Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA986860 |
T |
C |
1: 130,668,725 (GRCm39) |
|
probably benign |
Het |
Adcy4 |
C |
T |
14: 56,016,486 (GRCm39) |
D322N |
probably damaging |
Het |
Adgrb3 |
T |
C |
1: 25,260,908 (GRCm39) |
N916S |
probably damaging |
Het |
Aox1 |
T |
C |
1: 58,373,862 (GRCm39) |
V841A |
probably benign |
Het |
Baz2b |
A |
T |
2: 59,756,383 (GRCm39) |
M983K |
probably damaging |
Het |
C2cd2l |
A |
G |
9: 44,222,430 (GRCm39) |
F682L |
probably damaging |
Het |
Ccsap |
T |
G |
8: 124,572,160 (GRCm39) |
E114A |
possibly damaging |
Het |
Cept1 |
T |
A |
3: 106,413,123 (GRCm39) |
T201S |
probably damaging |
Het |
Cfap221 |
T |
C |
1: 119,883,476 (GRCm39) |
M232V |
probably benign |
Het |
Chsy1 |
A |
G |
7: 65,759,974 (GRCm39) |
R106G |
probably benign |
Het |
Cit |
C |
T |
5: 116,126,182 (GRCm39) |
|
probably benign |
Het |
Cldn7 |
G |
A |
11: 69,857,918 (GRCm39) |
V42I |
probably benign |
Het |
Cnnm4 |
T |
A |
1: 36,511,345 (GRCm39) |
V191E |
probably benign |
Het |
Cntf |
A |
T |
19: 12,741,326 (GRCm39) |
V178D |
possibly damaging |
Het |
Ctsz |
C |
A |
2: 174,270,393 (GRCm39) |
R263L |
probably damaging |
Het |
Dclk1 |
T |
C |
3: 55,429,353 (GRCm39) |
M407T |
probably benign |
Het |
Dnhd1 |
A |
G |
7: 105,306,164 (GRCm39) |
I368V |
possibly damaging |
Het |
Gak |
A |
T |
5: 108,728,742 (GRCm39) |
|
probably benign |
Het |
Hepacam2 |
A |
T |
6: 3,487,231 (GRCm39) |
V42D |
probably damaging |
Het |
Il1rl2 |
CTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATT |
CTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATT |
1: 40,366,470 (GRCm39) |
|
probably benign |
Het |
Insr |
T |
A |
8: 3,248,234 (GRCm39) |
Q437L |
probably benign |
Het |
Itga8 |
G |
A |
2: 12,198,102 (GRCm39) |
|
probably benign |
Het |
Kansl1 |
A |
T |
11: 104,233,868 (GRCm39) |
C732S |
probably benign |
Het |
Kdsr |
T |
C |
1: 106,680,964 (GRCm39) |
K78R |
probably benign |
Het |
Kif14 |
T |
C |
1: 136,414,868 (GRCm39) |
S785P |
possibly damaging |
Het |
Lbr |
C |
A |
1: 181,645,133 (GRCm39) |
L506F |
probably benign |
Het |
Macf1 |
C |
A |
4: 123,342,031 (GRCm39) |
C2720F |
probably damaging |
Het |
Mapt |
G |
A |
11: 104,218,975 (GRCm39) |
D738N |
probably damaging |
Het |
Mroh9 |
T |
C |
1: 162,854,093 (GRCm39) |
Y769C |
probably damaging |
Het |
Mylk2 |
A |
G |
2: 152,762,274 (GRCm39) |
N515S |
possibly damaging |
Het |
Myorg |
G |
A |
4: 41,498,877 (GRCm39) |
T251M |
probably benign |
Het |
Nek10 |
T |
A |
14: 14,860,986 (GRCm38) |
L513M |
possibly damaging |
Het |
Nrxn2 |
A |
T |
19: 6,498,308 (GRCm39) |
S258C |
possibly damaging |
Het |
Nudt16l2 |
A |
T |
9: 105,021,786 (GRCm39) |
S87T |
possibly damaging |
Het |
Or52e15 |
G |
A |
7: 104,645,311 (GRCm39) |
H267Y |
probably benign |
Het |
Or5m12 |
C |
T |
2: 85,735,092 (GRCm39) |
C102Y |
possibly damaging |
Het |
Or6c1b |
C |
T |
10: 129,272,948 (GRCm39) |
T89I |
probably benign |
Het |
Or6z5 |
T |
A |
7: 6,477,848 (GRCm39) |
C246* |
probably null |
Het |
Or8c15 |
G |
T |
9: 38,120,586 (GRCm39) |
C79F |
probably benign |
Het |
Osgin2 |
G |
A |
4: 16,013,739 (GRCm39) |
|
probably benign |
Het |
Otud3 |
G |
A |
4: 138,641,060 (GRCm39) |
R27W |
probably damaging |
Het |
Pcare |
C |
T |
17: 72,059,306 (GRCm39) |
V124I |
possibly damaging |
Het |
Pcdhga12 |
T |
A |
18: 37,901,290 (GRCm39) |
F707L |
possibly damaging |
Het |
Pik3r1 |
T |
C |
13: 101,894,118 (GRCm39) |
E17G |
probably damaging |
Het |
Pramel19 |
A |
G |
4: 101,798,788 (GRCm39) |
E253G |
probably damaging |
Het |
Prickle4 |
AAGAGAGAGAGAGAGA |
AAGAGAGAGAGAGA |
17: 48,000,806 (GRCm39) |
|
probably benign |
Het |
Prokr1 |
G |
A |
6: 87,565,678 (GRCm39) |
R56W |
probably benign |
Het |
Ptprz1 |
G |
A |
6: 23,024,957 (GRCm39) |
C1731Y |
probably damaging |
Het |
Rbm15b |
A |
T |
9: 106,763,028 (GRCm39) |
F380Y |
possibly damaging |
Het |
Rfc5 |
G |
A |
5: 117,524,885 (GRCm39) |
L56F |
probably damaging |
Het |
Rhpn2 |
A |
T |
7: 35,090,228 (GRCm39) |
M617L |
probably benign |
Het |
Rusc1 |
T |
C |
3: 88,995,577 (GRCm39) |
|
probably null |
Het |
Sec23ip |
A |
G |
7: 128,354,634 (GRCm39) |
N297D |
probably damaging |
Het |
Sema3c |
A |
T |
5: 17,880,157 (GRCm39) |
H259L |
probably benign |
Het |
Sgsm1 |
G |
A |
5: 113,428,328 (GRCm39) |
|
probably benign |
Het |
Shisal2a |
A |
G |
4: 108,224,998 (GRCm39) |
V188A |
probably benign |
Het |
Sipa1l2 |
T |
A |
8: 126,218,606 (GRCm39) |
S244C |
probably damaging |
Het |
Slc39a5 |
T |
C |
10: 128,234,316 (GRCm39) |
I196V |
probably benign |
Het |
Smim22 |
G |
A |
16: 4,825,722 (GRCm39) |
A36T |
probably damaging |
Het |
Spag6 |
A |
G |
2: 18,747,588 (GRCm39) |
I408V |
probably benign |
Het |
Sult2a5 |
A |
G |
7: 13,359,311 (GRCm39) |
I96V |
probably benign |
Het |
Tmcc2 |
C |
A |
1: 132,308,517 (GRCm39) |
A126S |
probably benign |
Het |
Tsc2 |
A |
T |
17: 24,819,009 (GRCm39) |
S1276T |
probably damaging |
Het |
Ttc21a |
A |
G |
9: 119,788,103 (GRCm39) |
S843G |
probably benign |
Het |
Tubd1 |
G |
C |
11: 86,443,621 (GRCm39) |
V110L |
possibly damaging |
Het |
Ugt1a2 |
T |
A |
1: 88,128,534 (GRCm39) |
V59D |
probably damaging |
Het |
Vmn2r-ps158 |
A |
G |
7: 42,697,024 (GRCm39) |
R687G |
probably damaging |
Het |
Vsig8 |
T |
A |
1: 172,389,142 (GRCm39) |
H131Q |
probably benign |
Het |
Zbtb42 |
C |
A |
12: 112,646,861 (GRCm39) |
Y345* |
probably null |
Het |
Zfp612 |
T |
A |
8: 110,816,576 (GRCm39) |
C594* |
probably null |
Het |
Zfp940 |
A |
G |
7: 29,544,824 (GRCm39) |
V361A |
probably benign |
Het |
|
Other mutations in Dennd1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:Dennd1a
|
APN |
2 |
38,133,454 (GRCm39) |
nonsense |
probably null |
|
IGL00490:Dennd1a
|
APN |
2 |
37,691,164 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00839:Dennd1a
|
APN |
2 |
37,706,994 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01065:Dennd1a
|
APN |
2 |
37,734,917 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01621:Dennd1a
|
APN |
2 |
37,734,821 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01792:Dennd1a
|
APN |
2 |
38,016,592 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01799:Dennd1a
|
APN |
2 |
37,938,754 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02516:Dennd1a
|
APN |
2 |
37,742,406 (GRCm39) |
critical splice donor site |
probably null |
|
contract
|
UTSW |
2 |
37,742,453 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0018:Dennd1a
|
UTSW |
2 |
37,748,472 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0018:Dennd1a
|
UTSW |
2 |
37,748,472 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0144:Dennd1a
|
UTSW |
2 |
38,016,652 (GRCm39) |
missense |
probably damaging |
0.96 |
R0784:Dennd1a
|
UTSW |
2 |
37,911,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R1199:Dennd1a
|
UTSW |
2 |
37,851,728 (GRCm39) |
missense |
probably damaging |
0.99 |
R1439:Dennd1a
|
UTSW |
2 |
37,933,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R1563:Dennd1a
|
UTSW |
2 |
37,748,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R1608:Dennd1a
|
UTSW |
2 |
37,742,446 (GRCm39) |
missense |
probably benign |
0.18 |
R1720:Dennd1a
|
UTSW |
2 |
37,690,209 (GRCm39) |
nonsense |
probably null |
|
R1967:Dennd1a
|
UTSW |
2 |
37,734,845 (GRCm39) |
missense |
probably benign |
|
R2570:Dennd1a
|
UTSW |
2 |
37,734,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R3886:Dennd1a
|
UTSW |
2 |
37,748,089 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4464:Dennd1a
|
UTSW |
2 |
38,133,402 (GRCm39) |
splice site |
probably benign |
|
R5395:Dennd1a
|
UTSW |
2 |
37,692,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R5652:Dennd1a
|
UTSW |
2 |
37,691,138 (GRCm39) |
missense |
probably benign |
0.00 |
R5882:Dennd1a
|
UTSW |
2 |
37,851,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R6285:Dennd1a
|
UTSW |
2 |
37,742,453 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6520:Dennd1a
|
UTSW |
2 |
37,851,759 (GRCm39) |
splice site |
probably null |
|
R6934:Dennd1a
|
UTSW |
2 |
37,691,225 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7053:Dennd1a
|
UTSW |
2 |
37,851,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R7109:Dennd1a
|
UTSW |
2 |
37,938,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R7204:Dennd1a
|
UTSW |
2 |
37,929,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R7235:Dennd1a
|
UTSW |
2 |
37,691,073 (GRCm39) |
missense |
probably benign |
|
R7408:Dennd1a
|
UTSW |
2 |
37,742,184 (GRCm39) |
splice site |
probably null |
|
R7446:Dennd1a
|
UTSW |
2 |
37,706,991 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7579:Dennd1a
|
UTSW |
2 |
37,748,444 (GRCm39) |
missense |
probably damaging |
0.99 |
R7645:Dennd1a
|
UTSW |
2 |
37,911,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R7661:Dennd1a
|
UTSW |
2 |
37,734,841 (GRCm39) |
missense |
probably benign |
|
R8132:Dennd1a
|
UTSW |
2 |
37,748,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R8305:Dennd1a
|
UTSW |
2 |
37,748,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R8369:Dennd1a
|
UTSW |
2 |
37,938,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R8418:Dennd1a
|
UTSW |
2 |
37,748,403 (GRCm39) |
missense |
probably benign |
0.36 |
R8438:Dennd1a
|
UTSW |
2 |
37,746,150 (GRCm39) |
missense |
probably benign |
0.08 |
R8544:Dennd1a
|
UTSW |
2 |
37,872,920 (GRCm39) |
splice site |
probably null |
|
R8997:Dennd1a
|
UTSW |
2 |
37,690,497 (GRCm39) |
missense |
probably benign |
0.14 |
R9052:Dennd1a
|
UTSW |
2 |
37,911,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R9087:Dennd1a
|
UTSW |
2 |
37,911,366 (GRCm39) |
critical splice donor site |
probably null |
|
R9096:Dennd1a
|
UTSW |
2 |
37,690,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R9346:Dennd1a
|
UTSW |
2 |
37,911,447 (GRCm39) |
missense |
probably benign |
0.12 |
Z1088:Dennd1a
|
UTSW |
2 |
37,690,704 (GRCm39) |
missense |
probably benign |
|
Z1177:Dennd1a
|
UTSW |
2 |
37,690,269 (GRCm39) |
missense |
probably damaging |
1.00 |
|