Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
G |
3: 137,771,456 (GRCm39) |
E215G |
probably benign |
Het |
Adam8 |
T |
A |
7: 139,572,394 (GRCm39) |
|
probably benign |
Het |
Ankrd35 |
A |
G |
3: 96,592,104 (GRCm39) |
S797G |
not run |
Het |
Anxa3 |
T |
A |
5: 96,982,680 (GRCm39) |
H259Q |
probably benign |
Het |
Ap3d1 |
T |
A |
10: 80,557,426 (GRCm39) |
Q302L |
probably damaging |
Het |
Atg2a |
T |
C |
19: 6,305,682 (GRCm39) |
V1294A |
probably benign |
Het |
Atp13a5 |
G |
A |
16: 29,116,278 (GRCm39) |
Q613* |
probably null |
Het |
Bltp1 |
T |
A |
3: 37,002,490 (GRCm39) |
H1478Q |
probably benign |
Het |
Bltp1 |
A |
T |
3: 37,037,543 (GRCm39) |
H2448L |
probably benign |
Het |
Bmpr2 |
T |
G |
1: 59,906,510 (GRCm39) |
N534K |
probably benign |
Het |
C1qbp |
T |
C |
11: 70,869,072 (GRCm39) |
|
probably null |
Het |
C1qbp |
G |
T |
11: 70,869,073 (GRCm39) |
|
probably null |
Het |
C1ql3 |
T |
G |
2: 13,015,229 (GRCm39) |
K144Q |
possibly damaging |
Het |
C3 |
T |
C |
17: 57,511,039 (GRCm39) |
M1656V |
possibly damaging |
Het |
Cand1 |
A |
T |
10: 119,052,148 (GRCm39) |
Y252N |
probably benign |
Het |
Capn13 |
T |
C |
17: 73,625,053 (GRCm39) |
I632M |
probably benign |
Het |
Catsperb |
A |
G |
12: 101,557,757 (GRCm39) |
E776G |
probably damaging |
Het |
Ccnl1 |
A |
T |
3: 65,856,179 (GRCm39) |
V242D |
probably damaging |
Het |
Cd68 |
T |
C |
11: 69,555,938 (GRCm39) |
D200G |
probably benign |
Het |
Cela3a |
T |
C |
4: 137,132,899 (GRCm39) |
N118D |
probably benign |
Het |
Celsr2 |
A |
G |
3: 108,309,773 (GRCm39) |
C1609R |
probably damaging |
Het |
Cep85l |
G |
C |
10: 53,177,666 (GRCm39) |
Q458E |
probably damaging |
Het |
Cnga1 |
T |
G |
5: 72,766,868 (GRCm39) |
E190D |
probably benign |
Het |
Cntnap3 |
G |
A |
13: 64,906,066 (GRCm39) |
R847C |
probably damaging |
Het |
Cntrob |
G |
A |
11: 69,205,560 (GRCm39) |
Q425* |
probably null |
Het |
Commd9 |
G |
A |
2: 101,730,245 (GRCm39) |
W128* |
probably null |
Het |
Csnk1a1 |
C |
T |
18: 61,718,330 (GRCm39) |
S352L |
unknown |
Het |
Dact2 |
A |
G |
17: 14,416,593 (GRCm39) |
S536P |
probably damaging |
Het |
Ddx25 |
A |
G |
9: 35,465,882 (GRCm39) |
I113T |
probably benign |
Het |
Fndc7 |
A |
C |
3: 108,783,975 (GRCm39) |
F211L |
probably benign |
Het |
Fryl |
T |
C |
5: 73,262,091 (GRCm39) |
T559A |
probably damaging |
Het |
Hpx |
C |
A |
7: 105,241,068 (GRCm39) |
D402Y |
probably damaging |
Het |
Ints13 |
A |
G |
6: 146,476,198 (GRCm39) |
|
probably null |
Het |
Ipcef1 |
T |
C |
10: 6,906,066 (GRCm39) |
K76E |
probably damaging |
Het |
Kcnb2 |
A |
C |
1: 15,780,031 (GRCm39) |
Q301P |
probably damaging |
Het |
Lamp3 |
C |
T |
16: 19,518,362 (GRCm39) |
|
probably null |
Het |
Lmod2 |
A |
T |
6: 24,603,475 (GRCm39) |
H150L |
probably benign |
Het |
Lrch3 |
T |
C |
16: 32,826,077 (GRCm39) |
F718S |
probably damaging |
Het |
Mms22l |
T |
C |
4: 24,596,287 (GRCm39) |
V1082A |
probably benign |
Het |
Nbas |
G |
T |
12: 13,519,881 (GRCm39) |
V1598L |
probably damaging |
Het |
Nrxn3 |
C |
T |
12: 89,479,870 (GRCm39) |
R671* |
probably null |
Het |
Or4c110 |
A |
T |
2: 88,832,544 (GRCm39) |
F29L |
|
Het |
Or4c58 |
A |
G |
2: 89,674,789 (GRCm39) |
L176P |
probably damaging |
Het |
Or52e8 |
A |
T |
7: 104,624,268 (GRCm39) |
L312* |
probably null |
Het |
Or5a3 |
A |
C |
19: 12,400,204 (GRCm39) |
H177P |
probably damaging |
Het |
Or6d14 |
A |
T |
6: 116,533,398 (GRCm39) |
E4V |
possibly damaging |
Het |
Pcdhga6 |
T |
A |
18: 37,841,619 (GRCm39) |
N446K |
probably damaging |
Het |
Phlpp1 |
A |
T |
1: 106,320,303 (GRCm39) |
I1433F |
probably benign |
Het |
Pla2g6 |
G |
A |
15: 79,192,933 (GRCm39) |
R245C |
probably damaging |
Het |
Rgl3 |
G |
A |
9: 21,888,123 (GRCm39) |
Q464* |
probably null |
Het |
Ryr2 |
T |
C |
13: 11,720,530 (GRCm39) |
D2706G |
probably benign |
Het |
Sbf2 |
G |
A |
7: 109,974,984 (GRCm39) |
Q718* |
probably null |
Het |
Sdad1 |
T |
C |
5: 92,447,980 (GRCm39) |
T252A |
probably benign |
Het |
Sgk1 |
T |
C |
10: 21,870,009 (GRCm39) |
L16P |
probably damaging |
Het |
Slc38a8 |
A |
G |
8: 120,212,327 (GRCm39) |
S339P |
possibly damaging |
Het |
Slc44a4 |
T |
C |
17: 35,140,667 (GRCm39) |
S287P |
possibly damaging |
Het |
Syne1 |
T |
C |
10: 5,375,760 (GRCm39) |
I111V |
probably damaging |
Het |
Synm |
A |
C |
7: 67,383,194 (GRCm39) |
S1489R |
probably damaging |
Het |
Tfb2m |
A |
G |
1: 179,365,269 (GRCm39) |
F232L |
probably benign |
Het |
Traf3 |
A |
T |
12: 111,227,095 (GRCm39) |
K328* |
probably null |
Het |
Trim38 |
C |
A |
13: 23,972,365 (GRCm39) |
Q229K |
probably benign |
Het |
Vcan |
A |
G |
13: 89,837,951 (GRCm39) |
I2531T |
probably damaging |
Het |
Virma |
T |
A |
4: 11,546,211 (GRCm39) |
I1683N |
possibly damaging |
Het |
Vmn1r18 |
A |
T |
6: 57,367,551 (GRCm39) |
M1K |
probably null |
Het |
Vmn2r87 |
T |
C |
10: 130,314,761 (GRCm39) |
N275S |
probably damaging |
Het |
Vps13a |
T |
A |
19: 16,701,066 (GRCm39) |
H701L |
probably benign |
Het |
Vrk3 |
T |
A |
7: 44,420,348 (GRCm39) |
|
probably null |
Het |
Zfp993 |
T |
A |
4: 146,742,098 (GRCm39) |
S141T |
possibly damaging |
Het |
|
Other mutations in Dscam |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00515:Dscam
|
APN |
16 |
96,409,265 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL00841:Dscam
|
APN |
16 |
96,621,077 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01289:Dscam
|
APN |
16 |
96,445,082 (GRCm39) |
nonsense |
probably null |
|
IGL01358:Dscam
|
APN |
16 |
96,411,543 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL01431:Dscam
|
APN |
16 |
96,453,278 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01444:Dscam
|
APN |
16 |
96,474,909 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01767:Dscam
|
APN |
16 |
96,456,136 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01866:Dscam
|
APN |
16 |
96,486,550 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02020:Dscam
|
APN |
16 |
96,517,269 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02023:Dscam
|
APN |
16 |
96,602,397 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02057:Dscam
|
APN |
16 |
96,517,273 (GRCm39) |
nonsense |
probably null |
|
IGL02389:Dscam
|
APN |
16 |
96,442,097 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02409:Dscam
|
APN |
16 |
96,621,088 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02694:Dscam
|
APN |
16 |
96,394,476 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02899:Dscam
|
APN |
16 |
96,510,447 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02956:Dscam
|
APN |
16 |
96,602,472 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03035:Dscam
|
APN |
16 |
96,621,170 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03191:Dscam
|
APN |
16 |
96,621,969 (GRCm39) |
missense |
probably benign |
0.36 |
growler
|
UTSW |
16 |
96,622,197 (GRCm39) |
missense |
probably damaging |
0.99 |
Twostep
|
UTSW |
16 |
96,626,982 (GRCm39) |
splice site |
probably null |
|
F6893:Dscam
|
UTSW |
16 |
96,857,660 (GRCm39) |
missense |
possibly damaging |
0.78 |
K3955:Dscam
|
UTSW |
16 |
96,474,887 (GRCm39) |
missense |
probably benign |
0.00 |
R0024:Dscam
|
UTSW |
16 |
96,394,585 (GRCm39) |
nonsense |
probably null |
|
R0057:Dscam
|
UTSW |
16 |
96,474,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R0057:Dscam
|
UTSW |
16 |
96,474,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R0117:Dscam
|
UTSW |
16 |
96,474,878 (GRCm39) |
missense |
probably benign |
0.33 |
R0211:Dscam
|
UTSW |
16 |
96,517,279 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0280:Dscam
|
UTSW |
16 |
96,840,206 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0355:Dscam
|
UTSW |
16 |
96,456,105 (GRCm39) |
missense |
probably benign |
0.00 |
R0380:Dscam
|
UTSW |
16 |
96,857,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R0445:Dscam
|
UTSW |
16 |
96,573,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R0492:Dscam
|
UTSW |
16 |
96,626,982 (GRCm39) |
splice site |
probably null |
|
R0534:Dscam
|
UTSW |
16 |
96,453,372 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0593:Dscam
|
UTSW |
16 |
96,573,608 (GRCm39) |
missense |
probably benign |
0.19 |
R0707:Dscam
|
UTSW |
16 |
96,626,982 (GRCm39) |
splice site |
probably null |
|
R0738:Dscam
|
UTSW |
16 |
96,620,981 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1017:Dscam
|
UTSW |
16 |
96,634,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R1377:Dscam
|
UTSW |
16 |
96,573,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R1440:Dscam
|
UTSW |
16 |
96,621,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R1442:Dscam
|
UTSW |
16 |
96,409,274 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1464:Dscam
|
UTSW |
16 |
96,602,453 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1464:Dscam
|
UTSW |
16 |
96,602,453 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1478:Dscam
|
UTSW |
16 |
96,592,110 (GRCm39) |
missense |
probably benign |
0.15 |
R1530:Dscam
|
UTSW |
16 |
96,621,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R1731:Dscam
|
UTSW |
16 |
96,621,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R1765:Dscam
|
UTSW |
16 |
96,486,579 (GRCm39) |
missense |
probably benign |
0.00 |
R1824:Dscam
|
UTSW |
16 |
96,626,781 (GRCm39) |
missense |
probably benign |
0.00 |
R1933:Dscam
|
UTSW |
16 |
96,394,414 (GRCm39) |
missense |
probably benign |
0.00 |
R2005:Dscam
|
UTSW |
16 |
96,840,120 (GRCm39) |
missense |
probably benign |
0.02 |
R2006:Dscam
|
UTSW |
16 |
96,621,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R2101:Dscam
|
UTSW |
16 |
96,411,549 (GRCm39) |
missense |
probably benign |
0.00 |
R2177:Dscam
|
UTSW |
16 |
96,411,524 (GRCm39) |
missense |
probably damaging |
0.98 |
R2342:Dscam
|
UTSW |
16 |
96,420,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R2851:Dscam
|
UTSW |
16 |
96,423,915 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2929:Dscam
|
UTSW |
16 |
96,486,612 (GRCm39) |
missense |
possibly damaging |
0.76 |
R3055:Dscam
|
UTSW |
16 |
96,602,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R3157:Dscam
|
UTSW |
16 |
96,479,710 (GRCm39) |
missense |
probably benign |
0.16 |
R3159:Dscam
|
UTSW |
16 |
96,479,710 (GRCm39) |
missense |
probably benign |
0.16 |
R3944:Dscam
|
UTSW |
16 |
96,622,197 (GRCm39) |
missense |
probably damaging |
0.99 |
R4080:Dscam
|
UTSW |
16 |
96,484,972 (GRCm39) |
missense |
probably benign |
0.01 |
R4285:Dscam
|
UTSW |
16 |
96,510,309 (GRCm39) |
critical splice donor site |
probably null |
|
R4384:Dscam
|
UTSW |
16 |
96,510,416 (GRCm39) |
missense |
probably damaging |
0.99 |
R4460:Dscam
|
UTSW |
16 |
96,411,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R4575:Dscam
|
UTSW |
16 |
96,626,823 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4594:Dscam
|
UTSW |
16 |
96,519,196 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4643:Dscam
|
UTSW |
16 |
96,486,501 (GRCm39) |
missense |
probably damaging |
0.96 |
R4698:Dscam
|
UTSW |
16 |
96,411,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R4716:Dscam
|
UTSW |
16 |
96,420,771 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4743:Dscam
|
UTSW |
16 |
96,631,256 (GRCm39) |
missense |
probably benign |
0.00 |
R4766:Dscam
|
UTSW |
16 |
96,445,188 (GRCm39) |
missense |
probably benign |
0.02 |
R4899:Dscam
|
UTSW |
16 |
96,485,018 (GRCm39) |
missense |
probably benign |
0.01 |
R4987:Dscam
|
UTSW |
16 |
96,498,721 (GRCm39) |
missense |
probably benign |
0.00 |
R4990:Dscam
|
UTSW |
16 |
96,626,715 (GRCm39) |
missense |
probably benign |
0.12 |
R5123:Dscam
|
UTSW |
16 |
96,573,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R5130:Dscam
|
UTSW |
16 |
96,620,979 (GRCm39) |
missense |
probably benign |
0.00 |
R5328:Dscam
|
UTSW |
16 |
96,474,878 (GRCm39) |
missense |
probably benign |
0.33 |
R5666:Dscam
|
UTSW |
16 |
96,519,364 (GRCm39) |
missense |
probably benign |
0.23 |
R5670:Dscam
|
UTSW |
16 |
96,519,364 (GRCm39) |
missense |
probably benign |
0.23 |
R5678:Dscam
|
UTSW |
16 |
96,592,100 (GRCm39) |
missense |
probably benign |
0.16 |
R5827:Dscam
|
UTSW |
16 |
96,451,191 (GRCm39) |
critical splice donor site |
probably null |
|
R5907:Dscam
|
UTSW |
16 |
96,622,120 (GRCm39) |
missense |
probably damaging |
0.97 |
R6032:Dscam
|
UTSW |
16 |
96,451,191 (GRCm39) |
critical splice donor site |
probably null |
|
R6032:Dscam
|
UTSW |
16 |
96,451,191 (GRCm39) |
critical splice donor site |
probably null |
|
R6103:Dscam
|
UTSW |
16 |
96,626,781 (GRCm39) |
missense |
probably benign |
|
R6240:Dscam
|
UTSW |
16 |
96,420,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Dscam
|
UTSW |
16 |
96,474,914 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6361:Dscam
|
UTSW |
16 |
96,424,011 (GRCm39) |
missense |
probably benign |
0.08 |
R6405:Dscam
|
UTSW |
16 |
96,479,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R6444:Dscam
|
UTSW |
16 |
96,420,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R6560:Dscam
|
UTSW |
16 |
96,626,935 (GRCm39) |
missense |
probably benign |
0.00 |
R6598:Dscam
|
UTSW |
16 |
96,620,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R6622:Dscam
|
UTSW |
16 |
96,446,273 (GRCm39) |
missense |
probably benign |
0.06 |
R6792:Dscam
|
UTSW |
16 |
96,449,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R6792:Dscam
|
UTSW |
16 |
96,394,455 (GRCm39) |
missense |
probably damaging |
0.96 |
R6827:Dscam
|
UTSW |
16 |
96,840,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R6868:Dscam
|
UTSW |
16 |
96,631,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R6898:Dscam
|
UTSW |
16 |
96,631,100 (GRCm39) |
missense |
probably benign |
0.02 |
R6903:Dscam
|
UTSW |
16 |
96,621,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R7051:Dscam
|
UTSW |
16 |
96,620,986 (GRCm39) |
missense |
probably benign |
0.01 |
R7146:Dscam
|
UTSW |
16 |
96,631,117 (GRCm39) |
nonsense |
probably null |
|
R7180:Dscam
|
UTSW |
16 |
96,626,764 (GRCm39) |
missense |
probably damaging |
0.97 |
R7209:Dscam
|
UTSW |
16 |
96,451,544 (GRCm39) |
splice site |
probably null |
|
R7247:Dscam
|
UTSW |
16 |
96,622,008 (GRCm39) |
missense |
probably damaging |
0.99 |
R7269:Dscam
|
UTSW |
16 |
96,479,601 (GRCm39) |
missense |
probably benign |
0.00 |
R7301:Dscam
|
UTSW |
16 |
96,857,732 (GRCm39) |
missense |
probably benign |
0.01 |
R7328:Dscam
|
UTSW |
16 |
96,446,235 (GRCm39) |
nonsense |
probably null |
|
R7368:Dscam
|
UTSW |
16 |
96,445,131 (GRCm39) |
missense |
probably benign |
0.00 |
R7474:Dscam
|
UTSW |
16 |
96,621,089 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7536:Dscam
|
UTSW |
16 |
96,442,226 (GRCm39) |
splice site |
probably null |
|
R7624:Dscam
|
UTSW |
16 |
96,411,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R7766:Dscam
|
UTSW |
16 |
96,592,101 (GRCm39) |
missense |
probably benign |
0.31 |
R7817:Dscam
|
UTSW |
16 |
96,442,064 (GRCm39) |
missense |
probably benign |
|
R7843:Dscam
|
UTSW |
16 |
96,626,830 (GRCm39) |
missense |
probably damaging |
0.99 |
R7911:Dscam
|
UTSW |
16 |
96,445,122 (GRCm39) |
missense |
probably benign |
0.01 |
R8108:Dscam
|
UTSW |
16 |
96,445,079 (GRCm39) |
missense |
probably benign |
0.01 |
R8128:Dscam
|
UTSW |
16 |
96,602,374 (GRCm39) |
splice site |
probably null |
|
R8770:Dscam
|
UTSW |
16 |
96,456,106 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8876:Dscam
|
UTSW |
16 |
96,420,828 (GRCm39) |
missense |
probably damaging |
0.96 |
R9005:Dscam
|
UTSW |
16 |
96,602,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R9009:Dscam
|
UTSW |
16 |
96,840,116 (GRCm39) |
missense |
probably benign |
0.10 |
R9168:Dscam
|
UTSW |
16 |
96,420,768 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9176:Dscam
|
UTSW |
16 |
96,486,553 (GRCm39) |
missense |
probably benign |
0.37 |
R9244:Dscam
|
UTSW |
16 |
96,486,429 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9339:Dscam
|
UTSW |
16 |
96,517,263 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9374:Dscam
|
UTSW |
16 |
96,857,857 (GRCm39) |
missense |
probably benign |
0.19 |
R9385:Dscam
|
UTSW |
16 |
96,840,203 (GRCm39) |
missense |
probably benign |
|
R9674:Dscam
|
UTSW |
16 |
96,442,036 (GRCm39) |
missense |
probably benign |
0.03 |
X0025:Dscam
|
UTSW |
16 |
96,510,361 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Dscam
|
UTSW |
16 |
96,573,761 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Dscam
|
UTSW |
16 |
96,409,389 (GRCm39) |
missense |
probably damaging |
0.98 |
|