Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrb2 |
G |
T |
4: 129,885,925 (GRCm39) |
D22Y |
probably damaging |
Het |
Ak7 |
T |
C |
12: 105,701,183 (GRCm39) |
V242A |
probably benign |
Het |
Cacna1b |
T |
C |
2: 24,551,769 (GRCm39) |
N1127S |
probably damaging |
Het |
Cacnb2 |
A |
T |
2: 14,976,380 (GRCm39) |
H267L |
probably benign |
Het |
Ces1b |
C |
T |
8: 93,806,059 (GRCm39) |
G61R |
probably damaging |
Het |
Cgnl1 |
T |
A |
9: 71,632,286 (GRCm39) |
D355V |
probably damaging |
Het |
Col24a1 |
T |
C |
3: 145,021,005 (GRCm39) |
S459P |
probably damaging |
Het |
Crygd |
T |
C |
1: 65,101,185 (GRCm39) |
T137A |
probably benign |
Het |
Dctn4 |
T |
A |
18: 60,677,202 (GRCm39) |
M174K |
probably benign |
Het |
Evi5 |
A |
G |
5: 107,964,790 (GRCm39) |
|
probably benign |
Het |
Fat2 |
T |
G |
11: 55,174,806 (GRCm39) |
D1969A |
probably benign |
Het |
Fcrl5 |
A |
T |
3: 87,353,606 (GRCm39) |
E317V |
probably damaging |
Het |
Foxf2 |
G |
T |
13: 31,810,697 (GRCm39) |
S212I |
probably damaging |
Het |
Gm21759 |
T |
A |
5: 8,230,685 (GRCm39) |
|
probably benign |
Het |
Gm5414 |
A |
G |
15: 101,534,105 (GRCm39) |
|
probably benign |
Het |
Gm7275 |
T |
C |
16: 47,893,946 (GRCm39) |
|
noncoding transcript |
Het |
Hspa9 |
T |
C |
18: 35,071,761 (GRCm39) |
E613G |
possibly damaging |
Het |
Il1rl1 |
A |
G |
1: 40,501,168 (GRCm39) |
I515V |
possibly damaging |
Het |
Ins1 |
G |
T |
19: 52,253,173 (GRCm39) |
A38S |
probably damaging |
Het |
Klhl31 |
A |
G |
9: 77,562,488 (GRCm39) |
N418D |
probably benign |
Het |
Magi3 |
T |
C |
3: 103,961,778 (GRCm39) |
K417E |
probably damaging |
Het |
Msh4 |
A |
G |
3: 153,563,226 (GRCm39) |
Y823H |
probably damaging |
Het |
Myo6 |
T |
A |
9: 80,168,100 (GRCm39) |
D421E |
probably damaging |
Het |
Myom3 |
T |
C |
4: 135,492,900 (GRCm39) |
S150P |
possibly damaging |
Het |
Nectin1 |
C |
T |
9: 43,703,871 (GRCm39) |
|
probably benign |
Het |
Nkx1-2 |
A |
T |
7: 132,201,203 (GRCm39) |
I18N |
probably damaging |
Het |
Or4s2b |
A |
G |
2: 88,509,077 (GRCm39) |
T286A |
probably damaging |
Het |
Or5b113 |
A |
T |
19: 13,342,807 (GRCm39) |
I272F |
probably benign |
Het |
Or8g33 |
A |
C |
9: 39,337,634 (GRCm39) |
H244Q |
probably damaging |
Het |
Or9g4 |
T |
C |
2: 85,505,285 (GRCm39) |
D70G |
probably damaging |
Het |
Pde8b |
T |
C |
13: 95,232,232 (GRCm39) |
R237G |
probably damaging |
Het |
Pp2d1 |
G |
A |
17: 53,822,167 (GRCm39) |
L300F |
probably damaging |
Het |
Ptpn21 |
A |
T |
12: 98,655,420 (GRCm39) |
Y516N |
probably damaging |
Het |
Ptprm |
T |
A |
17: 67,370,158 (GRCm39) |
|
probably benign |
Het |
Rabggtb |
A |
G |
3: 153,617,650 (GRCm39) |
V16A |
probably damaging |
Het |
Rangap1 |
A |
T |
15: 81,604,864 (GRCm39) |
C82S |
probably damaging |
Het |
Rasal2 |
T |
C |
1: 157,003,480 (GRCm39) |
E393G |
probably damaging |
Het |
Rasgrf1 |
A |
T |
9: 89,856,889 (GRCm39) |
E449V |
probably damaging |
Het |
Rrp12 |
A |
T |
19: 41,859,334 (GRCm39) |
H1143Q |
probably damaging |
Het |
Scap |
T |
C |
9: 110,208,549 (GRCm39) |
I530T |
probably benign |
Het |
Sel1l |
T |
A |
12: 91,783,021 (GRCm39) |
Q482L |
probably damaging |
Het |
Serpinb9b |
T |
C |
13: 33,223,648 (GRCm39) |
M280T |
probably damaging |
Het |
Slc39a10 |
T |
A |
1: 46,871,895 (GRCm39) |
H348L |
probably benign |
Het |
Slc7a2 |
T |
C |
8: 41,367,120 (GRCm39) |
L542P |
possibly damaging |
Het |
Tas1r2 |
A |
T |
4: 139,396,488 (GRCm39) |
Q609L |
probably damaging |
Het |
Tbc1d14 |
A |
T |
5: 36,665,781 (GRCm39) |
|
probably benign |
Het |
Tfb2m |
A |
G |
1: 179,365,262 (GRCm39) |
|
probably null |
Het |
Tpo |
T |
C |
12: 30,134,646 (GRCm39) |
T771A |
possibly damaging |
Het |
Tpr |
G |
A |
1: 150,289,496 (GRCm39) |
R609H |
possibly damaging |
Het |
Usp34 |
T |
A |
11: 23,295,141 (GRCm39) |
|
probably benign |
Het |
Vmn1r193 |
G |
T |
13: 22,403,893 (GRCm39) |
S33* |
probably null |
Het |
Vmn2r104 |
A |
C |
17: 20,250,187 (GRCm39) |
S695A |
probably damaging |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r24 |
A |
G |
6: 123,764,404 (GRCm39) |
D427G |
probably benign |
Het |
|
Other mutations in Zfp362 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01667:Zfp362
|
APN |
4 |
128,680,902 (GRCm39) |
missense |
probably damaging |
1.00 |
trek
|
UTSW |
4 |
128,679,769 (GRCm39) |
missense |
probably damaging |
1.00 |
Zax
|
UTSW |
4 |
128,684,053 (GRCm39) |
missense |
possibly damaging |
0.71 |
Zebulon
|
UTSW |
4 |
128,679,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R1471:Zfp362
|
UTSW |
4 |
128,680,993 (GRCm39) |
missense |
probably benign |
|
R1892:Zfp362
|
UTSW |
4 |
128,684,057 (GRCm39) |
missense |
probably benign |
0.17 |
R1901:Zfp362
|
UTSW |
4 |
128,684,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R2058:Zfp362
|
UTSW |
4 |
128,680,780 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3739:Zfp362
|
UTSW |
4 |
128,680,682 (GRCm39) |
splice site |
probably benign |
|
R6772:Zfp362
|
UTSW |
4 |
128,684,053 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6900:Zfp362
|
UTSW |
4 |
128,679,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R6901:Zfp362
|
UTSW |
4 |
128,679,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R7105:Zfp362
|
UTSW |
4 |
128,668,319 (GRCm39) |
missense |
probably damaging |
0.99 |
R7348:Zfp362
|
UTSW |
4 |
128,671,010 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7629:Zfp362
|
UTSW |
4 |
128,679,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R7712:Zfp362
|
UTSW |
4 |
128,671,203 (GRCm39) |
missense |
probably benign |
0.14 |
R7763:Zfp362
|
UTSW |
4 |
128,680,824 (GRCm39) |
missense |
probably benign |
|
R8434:Zfp362
|
UTSW |
4 |
128,679,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R8508:Zfp362
|
UTSW |
4 |
128,668,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R9432:Zfp362
|
UTSW |
4 |
128,670,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R9567:Zfp362
|
UTSW |
4 |
128,688,681 (GRCm39) |
start codon destroyed |
unknown |
|
Z1177:Zfp362
|
UTSW |
4 |
128,668,343 (GRCm39) |
missense |
probably damaging |
0.99 |
|