Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930563M21Rik |
T |
C |
9: 55,888,126 (GRCm39) |
D397G |
probably benign |
Het |
6820408C15Rik |
C |
T |
2: 152,270,873 (GRCm39) |
T32I |
possibly damaging |
Het |
Abca13 |
A |
G |
11: 9,384,188 (GRCm39) |
K3880R |
probably benign |
Het |
Ahnak |
C |
T |
19: 8,979,147 (GRCm39) |
L144F |
probably benign |
Het |
Antxr2 |
A |
T |
5: 98,086,266 (GRCm39) |
I447N |
probably damaging |
Het |
Cdc20 |
C |
T |
4: 118,290,257 (GRCm39) |
R468Q |
probably damaging |
Het |
Clip2 |
A |
G |
5: 134,564,051 (GRCm39) |
|
probably benign |
Het |
Cntnap2 |
A |
T |
6: 46,507,324 (GRCm39) |
|
probably benign |
Het |
Ddi1 |
A |
G |
9: 6,265,799 (GRCm39) |
M190T |
probably benign |
Het |
Dicer1 |
A |
G |
12: 104,695,487 (GRCm39) |
V148A |
possibly damaging |
Het |
Galnt11 |
G |
A |
5: 25,470,258 (GRCm39) |
R569Q |
probably benign |
Het |
Gpr6 |
T |
C |
10: 40,946,604 (GRCm39) |
N326S |
probably damaging |
Het |
Hexb |
T |
C |
13: 97,313,259 (GRCm39) |
|
probably benign |
Het |
Ighv3-4 |
A |
T |
12: 114,217,533 (GRCm39) |
D19E |
probably benign |
Het |
L3mbtl3 |
G |
A |
10: 26,216,846 (GRCm39) |
A181V |
unknown |
Het |
Lrrc37a |
G |
A |
11: 103,393,115 (GRCm39) |
T770I |
probably damaging |
Het |
Or12e8 |
T |
C |
2: 87,188,597 (GRCm39) |
S270P |
probably damaging |
Het |
Or2d2 |
A |
G |
7: 106,728,244 (GRCm39) |
S119P |
probably damaging |
Het |
Or6a2 |
T |
C |
7: 106,600,536 (GRCm39) |
N177S |
probably damaging |
Het |
Or7g32 |
C |
T |
9: 19,388,893 (GRCm39) |
V215I |
probably benign |
Het |
Phactr1 |
T |
A |
13: 43,248,363 (GRCm39) |
N437K |
possibly damaging |
Het |
Ppp1r13b |
T |
C |
12: 111,805,170 (GRCm39) |
T181A |
probably benign |
Het |
Prc1 |
G |
A |
7: 79,960,964 (GRCm39) |
|
probably benign |
Het |
Proca1 |
A |
G |
11: 78,095,752 (GRCm39) |
N128S |
probably benign |
Het |
Psmd8 |
G |
A |
7: 28,876,546 (GRCm39) |
P155L |
probably damaging |
Het |
Rad54l |
A |
G |
4: 115,956,646 (GRCm39) |
V500A |
probably damaging |
Het |
Scamp3 |
G |
A |
3: 89,089,234 (GRCm39) |
|
probably null |
Het |
Serpinb10 |
C |
T |
1: 107,466,179 (GRCm39) |
T55M |
probably benign |
Het |
Sipa1l2 |
T |
C |
8: 126,218,395 (GRCm39) |
E314G |
probably benign |
Het |
Slc14a2 |
G |
A |
18: 78,250,283 (GRCm39) |
R62C |
probably damaging |
Het |
Tdrd9 |
C |
T |
12: 112,034,059 (GRCm39) |
R1334* |
probably null |
Het |
Trank1 |
A |
G |
9: 111,196,103 (GRCm39) |
I1376V |
probably benign |
Het |
Trim28 |
T |
A |
7: 12,761,838 (GRCm39) |
H268Q |
possibly damaging |
Het |
Vmn2r76 |
T |
A |
7: 85,879,740 (GRCm39) |
I187L |
probably benign |
Het |
Wdr95 |
A |
T |
5: 149,486,802 (GRCm39) |
R160* |
probably null |
Het |
Wnt5a |
T |
C |
14: 28,244,823 (GRCm39) |
C357R |
probably damaging |
Het |
Zfp157 |
A |
G |
5: 138,445,803 (GRCm39) |
I53V |
probably damaging |
Het |
Zfp184 |
G |
A |
13: 22,142,948 (GRCm39) |
R218H |
probably 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 |
IGL03050:Dpp8
|
UTSW |
9 |
64,962,118 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
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 |
|
|