Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acss2 |
G |
A |
2: 155,416,610 (GRCm39) |
|
probably null |
Het |
Adamts10 |
G |
A |
17: 33,750,590 (GRCm39) |
R210H |
probably benign |
Het |
Aplp2 |
A |
T |
9: 31,063,652 (GRCm39) |
M652K |
possibly damaging |
Het |
Atrn |
A |
G |
2: 130,803,491 (GRCm39) |
I560M |
possibly damaging |
Het |
Bicc1 |
T |
C |
10: 70,782,434 (GRCm39) |
D602G |
possibly damaging |
Het |
Bnip5 |
G |
A |
17: 29,124,298 (GRCm39) |
R335W |
probably damaging |
Het |
Cd200l2 |
T |
A |
16: 45,348,855 (GRCm39) |
T106S |
possibly damaging |
Het |
Cdh4 |
A |
G |
2: 179,086,603 (GRCm39) |
|
probably null |
Het |
Clasp1 |
T |
A |
1: 118,470,727 (GRCm39) |
|
probably null |
Het |
Col6a6 |
A |
G |
9: 105,644,523 (GRCm39) |
I1255T |
probably damaging |
Het |
Comp |
G |
T |
8: 70,834,000 (GRCm39) |
V672L |
probably damaging |
Het |
Dbnl |
T |
G |
11: 5,745,486 (GRCm39) |
D122E |
probably damaging |
Het |
Dgkz |
G |
A |
2: 91,773,020 (GRCm39) |
R346C |
probably damaging |
Het |
Dnhd1 |
C |
T |
7: 105,327,516 (GRCm39) |
R54C |
probably damaging |
Het |
Elmo3 |
T |
C |
8: 106,033,346 (GRCm39) |
I121T |
probably damaging |
Het |
Fam184b |
A |
G |
5: 45,699,574 (GRCm39) |
L614P |
probably damaging |
Het |
Fbh1 |
T |
C |
2: 11,754,348 (GRCm39) |
R797G |
probably benign |
Het |
Fcgbpl1 |
T |
A |
7: 27,843,681 (GRCm39) |
C856* |
probably null |
Het |
Gata6 |
A |
G |
18: 11,059,108 (GRCm39) |
T392A |
probably damaging |
Het |
Gm29609 |
A |
G |
5: 31,311,576 (GRCm39) |
F855S |
probably benign |
Het |
Gm3424 |
T |
C |
14: 17,337,195 (GRCm39) |
N88D |
possibly damaging |
Het |
Gnas |
T |
A |
2: 174,139,892 (GRCm39) |
S80T |
unknown |
Het |
Hsd17b14 |
C |
A |
7: 45,215,570 (GRCm39) |
P190Q |
probably damaging |
Het |
Iqch |
C |
T |
9: 63,352,803 (GRCm39) |
V955I |
possibly damaging |
Het |
Kcnt2 |
T |
C |
1: 140,304,122 (GRCm39) |
V164A |
probably benign |
Het |
Krt87 |
A |
G |
15: 101,336,515 (GRCm39) |
L46P |
probably damaging |
Het |
Lef1 |
A |
G |
3: 130,984,748 (GRCm39) |
M237V |
probably benign |
Het |
Lmbr1l |
A |
T |
15: 98,807,267 (GRCm39) |
|
probably null |
Het |
Lrrc49 |
T |
C |
9: 60,517,686 (GRCm39) |
I408V |
probably damaging |
Het |
Luc7l3 |
T |
C |
11: 94,186,791 (GRCm39) |
S365G |
unknown |
Het |
Marchf2 |
A |
T |
17: 33,922,032 (GRCm39) |
C109* |
probably null |
Het |
Metrnl |
T |
A |
11: 121,606,796 (GRCm39) |
C284S |
probably damaging |
Het |
Mmachc |
G |
A |
4: 116,563,082 (GRCm39) |
T91I |
probably benign |
Het |
Mrps7 |
T |
G |
11: 115,497,696 (GRCm39) |
M187R |
probably damaging |
Het |
Ncapd3 |
A |
G |
9: 26,978,336 (GRCm39) |
E845G |
probably damaging |
Het |
Nscme3l |
G |
A |
19: 5,553,439 (GRCm39) |
P114L |
probably benign |
Het |
Ooep |
T |
A |
9: 78,285,347 (GRCm39) |
T90S |
possibly damaging |
Het |
Or13c25 |
A |
T |
4: 52,911,376 (GRCm39) |
D139E |
probably benign |
Het |
Or2y1g |
T |
A |
11: 49,171,160 (GRCm39) |
F62I |
probably damaging |
Het |
Pcdhb18 |
A |
T |
18: 37,624,662 (GRCm39) |
D664V |
probably damaging |
Het |
Pigz |
T |
C |
16: 31,763,949 (GRCm39) |
S336P |
probably benign |
Het |
Pou2f2 |
A |
T |
7: 24,815,553 (GRCm39) |
D71E |
probably benign |
Het |
Reep6 |
G |
T |
10: 80,171,033 (GRCm39) |
R303L |
possibly damaging |
Het |
Rmdn2 |
A |
T |
17: 79,935,297 (GRCm39) |
S137C |
|
Het |
Rnf220 |
A |
T |
4: 117,347,127 (GRCm39) |
L95H |
probably damaging |
Het |
Rsf1 |
CGGCGGCGG |
CGGCGGCGGGGGCGGCGG |
7: 97,229,118 (GRCm39) |
|
probably benign |
Het |
Stxbp1 |
A |
T |
2: 32,708,517 (GRCm39) |
S83T |
probably damaging |
Het |
Tcstv7b |
A |
T |
13: 120,702,515 (GRCm39) |
M104L |
probably benign |
Het |
Trappc11 |
T |
C |
8: 47,958,617 (GRCm39) |
|
probably null |
Het |
Ttn |
G |
T |
2: 76,621,645 (GRCm39) |
D15598E |
probably damaging |
Het |
Vav2 |
T |
A |
2: 27,165,014 (GRCm39) |
R645W |
probably damaging |
Het |
Vmn1r169 |
T |
A |
7: 23,277,412 (GRCm39) |
V268D |
probably benign |
Het |
Zp2 |
A |
T |
7: 119,735,279 (GRCm39) |
C365S |
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 |
R6012:Als2
|
UTSW |
1 |
59,224,374 (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 |
|
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 |
|