Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg7 |
G |
A |
16: 56,590,725 (GRCm39) |
|
probably benign |
Het |
Afap1l1 |
T |
C |
18: 61,866,902 (GRCm39) |
D719G |
probably benign |
Het |
Amph |
C |
T |
13: 19,287,113 (GRCm39) |
T274M |
probably damaging |
Het |
Atp2c2 |
T |
A |
8: 120,469,414 (GRCm39) |
D396E |
possibly damaging |
Het |
Atpaf1 |
T |
C |
4: 115,648,475 (GRCm39) |
I164T |
probably damaging |
Het |
Avpr1b |
C |
A |
1: 131,528,257 (GRCm39) |
P260Q |
probably damaging |
Het |
Cacna1a |
T |
C |
8: 85,189,305 (GRCm39) |
|
probably benign |
Het |
Cald1 |
A |
G |
6: 34,741,963 (GRCm39) |
I449V |
probably damaging |
Het |
Ccdc24 |
A |
G |
4: 117,728,942 (GRCm39) |
|
probably null |
Het |
Cdcp3 |
A |
G |
7: 130,798,243 (GRCm39) |
Q84R |
possibly damaging |
Het |
Cenpk |
C |
A |
13: 104,378,885 (GRCm39) |
Q134K |
probably damaging |
Het |
Clasp1 |
A |
G |
1: 118,438,007 (GRCm39) |
N373D |
probably damaging |
Het |
Col7a1 |
T |
A |
9: 108,790,751 (GRCm39) |
S1042T |
unknown |
Het |
Cry2 |
G |
A |
2: 92,243,640 (GRCm39) |
R439C |
probably damaging |
Het |
Dlgap3 |
T |
C |
4: 127,089,018 (GRCm39) |
S205P |
possibly damaging |
Het |
Echdc2 |
T |
A |
4: 108,022,777 (GRCm39) |
S18T |
probably benign |
Het |
Efcab2 |
T |
A |
1: 178,265,042 (GRCm39) |
V36E |
probably damaging |
Het |
Galk1 |
A |
T |
11: 115,901,065 (GRCm39) |
|
probably null |
Het |
Hoxc11 |
A |
T |
15: 102,863,390 (GRCm39) |
N144Y |
probably damaging |
Het |
Ift140 |
T |
A |
17: 25,305,884 (GRCm39) |
C824S |
probably damaging |
Het |
Inf2 |
A |
G |
12: 112,570,663 (GRCm39) |
S401G |
probably benign |
Het |
Kcnn1 |
T |
G |
8: 71,307,724 (GRCm39) |
D106A |
probably damaging |
Het |
Lama4 |
A |
G |
10: 38,943,959 (GRCm39) |
N754S |
probably benign |
Het |
Marchf6 |
A |
G |
15: 31,478,439 (GRCm39) |
|
probably null |
Het |
Nlrp1b |
A |
C |
11: 71,072,659 (GRCm39) |
C395G |
probably benign |
Het |
Or2n1d |
T |
C |
17: 38,646,192 (GRCm39) |
V48A |
probably benign |
Het |
Or4k2 |
A |
T |
14: 50,424,461 (GRCm39) |
M71K |
probably damaging |
Het |
Or5ac15 |
T |
C |
16: 58,939,801 (GRCm39) |
M211V |
probably benign |
Het |
Or9q1 |
A |
G |
19: 13,805,014 (GRCm39) |
S249P |
possibly damaging |
Het |
Scel |
A |
G |
14: 103,836,842 (GRCm39) |
R477G |
possibly damaging |
Het |
Sdk2 |
A |
G |
11: 113,732,894 (GRCm39) |
S984P |
probably damaging |
Het |
Slc4a7 |
C |
T |
14: 14,782,040 (GRCm38) |
|
probably benign |
Het |
Tas2r103 |
A |
G |
6: 133,013,872 (GRCm39) |
S65P |
probably damaging |
Het |
Tnip2 |
T |
C |
5: 34,661,095 (GRCm39) |
E119G |
possibly damaging |
Het |
Zgrf1 |
T |
A |
3: 127,381,782 (GRCm39) |
L310M |
possibly damaging |
Het |
|
Other mutations in Dip2a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00422:Dip2a
|
APN |
10 |
76,149,070 (GRCm39) |
missense |
probably benign |
|
IGL00849:Dip2a
|
APN |
10 |
76,128,152 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01685:Dip2a
|
APN |
10 |
76,163,583 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01825:Dip2a
|
APN |
10 |
76,108,514 (GRCm39) |
nonsense |
probably null |
|
IGL02343:Dip2a
|
APN |
10 |
76,155,312 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02437:Dip2a
|
APN |
10 |
76,134,101 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02981:Dip2a
|
APN |
10 |
76,112,255 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03261:Dip2a
|
APN |
10 |
76,140,982 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0369:Dip2a
|
UTSW |
10 |
76,134,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R0522:Dip2a
|
UTSW |
10 |
76,157,365 (GRCm39) |
missense |
probably benign |
0.03 |
R0962:Dip2a
|
UTSW |
10 |
76,128,266 (GRCm39) |
unclassified |
probably benign |
|
R1164:Dip2a
|
UTSW |
10 |
76,112,231 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1309:Dip2a
|
UTSW |
10 |
76,115,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R1426:Dip2a
|
UTSW |
10 |
76,115,654 (GRCm39) |
unclassified |
probably benign |
|
R1636:Dip2a
|
UTSW |
10 |
76,157,412 (GRCm39) |
missense |
probably benign |
0.01 |
R1823:Dip2a
|
UTSW |
10 |
76,114,336 (GRCm39) |
nonsense |
probably null |
|
R1830:Dip2a
|
UTSW |
10 |
76,153,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R1876:Dip2a
|
UTSW |
10 |
76,153,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R2284:Dip2a
|
UTSW |
10 |
76,149,027 (GRCm39) |
missense |
probably benign |
0.01 |
R2369:Dip2a
|
UTSW |
10 |
76,149,030 (GRCm39) |
missense |
probably benign |
|
R4050:Dip2a
|
UTSW |
10 |
76,114,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R4089:Dip2a
|
UTSW |
10 |
76,114,323 (GRCm39) |
splice site |
probably null |
|
R4231:Dip2a
|
UTSW |
10 |
76,155,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R4715:Dip2a
|
UTSW |
10 |
76,132,240 (GRCm39) |
missense |
probably benign |
0.34 |
R4752:Dip2a
|
UTSW |
10 |
76,112,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R4846:Dip2a
|
UTSW |
10 |
76,157,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R4849:Dip2a
|
UTSW |
10 |
76,130,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R4892:Dip2a
|
UTSW |
10 |
76,116,593 (GRCm39) |
missense |
probably benign |
0.02 |
R4998:Dip2a
|
UTSW |
10 |
76,155,390 (GRCm39) |
nonsense |
probably null |
|
R5068:Dip2a
|
UTSW |
10 |
76,153,877 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5141:Dip2a
|
UTSW |
10 |
76,106,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R5253:Dip2a
|
UTSW |
10 |
76,135,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R5304:Dip2a
|
UTSW |
10 |
76,130,357 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5324:Dip2a
|
UTSW |
10 |
76,132,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R5369:Dip2a
|
UTSW |
10 |
76,128,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R6272:Dip2a
|
UTSW |
10 |
76,122,241 (GRCm39) |
makesense |
probably null |
|
R6884:Dip2a
|
UTSW |
10 |
76,108,366 (GRCm39) |
critical splice donor site |
probably null |
|
R7143:Dip2a
|
UTSW |
10 |
76,133,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R7247:Dip2a
|
UTSW |
10 |
76,108,366 (GRCm39) |
critical splice donor site |
probably null |
|
R7252:Dip2a
|
UTSW |
10 |
76,109,036 (GRCm39) |
missense |
not run |
|
R7327:Dip2a
|
UTSW |
10 |
76,108,396 (GRCm39) |
missense |
probably benign |
0.41 |
R7334:Dip2a
|
UTSW |
10 |
76,110,080 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7349:Dip2a
|
UTSW |
10 |
76,121,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R7360:Dip2a
|
UTSW |
10 |
76,114,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R7513:Dip2a
|
UTSW |
10 |
76,149,069 (GRCm39) |
missense |
probably benign |
|
R7793:Dip2a
|
UTSW |
10 |
76,114,417 (GRCm39) |
missense |
probably benign |
0.06 |
R7794:Dip2a
|
UTSW |
10 |
76,112,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R7819:Dip2a
|
UTSW |
10 |
76,126,862 (GRCm39) |
missense |
probably benign |
0.06 |
R8079:Dip2a
|
UTSW |
10 |
76,123,155 (GRCm39) |
missense |
probably benign |
|
R8280:Dip2a
|
UTSW |
10 |
76,100,610 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8281:Dip2a
|
UTSW |
10 |
76,112,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R8286:Dip2a
|
UTSW |
10 |
76,122,297 (GRCm39) |
missense |
probably benign |
|
R8350:Dip2a
|
UTSW |
10 |
76,100,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R8450:Dip2a
|
UTSW |
10 |
76,100,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R8525:Dip2a
|
UTSW |
10 |
76,110,115 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8824:Dip2a
|
UTSW |
10 |
76,114,320 (GRCm39) |
critical splice donor site |
probably null |
|
R8897:Dip2a
|
UTSW |
10 |
76,110,098 (GRCm39) |
missense |
probably benign |
0.22 |
R9039:Dip2a
|
UTSW |
10 |
76,163,553 (GRCm39) |
missense |
probably benign |
0.00 |
R9286:Dip2a
|
UTSW |
10 |
76,138,096 (GRCm39) |
missense |
probably benign |
0.05 |
R9504:Dip2a
|
UTSW |
10 |
76,132,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R9523:Dip2a
|
UTSW |
10 |
76,112,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R9628:Dip2a
|
UTSW |
10 |
76,142,993 (GRCm39) |
missense |
probably damaging |
0.99 |
R9732:Dip2a
|
UTSW |
10 |
76,110,077 (GRCm39) |
missense |
probably benign |
0.11 |
Z1088:Dip2a
|
UTSW |
10 |
76,121,462 (GRCm39) |
missense |
probably benign |
0.06 |
Z1176:Dip2a
|
UTSW |
10 |
76,116,654 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1176:Dip2a
|
UTSW |
10 |
76,102,157 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1177:Dip2a
|
UTSW |
10 |
76,132,234 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Dip2a
|
UTSW |
10 |
76,102,156 (GRCm39) |
missense |
possibly damaging |
0.51 |
|