Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acbd5 |
T |
A |
2: 22,977,507 (GRCm39) |
N168K |
possibly damaging |
Het |
Aig1 |
T |
C |
10: 13,744,418 (GRCm39) |
M29V |
probably damaging |
Het |
Albfm1 |
C |
A |
5: 90,727,473 (GRCm39) |
H364N |
probably damaging |
Het |
Apba2 |
A |
G |
7: 64,344,894 (GRCm39) |
E28G |
probably damaging |
Het |
Bglap3 |
T |
C |
3: 88,276,423 (GRCm39) |
N45S |
possibly damaging |
Het |
Cables2 |
A |
G |
2: 179,902,072 (GRCm39) |
|
probably null |
Het |
Cd109 |
A |
G |
9: 78,596,237 (GRCm39) |
|
probably benign |
Het |
Cdk1 |
T |
C |
10: 69,176,331 (GRCm39) |
N259D |
probably benign |
Het |
Ces1h |
A |
G |
8: 94,078,654 (GRCm39) |
*563R |
probably null |
Het |
Cfap46 |
C |
T |
7: 139,262,425 (GRCm39) |
A115T |
probably damaging |
Het |
Cry2 |
A |
T |
2: 92,257,266 (GRCm39) |
V101E |
possibly damaging |
Het |
Cyp4a31 |
A |
G |
4: 115,421,026 (GRCm39) |
Y38C |
probably damaging |
Het |
Eps8l1 |
A |
G |
7: 4,475,123 (GRCm39) |
T366A |
probably benign |
Het |
Esr2 |
C |
T |
12: 76,192,119 (GRCm39) |
R303H |
probably benign |
Het |
Fbxo41 |
T |
G |
6: 85,455,153 (GRCm39) |
L617F |
possibly damaging |
Het |
Fbxw15 |
A |
T |
9: 109,381,723 (GRCm39) |
|
probably benign |
Het |
Lrriq1 |
T |
A |
10: 103,070,024 (GRCm39) |
|
probably benign |
Het |
Me1 |
A |
T |
9: 86,536,694 (GRCm39) |
|
probably null |
Het |
Moxd1 |
G |
A |
10: 24,155,762 (GRCm39) |
V289I |
probably damaging |
Het |
Muc19 |
T |
G |
15: 91,778,428 (GRCm39) |
|
noncoding transcript |
Het |
Myo15b |
A |
G |
11: 115,764,226 (GRCm39) |
|
probably benign |
Het |
Nav1 |
A |
T |
1: 135,382,490 (GRCm39) |
L1264* |
probably null |
Het |
Nhlrc4 |
T |
C |
17: 26,162,335 (GRCm39) |
*137W |
probably null |
Het |
Nrxn3 |
A |
G |
12: 88,762,123 (GRCm39) |
T57A |
probably damaging |
Het |
Or10g3 |
T |
A |
14: 52,609,934 (GRCm39) |
D192V |
probably damaging |
Het |
Orc2 |
A |
T |
1: 58,508,825 (GRCm39) |
|
probably null |
Het |
Rpap2 |
G |
A |
5: 107,766,047 (GRCm39) |
|
probably null |
Het |
S100a9 |
T |
C |
3: 90,602,531 (GRCm39) |
H21R |
probably damaging |
Het |
Spz1 |
T |
A |
13: 92,712,054 (GRCm39) |
M141L |
probably benign |
Het |
Stk40 |
A |
G |
4: 126,030,695 (GRCm39) |
Y305C |
probably damaging |
Het |
Stra6l |
A |
G |
4: 45,869,588 (GRCm39) |
Q218R |
probably damaging |
Het |
T |
C |
A |
17: 8,658,732 (GRCm39) |
|
probably benign |
Het |
Tep1 |
T |
C |
14: 51,066,704 (GRCm39) |
D2298G |
probably damaging |
Het |
Trim40 |
A |
T |
17: 37,200,030 (GRCm39) |
L16Q |
probably benign |
Het |
Tubb4a |
T |
C |
17: 57,388,538 (GRCm39) |
I163V |
probably benign |
Het |
Vwc2 |
T |
A |
11: 11,066,532 (GRCm39) |
C207S |
probably damaging |
Het |
Zfp407 |
A |
G |
18: 84,227,849 (GRCm39) |
I1920T |
possibly damaging |
Het |
Zfp429 |
T |
C |
13: 67,538,844 (GRCm39) |
E200G |
probably damaging |
Het |
Zfp451 |
C |
T |
1: 33,815,574 (GRCm39) |
C792Y |
probably 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 |
|
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 |
IGL03122:Dip2a
|
APN |
10 |
76,110,880 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
|