Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aacs |
C |
T |
5: 125,583,326 (GRCm39) |
T294M |
probably damaging |
Het |
Brf2 |
G |
T |
8: 27,614,496 (GRCm39) |
T230N |
possibly damaging |
Het |
Ccne2 |
A |
G |
4: 11,199,293 (GRCm39) |
|
probably benign |
Het |
Crbn |
T |
C |
6: 106,771,987 (GRCm39) |
K106E |
possibly damaging |
Het |
Cttnbp2nl |
G |
A |
3: 104,912,117 (GRCm39) |
T589I |
probably benign |
Het |
Dock10 |
A |
G |
1: 80,514,643 (GRCm39) |
S1091P |
probably damaging |
Het |
Fh1 |
A |
G |
1: 175,442,316 (GRCm39) |
V178A |
probably damaging |
Het |
Fndc1 |
A |
G |
17: 8,003,253 (GRCm39) |
S111P |
probably damaging |
Het |
Frk |
A |
G |
10: 34,360,001 (GRCm39) |
M1V |
probably null |
Het |
Gm29394 |
C |
T |
15: 57,912,024 (GRCm39) |
|
probably benign |
Het |
Herc2 |
A |
G |
7: 55,813,572 (GRCm39) |
D2601G |
probably damaging |
Het |
Hspa13 |
T |
C |
16: 75,561,974 (GRCm39) |
D75G |
probably benign |
Het |
Itgav |
T |
C |
2: 83,632,229 (GRCm39) |
|
probably null |
Het |
Kif6 |
A |
T |
17: 50,065,671 (GRCm39) |
|
probably benign |
Het |
Lypla1 |
G |
A |
1: 4,911,201 (GRCm39) |
R104Q |
probably benign |
Het |
Map1b |
T |
C |
13: 99,570,595 (GRCm39) |
K709E |
unknown |
Het |
Or52l1 |
A |
T |
7: 104,830,088 (GRCm39) |
I159K |
probably damaging |
Het |
Or56b1b |
G |
A |
7: 108,164,402 (GRCm39) |
P200L |
probably benign |
Het |
Pcdhb16 |
A |
T |
18: 37,611,249 (GRCm39) |
K70* |
probably null |
Het |
Pex5l |
T |
G |
3: 33,061,327 (GRCm39) |
D174A |
probably benign |
Het |
Plac8l1 |
A |
T |
18: 42,313,460 (GRCm39) |
M94K |
probably benign |
Het |
Plxna1 |
T |
C |
6: 89,311,757 (GRCm39) |
|
probably benign |
Het |
Psg26 |
T |
C |
7: 18,208,996 (GRCm39) |
T471A |
probably benign |
Het |
Pus3 |
C |
A |
9: 35,477,968 (GRCm39) |
T400K |
probably benign |
Het |
Pxk |
T |
C |
14: 8,136,863 (GRCm38) |
|
probably benign |
Het |
Rapgef2 |
T |
C |
3: 78,996,057 (GRCm39) |
T569A |
probably benign |
Het |
Sall4 |
T |
C |
2: 168,597,964 (GRCm39) |
Q292R |
possibly damaging |
Het |
Slc18b1 |
A |
G |
10: 23,674,647 (GRCm39) |
D34G |
probably damaging |
Het |
Slc45a1 |
T |
C |
4: 150,722,517 (GRCm39) |
R456G |
probably damaging |
Het |
Sox13 |
T |
C |
1: 133,318,536 (GRCm39) |
R81G |
possibly damaging |
Het |
Spag9 |
A |
G |
11: 93,951,109 (GRCm39) |
|
probably benign |
Het |
Ston1 |
C |
T |
17: 88,942,788 (GRCm39) |
P65S |
probably damaging |
Het |
Tada2b |
A |
T |
5: 36,633,761 (GRCm39) |
D197E |
probably benign |
Het |
Tcim |
T |
A |
8: 24,928,765 (GRCm39) |
R50W |
probably damaging |
Het |
Tnpo3 |
T |
C |
6: 29,579,688 (GRCm39) |
D235G |
probably benign |
Het |
Trim59 |
A |
G |
3: 68,944,137 (GRCm39) |
V401A |
probably benign |
Het |
Trpm3 |
A |
C |
19: 22,425,741 (GRCm39) |
Q32P |
probably benign |
Het |
Tubgcp5 |
T |
A |
7: 55,480,614 (GRCm39) |
M1018K |
probably damaging |
Het |
Ube2o |
A |
G |
11: 116,437,689 (GRCm39) |
|
probably benign |
Het |
Uvrag |
G |
T |
7: 98,537,350 (GRCm39) |
S615* |
probably null |
Het |
Vmn2r6 |
T |
A |
3: 64,463,929 (GRCm39) |
I302L |
probably benign |
Het |
Vmn2r73 |
C |
T |
7: 85,521,198 (GRCm39) |
V257I |
probably benign |
Het |
|
Other mutations in Ugcg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01447:Ugcg
|
APN |
4 |
59,213,865 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01768:Ugcg
|
APN |
4 |
59,217,216 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02636:Ugcg
|
APN |
4 |
59,207,763 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02672:Ugcg
|
APN |
4 |
59,218,587 (GRCm39) |
splice site |
probably benign |
|
IGL02798:Ugcg
|
APN |
4 |
59,220,346 (GRCm39) |
missense |
probably damaging |
1.00 |
congee
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
cream_o_wheat
|
UTSW |
4 |
59,220,387 (GRCm39) |
missense |
possibly damaging |
0.91 |
gruel
|
UTSW |
4 |
59,189,690 (GRCm39) |
missense |
probably benign |
|
Porridge
|
UTSW |
4 |
59,219,530 (GRCm39) |
missense |
possibly damaging |
0.86 |
slop
|
UTSW |
4 |
59,211,883 (GRCm39) |
missense |
probably benign |
0.16 |
wheatina
|
UTSW |
4 |
59,220,272 (GRCm39) |
missense |
probably damaging |
0.96 |
PIT4382001:Ugcg
|
UTSW |
4 |
59,213,246 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0013:Ugcg
|
UTSW |
4 |
59,213,931 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0013:Ugcg
|
UTSW |
4 |
59,213,931 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0068:Ugcg
|
UTSW |
4 |
59,217,130 (GRCm39) |
missense |
probably benign |
0.16 |
R0068:Ugcg
|
UTSW |
4 |
59,217,130 (GRCm39) |
missense |
probably benign |
0.16 |
R0119:Ugcg
|
UTSW |
4 |
59,217,036 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0230:Ugcg
|
UTSW |
4 |
59,189,739 (GRCm39) |
nonsense |
probably null |
|
R0299:Ugcg
|
UTSW |
4 |
59,217,036 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0384:Ugcg
|
UTSW |
4 |
59,220,387 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0499:Ugcg
|
UTSW |
4 |
59,217,036 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0645:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R0688:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R0726:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R0802:Ugcg
|
UTSW |
4 |
59,189,685 (GRCm39) |
missense |
probably benign |
0.00 |
R0803:Ugcg
|
UTSW |
4 |
59,189,685 (GRCm39) |
missense |
probably benign |
0.00 |
R0811:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R0812:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R0828:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R0831:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R0944:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R0945:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R0947:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1104:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1209:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1210:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1252:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1253:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1255:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1488:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1490:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1548:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1698:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1771:Ugcg
|
UTSW |
4 |
59,207,775 (GRCm39) |
missense |
probably benign |
0.05 |
R1776:Ugcg
|
UTSW |
4 |
59,207,775 (GRCm39) |
missense |
probably benign |
0.05 |
R1781:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1794:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1840:Ugcg
|
UTSW |
4 |
59,219,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R1942:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2228:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2229:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2237:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2239:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2314:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2337:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2338:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2340:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2422:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2426:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2433:Ugcg
|
UTSW |
4 |
59,207,876 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2680:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3076:Ugcg
|
UTSW |
4 |
59,213,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R3078:Ugcg
|
UTSW |
4 |
59,213,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R3689:Ugcg
|
UTSW |
4 |
59,211,883 (GRCm39) |
missense |
probably benign |
0.16 |
R3732:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3732:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3733:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3767:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3768:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3769:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3771:Ugcg
|
UTSW |
4 |
59,189,690 (GRCm39) |
missense |
probably benign |
|
R3847:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3848:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3916:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3917:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3958:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3959:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R4023:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R4024:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R4025:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R4065:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R4066:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R4427:Ugcg
|
UTSW |
4 |
59,219,555 (GRCm39) |
missense |
probably benign |
0.02 |
R5842:Ugcg
|
UTSW |
4 |
59,219,545 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6012:Ugcg
|
UTSW |
4 |
59,220,272 (GRCm39) |
missense |
probably damaging |
0.96 |
R6080:Ugcg
|
UTSW |
4 |
59,218,524 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6762:Ugcg
|
UTSW |
4 |
59,219,530 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7194:Ugcg
|
UTSW |
4 |
59,213,210 (GRCm39) |
missense |
probably damaging |
0.99 |
R7286:Ugcg
|
UTSW |
4 |
59,217,111 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7362:Ugcg
|
UTSW |
4 |
59,217,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R7472:Ugcg
|
UTSW |
4 |
59,217,156 (GRCm39) |
missense |
probably benign |
|
R7638:Ugcg
|
UTSW |
4 |
59,220,299 (GRCm39) |
missense |
probably benign |
0.26 |
R7866:Ugcg
|
UTSW |
4 |
59,211,927 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8170:Ugcg
|
UTSW |
4 |
59,211,974 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8488:Ugcg
|
UTSW |
4 |
59,213,896 (GRCm39) |
missense |
probably benign |
0.00 |
R8793:Ugcg
|
UTSW |
4 |
59,207,794 (GRCm39) |
missense |
probably benign |
0.22 |
R9441:Ugcg
|
UTSW |
4 |
59,207,843 (GRCm39) |
missense |
probably damaging |
1.00 |
Y4336:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
Y4337:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|