Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310061I04Rik |
C |
G |
17: 36,203,963 (GRCm39) |
S185T |
probably benign |
Het |
Agfg1 |
T |
G |
1: 82,872,216 (GRCm39) |
F516L |
possibly damaging |
Het |
Akap5 |
T |
A |
12: 76,374,592 (GRCm39) |
M8K |
possibly damaging |
Het |
Aldh1l2 |
C |
T |
10: 83,342,545 (GRCm39) |
V535I |
probably benign |
Het |
Atg3 |
T |
C |
16: 45,006,564 (GRCm39) |
V277A |
probably damaging |
Het |
Bloc1s6 |
C |
T |
2: 122,588,534 (GRCm39) |
P168L |
probably damaging |
Het |
Ccr7 |
A |
G |
11: 99,036,086 (GRCm39) |
Y279H |
probably damaging |
Het |
Cfap210 |
G |
T |
2: 69,612,103 (GRCm39) |
S175* |
probably null |
Het |
Clint1 |
A |
G |
11: 45,781,562 (GRCm39) |
T211A |
probably damaging |
Het |
Dchs2 |
T |
G |
3: 83,176,662 (GRCm39) |
D873E |
probably benign |
Het |
Dhx30 |
A |
G |
9: 109,926,164 (GRCm39) |
L149P |
probably damaging |
Het |
Dnah1 |
T |
C |
14: 31,033,581 (GRCm39) |
|
probably benign |
Het |
Dtx1 |
A |
G |
5: 120,848,356 (GRCm39) |
V8A |
probably benign |
Het |
Enpp3 |
T |
A |
10: 24,702,078 (GRCm39) |
K91N |
possibly damaging |
Het |
Fcho1 |
C |
T |
8: 72,164,712 (GRCm39) |
G523E |
possibly damaging |
Het |
Ffar2 |
T |
C |
7: 30,518,616 (GRCm39) |
E308G |
probably damaging |
Het |
Foxb2 |
T |
C |
19: 16,850,758 (GRCm39) |
K83E |
unknown |
Het |
Git2 |
A |
G |
5: 114,887,621 (GRCm39) |
|
probably null |
Het |
Gm10024 |
T |
C |
10: 77,547,339 (GRCm39) |
S17P |
unknown |
Het |
Greb1l |
A |
T |
18: 10,542,422 (GRCm39) |
Y1339F |
probably benign |
Het |
Grhl2 |
T |
A |
15: 37,270,912 (GRCm39) |
D33E |
probably damaging |
Het |
Herc4 |
C |
A |
10: 63,126,300 (GRCm39) |
L551I |
probably benign |
Het |
Igfn1 |
T |
A |
1: 135,902,528 (GRCm39) |
T390S |
probably benign |
Het |
Ighv3-1 |
T |
A |
12: 113,928,089 (GRCm39) |
H90L |
probably benign |
Het |
Jag2 |
G |
T |
12: 112,877,279 (GRCm39) |
Y697* |
probably null |
Het |
Kif1c |
T |
C |
11: 70,595,798 (GRCm39) |
V168A |
probably damaging |
Het |
Lipn |
T |
C |
19: 34,046,041 (GRCm39) |
W5R |
probably damaging |
Het |
Mavs |
G |
A |
2: 131,087,245 (GRCm39) |
A248T |
probably benign |
Het |
Megf10 |
G |
A |
18: 57,392,773 (GRCm39) |
G390D |
probably damaging |
Het |
Mib1 |
A |
G |
18: 10,793,023 (GRCm39) |
H653R |
probably benign |
Het |
Mrps9 |
T |
G |
1: 42,942,537 (GRCm39) |
S332A |
probably benign |
Het |
Muc5b |
T |
C |
7: 141,423,070 (GRCm39) |
C4498R |
possibly damaging |
Het |
Myo15b |
T |
A |
11: 115,778,743 (GRCm39) |
I1157N |
possibly damaging |
Het |
Myo9b |
C |
T |
8: 71,800,451 (GRCm39) |
T1002M |
probably benign |
Het |
Nav3 |
T |
A |
10: 109,520,100 (GRCm39) |
M2328L |
probably benign |
Het |
Or5h18 |
T |
C |
16: 58,847,653 (GRCm39) |
I206V |
probably benign |
Het |
Or8b52 |
T |
A |
9: 38,577,106 (GRCm39) |
E11D |
probably benign |
Het |
Pawr |
T |
C |
10: 108,169,140 (GRCm39) |
S155P |
probably damaging |
Het |
Pcdhb15 |
G |
T |
18: 37,608,090 (GRCm39) |
V441F |
probably damaging |
Het |
Plekhg3 |
A |
G |
12: 76,624,905 (GRCm39) |
D1250G |
probably benign |
Het |
Ptprs |
T |
A |
17: 56,742,853 (GRCm39) |
M430L |
possibly damaging |
Het |
Raly |
T |
A |
2: 154,703,785 (GRCm39) |
S119T |
probably damaging |
Het |
Serpinb6a |
A |
T |
13: 34,109,412 (GRCm39) |
S128T |
probably benign |
Het |
Sirt3 |
C |
T |
7: 140,449,362 (GRCm39) |
|
probably benign |
Het |
Speg |
G |
T |
1: 75,364,444 (GRCm39) |
S275I |
probably damaging |
Het |
Stk32c |
C |
T |
7: 138,768,141 (GRCm39) |
D47N |
unknown |
Het |
Stra6 |
T |
G |
9: 58,059,822 (GRCm39) |
S594R |
probably benign |
Het |
Sun2 |
T |
C |
15: 79,614,517 (GRCm39) |
H295R |
probably benign |
Het |
Syne1 |
T |
C |
10: 5,053,667 (GRCm39) |
Q7470R |
probably damaging |
Het |
Syt14 |
A |
T |
1: 192,666,126 (GRCm39) |
H259Q |
unknown |
Het |
Toporsl |
A |
T |
4: 52,609,943 (GRCm39) |
|
probably benign |
Het |
Trim50 |
A |
G |
5: 135,382,537 (GRCm39) |
S130G |
possibly damaging |
Het |
Tyw1 |
G |
A |
5: 130,298,065 (GRCm39) |
R202Q |
probably damaging |
Het |
Wdr18 |
T |
C |
10: 79,801,154 (GRCm39) |
V189A |
probably benign |
Het |
Zfat |
C |
A |
15: 68,058,918 (GRCm39) |
A206S |
probably damaging |
Het |
|
Other mutations in Slc22a7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01638:Slc22a7
|
APN |
17 |
46,748,920 (GRCm39) |
splice site |
probably null |
|
R0755:Slc22a7
|
UTSW |
17 |
46,749,113 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0898:Slc22a7
|
UTSW |
17 |
46,744,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R1594:Slc22a7
|
UTSW |
17 |
46,748,957 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1794:Slc22a7
|
UTSW |
17 |
46,744,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R1900:Slc22a7
|
UTSW |
17 |
46,749,157 (GRCm39) |
missense |
probably benign |
0.00 |
R1973:Slc22a7
|
UTSW |
17 |
46,748,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R2117:Slc22a7
|
UTSW |
17 |
46,744,898 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4467:Slc22a7
|
UTSW |
17 |
46,743,436 (GRCm39) |
missense |
probably benign |
|
R4739:Slc22a7
|
UTSW |
17 |
46,745,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R4921:Slc22a7
|
UTSW |
17 |
46,747,859 (GRCm39) |
missense |
probably benign |
0.00 |
R6982:Slc22a7
|
UTSW |
17 |
46,745,563 (GRCm39) |
missense |
probably benign |
0.02 |
R7122:Slc22a7
|
UTSW |
17 |
46,749,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R7412:Slc22a7
|
UTSW |
17 |
46,745,553 (GRCm39) |
missense |
probably benign |
0.00 |
R7634:Slc22a7
|
UTSW |
17 |
46,749,156 (GRCm39) |
missense |
probably benign |
0.02 |
R8112:Slc22a7
|
UTSW |
17 |
46,747,756 (GRCm39) |
missense |
probably benign |
0.00 |
R8703:Slc22a7
|
UTSW |
17 |
46,744,951 (GRCm39) |
missense |
probably damaging |
0.98 |
R9541:Slc22a7
|
UTSW |
17 |
46,749,084 (GRCm39) |
missense |
probably damaging |
1.00 |
|