Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acox3 |
T |
A |
5: 35,762,543 (GRCm39) |
|
probably null |
Het |
Ahnak2 |
A |
T |
12: 112,742,100 (GRCm39) |
Y657* |
probably null |
Het |
Anxa3 |
T |
A |
5: 96,968,331 (GRCm39) |
I128N |
probably damaging |
Het |
Bsnd |
T |
C |
4: 106,345,198 (GRCm39) |
T83A |
probably benign |
Het |
Capn10 |
A |
G |
1: 92,871,635 (GRCm39) |
Y411C |
probably benign |
Het |
Capn3 |
G |
A |
2: 120,315,075 (GRCm39) |
W201* |
probably null |
Het |
Crtap |
T |
C |
9: 114,207,164 (GRCm39) |
T365A |
probably benign |
Het |
Daam1 |
A |
G |
12: 71,992,272 (GRCm39) |
D329G |
unknown |
Het |
Dmxl2 |
A |
T |
9: 54,283,550 (GRCm39) |
L2761Q |
possibly damaging |
Het |
Fcho2 |
A |
C |
13: 98,926,310 (GRCm39) |
V91G |
probably damaging |
Het |
Fen1 |
A |
T |
19: 10,178,022 (GRCm39) |
C141S |
possibly damaging |
Het |
Fkbp15 |
G |
C |
4: 62,225,166 (GRCm39) |
A831G |
probably benign |
Het |
Frmd4a |
A |
T |
2: 4,305,768 (GRCm39) |
R14S |
possibly damaging |
Het |
Fzr1 |
A |
G |
10: 81,206,160 (GRCm39) |
F176L |
possibly damaging |
Het |
Garem2 |
A |
G |
5: 30,321,336 (GRCm39) |
D565G |
probably damaging |
Het |
Garre1 |
A |
T |
7: 33,944,505 (GRCm39) |
S76T |
probably damaging |
Het |
Iqca1 |
G |
T |
1: 89,998,257 (GRCm39) |
T549K |
probably damaging |
Het |
Itgax |
T |
A |
7: 127,739,647 (GRCm39) |
S686R |
probably damaging |
Het |
Knop1 |
C |
A |
7: 118,445,305 (GRCm39) |
G220C |
probably damaging |
Het |
Lyzl1 |
T |
A |
18: 4,169,142 (GRCm39) |
C49S |
probably damaging |
Het |
Mpzl1 |
A |
T |
1: 165,433,180 (GRCm39) |
I157K |
probably benign |
Het |
Mrgprb2 |
T |
C |
7: 48,202,261 (GRCm39) |
I155V |
probably benign |
Het |
Mucl3 |
T |
C |
17: 35,949,102 (GRCm39) |
M166V |
probably benign |
Het |
Mvb12b |
T |
C |
2: 33,717,728 (GRCm39) |
T167A |
probably benign |
Het |
Myh3 |
A |
G |
11: 66,979,445 (GRCm39) |
N491S |
probably benign |
Het |
Myo5b |
A |
G |
18: 74,787,128 (GRCm39) |
D511G |
possibly damaging |
Het |
Or10ak8 |
C |
T |
4: 118,774,035 (GRCm39) |
V210I |
probably benign |
Het |
Or11h4 |
T |
C |
14: 50,974,509 (GRCm39) |
T37A |
probably benign |
Het |
Or6b1 |
C |
T |
6: 42,815,180 (GRCm39) |
R122C |
probably damaging |
Het |
Or8k21 |
T |
G |
2: 86,145,558 (GRCm39) |
Q24P |
probably damaging |
Het |
Ptcd1 |
A |
G |
5: 145,091,671 (GRCm39) |
M476T |
probably damaging |
Het |
Pum3 |
A |
G |
19: 27,398,695 (GRCm39) |
|
probably null |
Het |
Ranbp2 |
G |
A |
10: 58,321,658 (GRCm39) |
D2652N |
probably damaging |
Het |
Rassf1 |
T |
C |
9: 107,435,213 (GRCm39) |
V166A |
probably damaging |
Het |
Rictor |
A |
G |
15: 6,812,585 (GRCm39) |
H907R |
probably benign |
Het |
Rorb |
T |
C |
19: 18,965,471 (GRCm39) |
E6G |
probably damaging |
Het |
Serpina3f |
A |
T |
12: 104,183,182 (GRCm39) |
T15S |
possibly damaging |
Het |
Sorbs2 |
T |
C |
8: 46,212,226 (GRCm39) |
L100P |
probably damaging |
Het |
Sprr2k |
T |
C |
3: 92,340,655 (GRCm39) |
|
probably benign |
Het |
Srrm2 |
T |
A |
17: 24,040,360 (GRCm39) |
S2431T |
probably damaging |
Het |
Stox2 |
T |
A |
8: 47,866,172 (GRCm39) |
K57* |
probably null |
Het |
Ttc21a |
G |
A |
9: 119,770,327 (GRCm39) |
V133I |
probably benign |
Het |
Vasn |
T |
C |
16: 4,468,026 (GRCm39) |
Y658H |
possibly damaging |
Het |
|
Other mutations in Zfp251 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01433:Zfp251
|
APN |
15 |
76,738,755 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02868:Zfp251
|
APN |
15 |
76,738,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R0011:Zfp251
|
UTSW |
15 |
76,738,754 (GRCm39) |
missense |
probably benign |
0.42 |
R0011:Zfp251
|
UTSW |
15 |
76,738,754 (GRCm39) |
missense |
probably benign |
0.42 |
R1199:Zfp251
|
UTSW |
15 |
76,738,436 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1201:Zfp251
|
UTSW |
15 |
76,738,436 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1321:Zfp251
|
UTSW |
15 |
76,738,436 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1322:Zfp251
|
UTSW |
15 |
76,738,436 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1565:Zfp251
|
UTSW |
15 |
76,737,239 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1565:Zfp251
|
UTSW |
15 |
76,737,238 (GRCm39) |
missense |
probably damaging |
0.96 |
R1587:Zfp251
|
UTSW |
15 |
76,754,484 (GRCm39) |
missense |
probably damaging |
0.98 |
R1752:Zfp251
|
UTSW |
15 |
76,737,863 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3771:Zfp251
|
UTSW |
15 |
76,737,836 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3772:Zfp251
|
UTSW |
15 |
76,737,836 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3773:Zfp251
|
UTSW |
15 |
76,737,836 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4684:Zfp251
|
UTSW |
15 |
76,738,607 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6341:Zfp251
|
UTSW |
15 |
76,738,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R7050:Zfp251
|
UTSW |
15 |
76,738,496 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7605:Zfp251
|
UTSW |
15 |
76,738,557 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8783:Zfp251
|
UTSW |
15 |
76,737,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R9662:Zfp251
|
UTSW |
15 |
76,737,520 (GRCm39) |
missense |
possibly damaging |
0.53 |
|