Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1a |
T |
G |
5: 8,790,428 (GRCm39) |
I1097R |
possibly damaging |
Het |
Abcd4 |
A |
G |
12: 84,650,762 (GRCm39) |
S533P |
probably damaging |
Het |
Adat1 |
C |
T |
8: 112,705,946 (GRCm39) |
V387I |
probably benign |
Het |
Aff3 |
T |
A |
1: 38,249,266 (GRCm39) |
T614S |
probably benign |
Het |
Aldh1a1 |
T |
A |
19: 20,597,417 (GRCm39) |
C133S |
probably benign |
Het |
Ankrd12 |
A |
G |
17: 66,290,415 (GRCm39) |
S1673P |
probably damaging |
Het |
Aox1 |
T |
A |
1: 58,370,055 (GRCm39) |
|
probably null |
Het |
Arsi |
A |
G |
18: 61,050,160 (GRCm39) |
T348A |
probably damaging |
Het |
Baz2b |
T |
C |
2: 59,799,300 (GRCm39) |
R275G |
probably benign |
Het |
Cdh2 |
T |
A |
18: 16,803,112 (GRCm39) |
|
probably benign |
Het |
Cela1 |
C |
T |
15: 100,573,261 (GRCm39) |
A243T |
probably benign |
Het |
Cep192 |
G |
T |
18: 67,980,465 (GRCm39) |
V1409F |
probably damaging |
Het |
Chia1 |
T |
C |
3: 106,035,879 (GRCm39) |
Y240H |
possibly damaging |
Het |
Dact1 |
A |
T |
12: 71,365,619 (GRCm39) |
K763M |
probably damaging |
Het |
Dip2b |
C |
A |
15: 100,079,255 (GRCm39) |
N822K |
probably damaging |
Het |
Dnah12 |
C |
T |
14: 26,491,985 (GRCm39) |
T1140I |
probably damaging |
Het |
Drc7 |
T |
C |
8: 95,785,782 (GRCm39) |
S213P |
probably damaging |
Het |
Ell2 |
A |
G |
13: 75,912,148 (GRCm39) |
D478G |
probably benign |
Het |
Evpl |
G |
A |
11: 116,120,660 (GRCm39) |
T483M |
probably benign |
Het |
Farp1 |
A |
T |
14: 121,480,841 (GRCm39) |
E414V |
probably benign |
Het |
Fbxl17 |
A |
G |
17: 63,806,525 (GRCm39) |
V163A |
probably benign |
Het |
Foxn3 |
C |
T |
12: 99,163,035 (GRCm39) |
E289K |
probably damaging |
Het |
Fscb |
T |
A |
12: 64,521,122 (GRCm39) |
I115F |
probably benign |
Het |
Gm14496 |
A |
T |
2: 181,642,047 (GRCm39) |
T573S |
probably benign |
Het |
Golga1 |
G |
T |
2: 38,909,573 (GRCm39) |
D677E |
probably damaging |
Het |
Herc6 |
A |
T |
6: 57,635,101 (GRCm39) |
K772N |
probably damaging |
Het |
Ikbkb |
T |
C |
8: 23,155,575 (GRCm39) |
D639G |
probably damaging |
Het |
Lrrc61 |
G |
A |
6: 48,545,653 (GRCm39) |
V159I |
possibly damaging |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Mib1 |
A |
G |
18: 10,775,701 (GRCm39) |
D551G |
possibly damaging |
Het |
Muc5ac |
G |
T |
7: 141,363,799 (GRCm39) |
R2370L |
unknown |
Het |
Mybpc3 |
A |
G |
2: 90,949,616 (GRCm39) |
D53G |
probably benign |
Het |
Myo9b |
C |
T |
8: 71,812,543 (GRCm39) |
P2105S |
probably benign |
Het |
Naip5 |
G |
T |
13: 100,351,194 (GRCm39) |
H1271Q |
probably benign |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Nmt2 |
T |
C |
2: 3,317,212 (GRCm39) |
V340A |
possibly damaging |
Het |
Nos1 |
A |
G |
5: 118,043,459 (GRCm39) |
E578G |
probably damaging |
Het |
Nox3 |
G |
A |
17: 3,700,328 (GRCm39) |
R462W |
possibly damaging |
Het |
Or10h28 |
C |
A |
17: 33,487,995 (GRCm39) |
A99D |
probably damaging |
Het |
Or52a20 |
A |
G |
7: 103,365,788 (GRCm39) |
|
probably benign |
Het |
Pcdhgc4 |
A |
G |
18: 37,950,189 (GRCm39) |
Q535R |
probably benign |
Het |
Pcsk5 |
T |
C |
19: 17,432,196 (GRCm39) |
D1473G |
probably benign |
Het |
Pdilt |
A |
T |
7: 119,099,633 (GRCm39) |
F212I |
probably damaging |
Het |
Ptk2b |
A |
T |
14: 66,450,789 (GRCm39) |
V59D |
probably damaging |
Het |
Ptprf |
T |
C |
4: 118,092,257 (GRCm39) |
D571G |
probably benign |
Het |
Ptprq |
A |
T |
10: 107,547,771 (GRCm39) |
V209E |
possibly damaging |
Het |
Rsf1 |
GGCGGCGGC |
GGCGGCGGCCGCGGCGGC |
7: 97,229,125 (GRCm39) |
|
probably benign |
Het |
Sec16a |
C |
T |
2: 26,328,647 (GRCm39) |
V142I |
|
Het |
Slamf6 |
A |
G |
1: 171,761,897 (GRCm39) |
Y106C |
|
Het |
Strc |
A |
G |
2: 121,207,928 (GRCm39) |
V481A |
probably damaging |
Het |
Sulf1 |
A |
T |
1: 12,875,478 (GRCm39) |
I163F |
possibly damaging |
Het |
Tjp1 |
A |
G |
7: 64,949,472 (GRCm39) |
S1637P |
probably damaging |
Het |
Tlr9 |
A |
G |
9: 106,101,510 (GRCm39) |
E267G |
probably damaging |
Het |
Tmem117 |
T |
A |
15: 94,992,268 (GRCm39) |
F309L |
probably benign |
Het |
Tmtc4 |
T |
C |
14: 123,187,998 (GRCm39) |
N196S |
probably benign |
Het |
Trim16 |
T |
A |
11: 62,727,557 (GRCm39) |
I293K |
probably damaging |
Het |
Trim7 |
T |
C |
11: 48,738,887 (GRCm39) |
V95A |
probably damaging |
Het |
Ttll6 |
A |
T |
11: 96,049,572 (GRCm39) |
K763N |
probably benign |
Het |
Tut1 |
T |
C |
19: 8,941,981 (GRCm39) |
S483P |
probably benign |
Het |
Zfp101 |
A |
T |
17: 33,605,730 (GRCm39) |
L26* |
probably null |
Het |
Zfp106 |
C |
T |
2: 120,365,807 (GRCm39) |
R155K |
|
Het |
Zfp518a |
T |
A |
19: 40,900,156 (GRCm39) |
D28E |
probably damaging |
Het |
Zfp90 |
T |
A |
8: 107,151,714 (GRCm39) |
S476T |
probably benign |
Het |
|
Other mutations in Schip1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01431:Schip1
|
APN |
3 |
68,525,110 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03354:Schip1
|
APN |
3 |
68,402,298 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0190:Schip1
|
UTSW |
3 |
68,533,177 (GRCm39) |
missense |
probably benign |
0.09 |
R0413:Schip1
|
UTSW |
3 |
68,401,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R1256:Schip1
|
UTSW |
3 |
68,402,375 (GRCm39) |
missense |
probably benign |
0.12 |
R1777:Schip1
|
UTSW |
3 |
68,525,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R2067:Schip1
|
UTSW |
3 |
68,525,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R3027:Schip1
|
UTSW |
3 |
68,401,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R4258:Schip1
|
UTSW |
3 |
68,525,963 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4646:Schip1
|
UTSW |
3 |
67,972,297 (GRCm39) |
missense |
probably benign |
|
R4917:Schip1
|
UTSW |
3 |
68,315,818 (GRCm39) |
intron |
probably benign |
|
R4918:Schip1
|
UTSW |
3 |
68,315,818 (GRCm39) |
intron |
probably benign |
|
R5021:Schip1
|
UTSW |
3 |
68,402,585 (GRCm39) |
missense |
probably benign |
0.03 |
R5194:Schip1
|
UTSW |
3 |
68,402,205 (GRCm39) |
missense |
probably benign |
0.15 |
R5225:Schip1
|
UTSW |
3 |
68,402,270 (GRCm39) |
missense |
probably benign |
|
R5719:Schip1
|
UTSW |
3 |
68,315,560 (GRCm39) |
intron |
probably benign |
|
R6460:Schip1
|
UTSW |
3 |
68,402,227 (GRCm39) |
missense |
probably benign |
0.37 |
R7189:Schip1
|
UTSW |
3 |
68,525,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R7189:Schip1
|
UTSW |
3 |
68,525,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R7727:Schip1
|
UTSW |
3 |
67,972,317 (GRCm39) |
missense |
probably benign |
0.09 |
R7757:Schip1
|
UTSW |
3 |
68,525,028 (GRCm39) |
missense |
probably damaging |
0.99 |
R7793:Schip1
|
UTSW |
3 |
68,401,911 (GRCm39) |
missense |
probably benign |
0.00 |
R8496:Schip1
|
UTSW |
3 |
68,401,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R8500:Schip1
|
UTSW |
3 |
68,401,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R8904:Schip1
|
UTSW |
3 |
68,402,436 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9098:Schip1
|
UTSW |
3 |
67,972,318 (GRCm39) |
missense |
|
|
R9582:Schip1
|
UTSW |
3 |
68,525,060 (GRCm39) |
frame shift |
probably null |
|
|