Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abat |
T |
A |
16: 8,400,691 (GRCm39) |
Y97N |
probably damaging |
Het |
Adrm1b |
C |
A |
3: 92,336,791 (GRCm39) |
|
probably null |
Het |
Akr1b10 |
A |
T |
6: 34,364,715 (GRCm39) |
I59F |
probably damaging |
Het |
Bank1 |
T |
C |
3: 135,919,598 (GRCm39) |
D266G |
probably benign |
Het |
Bmp2k |
T |
A |
5: 97,211,467 (GRCm39) |
|
probably null |
Het |
Cdc42bpa |
A |
G |
1: 179,892,655 (GRCm39) |
Y273C |
probably damaging |
Het |
Chfr |
G |
T |
5: 110,292,517 (GRCm39) |
|
probably null |
Het |
Dapk1 |
A |
T |
13: 60,909,476 (GRCm39) |
Q1363L |
probably benign |
Het |
Ddx23 |
A |
T |
15: 98,548,651 (GRCm39) |
D352E |
possibly damaging |
Het |
Ect2 |
T |
C |
3: 27,152,474 (GRCm39) |
|
probably benign |
Het |
Efcab10 |
A |
C |
12: 33,448,592 (GRCm39) |
D107A |
probably damaging |
Het |
Fcgr4 |
G |
A |
1: 170,853,233 (GRCm39) |
G146D |
possibly damaging |
Het |
Fgd5 |
A |
G |
6: 91,966,322 (GRCm39) |
T694A |
possibly damaging |
Het |
Ghr |
T |
C |
15: 3,370,409 (GRCm39) |
D152G |
probably damaging |
Het |
Gli2 |
A |
C |
1: 118,765,445 (GRCm39) |
L902R |
probably damaging |
Het |
Glis2 |
G |
A |
16: 4,429,172 (GRCm39) |
G125D |
possibly damaging |
Het |
Gmcl1 |
A |
G |
6: 86,698,394 (GRCm39) |
Y168H |
probably damaging |
Het |
Golga4 |
A |
G |
9: 118,388,764 (GRCm39) |
K1962R |
possibly damaging |
Het |
Hebp1 |
T |
A |
6: 135,145,055 (GRCm39) |
E14V |
probably damaging |
Het |
Hhla1 |
A |
C |
15: 65,820,339 (GRCm39) |
I137S |
probably damaging |
Het |
Hivep1 |
A |
G |
13: 42,337,934 (GRCm39) |
H2671R |
possibly damaging |
Het |
Hltf |
A |
G |
3: 20,113,098 (GRCm39) |
Y19C |
probably damaging |
Het |
Hsd3b2 |
A |
T |
3: 98,619,333 (GRCm39) |
M204K |
probably benign |
Het |
Hspa4l |
A |
T |
3: 40,736,031 (GRCm39) |
I551F |
probably benign |
Het |
Itpkc |
A |
T |
7: 26,927,490 (GRCm39) |
D141E |
probably damaging |
Het |
Kcnc3 |
A |
G |
7: 44,248,296 (GRCm39) |
D757G |
probably benign |
Het |
Mettl16 |
A |
T |
11: 74,678,474 (GRCm39) |
Y141F |
probably damaging |
Het |
Mfng |
G |
A |
15: 78,640,840 (GRCm39) |
R302C |
probably damaging |
Het |
Mogs |
T |
A |
6: 83,094,363 (GRCm39) |
S393R |
probably damaging |
Het |
Mrps28 |
A |
G |
3: 8,965,044 (GRCm39) |
|
probably null |
Het |
Nfat5 |
T |
C |
8: 108,093,765 (GRCm39) |
S150P |
probably benign |
Het |
Or2w1 |
T |
C |
13: 21,316,978 (GRCm39) |
V11A |
probably benign |
Het |
Or7d10 |
A |
T |
9: 19,832,237 (GRCm39) |
H244L |
probably damaging |
Het |
Pcdh12 |
A |
G |
18: 38,416,805 (GRCm39) |
S107P |
probably damaging |
Het |
Phf21a |
G |
A |
2: 92,182,120 (GRCm39) |
D463N |
probably damaging |
Het |
Picalm |
A |
C |
7: 89,844,908 (GRCm39) |
I567L |
probably benign |
Het |
Pla2g4a |
T |
A |
1: 149,808,428 (GRCm39) |
D5V |
possibly damaging |
Het |
Sspo |
C |
T |
6: 48,428,305 (GRCm39) |
T222M |
probably benign |
Het |
Stard9 |
T |
C |
2: 120,535,067 (GRCm39) |
S3775P |
probably damaging |
Het |
Stk31 |
A |
T |
6: 49,446,243 (GRCm39) |
D982V |
probably damaging |
Het |
Tas2r113 |
C |
T |
6: 132,870,644 (GRCm39) |
T224I |
probably damaging |
Het |
Tbc1d15 |
T |
C |
10: 115,055,112 (GRCm39) |
D310G |
probably damaging |
Het |
Tcf12 |
G |
T |
9: 71,766,229 (GRCm39) |
T468K |
possibly damaging |
Het |
Tenm4 |
A |
G |
7: 96,171,640 (GRCm39) |
|
probably benign |
Het |
Tet2 |
A |
G |
3: 133,172,542 (GRCm39) |
Y1907H |
possibly damaging |
Het |
Thsd7a |
T |
C |
6: 12,379,388 (GRCm39) |
|
probably null |
Het |
Tln1 |
T |
A |
4: 43,539,508 (GRCm39) |
T1605S |
probably benign |
Het |
Trp53bp1 |
T |
C |
2: 121,087,083 (GRCm39) |
Y191C |
probably benign |
Het |
Ugcg |
T |
A |
4: 59,220,272 (GRCm39) |
I355N |
probably damaging |
Het |
Vmn1r21 |
A |
T |
6: 57,820,891 (GRCm39) |
D184E |
probably damaging |
Het |
Vsig10l |
T |
A |
7: 43,117,439 (GRCm39) |
D575E |
probably damaging |
Het |
Zan |
G |
A |
5: 137,462,791 (GRCm39) |
T796I |
unknown |
Het |
Zfp639 |
A |
G |
3: 32,573,271 (GRCm39) |
D61G |
probably damaging |
Het |
|
Other mutations in Als2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00772:Als2
|
APN |
1 |
59,209,055 (GRCm39) |
nonsense |
probably null |
|
IGL00924:Als2
|
APN |
1 |
59,255,021 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00949:Als2
|
APN |
1 |
59,254,731 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00950:Als2
|
APN |
1 |
59,254,541 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01090:Als2
|
APN |
1 |
59,254,775 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01116:Als2
|
APN |
1 |
59,225,163 (GRCm39) |
splice site |
probably benign |
|
IGL02001:Als2
|
APN |
1 |
59,219,347 (GRCm39) |
splice site |
probably benign |
|
IGL02075:Als2
|
APN |
1 |
59,246,945 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02441:Als2
|
APN |
1 |
59,254,631 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02728:Als2
|
APN |
1 |
59,235,506 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02740:Als2
|
APN |
1 |
59,209,078 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02885:Als2
|
APN |
1 |
59,206,650 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02896:Als2
|
APN |
1 |
59,222,946 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02978:Als2
|
APN |
1 |
59,254,324 (GRCm39) |
missense |
probably benign |
0.32 |
IGL03032:Als2
|
APN |
1 |
59,255,189 (GRCm39) |
splice site |
probably benign |
|
IGL03065:Als2
|
APN |
1 |
59,255,031 (GRCm39) |
missense |
probably benign |
|
IGL03212:Als2
|
APN |
1 |
59,242,085 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03226:Als2
|
APN |
1 |
59,225,679 (GRCm39) |
missense |
probably benign |
0.43 |
R0014:Als2
|
UTSW |
1 |
59,250,547 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0243:Als2
|
UTSW |
1 |
59,254,546 (GRCm39) |
missense |
probably benign |
|
R0326:Als2
|
UTSW |
1 |
59,219,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R0376:Als2
|
UTSW |
1 |
59,254,724 (GRCm39) |
missense |
probably benign |
0.00 |
R0605:Als2
|
UTSW |
1 |
59,207,573 (GRCm39) |
missense |
probably benign |
0.02 |
R1607:Als2
|
UTSW |
1 |
59,219,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R1631:Als2
|
UTSW |
1 |
59,257,226 (GRCm39) |
missense |
probably benign |
0.00 |
R1657:Als2
|
UTSW |
1 |
59,219,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R1763:Als2
|
UTSW |
1 |
59,214,150 (GRCm39) |
missense |
probably benign |
|
R1950:Als2
|
UTSW |
1 |
59,224,760 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1970:Als2
|
UTSW |
1 |
59,254,328 (GRCm39) |
missense |
probably benign |
0.34 |
R2151:Als2
|
UTSW |
1 |
59,246,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R2292:Als2
|
UTSW |
1 |
59,226,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R2513:Als2
|
UTSW |
1 |
59,254,276 (GRCm39) |
missense |
probably benign |
0.00 |
R2849:Als2
|
UTSW |
1 |
59,245,697 (GRCm39) |
missense |
probably damaging |
0.97 |
R2869:Als2
|
UTSW |
1 |
59,250,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R2869:Als2
|
UTSW |
1 |
59,250,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R2870:Als2
|
UTSW |
1 |
59,250,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R2870:Als2
|
UTSW |
1 |
59,250,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R2872:Als2
|
UTSW |
1 |
59,250,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R2872:Als2
|
UTSW |
1 |
59,250,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R2873:Als2
|
UTSW |
1 |
59,250,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R3054:Als2
|
UTSW |
1 |
59,254,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R3081:Als2
|
UTSW |
1 |
59,226,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R3176:Als2
|
UTSW |
1 |
59,209,167 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3276:Als2
|
UTSW |
1 |
59,209,167 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3801:Als2
|
UTSW |
1 |
59,206,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R3803:Als2
|
UTSW |
1 |
59,206,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R3808:Als2
|
UTSW |
1 |
59,209,609 (GRCm39) |
missense |
probably benign |
0.08 |
R3884:Als2
|
UTSW |
1 |
59,224,727 (GRCm39) |
missense |
probably damaging |
0.99 |
R4012:Als2
|
UTSW |
1 |
59,226,575 (GRCm39) |
missense |
probably benign |
0.09 |
R4033:Als2
|
UTSW |
1 |
59,235,400 (GRCm39) |
missense |
probably benign |
|
R4201:Als2
|
UTSW |
1 |
59,219,313 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4321:Als2
|
UTSW |
1 |
59,206,613 (GRCm39) |
splice site |
probably benign |
|
R4707:Als2
|
UTSW |
1 |
59,254,472 (GRCm39) |
missense |
probably benign |
|
R4784:Als2
|
UTSW |
1 |
59,254,472 (GRCm39) |
missense |
probably benign |
|
R4785:Als2
|
UTSW |
1 |
59,254,472 (GRCm39) |
missense |
probably benign |
|
R4991:Als2
|
UTSW |
1 |
59,246,927 (GRCm39) |
missense |
probably benign |
0.10 |
R5068:Als2
|
UTSW |
1 |
59,250,433 (GRCm39) |
missense |
probably benign |
0.13 |
R5110:Als2
|
UTSW |
1 |
59,224,600 (GRCm39) |
missense |
probably damaging |
0.98 |
R5141:Als2
|
UTSW |
1 |
59,209,611 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5394:Als2
|
UTSW |
1 |
59,214,105 (GRCm39) |
missense |
probably benign |
0.06 |
R5621:Als2
|
UTSW |
1 |
59,231,049 (GRCm39) |
missense |
probably benign |
0.33 |
R5685:Als2
|
UTSW |
1 |
59,218,250 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5987:Als2
|
UTSW |
1 |
59,245,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R6118:Als2
|
UTSW |
1 |
59,242,228 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6222:Als2
|
UTSW |
1 |
59,219,284 (GRCm39) |
missense |
probably benign |
0.04 |
R6367:Als2
|
UTSW |
1 |
59,238,299 (GRCm39) |
missense |
probably benign |
0.04 |
R6394:Als2
|
UTSW |
1 |
59,206,356 (GRCm39) |
missense |
probably damaging |
0.99 |
R6866:Als2
|
UTSW |
1 |
59,250,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R6965:Als2
|
UTSW |
1 |
59,209,716 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7038:Als2
|
UTSW |
1 |
59,206,673 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7178:Als2
|
UTSW |
1 |
59,246,971 (GRCm39) |
missense |
probably damaging |
0.96 |
R7494:Als2
|
UTSW |
1 |
59,222,325 (GRCm39) |
splice site |
probably null |
|
R7541:Als2
|
UTSW |
1 |
59,206,775 (GRCm39) |
splice site |
probably null |
|
R7601:Als2
|
UTSW |
1 |
59,209,161 (GRCm39) |
missense |
probably benign |
0.17 |
R8380:Als2
|
UTSW |
1 |
59,250,467 (GRCm39) |
missense |
probably benign |
|
R8478:Als2
|
UTSW |
1 |
59,225,175 (GRCm39) |
missense |
probably damaging |
0.96 |
R8492:Als2
|
UTSW |
1 |
59,250,503 (GRCm39) |
missense |
probably damaging |
0.98 |
R9048:Als2
|
UTSW |
1 |
59,225,670 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9090:Als2
|
UTSW |
1 |
59,242,189 (GRCm39) |
missense |
probably benign |
0.01 |
R9128:Als2
|
UTSW |
1 |
59,219,709 (GRCm39) |
missense |
probably benign |
0.00 |
R9206:Als2
|
UTSW |
1 |
59,224,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R9271:Als2
|
UTSW |
1 |
59,242,189 (GRCm39) |
missense |
probably benign |
0.01 |
R9430:Als2
|
UTSW |
1 |
59,231,198 (GRCm39) |
missense |
probably benign |
0.00 |
R9455:Als2
|
UTSW |
1 |
59,219,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R9482:Als2
|
UTSW |
1 |
59,231,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R9494:Als2
|
UTSW |
1 |
59,206,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R9544:Als2
|
UTSW |
1 |
59,250,468 (GRCm39) |
missense |
probably benign |
0.00 |
R9796:Als2
|
UTSW |
1 |
59,209,601 (GRCm39) |
missense |
probably benign |
0.04 |
|