Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Apc2 |
G |
A |
10: 80,143,393 (GRCm39) |
G498R |
possibly damaging |
Het |
Bltp1 |
T |
A |
3: 36,939,547 (GRCm39) |
F134I |
possibly damaging |
Het |
Bub1 |
A |
G |
2: 127,656,676 (GRCm39) |
|
probably benign |
Het |
Cttnbp2 |
C |
T |
6: 18,434,905 (GRCm39) |
V318M |
probably benign |
Het |
D430041D05Rik |
T |
C |
2: 104,044,522 (GRCm39) |
I825M |
possibly damaging |
Het |
Enpp6 |
A |
G |
8: 47,519,027 (GRCm39) |
Q265R |
probably benign |
Het |
Eri1 |
A |
G |
8: 35,958,448 (GRCm39) |
V61A |
possibly damaging |
Het |
Evi2 |
T |
A |
11: 79,406,472 (GRCm39) |
I368F |
probably benign |
Het |
Fat3 |
G |
A |
9: 15,909,567 (GRCm39) |
S2145F |
probably damaging |
Het |
Fkbp9 |
A |
G |
6: 56,845,890 (GRCm39) |
T409A |
probably benign |
Het |
Gtpbp4 |
A |
G |
13: 9,040,834 (GRCm39) |
V97A |
probably damaging |
Het |
Hapln1 |
C |
T |
13: 89,753,418 (GRCm39) |
Q195* |
probably null |
Het |
Helt |
G |
T |
8: 46,745,315 (GRCm39) |
N189K |
probably benign |
Het |
Hint2 |
A |
G |
4: 43,654,771 (GRCm39) |
V91A |
probably damaging |
Het |
Ighv1-7 |
A |
G |
12: 114,502,266 (GRCm39) |
I67T |
probably damaging |
Het |
Kif26a |
A |
G |
12: 112,146,323 (GRCm39) |
E1803G |
probably benign |
Het |
Lrrd1 |
G |
A |
5: 3,901,248 (GRCm39) |
V518I |
probably benign |
Het |
Marchf11 |
C |
T |
15: 26,387,952 (GRCm39) |
A269V |
probably damaging |
Het |
Mep1b |
A |
G |
18: 21,217,226 (GRCm39) |
N115S |
possibly damaging |
Het |
Naif1 |
A |
G |
2: 32,342,637 (GRCm39) |
R63G |
probably damaging |
Het |
Nsmaf |
A |
G |
4: 6,435,064 (GRCm39) |
I126T |
probably benign |
Het |
Obscn |
T |
C |
11: 59,022,472 (GRCm39) |
R758G |
possibly damaging |
Het |
Or52h7 |
G |
A |
7: 104,214,145 (GRCm39) |
R239H |
probably benign |
Het |
Or8g53 |
T |
A |
9: 39,683,920 (GRCm39) |
M59L |
probably benign |
Het |
Pcdhb3 |
A |
G |
18: 37,436,329 (GRCm39) |
E765G |
probably damaging |
Het |
Ppp4r4 |
C |
T |
12: 103,562,680 (GRCm39) |
R550* |
probably null |
Het |
Sgcz |
T |
C |
8: 37,990,565 (GRCm39) |
I263V |
probably benign |
Het |
Slc15a1 |
C |
T |
14: 121,722,269 (GRCm39) |
V211I |
probably benign |
Het |
Slc25a21 |
G |
T |
12: 56,764,920 (GRCm39) |
|
probably benign |
Het |
Snrnp200 |
C |
A |
2: 127,075,019 (GRCm39) |
|
probably benign |
Het |
Spata31e5 |
T |
C |
1: 28,816,722 (GRCm39) |
T437A |
probably damaging |
Het |
Sptbn1 |
G |
T |
11: 30,092,329 (GRCm39) |
Q479K |
possibly damaging |
Het |
Stag1 |
T |
A |
9: 100,826,838 (GRCm39) |
V935D |
probably benign |
Het |
Veph1 |
C |
T |
3: 66,162,313 (GRCm39) |
C115Y |
probably damaging |
Het |
Zc3h12a |
T |
C |
4: 125,020,732 (GRCm39) |
D37G |
probably benign |
Het |
Zfand4 |
A |
T |
6: 116,270,776 (GRCm39) |
|
probably benign |
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 |
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 |
R8172:Scgb2b3
|
UTSW |
7 |
31,058,476 (GRCm39) |
missense |
possibly damaging |
0.78 |
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 |
|
|