Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810030O07Rik |
T |
C |
X: 12,535,892 (GRCm39) |
|
probably benign |
Het |
9530068E07Rik |
A |
G |
11: 52,294,331 (GRCm39) |
I199V |
probably benign |
Het |
Aasdh |
A |
T |
5: 77,049,936 (GRCm39) |
|
probably null |
Het |
Aatk |
T |
C |
11: 119,907,577 (GRCm39) |
I84V |
probably benign |
Het |
Adcy1 |
A |
G |
11: 7,100,071 (GRCm39) |
H727R |
probably benign |
Het |
Aff2 |
T |
C |
X: 68,878,092 (GRCm39) |
V626A |
probably benign |
Het |
Ano2 |
C |
A |
6: 125,957,134 (GRCm39) |
Y634* |
probably null |
Het |
Apob |
C |
A |
12: 8,066,350 (GRCm39) |
Q4407K |
probably damaging |
Het |
Asz1 |
T |
C |
6: 18,076,642 (GRCm39) |
|
probably benign |
Het |
Atp2b4 |
T |
G |
1: 133,656,506 (GRCm39) |
T715P |
possibly damaging |
Het |
Brip1 |
G |
T |
11: 85,955,735 (GRCm39) |
S926* |
probably null |
Het |
Cpd |
A |
T |
11: 76,702,539 (GRCm39) |
Y610N |
probably damaging |
Het |
Dennd4c |
T |
C |
4: 86,707,057 (GRCm39) |
|
probably benign |
Het |
Dido1 |
G |
A |
2: 180,312,772 (GRCm39) |
T1041I |
probably damaging |
Het |
Efcab3 |
T |
A |
11: 104,612,359 (GRCm39) |
S661T |
probably benign |
Het |
Fcer1a |
G |
A |
1: 173,049,128 (GRCm39) |
Q172* |
probably null |
Het |
Frem3 |
A |
G |
8: 81,339,435 (GRCm39) |
E576G |
possibly damaging |
Het |
Gcsam |
T |
C |
16: 45,440,431 (GRCm39) |
F136S |
possibly damaging |
Het |
Glmn |
T |
G |
5: 107,698,949 (GRCm39) |
T430P |
probably damaging |
Het |
Gm5934 |
T |
C |
X: 24,340,931 (GRCm39) |
N194S |
probably benign |
Het |
Gpatch11 |
T |
A |
17: 79,151,282 (GRCm39) |
L231* |
probably null |
Het |
Hibadh |
A |
T |
6: 52,525,917 (GRCm39) |
N244K |
probably damaging |
Het |
Kank2 |
A |
G |
9: 21,684,060 (GRCm39) |
V723A |
probably damaging |
Het |
Kcnn2 |
A |
T |
18: 45,788,273 (GRCm39) |
D192V |
probably damaging |
Het |
Ksr2 |
G |
A |
5: 117,846,022 (GRCm39) |
E630K |
probably benign |
Het |
Lmod3 |
T |
C |
6: 97,224,156 (GRCm39) |
H555R |
possibly damaging |
Het |
Mycs |
A |
G |
X: 5,380,922 (GRCm39) |
F53L |
probably damaging |
Het |
Ndufa10 |
G |
A |
1: 92,392,109 (GRCm39) |
Q215* |
probably null |
Het |
Ninl |
C |
T |
2: 150,806,139 (GRCm39) |
A361T |
probably damaging |
Het |
Pbsn |
A |
G |
X: 76,891,624 (GRCm39) |
C58R |
probably damaging |
Het |
Pcsk1 |
T |
A |
13: 75,280,335 (GRCm39) |
L720Q |
probably damaging |
Het |
Prss12 |
T |
C |
3: 123,299,925 (GRCm39) |
F679L |
probably benign |
Het |
Sohlh1 |
C |
T |
2: 25,735,660 (GRCm39) |
|
probably null |
Het |
Sspo |
T |
C |
6: 48,471,035 (GRCm39) |
F701L |
probably benign |
Het |
Tdp1 |
T |
C |
12: 99,921,290 (GRCm39) |
S609P |
probably benign |
Het |
Tmtc4 |
T |
A |
14: 123,165,044 (GRCm39) |
N605I |
probably benign |
Het |
Tnc |
G |
A |
4: 63,932,270 (GRCm39) |
P715S |
probably damaging |
Het |
Ubn2 |
T |
C |
6: 38,468,834 (GRCm39) |
S1181P |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,206,892 (GRCm39) |
|
probably benign |
Het |
Vmn1r46 |
T |
C |
6: 89,953,898 (GRCm39) |
F249S |
probably benign |
Het |
Zfp382 |
T |
C |
7: 29,833,614 (GRCm39) |
S422P |
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 |
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 |
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 |
|
|