Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actn4 |
A |
T |
7: 28,596,467 (GRCm39) |
I676N |
possibly damaging |
Het |
Adamts10 |
T |
C |
17: 33,770,126 (GRCm39) |
C1002R |
probably damaging |
Het |
Agbl2 |
A |
C |
2: 90,619,349 (GRCm39) |
N58T |
probably benign |
Het |
Akap12 |
A |
T |
10: 4,306,082 (GRCm39) |
D1069V |
probably damaging |
Het |
Bltp2 |
C |
A |
11: 78,159,570 (GRCm39) |
Q540K |
probably benign |
Het |
Cfap65 |
T |
A |
1: 74,967,527 (GRCm39) |
T184S |
probably benign |
Het |
Chd1 |
T |
C |
17: 15,987,737 (GRCm39) |
V1517A |
probably benign |
Het |
CN725425 |
T |
A |
15: 91,119,993 (GRCm39) |
V38D |
possibly damaging |
Het |
Copg1 |
T |
A |
6: 87,884,940 (GRCm39) |
L712Q |
probably benign |
Het |
Ctsf |
T |
G |
19: 4,906,567 (GRCm39) |
F165V |
probably damaging |
Het |
Ddx21 |
T |
C |
10: 62,429,865 (GRCm39) |
Y293C |
probably damaging |
Het |
Ddx46 |
C |
T |
13: 55,821,832 (GRCm39) |
P839S |
probably benign |
Het |
Dennd5a |
A |
G |
7: 109,496,174 (GRCm39) |
V1164A |
possibly damaging |
Het |
Dync1h1 |
T |
A |
12: 110,632,200 (GRCm39) |
I4490N |
probably damaging |
Het |
Ecm1 |
A |
C |
3: 95,643,843 (GRCm39) |
Y236D |
probably damaging |
Het |
Fat2 |
T |
C |
11: 55,175,173 (GRCm39) |
T1847A |
probably benign |
Het |
Galc |
T |
A |
12: 98,175,102 (GRCm39) |
I567L |
probably benign |
Het |
Gask1a |
C |
T |
9: 121,780,151 (GRCm39) |
|
probably benign |
Het |
H6pd |
T |
C |
4: 150,067,360 (GRCm39) |
D350G |
probably benign |
Het |
Ifi44 |
A |
G |
3: 151,438,061 (GRCm39) |
Y409H |
probably benign |
Het |
Kdm5a |
T |
G |
6: 120,404,025 (GRCm39) |
F1210C |
probably damaging |
Het |
Kdm5b |
C |
T |
1: 134,515,669 (GRCm39) |
R98C |
probably damaging |
Het |
Lipt1 |
T |
A |
1: 37,915,043 (GRCm39) |
C366* |
probably null |
Het |
Med13 |
G |
A |
11: 86,236,744 (GRCm39) |
R138* |
probably null |
Het |
Mterf1a |
A |
G |
5: 3,941,845 (GRCm39) |
C8R |
probably benign |
Het |
Ncapg2 |
A |
T |
12: 116,382,897 (GRCm39) |
I243F |
probably damaging |
Het |
Nop58 |
T |
C |
1: 59,744,754 (GRCm39) |
S304P |
probably damaging |
Het |
Nsd2 |
T |
C |
5: 34,028,811 (GRCm39) |
*167Q |
probably null |
Het |
Or1e30 |
T |
G |
11: 73,678,616 (GRCm39) |
M284R |
probably damaging |
Het |
Or2t35 |
T |
A |
14: 14,407,867 (GRCm38) |
I213N |
probably damaging |
Het |
Or52ab2 |
T |
A |
7: 102,969,978 (GRCm39) |
M120K |
|
Het |
Pramel29 |
C |
T |
4: 143,935,091 (GRCm39) |
V217I |
possibly damaging |
Het |
Prdm16 |
C |
T |
4: 154,425,947 (GRCm39) |
G613R |
probably damaging |
Het |
Prss46 |
T |
C |
9: 110,679,065 (GRCm39) |
S89P |
probably damaging |
Het |
Scin |
T |
C |
12: 40,174,687 (GRCm39) |
N132S |
possibly damaging |
Het |
Sec14l2 |
T |
C |
11: 4,058,574 (GRCm39) |
K196R |
probably benign |
Het |
Sox17 |
C |
A |
1: 4,563,895 (GRCm39) |
|
probably benign |
Het |
Tango6 |
A |
G |
8: 107,425,621 (GRCm39) |
T394A |
probably benign |
Het |
Tbc1d22a |
T |
A |
15: 86,250,876 (GRCm39) |
I398N |
probably damaging |
Het |
Tdpoz8 |
A |
G |
3: 92,981,752 (GRCm39) |
I183V |
probably benign |
Het |
Tmem8b |
T |
C |
4: 43,689,461 (GRCm39) |
V285A |
probably damaging |
Het |
Tnfrsf11b |
T |
A |
15: 54,123,497 (GRCm39) |
T35S |
probably benign |
Het |
Unc13c |
T |
A |
9: 73,606,494 (GRCm39) |
I1289F |
probably benign |
Het |
Ust |
C |
T |
10: 8,205,987 (GRCm39) |
V99I |
probably benign |
Het |
Vmn1r76 |
A |
G |
7: 11,664,344 (GRCm39) |
V290A |
probably benign |
Het |
Vmn2r50 |
T |
C |
7: 9,781,665 (GRCm39) |
N360S |
probably benign |
Het |
Vmn2r93 |
T |
C |
17: 18,536,910 (GRCm39) |
I531T |
probably benign |
Het |
Zap70 |
T |
C |
1: 36,818,395 (GRCm39) |
|
probably null |
Het |
Zfp932 |
A |
G |
5: 110,157,630 (GRCm39) |
N443D |
probably benign |
Het |
|
Other mutations in Abcc8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01114:Abcc8
|
APN |
7 |
45,754,088 (GRCm39) |
missense |
probably benign |
|
IGL01457:Abcc8
|
APN |
7 |
45,784,917 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL01645:Abcc8
|
APN |
7 |
45,764,477 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01683:Abcc8
|
APN |
7 |
45,801,091 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01826:Abcc8
|
APN |
7 |
45,774,273 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01912:Abcc8
|
APN |
7 |
45,769,934 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02218:Abcc8
|
APN |
7 |
45,769,860 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02326:Abcc8
|
APN |
7 |
45,772,281 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02403:Abcc8
|
APN |
7 |
45,755,227 (GRCm39) |
splice site |
probably null |
|
IGL02411:Abcc8
|
APN |
7 |
45,756,431 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02653:Abcc8
|
APN |
7 |
45,765,191 (GRCm39) |
splice site |
probably benign |
|
IGL02706:Abcc8
|
APN |
7 |
45,816,345 (GRCm39) |
missense |
probably benign |
0.08 |
R0295:Abcc8
|
UTSW |
7 |
45,767,478 (GRCm39) |
missense |
probably benign |
|
R0381:Abcc8
|
UTSW |
7 |
45,757,858 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0391:Abcc8
|
UTSW |
7 |
45,771,597 (GRCm39) |
missense |
probably damaging |
0.98 |
R0408:Abcc8
|
UTSW |
7 |
45,756,457 (GRCm39) |
missense |
probably damaging |
0.99 |
R0496:Abcc8
|
UTSW |
7 |
45,758,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1126:Abcc8
|
UTSW |
7 |
45,759,062 (GRCm39) |
missense |
probably damaging |
0.99 |
R1323:Abcc8
|
UTSW |
7 |
45,766,786 (GRCm39) |
missense |
probably benign |
0.07 |
R1323:Abcc8
|
UTSW |
7 |
45,766,786 (GRCm39) |
missense |
probably benign |
0.07 |
R1352:Abcc8
|
UTSW |
7 |
45,784,892 (GRCm39) |
splice site |
probably benign |
|
R1368:Abcc8
|
UTSW |
7 |
45,772,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R1437:Abcc8
|
UTSW |
7 |
45,829,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R1463:Abcc8
|
UTSW |
7 |
45,803,936 (GRCm39) |
missense |
probably benign |
0.12 |
R1689:Abcc8
|
UTSW |
7 |
45,769,827 (GRCm39) |
missense |
probably benign |
0.16 |
R1717:Abcc8
|
UTSW |
7 |
45,765,239 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1804:Abcc8
|
UTSW |
7 |
45,769,903 (GRCm39) |
missense |
probably benign |
0.02 |
R1848:Abcc8
|
UTSW |
7 |
45,816,326 (GRCm39) |
missense |
probably benign |
|
R1870:Abcc8
|
UTSW |
7 |
45,773,339 (GRCm39) |
missense |
probably benign |
0.05 |
R1938:Abcc8
|
UTSW |
7 |
45,824,795 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1993:Abcc8
|
UTSW |
7 |
45,766,847 (GRCm39) |
splice site |
probably null |
|
R1994:Abcc8
|
UTSW |
7 |
45,806,543 (GRCm39) |
missense |
probably benign |
0.02 |
R2511:Abcc8
|
UTSW |
7 |
45,800,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R3840:Abcc8
|
UTSW |
7 |
45,757,524 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3879:Abcc8
|
UTSW |
7 |
45,754,051 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4444:Abcc8
|
UTSW |
7 |
45,785,618 (GRCm39) |
missense |
probably benign |
0.09 |
R4463:Abcc8
|
UTSW |
7 |
45,756,005 (GRCm39) |
splice site |
probably null |
|
R4761:Abcc8
|
UTSW |
7 |
45,762,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R4816:Abcc8
|
UTSW |
7 |
45,754,131 (GRCm39) |
missense |
probably benign |
0.01 |
R4841:Abcc8
|
UTSW |
7 |
45,800,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R4842:Abcc8
|
UTSW |
7 |
45,800,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R4870:Abcc8
|
UTSW |
7 |
45,756,683 (GRCm39) |
nonsense |
probably null |
|
R4969:Abcc8
|
UTSW |
7 |
45,754,943 (GRCm39) |
missense |
probably benign |
0.02 |
R4975:Abcc8
|
UTSW |
7 |
45,800,291 (GRCm39) |
missense |
probably damaging |
0.98 |
R5258:Abcc8
|
UTSW |
7 |
45,806,572 (GRCm39) |
missense |
probably benign |
0.17 |
R5258:Abcc8
|
UTSW |
7 |
45,757,811 (GRCm39) |
missense |
probably benign |
|
R5502:Abcc8
|
UTSW |
7 |
45,758,262 (GRCm39) |
missense |
probably benign |
0.00 |
R5518:Abcc8
|
UTSW |
7 |
45,769,873 (GRCm39) |
missense |
probably benign |
|
R5660:Abcc8
|
UTSW |
7 |
45,757,828 (GRCm39) |
missense |
probably benign |
0.15 |
R5902:Abcc8
|
UTSW |
7 |
45,764,463 (GRCm39) |
missense |
probably benign |
|
R5907:Abcc8
|
UTSW |
7 |
45,773,330 (GRCm39) |
missense |
probably benign |
0.01 |
R6023:Abcc8
|
UTSW |
7 |
45,757,843 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6026:Abcc8
|
UTSW |
7 |
45,816,424 (GRCm39) |
missense |
probably benign |
|
R6078:Abcc8
|
UTSW |
7 |
45,755,268 (GRCm39) |
missense |
probably benign |
0.01 |
R6079:Abcc8
|
UTSW |
7 |
45,755,268 (GRCm39) |
missense |
probably benign |
0.01 |
R6103:Abcc8
|
UTSW |
7 |
45,768,445 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6221:Abcc8
|
UTSW |
7 |
45,824,874 (GRCm39) |
missense |
probably benign |
0.01 |
R6511:Abcc8
|
UTSW |
7 |
45,800,285 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7046:Abcc8
|
UTSW |
7 |
45,772,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R7230:Abcc8
|
UTSW |
7 |
45,766,812 (GRCm39) |
missense |
probably benign |
|
R7287:Abcc8
|
UTSW |
7 |
45,762,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R7292:Abcc8
|
UTSW |
7 |
45,784,950 (GRCm39) |
missense |
probably benign |
|
R7299:Abcc8
|
UTSW |
7 |
45,754,922 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7411:Abcc8
|
UTSW |
7 |
45,815,341 (GRCm39) |
critical splice donor site |
probably null |
|
R7693:Abcc8
|
UTSW |
7 |
45,827,968 (GRCm39) |
missense |
probably damaging |
0.99 |
R7911:Abcc8
|
UTSW |
7 |
45,803,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R7947:Abcc8
|
UTSW |
7 |
45,754,886 (GRCm39) |
critical splice donor site |
probably null |
|
R8089:Abcc8
|
UTSW |
7 |
45,757,780 (GRCm39) |
missense |
probably benign |
0.00 |
R8120:Abcc8
|
UTSW |
7 |
45,786,108 (GRCm39) |
missense |
probably benign |
0.01 |
R8394:Abcc8
|
UTSW |
7 |
45,803,977 (GRCm39) |
missense |
probably benign |
0.03 |
R8731:Abcc8
|
UTSW |
7 |
45,803,986 (GRCm39) |
missense |
probably damaging |
0.98 |
R8848:Abcc8
|
UTSW |
7 |
45,766,769 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8938:Abcc8
|
UTSW |
7 |
45,816,418 (GRCm39) |
missense |
|
|
R9246:Abcc8
|
UTSW |
7 |
45,774,289 (GRCm39) |
missense |
probably benign |
0.00 |
R9293:Abcc8
|
UTSW |
7 |
45,756,092 (GRCm39) |
missense |
probably benign |
0.00 |
R9476:Abcc8
|
UTSW |
7 |
45,819,270 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9516:Abcc8
|
UTSW |
7 |
45,787,429 (GRCm39) |
missense |
probably benign |
0.30 |
R9541:Abcc8
|
UTSW |
7 |
45,801,079 (GRCm39) |
missense |
probably benign |
0.04 |
R9701:Abcc8
|
UTSW |
7 |
45,786,054 (GRCm39) |
missense |
probably benign |
|
R9802:Abcc8
|
UTSW |
7 |
45,786,054 (GRCm39) |
missense |
probably benign |
|
U15987:Abcc8
|
UTSW |
7 |
45,755,268 (GRCm39) |
missense |
probably benign |
0.01 |
Z1088:Abcc8
|
UTSW |
7 |
45,787,489 (GRCm39) |
missense |
probably benign |
|
Z1176:Abcc8
|
UTSW |
7 |
45,756,389 (GRCm39) |
missense |
possibly damaging |
0.76 |
Z1177:Abcc8
|
UTSW |
7 |
45,803,933 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Abcc8
|
UTSW |
7 |
45,772,309 (GRCm39) |
missense |
probably benign |
0.00 |
|