Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930012K11Rik |
A |
G |
14: 70,395,058 (GRCm39) |
V32A |
probably damaging |
Het |
Bcat2 |
T |
A |
7: 45,237,778 (GRCm39) |
V348E |
probably damaging |
Het |
Bnip2 |
A |
G |
9: 69,903,456 (GRCm39) |
D36G |
probably benign |
Het |
C2cd5 |
T |
A |
6: 143,018,292 (GRCm39) |
D310V |
possibly damaging |
Het |
Cltc |
G |
A |
11: 86,611,113 (GRCm39) |
T582M |
probably damaging |
Het |
Cplx3 |
A |
T |
9: 57,517,290 (GRCm39) |
Y365N |
probably benign |
Het |
Dync2h1 |
T |
C |
9: 7,125,918 (GRCm39) |
H1896R |
probably benign |
Het |
Efcab5 |
T |
C |
11: 77,028,501 (GRCm39) |
R413G |
possibly damaging |
Het |
Fam131b |
C |
T |
6: 42,295,888 (GRCm39) |
M169I |
possibly damaging |
Het |
Fam241b |
A |
G |
10: 61,945,671 (GRCm39) |
S52P |
probably benign |
Het |
Gpd2 |
G |
A |
2: 57,194,498 (GRCm39) |
|
probably null |
Het |
Gucy1a1 |
T |
A |
3: 82,026,331 (GRCm39) |
Q41L |
probably benign |
Het |
Ifna16 |
T |
C |
4: 88,594,741 (GRCm39) |
D118G |
probably benign |
Het |
Kcnn1 |
T |
C |
8: 71,299,135 (GRCm39) |
|
probably benign |
Het |
Lyl1 |
C |
T |
8: 85,429,300 (GRCm39) |
P3L |
possibly damaging |
Het |
Lyst |
A |
T |
13: 13,884,144 (GRCm39) |
H2984L |
probably benign |
Het |
Myh7b |
C |
T |
2: 155,462,403 (GRCm39) |
Q369* |
probably null |
Het |
Nalcn |
A |
C |
14: 123,518,527 (GRCm39) |
W1671G |
probably benign |
Het |
Ndrg2 |
G |
A |
14: 52,144,026 (GRCm39) |
|
probably benign |
Het |
Nfia |
C |
A |
4: 97,951,286 (GRCm39) |
P371Q |
probably damaging |
Het |
Or10d5 |
A |
C |
9: 39,861,719 (GRCm39) |
|
probably null |
Het |
Pcdhb22 |
A |
G |
18: 37,652,009 (GRCm39) |
D159G |
probably damaging |
Het |
Plekhm3 |
A |
T |
1: 64,960,959 (GRCm39) |
D432E |
possibly damaging |
Het |
Pramel17 |
T |
A |
4: 101,692,594 (GRCm39) |
T469S |
probably benign |
Het |
Rab2a |
A |
G |
4: 8,606,448 (GRCm39) |
N195S |
probably benign |
Het |
Sbf1 |
A |
G |
15: 89,173,308 (GRCm39) |
Y1764H |
possibly damaging |
Het |
Scap |
A |
G |
9: 110,213,335 (GRCm39) |
T1127A |
possibly damaging |
Het |
Shld2 |
T |
C |
14: 33,990,328 (GRCm39) |
T193A |
probably benign |
Het |
Slc45a2 |
A |
G |
15: 11,022,278 (GRCm39) |
D340G |
probably damaging |
Het |
Tbc1d23 |
A |
T |
16: 57,034,625 (GRCm39) |
L58Q |
probably damaging |
Het |
Tmcc1 |
T |
C |
6: 116,110,937 (GRCm39) |
T119A |
probably damaging |
Het |
Tnfsf10 |
C |
A |
3: 27,389,597 (GRCm39) |
Y219* |
probably null |
Het |
Traip |
G |
A |
9: 107,848,192 (GRCm39) |
R437Q |
probably damaging |
Het |
Tyw3 |
T |
C |
3: 154,293,187 (GRCm39) |
T163A |
possibly 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 |
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 |
|
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 |
|