Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adora2b |
A |
G |
11: 62,156,010 (GRCm39) |
N153S |
possibly damaging |
Het |
Afm |
C |
T |
5: 90,672,765 (GRCm39) |
T200I |
probably benign |
Het |
Cyp2c67 |
T |
C |
19: 39,604,165 (GRCm39) |
D397G |
probably damaging |
Het |
Dnah9 |
A |
G |
11: 65,998,952 (GRCm39) |
V1032A |
probably benign |
Het |
Elovl7 |
T |
G |
13: 108,410,854 (GRCm39) |
V143G |
probably damaging |
Het |
Fhl4 |
T |
C |
10: 84,934,734 (GRCm39) |
K16E |
probably damaging |
Het |
Golga1 |
C |
T |
2: 38,924,161 (GRCm39) |
C383Y |
probably benign |
Het |
Gucy1a2 |
C |
T |
9: 3,865,409 (GRCm39) |
R628* |
probably null |
Het |
Hectd4 |
A |
G |
5: 121,466,481 (GRCm39) |
D2432G |
possibly damaging |
Het |
Iqcf5 |
T |
A |
9: 106,393,189 (GRCm39) |
*149R |
probably null |
Het |
Kcnab1 |
T |
A |
3: 65,226,875 (GRCm39) |
Y185N |
probably damaging |
Het |
Lars1 |
G |
T |
18: 42,335,615 (GRCm39) |
T1167K |
probably benign |
Het |
Mib2 |
A |
T |
4: 155,739,715 (GRCm39) |
|
probably null |
Het |
Mrps2 |
T |
C |
2: 28,358,348 (GRCm39) |
V46A |
probably benign |
Het |
Myo18b |
T |
C |
5: 113,025,916 (GRCm39) |
T45A |
unknown |
Het |
Myo1e |
C |
T |
9: 70,250,322 (GRCm39) |
|
probably benign |
Het |
Or10ag59 |
A |
G |
2: 87,405,823 (GRCm39) |
I132V |
probably damaging |
Het |
Or4k39 |
T |
A |
2: 111,239,078 (GRCm39) |
V106E |
probably damaging |
Het |
Osbp2 |
A |
T |
11: 3,667,127 (GRCm39) |
I8N |
probably damaging |
Het |
Pcdhb22 |
A |
T |
18: 37,652,974 (GRCm39) |
N481Y |
probably damaging |
Het |
Pde3a |
T |
C |
6: 141,433,263 (GRCm39) |
W765R |
probably damaging |
Het |
Phf11c |
T |
C |
14: 59,630,586 (GRCm39) |
T40A |
probably benign |
Het |
Pih1d2 |
T |
A |
9: 50,533,177 (GRCm39) |
S268R |
probably benign |
Het |
Pkd1l2 |
T |
C |
8: 117,724,913 (GRCm39) |
N2333D |
probably damaging |
Het |
Ptcd2 |
T |
C |
13: 99,463,219 (GRCm39) |
N245S |
possibly damaging |
Het |
Ripor3 |
C |
A |
2: 167,822,763 (GRCm39) |
V933F |
probably damaging |
Het |
Sanbr |
A |
G |
11: 23,534,561 (GRCm39) |
S105P |
probably benign |
Het |
Sphk2 |
A |
G |
7: 45,360,480 (GRCm39) |
|
probably null |
Het |
Tfcp2 |
T |
G |
15: 100,402,320 (GRCm39) |
E492D |
probably benign |
Het |
Ttn |
C |
T |
2: 76,629,106 (GRCm39) |
V14411I |
possibly damaging |
Het |
Utp20 |
T |
C |
10: 88,628,549 (GRCm39) |
Q915R |
probably damaging |
Het |
Vmn2r45 |
C |
A |
7: 8,488,556 (GRCm39) |
S158I |
probably benign |
Het |
|
Other mutations in Prex1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00161:Prex1
|
APN |
2 |
166,480,321 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00309:Prex1
|
APN |
2 |
166,451,743 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00953:Prex1
|
APN |
2 |
166,480,329 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00961:Prex1
|
APN |
2 |
166,427,656 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01300:Prex1
|
APN |
2 |
166,480,327 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL01318:Prex1
|
APN |
2 |
166,411,260 (GRCm39) |
splice site |
probably benign |
|
IGL01753:Prex1
|
APN |
2 |
166,444,802 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02058:Prex1
|
APN |
2 |
166,427,103 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02251:Prex1
|
APN |
2 |
166,419,806 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02326:Prex1
|
APN |
2 |
166,463,105 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02366:Prex1
|
APN |
2 |
166,422,347 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02414:Prex1
|
APN |
2 |
166,451,748 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02660:Prex1
|
APN |
2 |
166,435,787 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02666:Prex1
|
APN |
2 |
166,414,909 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02874:Prex1
|
APN |
2 |
166,426,967 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02935:Prex1
|
APN |
2 |
166,412,265 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03179:Prex1
|
APN |
2 |
166,427,114 (GRCm39) |
missense |
probably benign |
0.31 |
R0207:Prex1
|
UTSW |
2 |
166,427,818 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0415:Prex1
|
UTSW |
2 |
166,428,619 (GRCm39) |
unclassified |
probably benign |
|
R0420:Prex1
|
UTSW |
2 |
166,431,491 (GRCm39) |
missense |
probably benign |
0.13 |
R0449:Prex1
|
UTSW |
2 |
166,411,297 (GRCm39) |
missense |
probably benign |
0.16 |
R0458:Prex1
|
UTSW |
2 |
166,427,743 (GRCm39) |
missense |
probably damaging |
0.99 |
R0927:Prex1
|
UTSW |
2 |
166,428,457 (GRCm39) |
missense |
probably benign |
0.01 |
R1299:Prex1
|
UTSW |
2 |
166,427,827 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1414:Prex1
|
UTSW |
2 |
166,435,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R1440:Prex1
|
UTSW |
2 |
166,422,383 (GRCm39) |
missense |
probably damaging |
0.98 |
R1506:Prex1
|
UTSW |
2 |
166,429,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R1725:Prex1
|
UTSW |
2 |
166,443,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R1831:Prex1
|
UTSW |
2 |
166,427,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R1883:Prex1
|
UTSW |
2 |
166,425,192 (GRCm39) |
missense |
probably benign |
0.20 |
R1896:Prex1
|
UTSW |
2 |
166,428,574 (GRCm39) |
missense |
probably benign |
0.01 |
R2022:Prex1
|
UTSW |
2 |
166,417,534 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2091:Prex1
|
UTSW |
2 |
166,411,285 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2258:Prex1
|
UTSW |
2 |
166,429,077 (GRCm39) |
missense |
probably benign |
0.00 |
R2263:Prex1
|
UTSW |
2 |
166,430,988 (GRCm39) |
splice site |
probably benign |
|
R2276:Prex1
|
UTSW |
2 |
166,419,875 (GRCm39) |
missense |
probably benign |
0.34 |
R2279:Prex1
|
UTSW |
2 |
166,419,875 (GRCm39) |
missense |
probably benign |
0.34 |
R2680:Prex1
|
UTSW |
2 |
166,443,692 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3024:Prex1
|
UTSW |
2 |
166,430,956 (GRCm39) |
missense |
probably benign |
0.04 |
R3421:Prex1
|
UTSW |
2 |
166,459,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R3614:Prex1
|
UTSW |
2 |
166,451,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R4244:Prex1
|
UTSW |
2 |
166,412,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R4605:Prex1
|
UTSW |
2 |
166,555,464 (GRCm39) |
missense |
probably benign |
0.45 |
R4685:Prex1
|
UTSW |
2 |
166,480,252 (GRCm39) |
missense |
probably damaging |
0.97 |
R4787:Prex1
|
UTSW |
2 |
166,480,260 (GRCm39) |
missense |
probably benign |
0.01 |
R4796:Prex1
|
UTSW |
2 |
166,434,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R4825:Prex1
|
UTSW |
2 |
166,427,777 (GRCm39) |
nonsense |
probably null |
|
R4955:Prex1
|
UTSW |
2 |
166,415,143 (GRCm39) |
missense |
probably damaging |
0.99 |
R5046:Prex1
|
UTSW |
2 |
166,414,883 (GRCm39) |
missense |
probably benign |
0.00 |
R5095:Prex1
|
UTSW |
2 |
166,423,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R5408:Prex1
|
UTSW |
2 |
166,417,573 (GRCm39) |
small insertion |
probably benign |
|
R5462:Prex1
|
UTSW |
2 |
166,486,728 (GRCm39) |
missense |
probably benign |
0.02 |
R5535:Prex1
|
UTSW |
2 |
166,422,193 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5777:Prex1
|
UTSW |
2 |
166,428,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R5813:Prex1
|
UTSW |
2 |
166,425,127 (GRCm39) |
missense |
probably benign |
|
R5860:Prex1
|
UTSW |
2 |
166,486,604 (GRCm39) |
intron |
probably benign |
|
R5984:Prex1
|
UTSW |
2 |
166,427,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R6009:Prex1
|
UTSW |
2 |
166,423,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R6174:Prex1
|
UTSW |
2 |
166,414,883 (GRCm39) |
missense |
probably benign |
0.00 |
R6345:Prex1
|
UTSW |
2 |
166,414,880 (GRCm39) |
missense |
probably null |
0.81 |
R6897:Prex1
|
UTSW |
2 |
166,423,913 (GRCm39) |
missense |
probably damaging |
0.99 |
R6935:Prex1
|
UTSW |
2 |
166,441,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R7025:Prex1
|
UTSW |
2 |
166,455,107 (GRCm39) |
small insertion |
probably benign |
|
R7037:Prex1
|
UTSW |
2 |
166,429,100 (GRCm39) |
missense |
probably benign |
0.05 |
R7076:Prex1
|
UTSW |
2 |
166,475,302 (GRCm39) |
missense |
probably damaging |
0.99 |
R7181:Prex1
|
UTSW |
2 |
166,412,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R7361:Prex1
|
UTSW |
2 |
166,555,490 (GRCm39) |
missense |
probably benign |
0.04 |
R7381:Prex1
|
UTSW |
2 |
166,429,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R7721:Prex1
|
UTSW |
2 |
166,419,810 (GRCm39) |
nonsense |
probably null |
|
R7763:Prex1
|
UTSW |
2 |
166,555,629 (GRCm39) |
missense |
unknown |
|
R7809:Prex1
|
UTSW |
2 |
166,415,164 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7915:Prex1
|
UTSW |
2 |
166,463,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R7971:Prex1
|
UTSW |
2 |
166,423,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R7998:Prex1
|
UTSW |
2 |
166,428,965 (GRCm39) |
critical splice donor site |
probably null |
|
R8029:Prex1
|
UTSW |
2 |
166,417,523 (GRCm39) |
missense |
probably benign |
0.01 |
R8193:Prex1
|
UTSW |
2 |
166,435,780 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8352:Prex1
|
UTSW |
2 |
166,431,493 (GRCm39) |
missense |
probably benign |
0.05 |
R8452:Prex1
|
UTSW |
2 |
166,431,493 (GRCm39) |
missense |
probably benign |
0.05 |
R8927:Prex1
|
UTSW |
2 |
166,426,995 (GRCm39) |
missense |
probably damaging |
0.97 |
R8928:Prex1
|
UTSW |
2 |
166,426,995 (GRCm39) |
missense |
probably damaging |
0.97 |
R9021:Prex1
|
UTSW |
2 |
166,432,429 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9070:Prex1
|
UTSW |
2 |
166,427,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R9213:Prex1
|
UTSW |
2 |
166,417,669 (GRCm39) |
missense |
probably damaging |
0.99 |
R9511:Prex1
|
UTSW |
2 |
166,413,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R9514:Prex1
|
UTSW |
2 |
166,419,896 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9529:Prex1
|
UTSW |
2 |
166,431,518 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Prex1
|
UTSW |
2 |
166,428,545 (GRCm39) |
missense |
probably benign |
|
Z1176:Prex1
|
UTSW |
2 |
166,414,890 (GRCm39) |
nonsense |
probably null |
|
Z1177:Prex1
|
UTSW |
2 |
166,434,148 (GRCm39) |
missense |
probably damaging |
0.98 |
|