Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam6a |
T |
G |
12: 113,508,886 (GRCm39) |
F420V |
probably benign |
Het |
Alpl |
T |
C |
4: 137,473,740 (GRCm39) |
T321A |
probably benign |
Het |
Asxl3 |
A |
G |
18: 22,586,666 (GRCm39) |
D152G |
probably damaging |
Het |
B4galt4 |
A |
G |
16: 38,578,173 (GRCm39) |
T207A |
probably benign |
Het |
Bsph2 |
A |
T |
7: 13,304,972 (GRCm39) |
M1K |
probably null |
Het |
Cacna2d1 |
T |
A |
5: 16,531,338 (GRCm39) |
L535Q |
probably damaging |
Het |
Cacna2d3 |
T |
C |
14: 28,846,642 (GRCm39) |
|
probably null |
Het |
Chrdl2 |
T |
C |
7: 99,659,328 (GRCm39) |
|
probably null |
Het |
Ctdnep1 |
A |
G |
11: 69,875,138 (GRCm39) |
N54S |
probably benign |
Het |
Dclre1a |
A |
T |
19: 56,533,501 (GRCm39) |
D364E |
probably benign |
Het |
Dock1 |
A |
G |
7: 134,735,615 (GRCm39) |
I1328V |
possibly damaging |
Het |
Eno4 |
A |
T |
19: 58,959,112 (GRCm39) |
E411D |
probably benign |
Het |
Fbxl14 |
A |
G |
6: 119,457,716 (GRCm39) |
Y299C |
probably benign |
Het |
Fhdc1 |
T |
C |
3: 84,353,729 (GRCm39) |
S499G |
probably damaging |
Het |
Hectd4 |
C |
T |
5: 121,458,147 (GRCm39) |
T771I |
possibly damaging |
Het |
Kansl3 |
A |
G |
1: 36,383,995 (GRCm39) |
|
probably null |
Het |
Letm2 |
G |
A |
8: 26,083,977 (GRCm39) |
H85Y |
probably benign |
Het |
Map3k6 |
A |
T |
4: 132,978,250 (GRCm39) |
K1031* |
probably null |
Het |
Mfsd4b5 |
T |
A |
10: 39,862,413 (GRCm39) |
T37S |
probably benign |
Het |
Mgam |
T |
A |
6: 40,721,720 (GRCm39) |
V346D |
probably benign |
Het |
Myrip |
C |
T |
9: 120,217,359 (GRCm39) |
H98Y |
possibly damaging |
Het |
Nos2 |
A |
G |
11: 78,835,549 (GRCm39) |
N443D |
possibly damaging |
Het |
Notch2 |
A |
T |
3: 98,045,746 (GRCm39) |
D1637V |
possibly damaging |
Het |
Or4c35 |
T |
A |
2: 89,808,929 (GRCm39) |
V269E |
probably damaging |
Het |
Or6z6 |
G |
A |
7: 6,491,049 (GRCm39) |
R275C |
probably damaging |
Het |
Pank1 |
C |
T |
19: 34,789,786 (GRCm39) |
G530D |
probably damaging |
Het |
Pde4dip |
G |
T |
3: 97,648,709 (GRCm39) |
R1036S |
probably damaging |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Plin2 |
T |
C |
4: 86,578,357 (GRCm39) |
T247A |
probably benign |
Het |
Rp1 |
T |
A |
1: 4,212,887 (GRCm39) |
I1067F |
unknown |
Het |
Serpinb9d |
T |
A |
13: 33,380,541 (GRCm39) |
N142K |
probably benign |
Het |
Slc12a5 |
A |
G |
2: 164,830,509 (GRCm39) |
Y639C |
probably damaging |
Het |
Tfap2c |
A |
G |
2: 172,399,276 (GRCm39) |
M508V |
probably benign |
Het |
Tmprss11d |
T |
C |
5: 86,478,962 (GRCm39) |
N147S |
probably benign |
Het |
Togaram1 |
T |
A |
12: 65,049,383 (GRCm39) |
N1273K |
probably benign |
Het |
Ttn |
G |
A |
2: 76,709,687 (GRCm39) |
R1581* |
probably null |
Het |
Uggt2 |
T |
A |
14: 119,308,293 (GRCm39) |
I363F |
probably damaging |
Het |
Vmn2r63 |
T |
A |
7: 42,578,001 (GRCm39) |
D179V |
probably damaging |
Het |
|
Other mutations in Adam34 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00545:Adam34
|
APN |
8 |
44,105,227 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01296:Adam34
|
APN |
8 |
44,104,178 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01369:Adam34
|
APN |
8 |
44,104,094 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01933:Adam34
|
APN |
8 |
44,104,569 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01938:Adam34
|
APN |
8 |
44,104,053 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02112:Adam34
|
APN |
8 |
44,104,175 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02182:Adam34
|
APN |
8 |
44,104,790 (GRCm39) |
missense |
probably benign |
|
IGL02306:Adam34
|
APN |
8 |
44,103,522 (GRCm39) |
missense |
probably benign |
0.44 |
IGL02661:Adam34
|
APN |
8 |
44,104,572 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02888:Adam34
|
APN |
8 |
44,104,610 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02979:Adam34
|
APN |
8 |
44,104,408 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03073:Adam34
|
APN |
8 |
44,103,940 (GRCm39) |
missense |
probably damaging |
0.99 |
BB010:Adam34
|
UTSW |
8 |
44,103,911 (GRCm39) |
missense |
probably damaging |
1.00 |
BB020:Adam34
|
UTSW |
8 |
44,103,911 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4453001:Adam34
|
UTSW |
8 |
44,104,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R0060:Adam34
|
UTSW |
8 |
44,128,920 (GRCm39) |
intron |
probably benign |
|
R0317:Adam34
|
UTSW |
8 |
44,105,288 (GRCm39) |
missense |
probably benign |
0.14 |
R0322:Adam34
|
UTSW |
8 |
44,104,958 (GRCm39) |
missense |
probably benign |
0.00 |
R0427:Adam34
|
UTSW |
8 |
44,105,493 (GRCm39) |
missense |
probably benign |
0.15 |
R0593:Adam34
|
UTSW |
8 |
44,104,724 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0837:Adam34
|
UTSW |
8 |
44,104,537 (GRCm39) |
missense |
probably benign |
0.00 |
R0927:Adam34
|
UTSW |
8 |
44,104,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R1634:Adam34
|
UTSW |
8 |
44,105,127 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1653:Adam34
|
UTSW |
8 |
44,103,682 (GRCm39) |
nonsense |
probably null |
|
R1826:Adam34
|
UTSW |
8 |
44,104,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R1873:Adam34
|
UTSW |
8 |
44,104,843 (GRCm39) |
missense |
probably benign |
0.02 |
R1943:Adam34
|
UTSW |
8 |
44,104,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R1943:Adam34
|
UTSW |
8 |
44,103,864 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2147:Adam34
|
UTSW |
8 |
44,105,538 (GRCm39) |
missense |
probably benign |
0.01 |
R2150:Adam34
|
UTSW |
8 |
44,105,538 (GRCm39) |
missense |
probably benign |
0.01 |
R2206:Adam34
|
UTSW |
8 |
44,105,274 (GRCm39) |
missense |
probably benign |
0.02 |
R2207:Adam34
|
UTSW |
8 |
44,105,274 (GRCm39) |
missense |
probably benign |
0.02 |
R2268:Adam34
|
UTSW |
8 |
44,103,647 (GRCm39) |
missense |
probably benign |
0.00 |
R2349:Adam34
|
UTSW |
8 |
44,105,415 (GRCm39) |
missense |
probably damaging |
0.99 |
R3983:Adam34
|
UTSW |
8 |
44,103,806 (GRCm39) |
missense |
probably benign |
|
R4158:Adam34
|
UTSW |
8 |
44,103,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R4179:Adam34
|
UTSW |
8 |
44,104,128 (GRCm39) |
missense |
probably benign |
0.18 |
R5219:Adam34
|
UTSW |
8 |
44,104,461 (GRCm39) |
missense |
probably benign |
|
R5398:Adam34
|
UTSW |
8 |
44,104,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R5611:Adam34
|
UTSW |
8 |
44,104,749 (GRCm39) |
missense |
probably benign |
0.43 |
R5928:Adam34
|
UTSW |
8 |
44,105,067 (GRCm39) |
missense |
probably benign |
0.08 |
R6115:Adam34
|
UTSW |
8 |
44,105,098 (GRCm39) |
missense |
probably benign |
|
R6319:Adam34
|
UTSW |
8 |
44,104,952 (GRCm39) |
missense |
probably benign |
0.01 |
R6384:Adam34
|
UTSW |
8 |
44,103,836 (GRCm39) |
missense |
probably benign |
0.00 |
R6992:Adam34
|
UTSW |
8 |
44,105,642 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R7032:Adam34
|
UTSW |
8 |
44,105,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R7151:Adam34
|
UTSW |
8 |
44,104,499 (GRCm39) |
missense |
probably benign |
0.19 |
R7187:Adam34
|
UTSW |
8 |
44,105,565 (GRCm39) |
missense |
probably benign |
0.02 |
R7223:Adam34
|
UTSW |
8 |
44,105,041 (GRCm39) |
missense |
probably benign |
0.02 |
R7487:Adam34
|
UTSW |
8 |
44,104,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R7726:Adam34
|
UTSW |
8 |
44,104,208 (GRCm39) |
missense |
probably damaging |
0.99 |
R7789:Adam34
|
UTSW |
8 |
44,105,488 (GRCm39) |
missense |
probably benign |
0.00 |
R7810:Adam34
|
UTSW |
8 |
44,105,045 (GRCm39) |
missense |
probably benign |
0.01 |
R7933:Adam34
|
UTSW |
8 |
44,103,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R8192:Adam34
|
UTSW |
8 |
44,103,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R8231:Adam34
|
UTSW |
8 |
44,104,659 (GRCm39) |
missense |
probably benign |
|
R8238:Adam34
|
UTSW |
8 |
44,103,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R8259:Adam34
|
UTSW |
8 |
44,104,646 (GRCm39) |
missense |
probably benign |
0.03 |
R8339:Adam34
|
UTSW |
8 |
44,103,640 (GRCm39) |
missense |
probably benign |
0.20 |
R8381:Adam34
|
UTSW |
8 |
44,104,847 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8670:Adam34
|
UTSW |
8 |
44,105,126 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8693:Adam34
|
UTSW |
8 |
44,104,641 (GRCm39) |
missense |
probably benign |
|
R8932:Adam34
|
UTSW |
8 |
44,105,192 (GRCm39) |
missense |
probably benign |
0.19 |
R8936:Adam34
|
UTSW |
8 |
44,104,439 (GRCm39) |
missense |
probably benign |
0.00 |
R8981:Adam34
|
UTSW |
8 |
44,103,840 (GRCm39) |
missense |
probably benign |
0.05 |
R9040:Adam34
|
UTSW |
8 |
44,103,363 (GRCm39) |
unclassified |
probably benign |
|
R9105:Adam34
|
UTSW |
8 |
44,103,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R9305:Adam34
|
UTSW |
8 |
44,104,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R9321:Adam34
|
UTSW |
8 |
44,105,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R9641:Adam34
|
UTSW |
8 |
44,104,076 (GRCm39) |
missense |
probably damaging |
0.97 |
R9644:Adam34
|
UTSW |
8 |
44,104,766 (GRCm39) |
missense |
probably damaging |
0.96 |
|