Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Bbs9 |
A |
G |
9: 22,490,780 (GRCm39) |
T303A |
probably damaging |
Het |
Bet1 |
T |
A |
6: 4,086,795 (GRCm39) |
M1L |
probably benign |
Het |
Bicc1 |
A |
C |
10: 70,794,710 (GRCm39) |
V149G |
probably damaging |
Het |
Braf |
C |
A |
6: 39,604,662 (GRCm39) |
L655F |
possibly damaging |
Het |
Cd101 |
A |
G |
3: 100,925,881 (GRCm39) |
|
probably benign |
Het |
Cobll1 |
T |
C |
2: 64,956,389 (GRCm39) |
K290E |
probably damaging |
Het |
Col6a5 |
A |
T |
9: 105,811,506 (GRCm39) |
I671K |
unknown |
Het |
D130052B06Rik |
A |
C |
11: 33,573,864 (GRCm39) |
T154P |
probably benign |
Het |
Dglucy |
A |
C |
12: 100,837,663 (GRCm39) |
H602P |
probably damaging |
Het |
Fbxo34 |
A |
G |
14: 47,767,146 (GRCm39) |
I220V |
probably benign |
Het |
Gm42878 |
A |
G |
5: 121,675,266 (GRCm39) |
V101A |
probably damaging |
Het |
Gsdmc4 |
A |
G |
15: 63,764,497 (GRCm39) |
L381P |
probably benign |
Het |
Ifi208 |
C |
A |
1: 173,510,406 (GRCm39) |
P187H |
probably damaging |
Het |
Lrrc37a |
A |
T |
11: 103,382,000 (GRCm39) |
C2473S |
unknown |
Het |
Miip |
T |
A |
4: 147,947,518 (GRCm39) |
N214I |
probably benign |
Het |
Mrc2 |
A |
G |
11: 105,227,533 (GRCm39) |
T589A |
possibly damaging |
Het |
Mtss1 |
A |
G |
15: 58,930,277 (GRCm39) |
|
probably benign |
Het |
Mypn |
T |
C |
10: 63,028,365 (GRCm39) |
R233G |
probably benign |
Het |
Naip6 |
A |
T |
13: 100,437,273 (GRCm39) |
C417S |
probably benign |
Het |
Or13f5 |
C |
T |
4: 52,826,027 (GRCm39) |
P210L |
probably damaging |
Het |
Or4c111 |
A |
C |
2: 88,844,021 (GRCm39) |
L129W |
probably damaging |
Het |
Or8k37 |
T |
A |
2: 86,469,599 (GRCm39) |
Y151F |
possibly damaging |
Het |
Pcsk1 |
T |
C |
13: 75,274,955 (GRCm39) |
Y515H |
probably damaging |
Het |
Pla2g2e |
T |
A |
4: 138,607,747 (GRCm39) |
Y42* |
probably null |
Het |
Polh |
A |
T |
17: 46,483,828 (GRCm39) |
L479Q |
possibly damaging |
Het |
Prr36 |
T |
A |
8: 4,265,278 (GRCm39) |
R157S |
possibly damaging |
Het |
Reck |
T |
A |
4: 43,891,014 (GRCm39) |
C51S |
probably damaging |
Het |
Rev3l |
A |
G |
10: 39,701,236 (GRCm39) |
D1911G |
probably damaging |
Het |
Scgb1b27 |
A |
T |
7: 33,721,173 (GRCm39) |
|
probably null |
Het |
Sema4g |
G |
A |
19: 44,981,188 (GRCm39) |
R47Q |
possibly damaging |
Het |
Serinc1 |
A |
T |
10: 57,400,061 (GRCm39) |
Y158* |
probably null |
Het |
Slc15a2 |
C |
A |
16: 36,577,555 (GRCm39) |
G435C |
possibly damaging |
Het |
Tbc1d17 |
C |
A |
7: 44,498,296 (GRCm39) |
|
probably benign |
Het |
Tenm4 |
C |
T |
7: 96,544,205 (GRCm39) |
Q2074* |
probably null |
Het |
Tns3 |
A |
G |
11: 8,469,564 (GRCm39) |
C244R |
probably damaging |
Het |
Vmn2r2 |
A |
T |
3: 64,026,172 (GRCm39) |
|
probably benign |
Het |
Vmn2r44 |
T |
A |
7: 8,380,879 (GRCm39) |
Q338L |
possibly damaging |
Het |
Wdr70 |
C |
T |
15: 8,006,463 (GRCm39) |
D363N |
possibly damaging |
Het |
|
Other mutations in Yipf7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01160:Yipf7
|
APN |
5 |
69,676,660 (GRCm39) |
missense |
probably benign |
0.13 |
R0581:Yipf7
|
UTSW |
5 |
69,678,406 (GRCm39) |
missense |
probably benign |
0.37 |
R2104:Yipf7
|
UTSW |
5 |
69,678,462 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2697:Yipf7
|
UTSW |
5 |
69,698,483 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4329:Yipf7
|
UTSW |
5 |
69,678,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R4621:Yipf7
|
UTSW |
5 |
69,676,704 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6103:Yipf7
|
UTSW |
5 |
69,698,405 (GRCm39) |
missense |
probably benign |
|
R6652:Yipf7
|
UTSW |
5 |
69,698,504 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R6823:Yipf7
|
UTSW |
5 |
69,674,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R7674:Yipf7
|
UTSW |
5 |
69,676,572 (GRCm39) |
missense |
probably damaging |
0.99 |
R7796:Yipf7
|
UTSW |
5 |
69,684,596 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8115:Yipf7
|
UTSW |
5 |
69,684,570 (GRCm39) |
missense |
probably benign |
|
R8284:Yipf7
|
UTSW |
5 |
69,674,539 (GRCm39) |
missense |
probably benign |
0.25 |
R8512:Yipf7
|
UTSW |
5 |
69,674,387 (GRCm39) |
missense |
probably benign |
0.03 |
R9646:Yipf7
|
UTSW |
5 |
69,678,424 (GRCm39) |
missense |
probably benign |
0.29 |
|