Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
A |
G |
11: 110,046,003 (GRCm39) |
F307S |
probably damaging |
Het |
Abcc6 |
A |
T |
7: 45,652,096 (GRCm39) |
|
probably benign |
Het |
Akap6 |
T |
A |
12: 53,186,447 (GRCm39) |
L1287H |
probably damaging |
Het |
Ascl3 |
A |
G |
7: 109,327,245 (GRCm39) |
S25P |
probably benign |
Het |
Brd2 |
A |
G |
17: 34,336,016 (GRCm39) |
S66P |
probably damaging |
Het |
Cacna1i |
C |
A |
15: 80,271,960 (GRCm39) |
|
probably benign |
Het |
Cdc5l |
T |
C |
17: 45,715,602 (GRCm39) |
Y670C |
probably damaging |
Het |
Clybl |
T |
A |
14: 122,608,834 (GRCm39) |
I142N |
probably damaging |
Het |
Cyp2c66 |
T |
C |
19: 39,172,379 (GRCm39) |
|
probably null |
Het |
Dck |
C |
T |
5: 88,922,095 (GRCm39) |
|
probably benign |
Het |
Dsg1b |
T |
C |
18: 20,542,651 (GRCm39) |
Y1053H |
probably damaging |
Het |
Gm9912 |
T |
C |
3: 148,890,986 (GRCm39) |
D49G |
unknown |
Het |
Gpr107 |
T |
C |
2: 31,057,163 (GRCm39) |
|
probably benign |
Het |
Hsd3b7 |
T |
C |
7: 127,402,036 (GRCm39) |
F227S |
probably damaging |
Het |
Lrrtm2 |
T |
A |
18: 35,345,851 (GRCm39) |
N484Y |
probably damaging |
Het |
Muc19 |
A |
T |
15: 91,754,699 (GRCm39) |
|
noncoding transcript |
Het |
Nodal |
G |
A |
10: 61,254,176 (GRCm39) |
R33Q |
probably benign |
Het |
Or1a1 |
T |
C |
11: 74,086,587 (GRCm39) |
L86P |
probably damaging |
Het |
Plcb4 |
A |
G |
2: 135,809,038 (GRCm39) |
I569V |
probably benign |
Het |
Plekhg1 |
T |
C |
10: 3,913,631 (GRCm39) |
Y1118H |
probably benign |
Het |
Polr2a |
T |
G |
11: 69,632,020 (GRCm39) |
E1015D |
probably benign |
Het |
Recql5 |
A |
G |
11: 115,785,495 (GRCm39) |
F667S |
probably damaging |
Het |
Scube1 |
T |
C |
15: 83,496,754 (GRCm39) |
Y749C |
probably damaging |
Het |
Serpinb1c |
C |
A |
13: 33,070,155 (GRCm39) |
V136F |
probably damaging |
Het |
Slain2 |
T |
C |
5: 73,098,789 (GRCm39) |
|
probably benign |
Het |
Slc10a7 |
T |
C |
8: 79,456,369 (GRCm39) |
S296P |
probably damaging |
Het |
Sspo |
C |
T |
6: 48,428,112 (GRCm39) |
R320W |
probably damaging |
Het |
Usp16 |
G |
A |
16: 87,276,071 (GRCm39) |
A469T |
probably benign |
Het |
Vmn2r102 |
A |
T |
17: 19,899,066 (GRCm39) |
L469F |
probably benign |
Het |
Zfp772 |
A |
G |
7: 7,208,523 (GRCm39) |
F107S |
possibly damaging |
Het |
|
Other mutations in Adamts12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Adamts12
|
APN |
15 |
11,311,685 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00513:Adamts12
|
APN |
15 |
11,257,047 (GRCm39) |
missense |
probably benign |
0.28 |
IGL00579:Adamts12
|
APN |
15 |
11,152,100 (GRCm39) |
missense |
probably benign |
0.20 |
IGL00984:Adamts12
|
APN |
15 |
11,215,696 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01307:Adamts12
|
APN |
15 |
11,237,632 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01314:Adamts12
|
APN |
15 |
11,071,939 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01353:Adamts12
|
APN |
15 |
11,292,091 (GRCm39) |
splice site |
probably benign |
|
IGL01373:Adamts12
|
APN |
15 |
11,310,816 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01522:Adamts12
|
APN |
15 |
11,065,245 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01715:Adamts12
|
APN |
15 |
11,258,182 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL01966:Adamts12
|
APN |
15 |
11,258,269 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01994:Adamts12
|
APN |
15 |
11,345,680 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02058:Adamts12
|
APN |
15 |
11,215,696 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02216:Adamts12
|
APN |
15 |
11,241,571 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02252:Adamts12
|
APN |
15 |
11,311,101 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02336:Adamts12
|
APN |
15 |
11,311,331 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02445:Adamts12
|
APN |
15 |
11,286,798 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03115:Adamts12
|
APN |
15 |
11,263,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03131:Adamts12
|
APN |
15 |
11,345,650 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03161:Adamts12
|
APN |
15 |
11,292,168 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03403:Adamts12
|
APN |
15 |
11,241,574 (GRCm39) |
missense |
probably damaging |
1.00 |
I2289:Adamts12
|
UTSW |
15 |
11,071,894 (GRCm39) |
missense |
probably benign |
0.13 |
PIT4677001:Adamts12
|
UTSW |
15 |
11,286,896 (GRCm39) |
missense |
probably benign |
0.33 |
R0016:Adamts12
|
UTSW |
15 |
11,217,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R0016:Adamts12
|
UTSW |
15 |
11,217,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R0027:Adamts12
|
UTSW |
15 |
11,285,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R0027:Adamts12
|
UTSW |
15 |
11,285,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R0028:Adamts12
|
UTSW |
15 |
11,215,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R0108:Adamts12
|
UTSW |
15 |
11,311,184 (GRCm39) |
missense |
probably benign |
0.08 |
R0108:Adamts12
|
UTSW |
15 |
11,311,184 (GRCm39) |
missense |
probably benign |
0.08 |
R0122:Adamts12
|
UTSW |
15 |
11,215,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R0196:Adamts12
|
UTSW |
15 |
11,071,594 (GRCm39) |
missense |
probably benign |
0.11 |
R0308:Adamts12
|
UTSW |
15 |
11,311,646 (GRCm39) |
missense |
probably damaging |
0.98 |
R0335:Adamts12
|
UTSW |
15 |
11,311,144 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0667:Adamts12
|
UTSW |
15 |
11,215,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R0729:Adamts12
|
UTSW |
15 |
11,255,769 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1162:Adamts12
|
UTSW |
15 |
11,277,544 (GRCm39) |
critical splice donor site |
probably null |
|
R1173:Adamts12
|
UTSW |
15 |
11,071,843 (GRCm39) |
missense |
probably benign |
|
R1174:Adamts12
|
UTSW |
15 |
11,071,843 (GRCm39) |
missense |
probably benign |
|
R1319:Adamts12
|
UTSW |
15 |
11,286,877 (GRCm39) |
missense |
probably benign |
0.02 |
R1344:Adamts12
|
UTSW |
15 |
11,286,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R1367:Adamts12
|
UTSW |
15 |
11,256,980 (GRCm39) |
splice site |
probably benign |
|
R1396:Adamts12
|
UTSW |
15 |
11,311,558 (GRCm39) |
missense |
probably benign |
0.01 |
R1418:Adamts12
|
UTSW |
15 |
11,286,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R1447:Adamts12
|
UTSW |
15 |
11,263,447 (GRCm39) |
missense |
probably benign |
0.42 |
R1466:Adamts12
|
UTSW |
15 |
11,311,445 (GRCm39) |
missense |
probably benign |
|
R1466:Adamts12
|
UTSW |
15 |
11,311,445 (GRCm39) |
missense |
probably benign |
|
R1599:Adamts12
|
UTSW |
15 |
11,071,797 (GRCm39) |
missense |
probably damaging |
0.99 |
R1700:Adamts12
|
UTSW |
15 |
11,152,143 (GRCm39) |
missense |
probably benign |
0.00 |
R1748:Adamts12
|
UTSW |
15 |
11,241,548 (GRCm39) |
missense |
probably damaging |
0.99 |
R1826:Adamts12
|
UTSW |
15 |
11,071,606 (GRCm39) |
missense |
probably benign |
0.06 |
R1870:Adamts12
|
UTSW |
15 |
11,311,240 (GRCm39) |
missense |
probably benign |
0.06 |
R1871:Adamts12
|
UTSW |
15 |
11,311,240 (GRCm39) |
missense |
probably benign |
0.06 |
R1872:Adamts12
|
UTSW |
15 |
11,217,966 (GRCm39) |
nonsense |
probably null |
|
R1931:Adamts12
|
UTSW |
15 |
11,270,685 (GRCm39) |
missense |
probably benign |
0.00 |
R2041:Adamts12
|
UTSW |
15 |
11,215,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R2119:Adamts12
|
UTSW |
15 |
11,310,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R2120:Adamts12
|
UTSW |
15 |
11,310,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R2122:Adamts12
|
UTSW |
15 |
11,310,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R2161:Adamts12
|
UTSW |
15 |
11,215,821 (GRCm39) |
missense |
probably damaging |
0.99 |
R2655:Adamts12
|
UTSW |
15 |
11,065,174 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4010:Adamts12
|
UTSW |
15 |
11,286,169 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4208:Adamts12
|
UTSW |
15 |
11,071,840 (GRCm39) |
missense |
probably benign |
|
R4666:Adamts12
|
UTSW |
15 |
11,311,578 (GRCm39) |
missense |
probably benign |
0.08 |
R4731:Adamts12
|
UTSW |
15 |
11,270,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R4732:Adamts12
|
UTSW |
15 |
11,270,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:Adamts12
|
UTSW |
15 |
11,270,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R4766:Adamts12
|
UTSW |
15 |
11,285,987 (GRCm39) |
missense |
probably benign |
0.03 |
R4877:Adamts12
|
UTSW |
15 |
11,327,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R4929:Adamts12
|
UTSW |
15 |
11,259,108 (GRCm39) |
missense |
probably damaging |
0.96 |
R5060:Adamts12
|
UTSW |
15 |
11,300,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R5145:Adamts12
|
UTSW |
15 |
11,285,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R5191:Adamts12
|
UTSW |
15 |
11,327,843 (GRCm39) |
missense |
probably benign |
0.18 |
R5492:Adamts12
|
UTSW |
15 |
11,336,384 (GRCm39) |
missense |
probably benign |
0.05 |
R5580:Adamts12
|
UTSW |
15 |
11,152,086 (GRCm39) |
missense |
probably benign |
0.14 |
R5645:Adamts12
|
UTSW |
15 |
11,277,506 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5724:Adamts12
|
UTSW |
15 |
11,286,836 (GRCm39) |
missense |
probably benign |
0.15 |
R6240:Adamts12
|
UTSW |
15 |
11,286,044 (GRCm39) |
missense |
probably benign |
0.44 |
R6331:Adamts12
|
UTSW |
15 |
11,241,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R6381:Adamts12
|
UTSW |
15 |
11,257,080 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6393:Adamts12
|
UTSW |
15 |
11,255,721 (GRCm39) |
missense |
probably damaging |
0.97 |
R6419:Adamts12
|
UTSW |
15 |
11,215,759 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6571:Adamts12
|
UTSW |
15 |
11,065,187 (GRCm39) |
missense |
probably benign |
0.00 |
R6821:Adamts12
|
UTSW |
15 |
11,152,134 (GRCm39) |
missense |
probably benign |
0.14 |
R6913:Adamts12
|
UTSW |
15 |
11,215,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R6973:Adamts12
|
UTSW |
15 |
11,331,866 (GRCm39) |
nonsense |
probably null |
|
R7188:Adamts12
|
UTSW |
15 |
11,336,411 (GRCm39) |
nonsense |
probably null |
|
R7290:Adamts12
|
UTSW |
15 |
11,277,452 (GRCm39) |
missense |
probably benign |
0.08 |
R7307:Adamts12
|
UTSW |
15 |
11,217,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R7376:Adamts12
|
UTSW |
15 |
11,277,425 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7419:Adamts12
|
UTSW |
15 |
11,317,365 (GRCm39) |
missense |
probably benign |
0.00 |
R7484:Adamts12
|
UTSW |
15 |
11,345,734 (GRCm39) |
missense |
probably benign |
0.25 |
R7562:Adamts12
|
UTSW |
15 |
11,270,697 (GRCm39) |
missense |
probably benign |
0.01 |
R7653:Adamts12
|
UTSW |
15 |
11,257,115 (GRCm39) |
missense |
probably benign |
0.28 |
R7696:Adamts12
|
UTSW |
15 |
11,258,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R7957:Adamts12
|
UTSW |
15 |
11,317,298 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7980:Adamts12
|
UTSW |
15 |
11,263,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R7992:Adamts12
|
UTSW |
15 |
11,310,904 (GRCm39) |
missense |
probably benign |
|
R8032:Adamts12
|
UTSW |
15 |
11,259,189 (GRCm39) |
critical splice donor site |
probably null |
|
R8109:Adamts12
|
UTSW |
15 |
11,331,877 (GRCm39) |
missense |
probably benign |
0.02 |
R8402:Adamts12
|
UTSW |
15 |
11,263,376 (GRCm39) |
missense |
probably damaging |
0.96 |
R8751:Adamts12
|
UTSW |
15 |
11,215,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R8782:Adamts12
|
UTSW |
15 |
11,237,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R8934:Adamts12
|
UTSW |
15 |
11,300,015 (GRCm39) |
missense |
probably damaging |
0.99 |
R8952:Adamts12
|
UTSW |
15 |
11,286,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R8963:Adamts12
|
UTSW |
15 |
11,317,443 (GRCm39) |
critical splice donor site |
probably null |
|
R9042:Adamts12
|
UTSW |
15 |
11,152,134 (GRCm39) |
missense |
probably benign |
0.08 |
R9162:Adamts12
|
UTSW |
15 |
11,311,721 (GRCm39) |
missense |
probably benign |
0.29 |
R9190:Adamts12
|
UTSW |
15 |
11,336,446 (GRCm39) |
missense |
probably benign |
0.02 |
R9700:Adamts12
|
UTSW |
15 |
11,311,442 (GRCm39) |
missense |
probably benign |
0.04 |
R9748:Adamts12
|
UTSW |
15 |
11,310,628 (GRCm39) |
missense |
probably damaging |
0.99 |
V1662:Adamts12
|
UTSW |
15 |
11,071,894 (GRCm39) |
missense |
probably benign |
0.13 |
X0022:Adamts12
|
UTSW |
15 |
11,277,534 (GRCm39) |
missense |
probably benign |
0.30 |
Z1176:Adamts12
|
UTSW |
15 |
11,336,469 (GRCm39) |
missense |
not run |
|
Z1177:Adamts12
|
UTSW |
15 |
11,336,469 (GRCm39) |
missense |
not run |
|
Z1177:Adamts12
|
UTSW |
15 |
11,317,410 (GRCm39) |
missense |
probably damaging |
1.00 |
|