Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933416I08Rik |
TCC |
TCCC |
X: 52,692,862 (GRCm39) |
|
noncoding transcript |
Het |
Ankrd2 |
G |
A |
19: 42,028,533 (GRCm39) |
R63H |
probably damaging |
Het |
Bbs2 |
C |
A |
8: 94,801,041 (GRCm39) |
|
probably benign |
Het |
Btbd7 |
G |
T |
12: 102,779,065 (GRCm39) |
D400E |
probably benign |
Het |
Cilp |
TGGG |
TGG |
9: 65,187,412 (GRCm39) |
|
probably null |
Het |
Col17a1 |
C |
T |
19: 47,636,537 (GRCm39) |
|
probably null |
Het |
Col3a1 |
A |
G |
1: 45,368,085 (GRCm39) |
|
probably null |
Het |
Crb1 |
CG |
C |
1: 139,164,824 (GRCm39) |
|
probably null |
Het |
Dscaml1 |
A |
C |
9: 45,654,297 (GRCm39) |
D1443A |
probably damaging |
Het |
Dsp |
T |
C |
13: 38,372,421 (GRCm39) |
|
probably benign |
Het |
Elf2 |
C |
T |
3: 51,165,038 (GRCm39) |
R262Q |
probably benign |
Het |
Fat3 |
G |
A |
9: 15,907,896 (GRCm39) |
S2702F |
probably benign |
Het |
G530012D18Rik |
CAGAGAGA |
CAGAGAGAGA |
1: 85,504,945 (GRCm39) |
|
probably null |
Het |
Gabrb1 |
T |
A |
5: 72,279,497 (GRCm39) |
S347R |
probably benign |
Het |
Hivep1 |
T |
C |
13: 42,309,604 (GRCm39) |
S615P |
probably benign |
Het |
Kcnq3 |
T |
C |
15: 65,897,027 (GRCm39) |
D291G |
possibly damaging |
Het |
Lyl1 |
C |
T |
8: 85,429,300 (GRCm39) |
P3L |
possibly damaging |
Het |
Mirt1 |
A |
G |
19: 53,433,710 (GRCm39) |
|
noncoding transcript |
Het |
Mmp1a |
TG |
TGG |
9: 7,465,083 (GRCm38) |
|
probably null |
Het |
Mug1 |
T |
A |
6: 121,857,530 (GRCm39) |
S1085T |
possibly damaging |
Het |
Myo18a |
A |
T |
11: 77,709,596 (GRCm39) |
T190S |
probably benign |
Het |
Myo5a |
G |
A |
9: 75,054,191 (GRCm39) |
|
probably null |
Het |
Or1ak2 |
T |
A |
2: 36,827,635 (GRCm39) |
F168Y |
probably damaging |
Het |
Or1l8 |
A |
T |
2: 36,817,820 (GRCm39) |
M102K |
probably damaging |
Het |
Or1m1 |
A |
T |
9: 18,666,750 (GRCm39) |
Y60* |
probably null |
Het |
Or5an1 |
G |
T |
19: 12,260,876 (GRCm39) |
V155L |
probably benign |
Het |
Or9g3 |
A |
G |
2: 85,589,785 (GRCm39) |
*312Q |
probably null |
Het |
Relch |
T |
A |
1: 105,654,106 (GRCm39) |
V825E |
probably damaging |
Het |
Rgma |
G |
A |
7: 73,067,263 (GRCm39) |
V173M |
probably damaging |
Het |
Rgsl1 |
G |
A |
1: 153,701,422 (GRCm39) |
S379F |
possibly damaging |
Het |
Sec16a |
T |
A |
2: 26,305,759 (GRCm39) |
D2215V |
probably damaging |
Het |
Speer4c1 |
A |
C |
5: 15,919,214 (GRCm39) |
|
probably benign |
Het |
Thrap3 |
G |
A |
4: 126,059,335 (GRCm39) |
|
probably null |
Het |
Ttyh2 |
T |
A |
11: 114,599,680 (GRCm39) |
L370Q |
probably damaging |
Het |
Ugt8a |
T |
C |
3: 125,669,139 (GRCm39) |
R322G |
possibly damaging |
Het |
Vmn2r97 |
T |
C |
17: 19,167,900 (GRCm39) |
M718T |
possibly damaging |
Het |
Zhx2 |
T |
C |
15: 57,686,229 (GRCm39) |
F533L |
possibly damaging |
Het |
|
Other mutations in Dpp8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00519:Dpp8
|
APN |
9 |
64,985,290 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00576:Dpp8
|
APN |
9 |
64,951,111 (GRCm39) |
missense |
probably benign |
0.32 |
IGL01303:Dpp8
|
APN |
9 |
64,962,294 (GRCm39) |
splice site |
probably benign |
|
IGL01506:Dpp8
|
APN |
9 |
64,970,699 (GRCm39) |
splice site |
probably benign |
|
IGL01544:Dpp8
|
APN |
9 |
64,962,270 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02387:Dpp8
|
APN |
9 |
64,952,998 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02567:Dpp8
|
APN |
9 |
64,986,058 (GRCm39) |
nonsense |
probably null |
|
IGL02611:Dpp8
|
APN |
9 |
64,963,075 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02723:Dpp8
|
APN |
9 |
64,949,549 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02927:Dpp8
|
APN |
9 |
64,967,551 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03116:Dpp8
|
APN |
9 |
64,973,749 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03135:Dpp8
|
APN |
9 |
64,960,322 (GRCm39) |
splice site |
probably null |
|
IGL03356:Dpp8
|
APN |
9 |
64,953,069 (GRCm39) |
missense |
probably benign |
0.00 |
almaviva
|
UTSW |
9 |
64,983,085 (GRCm39) |
missense |
probably damaging |
1.00 |
bartolo
|
UTSW |
9 |
64,986,000 (GRCm39) |
missense |
probably damaging |
1.00 |
Cherubino
|
UTSW |
9 |
64,962,205 (GRCm39) |
missense |
probably benign |
|
rosina
|
UTSW |
9 |
64,983,066 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0498:Dpp8
|
UTSW |
9 |
64,953,077 (GRCm39) |
splice site |
probably benign |
|
R0594:Dpp8
|
UTSW |
9 |
64,944,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R0675:Dpp8
|
UTSW |
9 |
64,973,784 (GRCm39) |
splice site |
probably benign |
|
R0699:Dpp8
|
UTSW |
9 |
64,962,176 (GRCm39) |
missense |
probably benign |
0.01 |
R0831:Dpp8
|
UTSW |
9 |
64,985,961 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1148:Dpp8
|
UTSW |
9 |
64,961,114 (GRCm39) |
critical splice donor site |
probably null |
|
R1148:Dpp8
|
UTSW |
9 |
64,961,114 (GRCm39) |
critical splice donor site |
probably null |
|
R1512:Dpp8
|
UTSW |
9 |
64,971,096 (GRCm39) |
splice site |
probably benign |
|
R1515:Dpp8
|
UTSW |
9 |
64,986,030 (GRCm39) |
missense |
probably benign |
0.04 |
R1546:Dpp8
|
UTSW |
9 |
64,970,775 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1556:Dpp8
|
UTSW |
9 |
64,958,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R2027:Dpp8
|
UTSW |
9 |
64,986,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R2104:Dpp8
|
UTSW |
9 |
64,981,849 (GRCm39) |
splice site |
probably null |
|
R2113:Dpp8
|
UTSW |
9 |
64,971,150 (GRCm39) |
missense |
probably benign |
0.00 |
R2656:Dpp8
|
UTSW |
9 |
64,988,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R4237:Dpp8
|
UTSW |
9 |
64,962,205 (GRCm39) |
missense |
probably benign |
|
R4238:Dpp8
|
UTSW |
9 |
64,962,205 (GRCm39) |
missense |
probably benign |
|
R4239:Dpp8
|
UTSW |
9 |
64,962,205 (GRCm39) |
missense |
probably benign |
|
R4595:Dpp8
|
UTSW |
9 |
64,983,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R4614:Dpp8
|
UTSW |
9 |
64,973,678 (GRCm39) |
missense |
probably benign |
0.00 |
R4946:Dpp8
|
UTSW |
9 |
64,963,200 (GRCm39) |
missense |
probably benign |
0.00 |
R5338:Dpp8
|
UTSW |
9 |
64,971,206 (GRCm39) |
nonsense |
probably null |
|
R5378:Dpp8
|
UTSW |
9 |
64,985,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R5506:Dpp8
|
UTSW |
9 |
64,985,391 (GRCm39) |
splice site |
probably null |
|
R5644:Dpp8
|
UTSW |
9 |
64,953,017 (GRCm39) |
nonsense |
probably null |
|
R5862:Dpp8
|
UTSW |
9 |
64,953,004 (GRCm39) |
missense |
probably benign |
0.03 |
R6437:Dpp8
|
UTSW |
9 |
64,981,860 (GRCm39) |
missense |
probably benign |
0.01 |
R6783:Dpp8
|
UTSW |
9 |
64,970,844 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6863:Dpp8
|
UTSW |
9 |
64,942,290 (GRCm39) |
missense |
probably damaging |
0.98 |
R7192:Dpp8
|
UTSW |
9 |
64,953,068 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7461:Dpp8
|
UTSW |
9 |
64,960,402 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7514:Dpp8
|
UTSW |
9 |
64,986,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R7548:Dpp8
|
UTSW |
9 |
64,944,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R7584:Dpp8
|
UTSW |
9 |
64,986,064 (GRCm39) |
missense |
probably damaging |
0.98 |
R7605:Dpp8
|
UTSW |
9 |
64,962,240 (GRCm39) |
missense |
probably benign |
0.33 |
R7613:Dpp8
|
UTSW |
9 |
64,960,402 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7665:Dpp8
|
UTSW |
9 |
64,986,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R7698:Dpp8
|
UTSW |
9 |
64,949,618 (GRCm39) |
missense |
probably benign |
0.00 |
R7844:Dpp8
|
UTSW |
9 |
64,952,949 (GRCm39) |
missense |
probably damaging |
0.99 |
R7935:Dpp8
|
UTSW |
9 |
64,944,262 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8079:Dpp8
|
UTSW |
9 |
64,951,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R8121:Dpp8
|
UTSW |
9 |
64,985,362 (GRCm39) |
missense |
probably benign |
0.10 |
R8315:Dpp8
|
UTSW |
9 |
64,988,133 (GRCm39) |
makesense |
probably null |
|
R8419:Dpp8
|
UTSW |
9 |
64,988,037 (GRCm39) |
missense |
probably benign |
0.34 |
R8516:Dpp8
|
UTSW |
9 |
64,985,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R8524:Dpp8
|
UTSW |
9 |
64,950,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R8896:Dpp8
|
UTSW |
9 |
64,985,318 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8922:Dpp8
|
UTSW |
9 |
64,981,793 (GRCm39) |
missense |
probably benign |
0.02 |
R8935:Dpp8
|
UTSW |
9 |
64,983,066 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9463:Dpp8
|
UTSW |
9 |
64,973,700 (GRCm39) |
nonsense |
probably null |
|
R9518:Dpp8
|
UTSW |
9 |
64,981,866 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9732:Dpp8
|
UTSW |
9 |
64,970,862 (GRCm39) |
critical splice donor site |
probably null |
|
R9751:Dpp8
|
UTSW |
9 |
64,960,453 (GRCm39) |
missense |
probably null |
0.65 |
Z1177:Dpp8
|
UTSW |
9 |
64,973,767 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Dpp8
|
UTSW |
9 |
64,971,148 (GRCm39) |
frame shift |
probably null |
|
|