Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810009J06Rik |
A |
T |
6: 40,941,732 (GRCm39) |
I4F |
probably benign |
Het |
Aadacl4fm1 |
T |
C |
4: 144,246,511 (GRCm39) |
V19A |
probably benign |
Het |
Abca8a |
A |
T |
11: 109,943,928 (GRCm39) |
S1114T |
probably damaging |
Het |
Adgre1 |
A |
T |
17: 57,708,974 (GRCm39) |
Y55F |
possibly damaging |
Het |
Alb |
A |
C |
5: 90,611,910 (GRCm39) |
D113A |
possibly damaging |
Het |
Ankrd33b |
C |
T |
15: 31,305,155 (GRCm39) |
R203Q |
probably damaging |
Het |
Aqp6 |
T |
C |
15: 99,500,543 (GRCm39) |
V156A |
possibly damaging |
Het |
AU018091 |
T |
C |
7: 3,206,184 (GRCm39) |
S616G |
probably damaging |
Het |
Cfd |
T |
A |
10: 79,727,441 (GRCm39) |
D68E |
probably benign |
Het |
Cntn2 |
C |
T |
1: 132,446,936 (GRCm39) |
A725T |
probably damaging |
Het |
Copg2 |
A |
C |
6: 30,801,312 (GRCm39) |
D373E |
probably damaging |
Het |
Cyp2d11 |
T |
C |
15: 82,274,633 (GRCm39) |
T315A |
probably benign |
Het |
Cyp2j13 |
G |
T |
4: 95,950,304 (GRCm39) |
N232K |
probably damaging |
Het |
Dnah9 |
G |
A |
11: 65,805,980 (GRCm39) |
T3373M |
probably benign |
Het |
Eif2ak3 |
A |
G |
6: 70,864,790 (GRCm39) |
K549E |
probably damaging |
Het |
Epha3 |
C |
T |
16: 63,403,870 (GRCm39) |
V744I |
probably damaging |
Het |
Erich6 |
T |
C |
3: 58,523,868 (GRCm39) |
S669G |
probably benign |
Het |
Fam90a1a |
A |
T |
8: 22,451,464 (GRCm39) |
K108N |
probably damaging |
Het |
Fat1 |
G |
A |
8: 45,477,829 (GRCm39) |
V2292M |
probably damaging |
Het |
Fibp |
T |
C |
19: 5,513,822 (GRCm39) |
C255R |
probably null |
Het |
Fzd1 |
A |
G |
5: 4,805,791 (GRCm39) |
V597A |
possibly damaging |
Het |
Gm12790 |
G |
A |
4: 101,825,174 (GRCm39) |
A80V |
possibly damaging |
Het |
Gm2381 |
A |
T |
7: 42,469,649 (GRCm39) |
N158K |
probably benign |
Het |
Impg2 |
T |
A |
16: 56,085,441 (GRCm39) |
D940E |
probably benign |
Het |
Ints1 |
A |
T |
5: 139,748,594 (GRCm39) |
V1071E |
probably damaging |
Het |
Kat5 |
A |
T |
19: 5,659,507 (GRCm39) |
Y44* |
probably null |
Het |
Kif1c |
C |
T |
11: 70,619,223 (GRCm39) |
L953F |
probably damaging |
Het |
Klra6 |
A |
C |
6: 129,999,677 (GRCm39) |
L97* |
probably null |
Het |
Ly6c2 |
C |
T |
15: 74,983,469 (GRCm39) |
|
probably null |
Het |
Mon1a |
G |
A |
9: 107,775,917 (GRCm39) |
E12K |
probably benign |
Het |
Myo3b |
A |
T |
2: 70,075,729 (GRCm39) |
K578* |
probably null |
Het |
Myrip |
A |
T |
9: 120,293,840 (GRCm39) |
R778S |
possibly damaging |
Het |
Ncoa4-ps |
A |
G |
12: 119,225,968 (GRCm39) |
|
noncoding transcript |
Het |
Or2w4 |
C |
T |
13: 21,795,240 (GRCm39) |
A300T |
probably damaging |
Het |
Or3a4 |
G |
A |
11: 73,944,814 (GRCm39) |
T257I |
probably damaging |
Het |
Or4c35 |
A |
G |
2: 89,808,382 (GRCm39) |
R87G |
probably benign |
Het |
Or52n4b |
T |
A |
7: 108,143,781 (GRCm39) |
F14L |
probably benign |
Het |
Or5b121 |
T |
C |
19: 13,507,277 (GRCm39) |
V80A |
probably damaging |
Het |
Panx3 |
T |
C |
9: 37,572,687 (GRCm39) |
I288V |
probably benign |
Het |
Pcdh9 |
G |
A |
14: 94,125,741 (GRCm39) |
P143L |
probably damaging |
Het |
Pigc |
T |
A |
1: 161,798,293 (GRCm39) |
S92T |
probably benign |
Het |
Pou3f2 |
C |
A |
4: 22,487,255 (GRCm39) |
V293L |
possibly damaging |
Het |
Rbm15 |
A |
G |
3: 107,238,536 (GRCm39) |
S621P |
probably damaging |
Het |
Rnf220 |
T |
C |
4: 117,347,083 (GRCm39) |
S110G |
probably benign |
Het |
Rnf38 |
A |
T |
4: 44,143,593 (GRCm39) |
V115D |
probably damaging |
Het |
Rps6ka2 |
A |
G |
17: 7,544,929 (GRCm39) |
H347R |
probably damaging |
Het |
Ryr2 |
T |
C |
13: 11,602,328 (GRCm39) |
|
probably null |
Het |
Sema4f |
G |
T |
6: 82,894,975 (GRCm39) |
P407T |
probably damaging |
Het |
Setbp1 |
T |
C |
18: 78,901,682 (GRCm39) |
T662A |
probably damaging |
Het |
Slc27a1 |
C |
A |
8: 72,037,274 (GRCm39) |
|
probably null |
Het |
Slc41a2 |
T |
A |
10: 83,069,596 (GRCm39) |
I519F |
probably damaging |
Het |
Sntg2 |
C |
T |
12: 30,423,179 (GRCm39) |
S17N |
possibly damaging |
Het |
Sptb |
A |
G |
12: 76,659,348 (GRCm39) |
L1184P |
probably damaging |
Het |
Taf5l |
G |
A |
8: 124,736,509 (GRCm39) |
Q21* |
probably null |
Het |
Tbc1d32 |
A |
C |
10: 56,027,865 (GRCm39) |
S746A |
possibly damaging |
Het |
Tdrd1 |
T |
G |
19: 56,830,721 (GRCm39) |
S251R |
probably benign |
Het |
Thap7 |
C |
T |
16: 17,346,814 (GRCm39) |
R121Q |
probably benign |
Het |
Tmem50a |
A |
G |
4: 134,625,779 (GRCm39) |
V146A |
probably benign |
Het |
Tmprss15 |
T |
C |
16: 78,850,958 (GRCm39) |
I327V |
possibly damaging |
Het |
Tmt1a3 |
A |
G |
15: 100,233,150 (GRCm39) |
N114D |
probably damaging |
Het |
Ttc23 |
T |
C |
7: 67,316,924 (GRCm39) |
I65T |
probably damaging |
Het |
Vmn1r22 |
G |
T |
6: 57,877,481 (GRCm39) |
H165Q |
possibly damaging |
Het |
Vopp1 |
C |
T |
6: 57,739,497 (GRCm39) |
R17H |
probably damaging |
Het |
Vwa5a |
A |
G |
9: 38,639,128 (GRCm39) |
K337E |
probably benign |
Het |
Wrap53 |
G |
A |
11: 69,454,761 (GRCm39) |
R203* |
probably null |
Het |
Zfp944 |
T |
C |
17: 22,558,026 (GRCm39) |
Y407C |
probably damaging |
Het |
|
Other mutations in Cyp2j8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Cyp2j8
|
APN |
4 |
96,392,079 (GRCm39) |
missense |
probably benign |
0.06 |
IGL00418:Cyp2j8
|
APN |
4 |
96,332,853 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01577:Cyp2j8
|
APN |
4 |
96,367,308 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01629:Cyp2j8
|
APN |
4 |
96,387,840 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01928:Cyp2j8
|
APN |
4 |
96,358,713 (GRCm39) |
splice site |
probably benign |
|
IGL01978:Cyp2j8
|
APN |
4 |
96,392,246 (GRCm39) |
splice site |
probably null |
|
IGL02053:Cyp2j8
|
APN |
4 |
96,358,891 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02500:Cyp2j8
|
APN |
4 |
96,358,887 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02947:Cyp2j8
|
APN |
4 |
96,358,815 (GRCm39) |
missense |
probably damaging |
1.00 |
cyprus
|
UTSW |
4 |
96,387,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R0558:Cyp2j8
|
UTSW |
4 |
96,332,871 (GRCm39) |
missense |
probably benign |
0.01 |
R0718:Cyp2j8
|
UTSW |
4 |
96,389,433 (GRCm39) |
missense |
probably benign |
|
R1553:Cyp2j8
|
UTSW |
4 |
96,363,794 (GRCm39) |
missense |
probably benign |
|
R1557:Cyp2j8
|
UTSW |
4 |
96,358,713 (GRCm39) |
splice site |
probably benign |
|
R1632:Cyp2j8
|
UTSW |
4 |
96,335,561 (GRCm39) |
missense |
probably benign |
0.02 |
R2119:Cyp2j8
|
UTSW |
4 |
96,395,438 (GRCm39) |
missense |
probably benign |
|
R2220:Cyp2j8
|
UTSW |
4 |
96,332,862 (GRCm39) |
missense |
probably benign |
0.03 |
R3123:Cyp2j8
|
UTSW |
4 |
96,389,450 (GRCm39) |
splice site |
probably benign |
|
R3735:Cyp2j8
|
UTSW |
4 |
96,332,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R3736:Cyp2j8
|
UTSW |
4 |
96,332,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R4326:Cyp2j8
|
UTSW |
4 |
96,395,566 (GRCm39) |
missense |
probably benign |
0.10 |
R4327:Cyp2j8
|
UTSW |
4 |
96,395,566 (GRCm39) |
missense |
probably benign |
0.10 |
R4762:Cyp2j8
|
UTSW |
4 |
96,358,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R4901:Cyp2j8
|
UTSW |
4 |
96,367,323 (GRCm39) |
missense |
probably benign |
0.16 |
R4960:Cyp2j8
|
UTSW |
4 |
96,395,614 (GRCm39) |
missense |
probably benign |
|
R5260:Cyp2j8
|
UTSW |
4 |
96,389,301 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5562:Cyp2j8
|
UTSW |
4 |
96,358,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R5596:Cyp2j8
|
UTSW |
4 |
96,395,578 (GRCm39) |
missense |
probably benign |
0.00 |
R5741:Cyp2j8
|
UTSW |
4 |
96,332,880 (GRCm39) |
missense |
probably benign |
0.00 |
R5825:Cyp2j8
|
UTSW |
4 |
96,395,451 (GRCm39) |
missense |
probably benign |
0.01 |
R5903:Cyp2j8
|
UTSW |
4 |
96,395,514 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6122:Cyp2j8
|
UTSW |
4 |
96,332,877 (GRCm39) |
missense |
probably benign |
|
R6232:Cyp2j8
|
UTSW |
4 |
96,395,427 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6748:Cyp2j8
|
UTSW |
4 |
96,363,782 (GRCm39) |
missense |
probably benign |
0.01 |
R6931:Cyp2j8
|
UTSW |
4 |
96,333,018 (GRCm39) |
splice site |
probably null |
|
R7000:Cyp2j8
|
UTSW |
4 |
96,335,588 (GRCm39) |
missense |
probably benign |
0.06 |
R7183:Cyp2j8
|
UTSW |
4 |
96,367,418 (GRCm39) |
missense |
probably damaging |
0.97 |
R7186:Cyp2j8
|
UTSW |
4 |
96,363,787 (GRCm39) |
missense |
probably benign |
0.00 |
R7348:Cyp2j8
|
UTSW |
4 |
96,332,877 (GRCm39) |
missense |
probably benign |
0.00 |
R7575:Cyp2j8
|
UTSW |
4 |
96,358,785 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7648:Cyp2j8
|
UTSW |
4 |
96,387,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R7975:Cyp2j8
|
UTSW |
4 |
96,358,776 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7993:Cyp2j8
|
UTSW |
4 |
96,335,456 (GRCm39) |
critical splice donor site |
probably null |
|
R8878:Cyp2j8
|
UTSW |
4 |
96,358,807 (GRCm39) |
missense |
possibly damaging |
0.56 |
|