Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy5 |
T |
A |
16: 34,977,427 (GRCm39) |
L320Q |
probably damaging |
Het |
Adgre4 |
A |
T |
17: 56,104,769 (GRCm39) |
L278F |
probably benign |
Het |
Agfg2 |
C |
A |
5: 137,665,431 (GRCm39) |
R108L |
probably damaging |
Het |
Arap2 |
A |
T |
5: 62,779,324 (GRCm39) |
|
probably null |
Het |
Ascl2 |
G |
T |
7: 142,522,336 (GRCm39) |
N37K |
possibly damaging |
Het |
Baiap3 |
C |
A |
17: 25,463,096 (GRCm39) |
D1043Y |
probably damaging |
Het |
Cby2 |
T |
A |
14: 75,829,241 (GRCm39) |
|
probably null |
Het |
Ccdc18 |
T |
C |
5: 108,311,640 (GRCm39) |
|
probably null |
Het |
Cemip |
T |
A |
7: 83,646,433 (GRCm39) |
D205V |
probably damaging |
Het |
Cenpn |
G |
A |
8: 117,658,333 (GRCm39) |
G93D |
probably benign |
Het |
Clpsl2 |
T |
A |
17: 28,768,556 (GRCm39) |
S23R |
possibly damaging |
Het |
Cnot3 |
T |
A |
7: 3,661,724 (GRCm39) |
I672N |
possibly damaging |
Het |
Crygs |
A |
G |
16: 22,625,292 (GRCm39) |
Y50H |
probably damaging |
Het |
Cyp4x1 |
T |
C |
4: 114,968,874 (GRCm39) |
T403A |
possibly damaging |
Het |
Dnajc28 |
G |
A |
16: 91,413,795 (GRCm39) |
R150* |
probably null |
Het |
Fam184b |
C |
T |
5: 45,741,709 (GRCm39) |
G174D |
possibly damaging |
Het |
Fat2 |
T |
A |
11: 55,178,638 (GRCm39) |
D1474V |
probably damaging |
Het |
Flg2 |
T |
A |
3: 93,108,468 (GRCm39) |
D165E |
possibly damaging |
Het |
Fpr-rs7 |
A |
T |
17: 20,334,443 (GRCm39) |
F16I |
probably benign |
Het |
Gpr176 |
G |
A |
2: 118,114,615 (GRCm39) |
T65I |
probably damaging |
Het |
H2-Q10 |
C |
T |
17: 35,781,996 (GRCm39) |
T206I |
probably null |
Het |
Hadha |
C |
G |
5: 30,350,285 (GRCm39) |
A88P |
probably damaging |
Het |
Hlcs |
A |
T |
16: 94,068,485 (GRCm39) |
L245Q |
probably damaging |
Het |
Hnrnph1 |
T |
C |
11: 50,270,732 (GRCm39) |
V113A |
probably damaging |
Het |
Hsd3b7 |
G |
A |
7: 127,401,546 (GRCm39) |
V224M |
probably damaging |
Het |
Igha |
T |
C |
12: 113,223,592 (GRCm39) |
D88G |
|
Het |
Iqca1l |
T |
C |
5: 24,748,608 (GRCm39) |
M803V |
probably benign |
Het |
Kdm7a |
T |
C |
6: 39,125,965 (GRCm39) |
K610R |
probably benign |
Het |
Krt87 |
C |
T |
15: 101,383,284 (GRCm39) |
C474Y |
probably benign |
Het |
Lrrc74a |
T |
A |
12: 86,788,530 (GRCm39) |
L170H |
probably damaging |
Het |
Lyg2 |
T |
C |
1: 37,946,748 (GRCm39) |
T178A |
probably benign |
Het |
Map2k2 |
T |
A |
10: 80,959,442 (GRCm39) |
|
probably null |
Het |
Mast4 |
C |
T |
13: 103,089,633 (GRCm39) |
|
probably null |
Het |
Mtmr14 |
T |
A |
6: 113,216,529 (GRCm39) |
D8E |
probably benign |
Het |
Neu2 |
C |
T |
1: 87,524,633 (GRCm39) |
P206L |
probably damaging |
Het |
Oga |
C |
T |
19: 45,765,339 (GRCm39) |
R156H |
probably damaging |
Het |
Or10al6 |
A |
G |
17: 38,083,326 (GRCm39) |
T261A |
probably benign |
Het |
Or4c105 |
A |
T |
2: 88,647,986 (GRCm39) |
Q157L |
probably damaging |
Het |
Poc1b |
C |
A |
10: 98,980,338 (GRCm39) |
|
probably null |
Het |
Proser1 |
T |
A |
3: 53,386,272 (GRCm39) |
V718E |
possibly damaging |
Het |
Ptgr2 |
T |
A |
12: 84,360,783 (GRCm39) |
L351Q |
possibly damaging |
Het |
Ptprf |
A |
G |
4: 118,068,275 (GRCm39) |
Y1754H |
probably benign |
Het |
Scn2a |
A |
T |
2: 65,520,672 (GRCm39) |
H556L |
probably benign |
Het |
Scn7a |
A |
T |
2: 66,506,191 (GRCm39) |
M1566K |
possibly damaging |
Het |
Slco5a1 |
A |
T |
1: 13,060,490 (GRCm39) |
L77* |
probably null |
Het |
Stk31 |
T |
C |
6: 49,394,261 (GRCm39) |
F208L |
possibly damaging |
Het |
Tbcd |
C |
T |
11: 121,384,711 (GRCm39) |
T315M |
probably benign |
Het |
Tbx4 |
A |
G |
11: 85,801,933 (GRCm39) |
I189V |
probably benign |
Het |
Tia1 |
T |
A |
6: 86,404,682 (GRCm39) |
Y306N |
probably benign |
Het |
Ttc21b |
T |
A |
2: 66,082,500 (GRCm39) |
Y33F |
probably benign |
Het |
Usp47 |
T |
A |
7: 111,687,133 (GRCm39) |
L677* |
probably null |
Het |
|
Other mutations in Scgb2b3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1664:Scgb2b3
|
UTSW |
7 |
31,058,464 (GRCm39) |
makesense |
probably null |
|
R1772:Scgb2b3
|
UTSW |
7 |
31,059,621 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3862:Scgb2b3
|
UTSW |
7 |
31,061,430 (GRCm39) |
critical splice donor site |
probably null |
|
R5819:Scgb2b3
|
UTSW |
7 |
31,059,639 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6433:Scgb2b3
|
UTSW |
7 |
31,058,492 (GRCm39) |
missense |
probably benign |
0.15 |
R7135:Scgb2b3
|
UTSW |
7 |
31,059,639 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7145:Scgb2b3
|
UTSW |
7 |
31,059,573 (GRCm39) |
missense |
probably benign |
0.00 |
R7553:Scgb2b3
|
UTSW |
7 |
31,059,673 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7908:Scgb2b3
|
UTSW |
7 |
31,061,439 (GRCm39) |
missense |
probably damaging |
0.98 |
R8350:Scgb2b3
|
UTSW |
7 |
31,061,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R9276:Scgb2b3
|
UTSW |
7 |
31,059,528 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9371:Scgb2b3
|
UTSW |
7 |
31,059,642 (GRCm39) |
missense |
probably benign |
0.04 |
X0027:Scgb2b3
|
UTSW |
7 |
31,059,681 (GRCm39) |
missense |
probably benign |
0.00 |
Z1186:Scgb2b3
|
UTSW |
7 |
31,059,592 (GRCm39) |
missense |
probably benign |
|
Z1186:Scgb2b3
|
UTSW |
7 |
31,058,546 (GRCm39) |
missense |
probably benign |
|
|