm39) |
I623N |
probably benign |
Het |
Il17re |
A |
G |
6: 113,443,098 (GRCm39) |
E312G |
probably damaging |
Het |
Itgb7 |
G |
A |
15: 102,130,618 (GRCm39) |
|
probably benign |
Het |
Itpr3 |
A |
G |
17: 27,333,088 (GRCm39) |
Y1900C |
probably damaging |
Het |
Krt1c |
G |
A |
15: 101,721,626 (GRCm39) |
Q472* |
probably null |
Het |
Krtap5-1 |
A |
C |
7: 141,850,434 (GRCm39) |
C125G |
unknown |
Het |
Macf1 |
A |
G |
4: 123,328,709 (GRCm39) |
S2554P |
probably damaging |
Het |
Marchf10 |
C |
T |
11: 105,276,351 (GRCm39) |
G646R |
probably damaging |
Het |
Mrpl48 |
A |
C |
7: 100,195,560 (GRCm39) |
|
probably benign |
Het |
Myo16 |
A |
T |
8: 10,365,538 (GRCm39) |
|
probably benign |
Het |
Nrcam |
A |
T |
12: 44,631,628 (GRCm39) |
E1060D |
probably benign |
Het |
Nsd3 |
T |
A |
8: 26,170,709 (GRCm39) |
C731S |
probably damaging |
Het |
Nup85 |
T |
G |
11: 115,455,357 (GRCm39) |
M1R |
probably null |
Het |
Nxnl2 |
G |
T |
13: 51,325,483 (GRCm39) |
R42L |
probably damaging |
Het |
Oas3 |
G |
A |
5: 120,894,210 (GRCm39) |
R39C |
probably damaging |
Het |
Or13c25 |
G |
A |
4: 52,910,849 (GRCm39) |
T315M |
probably benign |
Het |
Orc1 |
C |
T |
4: 108,471,505 (GRCm39) |
R786* |
probably null |
Het |
P2ry6 |
A |
T |
7: 100,587,904 (GRCm39) |
W152R |
probably damaging |
Het |
Pex5l |
T |
C |
3: 33,047,102 (GRCm39) |
N283D |
possibly damaging |
Het |
Pgk2 |
T |
C |
17: 40,518,622 (GRCm39) |
I269V |
probably benign |
Het |
Phgdh |
T |
G |
3: 98,223,866 (GRCm39) |
|
probably benign |
Het |
Pzp |
A |
T |
6: 128,464,441 (GRCm39) |
L1362Q |
probably damaging |
Het |
Rbbp9 |
T |
C |
2: 144,390,026 (GRCm39) |
|
probably benign |
Het |
Rffl |
A |
G |
11: 82,700,989 (GRCm39) |
L244P |
probably damaging |
Het |
Serpina11 |
T |
C |
12: 103,952,131 (GRCm39) |
Y213C |
probably damaging |
Het |
Spopfm1 |
A |
G |
3: 94,173,229 (GRCm39) |
Y79C |
possibly damaging |
Het |
Srsf11 |
A |
G |
3: 157,742,172 (GRCm39) |
|
probably benign |
Het |
Sspo |
T |
A |
6: 48,463,570 (GRCm39) |
V3785E |
probably benign |
Het |
Svep1 |
A |
T |
4: 58,089,514 (GRCm39) |
S1632T |
possibly damaging |
Het |
Tm4sf1 |
T |
A |
3: 57,200,480 (GRCm39) |
D74V |
probably damaging |
Het |
Tmprss15 |
T |
A |
16: 78,831,222 (GRCm39) |
T393S |
probably benign |
Het |
Tnfaip3 |
A |
G |
10: 18,881,461 (GRCm39) |
L275P |
probably damaging |
Het |
Trim30c |
A |
G |
7: 104,031,636 (GRCm39) |
V393A |
probably benign |
Het |
Tssk2 |
T |
A |
16: 17,717,439 (GRCm39) |
S281T |
probably benign |
Het |
Tubb4a |
A |
G |
17: 57,388,499 (GRCm39) |
S176P |
probably damaging |
Het |
Unc45b |
T |
A |
11: 82,828,654 (GRCm39) |
M785K |
probably damaging |
Het |
Vldlr |
A |
T |
19: 27,215,786 (GRCm39) |
D261V |
probably damaging |
Het |
Vmn1r176 |
G |
T |
7: 23,535,010 (GRCm39) |
Q48K |
probably benign |
Het |
Vmn2r110 |
A |
T |
17: 20,794,317 (GRCm39) |
L784Q |
probably benign |
Het |
Vps13b |
A |
G |
15: 35,472,045 (GRCm39) |
T783A |
probably benign |
Het |
Zfp800 |
A |
G |
6: 28,243,846 (GRCm39) |
M373T |
probably damaging |
Het |
Zmym1 |
A |
G |
4: 126,941,704 (GRCm39) |
F895L |
possibly damaging |
Het |
|
Other mutations in Cngb3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00740:Cngb3
|
APN |
4 |
19,280,956 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01301:Cngb3
|
APN |
4 |
19,425,625 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01735:Cngb3
|
APN |
4 |
19,415,648 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01756:Cngb3
|
APN |
4 |
19,367,850 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01812:Cngb3
|
APN |
4 |
19,461,728 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02123:Cngb3
|
APN |
4 |
19,367,801 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02636:Cngb3
|
APN |
4 |
19,396,690 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02648:Cngb3
|
APN |
4 |
19,428,489 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02935:Cngb3
|
APN |
4 |
19,425,491 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03025:Cngb3
|
APN |
4 |
19,283,498 (GRCm39) |
splice site |
probably benign |
|
IGL03068:Cngb3
|
APN |
4 |
19,375,246 (GRCm39) |
missense |
possibly damaging |
0.92 |
braced
|
UTSW |
4 |
19,395,922 (GRCm39) |
splice site |
probably benign |
|
ANU18:Cngb3
|
UTSW |
4 |
19,425,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R0014:Cngb3
|
UTSW |
4 |
19,396,685 (GRCm39) |
missense |
probably benign |
0.33 |
R0014:Cngb3
|
UTSW |
4 |
19,396,685 (GRCm39) |
missense |
probably benign |
0.33 |
R0361:Cngb3
|
UTSW |
4 |
19,366,467 (GRCm39) |
missense |
probably benign |
0.00 |
R0480:Cngb3
|
UTSW |
4 |
19,309,517 (GRCm39) |
splice site |
probably benign |
|
R1103:Cngb3
|
UTSW |
4 |
19,309,658 (GRCm39) |
critical splice donor site |
probably null |
|
R1450:Cngb3
|
UTSW |
4 |
19,395,922 (GRCm39) |
splice site |
probably benign |
|
R1618:Cngb3
|
UTSW |
4 |
19,364,260 (GRCm39) |
missense |
probably benign |
|
R1891:Cngb3
|
UTSW |
4 |
19,366,446 (GRCm39) |
missense |
probably benign |
0.00 |
R2196:Cngb3
|
UTSW |
4 |
19,415,690 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2850:Cngb3
|
UTSW |
4 |
19,415,690 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3909:Cngb3
|
UTSW |
4 |
19,461,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R3941:Cngb3
|
UTSW |
4 |
19,396,786 (GRCm39) |
missense |
probably benign |
0.00 |
R4348:Cngb3
|
UTSW |
4 |
19,396,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R4490:Cngb3
|
UTSW |
4 |
19,415,684 (GRCm39) |
missense |
probably benign |
0.41 |
R4493:Cngb3
|
UTSW |
4 |
19,367,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R4578:Cngb3
|
UTSW |
4 |
19,425,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R4719:Cngb3
|
UTSW |
4 |
19,309,562 (GRCm39) |
missense |
probably benign |
|
R4774:Cngb3
|
UTSW |
4 |
19,415,713 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4860:Cngb3
|
UTSW |
4 |
19,425,569 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4860:Cngb3
|
UTSW |
4 |
19,425,569 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4898:Cngb3
|
UTSW |
4 |
19,395,926 (GRCm39) |
missense |
probably benign |
0.08 |
R5216:Cngb3
|
UTSW |
4 |
19,415,729 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5647:Cngb3
|
UTSW |
4 |
19,364,266 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5945:Cngb3
|
UTSW |
4 |
19,283,579 (GRCm39) |
missense |
probably null |
0.00 |
R6586:Cngb3
|
UTSW |
4 |
19,280,946 (GRCm39) |
missense |
probably damaging |
0.99 |
R6650:Cngb3
|
UTSW |
4 |
19,364,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R6651:Cngb3
|
UTSW |
4 |
19,375,231 (GRCm39) |
missense |
probably benign |
0.01 |
R7070:Cngb3
|
UTSW |
4 |
19,425,593 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7316:Cngb3
|
UTSW |
4 |
19,425,599 (GRCm39) |
missense |
probably benign |
0.16 |
R7371:Cngb3
|
UTSW |
4 |
19,425,575 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7554:Cngb3
|
UTSW |
4 |
19,461,753 (GRCm39) |
nonsense |
probably null |
|
R7755:Cngb3
|
UTSW |
4 |
19,461,684 (GRCm39) |
missense |
probably benign |
0.01 |
R8004:Cngb3
|
UTSW |
4 |
19,505,273 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8025:Cngb3
|
UTSW |
4 |
19,280,960 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9143:Cngb3
|
UTSW |
4 |
19,375,190 (GRCm39) |
splice site |
probably benign |
|
R9366:Cngb3
|
UTSW |
4 |
19,395,983 (GRCm39) |
missense |
probably benign |
0.03 |
R9489:Cngb3
|
UTSW |
4 |
19,505,187 (GRCm39) |
missense |
probably benign |
0.17 |
R9605:Cngb3
|
UTSW |
4 |
19,505,187 (GRCm39) |
missense |
probably benign |
0.17 |
X0062:Cngb3
|
UTSW |
4 |
19,364,189 (GRCm39) |
missense |
possibly damaging |
0.91 |
X0067:Cngb3
|
UTSW |
4 |
19,367,753 (GRCm39) |
missense |
probably damaging |
0.99 |
|