Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aldh16a1 |
C |
T |
7: 44,796,930 (GRCm39) |
W66* |
probably null |
Het |
Arhgap39 |
T |
C |
15: 76,636,007 (GRCm39) |
D76G |
probably damaging |
Het |
Arhgef2 |
G |
A |
3: 88,550,924 (GRCm39) |
|
probably null |
Het |
C1qtnf2 |
T |
C |
11: 43,376,835 (GRCm39) |
M99T |
probably damaging |
Het |
Cyren |
A |
G |
6: 34,851,593 (GRCm39) |
L87P |
probably damaging |
Het |
Eml3 |
G |
A |
19: 8,912,379 (GRCm39) |
C392Y |
possibly damaging |
Het |
Ephb4 |
C |
A |
5: 137,358,678 (GRCm39) |
P287Q |
probably benign |
Het |
Fat4 |
G |
T |
3: 38,941,485 (GRCm39) |
R126L |
probably benign |
Het |
Flt3 |
T |
C |
5: 147,271,719 (GRCm39) |
M858V |
probably damaging |
Het |
Gprin3 |
A |
C |
6: 59,331,698 (GRCm39) |
I203R |
probably benign |
Het |
Ipo13 |
G |
A |
4: 117,760,400 (GRCm39) |
T649I |
possibly damaging |
Het |
Krba1 |
A |
G |
6: 48,392,678 (GRCm39) |
D818G |
possibly damaging |
Het |
Llgl1 |
G |
A |
11: 60,603,806 (GRCm39) |
G1016R |
probably benign |
Het |
Loxl4 |
A |
G |
19: 42,596,066 (GRCm39) |
V142A |
probably benign |
Het |
Mthfd1 |
A |
G |
12: 76,340,992 (GRCm39) |
I464V |
probably benign |
Het |
Mycs |
C |
A |
X: 5,380,131 (GRCm39) |
K316N |
probably damaging |
Het |
Ncor2 |
A |
G |
5: 125,103,839 (GRCm39) |
|
probably benign |
Het |
Nlrc3 |
A |
G |
16: 3,781,909 (GRCm39) |
F516S |
probably damaging |
Het |
Oacyl |
A |
G |
18: 65,882,743 (GRCm39) |
S540G |
probably damaging |
Het |
Olfml2a |
A |
T |
2: 38,850,242 (GRCm39) |
T653S |
probably damaging |
Het |
Or8s16 |
C |
T |
15: 98,211,369 (GRCm39) |
V21I |
probably benign |
Het |
Pcnx2 |
A |
T |
8: 126,500,685 (GRCm39) |
N1468K |
probably damaging |
Het |
Plbd1 |
A |
G |
6: 136,611,503 (GRCm39) |
I258T |
probably damaging |
Het |
Ppargc1b |
C |
G |
18: 61,442,164 (GRCm39) |
D591H |
probably damaging |
Het |
Pramel21 |
A |
T |
4: 143,344,161 (GRCm39) |
Y487F |
possibly damaging |
Het |
Prop1 |
C |
T |
11: 50,844,153 (GRCm39) |
V27M |
probably damaging |
Het |
Rfx4 |
T |
G |
10: 84,650,625 (GRCm39) |
|
probably null |
Het |
Rgs11 |
C |
T |
17: 26,422,437 (GRCm39) |
|
probably benign |
Het |
Slc6a5 |
T |
A |
7: 49,595,260 (GRCm39) |
F541I |
probably damaging |
Het |
Srgap3 |
A |
T |
6: 112,699,807 (GRCm39) |
V1057E |
possibly damaging |
Het |
Synpo2 |
A |
T |
3: 122,907,946 (GRCm39) |
W457R |
probably damaging |
Het |
Tet2 |
T |
A |
3: 133,193,721 (GRCm39) |
N238Y |
possibly damaging |
Het |
Tiam2 |
T |
A |
17: 3,487,540 (GRCm39) |
M687K |
probably damaging |
Het |
Ticrr |
A |
G |
7: 79,346,438 (GRCm39) |
E1866G |
probably benign |
Het |
Tspan8 |
T |
C |
10: 115,669,156 (GRCm39) |
S64P |
possibly damaging |
Het |
Ugt2b37 |
C |
T |
5: 87,402,265 (GRCm39) |
G122D |
probably benign |
Het |
Uqcrc2 |
A |
G |
7: 120,237,111 (GRCm39) |
E53G |
probably damaging |
Het |
Vcan |
T |
C |
13: 89,852,071 (GRCm39) |
D963G |
probably damaging |
Het |
Vmn2r24 |
T |
A |
6: 123,764,226 (GRCm39) |
Y368N |
possibly damaging |
Het |
Wdr5 |
A |
G |
2: 27,418,323 (GRCm39) |
T208A |
probably benign |
Het |
Zbtb18 |
A |
G |
1: 177,275,936 (GRCm39) |
Y423C |
probably damaging |
Het |
Zc3h6 |
A |
G |
2: 128,839,696 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Insr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01099:Insr
|
APN |
8 |
3,308,682 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01986:Insr
|
APN |
8 |
3,208,817 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02135:Insr
|
APN |
8 |
3,308,741 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02203:Insr
|
APN |
8 |
3,205,817 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02220:Insr
|
APN |
8 |
3,209,578 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02678:Insr
|
APN |
8 |
3,223,570 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02961:Insr
|
APN |
8 |
3,308,785 (GRCm39) |
missense |
probably benign |
0.08 |
IGL03099:Insr
|
APN |
8 |
3,308,715 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03125:Insr
|
APN |
8 |
3,234,972 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03290:Insr
|
APN |
8 |
3,308,574 (GRCm39) |
missense |
probably damaging |
1.00 |
gummi_bear
|
UTSW |
8 |
3,211,770 (GRCm39) |
missense |
probably damaging |
1.00 |
jellybelly
|
UTSW |
8 |
3,308,841 (GRCm39) |
missense |
probably damaging |
1.00 |
Patently
|
UTSW |
8 |
3,209,475 (GRCm39) |
missense |
probably damaging |
1.00 |
trolli
|
UTSW |
8 |
3,248,111 (GRCm39) |
missense |
probably benign |
0.31 |
R0047:Insr
|
UTSW |
8 |
3,252,947 (GRCm39) |
missense |
probably damaging |
0.97 |
R0053:Insr
|
UTSW |
8 |
3,205,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R0053:Insr
|
UTSW |
8 |
3,205,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R0480:Insr
|
UTSW |
8 |
3,211,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R0748:Insr
|
UTSW |
8 |
3,308,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R0919:Insr
|
UTSW |
8 |
3,208,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R1348:Insr
|
UTSW |
8 |
3,242,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Insr
|
UTSW |
8 |
3,219,720 (GRCm39) |
missense |
probably damaging |
0.99 |
R1467:Insr
|
UTSW |
8 |
3,219,720 (GRCm39) |
missense |
probably damaging |
0.99 |
R1568:Insr
|
UTSW |
8 |
3,215,576 (GRCm39) |
missense |
probably benign |
|
R1768:Insr
|
UTSW |
8 |
3,209,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R2093:Insr
|
UTSW |
8 |
3,254,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R2111:Insr
|
UTSW |
8 |
3,219,748 (GRCm39) |
missense |
probably benign |
0.17 |
R2112:Insr
|
UTSW |
8 |
3,219,748 (GRCm39) |
missense |
probably benign |
0.17 |
R2352:Insr
|
UTSW |
8 |
3,242,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R2364:Insr
|
UTSW |
8 |
3,224,820 (GRCm39) |
missense |
probably benign |
|
R2842:Insr
|
UTSW |
8 |
3,252,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R3162:Insr
|
UTSW |
8 |
3,211,416 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3162:Insr
|
UTSW |
8 |
3,211,416 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4081:Insr
|
UTSW |
8 |
3,261,391 (GRCm39) |
missense |
probably benign |
0.00 |
R4441:Insr
|
UTSW |
8 |
3,244,902 (GRCm39) |
missense |
probably benign |
0.00 |
R4672:Insr
|
UTSW |
8 |
3,217,501 (GRCm39) |
critical splice donor site |
probably null |
|
R4687:Insr
|
UTSW |
8 |
3,211,709 (GRCm39) |
missense |
probably benign |
0.42 |
R4708:Insr
|
UTSW |
8 |
3,261,346 (GRCm39) |
intron |
probably benign |
|
R4890:Insr
|
UTSW |
8 |
3,248,234 (GRCm39) |
missense |
probably benign |
0.16 |
R4949:Insr
|
UTSW |
8 |
3,235,059 (GRCm39) |
missense |
probably benign |
0.04 |
R4996:Insr
|
UTSW |
8 |
3,242,665 (GRCm39) |
missense |
probably null |
0.98 |
R5073:Insr
|
UTSW |
8 |
3,209,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R5176:Insr
|
UTSW |
8 |
3,208,742 (GRCm39) |
missense |
probably benign |
0.03 |
R5200:Insr
|
UTSW |
8 |
3,248,059 (GRCm39) |
critical splice donor site |
probably null |
|
R5323:Insr
|
UTSW |
8 |
3,252,902 (GRCm39) |
missense |
probably benign |
0.02 |
R5453:Insr
|
UTSW |
8 |
3,205,694 (GRCm39) |
missense |
probably benign |
0.06 |
R5516:Insr
|
UTSW |
8 |
3,205,764 (GRCm39) |
nonsense |
probably null |
|
R5704:Insr
|
UTSW |
8 |
3,235,122 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5820:Insr
|
UTSW |
8 |
3,205,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R5894:Insr
|
UTSW |
8 |
3,224,869 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5937:Insr
|
UTSW |
8 |
3,224,808 (GRCm39) |
missense |
probably benign |
|
R5966:Insr
|
UTSW |
8 |
3,308,697 (GRCm39) |
missense |
probably benign |
0.04 |
R6134:Insr
|
UTSW |
8 |
3,242,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R6352:Insr
|
UTSW |
8 |
3,223,479 (GRCm39) |
critical splice donor site |
probably null |
|
R6423:Insr
|
UTSW |
8 |
3,223,566 (GRCm39) |
missense |
probably benign |
|
R6687:Insr
|
UTSW |
8 |
3,248,111 (GRCm39) |
missense |
probably benign |
0.31 |
R6985:Insr
|
UTSW |
8 |
3,211,372 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6993:Insr
|
UTSW |
8 |
3,308,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R7041:Insr
|
UTSW |
8 |
3,308,418 (GRCm39) |
missense |
probably benign |
|
R7109:Insr
|
UTSW |
8 |
3,308,481 (GRCm39) |
missense |
probably benign |
0.33 |
R7216:Insr
|
UTSW |
8 |
3,253,034 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7287:Insr
|
UTSW |
8 |
3,219,717 (GRCm39) |
missense |
probably benign |
0.00 |
R7378:Insr
|
UTSW |
8 |
3,248,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R7525:Insr
|
UTSW |
8 |
3,242,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R7572:Insr
|
UTSW |
8 |
3,223,602 (GRCm39) |
missense |
probably benign |
0.11 |
R7636:Insr
|
UTSW |
8 |
3,308,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R7684:Insr
|
UTSW |
8 |
3,219,753 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7840:Insr
|
UTSW |
8 |
3,308,415 (GRCm39) |
missense |
probably benign |
0.04 |
R8075:Insr
|
UTSW |
8 |
3,205,862 (GRCm39) |
missense |
probably benign |
0.17 |
R8161:Insr
|
UTSW |
8 |
3,308,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R8220:Insr
|
UTSW |
8 |
3,208,702 (GRCm39) |
missense |
probably benign |
0.01 |
R8434:Insr
|
UTSW |
8 |
3,215,514 (GRCm39) |
splice site |
probably benign |
|
R8810:Insr
|
UTSW |
8 |
3,219,714 (GRCm39) |
missense |
probably benign |
|
R8865:Insr
|
UTSW |
8 |
3,211,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R8884:Insr
|
UTSW |
8 |
3,205,679 (GRCm39) |
missense |
probably benign |
|
R9134:Insr
|
UTSW |
8 |
3,308,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R9359:Insr
|
UTSW |
8 |
3,208,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R9407:Insr
|
UTSW |
8 |
3,235,106 (GRCm39) |
missense |
probably benign |
|
R9647:Insr
|
UTSW |
8 |
3,205,874 (GRCm39) |
missense |
probably benign |
0.06 |
|