Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acr |
A |
G |
15: 89,458,165 (GRCm39) |
Y282C |
probably damaging |
Het |
Alkbh4 |
A |
G |
5: 136,169,123 (GRCm39) |
R136G |
probably damaging |
Het |
Bptf |
C |
A |
11: 106,938,166 (GRCm39) |
E2* |
probably null |
Het |
Cse1l |
T |
A |
2: 166,781,833 (GRCm39) |
F659Y |
probably damaging |
Het |
Ctrc |
A |
T |
4: 141,567,671 (GRCm39) |
L144Q |
probably damaging |
Het |
Elmo1 |
A |
G |
13: 20,470,902 (GRCm39) |
I265V |
probably benign |
Het |
Erich3 |
T |
C |
3: 154,419,553 (GRCm39) |
S19P |
probably benign |
Het |
Hmcn1 |
A |
T |
1: 150,540,629 (GRCm39) |
C2893* |
probably null |
Het |
Hnrnpll |
G |
A |
17: 80,346,152 (GRCm39) |
Q370* |
probably null |
Het |
Itpkb |
T |
C |
1: 180,160,059 (GRCm39) |
S62P |
probably damaging |
Het |
Lig3 |
T |
A |
11: 82,682,902 (GRCm39) |
C501S |
probably benign |
Het |
Nrxn1 |
C |
T |
17: 91,395,964 (GRCm39) |
R64H |
possibly damaging |
Het |
Ogfod2 |
T |
G |
5: 124,252,946 (GRCm39) |
C319G |
probably damaging |
Het |
Or51h1 |
A |
T |
7: 102,308,241 (GRCm39) |
D71V |
probably damaging |
Het |
Or5ac19 |
T |
C |
16: 59,089,472 (GRCm39) |
N186S |
probably benign |
Het |
Or5b118 |
A |
G |
19: 13,448,786 (GRCm39) |
I109V |
probably benign |
Het |
Or9k7 |
A |
G |
10: 130,046,729 (GRCm39) |
V90A |
probably benign |
Het |
Pabpc6 |
C |
A |
17: 9,888,302 (GRCm39) |
R83L |
probably damaging |
Het |
Pcdhgb2 |
A |
T |
18: 37,823,687 (GRCm39) |
Q226L |
probably benign |
Het |
Pole |
A |
T |
5: 110,460,600 (GRCm39) |
I1127F |
probably damaging |
Het |
Psg22 |
A |
T |
7: 18,453,671 (GRCm39) |
Q161L |
possibly damaging |
Het |
Slc17a7 |
A |
T |
7: 44,818,212 (GRCm39) |
T46S |
probably benign |
Het |
Smad4 |
A |
G |
18: 73,774,881 (GRCm39) |
S473P |
probably damaging |
Het |
Snap47 |
T |
A |
11: 59,329,180 (GRCm39) |
T41S |
probably benign |
Het |
Snx21 |
T |
C |
2: 164,628,657 (GRCm39) |
L100P |
probably benign |
Het |
Stc1 |
T |
A |
14: 69,275,844 (GRCm39) |
N212K |
probably benign |
Het |
Stk32a |
A |
T |
18: 43,448,209 (GRCm39) |
N396I |
possibly damaging |
Het |
Stox2 |
G |
A |
8: 47,639,512 (GRCm39) |
P894L |
probably benign |
Het |
Trav16d-dv11 |
A |
G |
14: 53,284,744 (GRCm39) |
M1V |
probably null |
Het |
Trim33 |
T |
C |
3: 103,218,831 (GRCm39) |
|
probably null |
Het |
Tyrp1 |
T |
C |
4: 80,758,907 (GRCm39) |
V260A |
probably benign |
Het |
Ush2a |
T |
C |
1: 188,643,261 (GRCm39) |
Y4208H |
probably damaging |
Het |
Vmn1r25 |
T |
A |
6: 57,956,065 (GRCm39) |
K75* |
probably null |
Het |
Vmn2r117 |
T |
A |
17: 23,698,381 (GRCm39) |
N64I |
possibly damaging |
Het |
Wdfy4 |
C |
T |
14: 32,695,492 (GRCm39) |
|
probably null |
Het |
Wnt8a |
A |
T |
18: 34,678,569 (GRCm39) |
I128F |
probably damaging |
Het |
Zc3h7b |
C |
A |
15: 81,663,461 (GRCm39) |
Y484* |
probably null |
Het |
Zfp619 |
A |
G |
7: 39,184,645 (GRCm39) |
K225R |
probably benign |
Het |
|
Other mutations in Mab21l4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01954:Mab21l4
|
APN |
1 |
93,079,794 (GRCm39) |
missense |
probably damaging |
0.98 |
R0018:Mab21l4
|
UTSW |
1 |
93,082,327 (GRCm39) |
missense |
probably benign |
0.00 |
R0115:Mab21l4
|
UTSW |
1 |
93,087,447 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0467:Mab21l4
|
UTSW |
1 |
93,080,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R1452:Mab21l4
|
UTSW |
1 |
93,080,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R1938:Mab21l4
|
UTSW |
1 |
93,079,730 (GRCm39) |
makesense |
probably null |
|
R3156:Mab21l4
|
UTSW |
1 |
93,087,764 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4740:Mab21l4
|
UTSW |
1 |
93,083,890 (GRCm39) |
missense |
probably benign |
0.01 |
R5260:Mab21l4
|
UTSW |
1 |
93,087,700 (GRCm39) |
missense |
probably damaging |
0.99 |
R5283:Mab21l4
|
UTSW |
1 |
93,087,575 (GRCm39) |
missense |
probably benign |
0.02 |
R5645:Mab21l4
|
UTSW |
1 |
93,080,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R6380:Mab21l4
|
UTSW |
1 |
93,088,613 (GRCm39) |
splice site |
probably null |
|
R6738:Mab21l4
|
UTSW |
1 |
93,087,707 (GRCm39) |
missense |
probably benign |
0.30 |
R7184:Mab21l4
|
UTSW |
1 |
93,082,237 (GRCm39) |
missense |
probably benign |
0.00 |
R7227:Mab21l4
|
UTSW |
1 |
93,079,736 (GRCm39) |
missense |
probably benign |
0.00 |
R7562:Mab21l4
|
UTSW |
1 |
93,087,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R8735:Mab21l4
|
UTSW |
1 |
93,082,208 (GRCm39) |
critical splice donor site |
probably null |
|
R8970:Mab21l4
|
UTSW |
1 |
93,087,533 (GRCm39) |
missense |
probably benign |
0.00 |
R9418:Mab21l4
|
UTSW |
1 |
93,087,710 (GRCm39) |
missense |
probably benign |
0.45 |
R9537:Mab21l4
|
UTSW |
1 |
93,080,884 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9599:Mab21l4
|
UTSW |
1 |
93,087,568 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9736:Mab21l4
|
UTSW |
1 |
93,087,661 (GRCm39) |
missense |
probably damaging |
0.99 |
|