Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
G |
11: 9,248,047 (GRCm39) |
D2598G |
probably benign |
Het |
Abcf2 |
T |
G |
5: 24,776,246 (GRCm39) |
|
probably null |
Het |
Acsl1 |
T |
A |
8: 46,946,031 (GRCm39) |
C55S |
possibly damaging |
Het |
Adam22 |
T |
A |
5: 8,199,210 (GRCm39) |
M249L |
possibly damaging |
Het |
Alk |
A |
G |
17: 72,206,159 (GRCm39) |
|
probably benign |
Het |
Apbb1ip |
T |
A |
2: 22,757,729 (GRCm39) |
V449D |
possibly damaging |
Het |
Atp13a5 |
A |
T |
16: 29,152,883 (GRCm39) |
Y194* |
probably null |
Het |
Cacul1 |
A |
T |
19: 60,531,489 (GRCm39) |
F260Y |
probably damaging |
Het |
Cfap46 |
A |
G |
7: 139,181,081 (GRCm39) |
I2640T |
probably damaging |
Het |
Chd7 |
T |
C |
4: 8,841,108 (GRCm39) |
S1446P |
probably damaging |
Het |
Cimap2 |
G |
T |
4: 106,464,601 (GRCm39) |
R353S |
possibly damaging |
Het |
Clcn2 |
G |
A |
16: 20,530,902 (GRCm39) |
T276I |
probably damaging |
Het |
Dcbld1 |
T |
G |
10: 52,195,721 (GRCm39) |
Y310D |
probably damaging |
Het |
Dennd4c |
G |
A |
4: 86,696,113 (GRCm39) |
V157I |
probably damaging |
Het |
Dennd5b |
G |
T |
6: 148,899,758 (GRCm39) |
T1213K |
possibly damaging |
Het |
Dusp8 |
A |
T |
7: 141,638,097 (GRCm39) |
L177* |
probably null |
Het |
Erbb4 |
T |
C |
1: 68,367,281 (GRCm39) |
S479G |
probably benign |
Het |
Gpbp1 |
T |
A |
13: 111,589,787 (GRCm39) |
|
probably benign |
Het |
Hmcn1 |
T |
A |
1: 150,608,661 (GRCm39) |
Q1507L |
probably damaging |
Het |
Inppl1 |
G |
T |
7: 101,473,587 (GRCm39) |
T1021K |
possibly damaging |
Het |
Klk1b9 |
A |
G |
7: 43,628,838 (GRCm39) |
E114G |
probably benign |
Het |
Klre1 |
T |
C |
6: 129,562,660 (GRCm39) |
|
probably benign |
Het |
Lancl1 |
T |
C |
1: 67,060,209 (GRCm39) |
Y72C |
probably damaging |
Het |
Lilra6 |
A |
G |
7: 3,917,647 (GRCm39) |
|
probably benign |
Het |
Magi2 |
T |
C |
5: 20,671,126 (GRCm39) |
V490A |
possibly damaging |
Het |
Myo3b |
T |
A |
2: 70,084,803 (GRCm39) |
N720K |
probably damaging |
Het |
Or2ah1 |
A |
C |
2: 85,653,729 (GRCm39) |
D138A |
probably benign |
Het |
Or7e166 |
T |
C |
9: 19,624,597 (GRCm39) |
V158A |
probably benign |
Het |
Ppp2r3d |
T |
A |
9: 101,003,630 (GRCm39) |
|
probably benign |
Het |
Rbm47 |
T |
C |
5: 66,184,036 (GRCm39) |
D189G |
probably damaging |
Het |
Scn2a |
G |
A |
2: 65,594,973 (GRCm39) |
D1941N |
probably benign |
Het |
Sgpp2 |
T |
C |
1: 78,367,200 (GRCm39) |
I111T |
probably benign |
Het |
Sh3bp2 |
T |
C |
5: 34,716,546 (GRCm39) |
V319A |
probably benign |
Het |
Slc12a3 |
A |
C |
8: 95,092,519 (GRCm39) |
Q980P |
possibly damaging |
Het |
Slc39a8 |
G |
T |
3: 135,590,474 (GRCm39) |
G389V |
probably damaging |
Het |
Slc5a3 |
T |
C |
16: 91,874,348 (GRCm39) |
I135T |
probably damaging |
Het |
Smu1 |
A |
G |
4: 40,739,568 (GRCm39) |
V414A |
possibly damaging |
Het |
Tlr12 |
A |
G |
4: 128,510,645 (GRCm39) |
F535S |
possibly damaging |
Het |
Trim47 |
A |
G |
11: 115,997,254 (GRCm39) |
V501A |
probably damaging |
Het |
Vmn1r16 |
A |
T |
6: 57,300,603 (GRCm39) |
N6K |
probably damaging |
Het |
Vwce |
G |
A |
19: 10,637,360 (GRCm39) |
C711Y |
possibly damaging |
Het |
Wdr25 |
C |
T |
12: 108,864,262 (GRCm39) |
L136F |
probably benign |
Het |
Xpo1 |
A |
G |
11: 23,234,306 (GRCm39) |
Q437R |
probably benign |
Het |
Zfp169 |
C |
A |
13: 48,644,270 (GRCm39) |
|
probably benign |
Het |
Zfp607b |
A |
T |
7: 27,403,295 (GRCm39) |
I584F |
probably damaging |
Het |
Zzef1 |
T |
A |
11: 72,808,099 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Ambn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01017:Ambn
|
APN |
5 |
88,607,218 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01139:Ambn
|
APN |
5 |
88,612,376 (GRCm39) |
splice site |
probably benign |
|
IGL01318:Ambn
|
APN |
5 |
88,608,554 (GRCm39) |
splice site |
probably benign |
|
IGL02139:Ambn
|
APN |
5 |
88,613,149 (GRCm39) |
missense |
probably benign |
|
IGL02261:Ambn
|
APN |
5 |
88,604,807 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02743:Ambn
|
APN |
5 |
88,612,343 (GRCm39) |
missense |
probably damaging |
0.99 |
R0242:Ambn
|
UTSW |
5 |
88,615,831 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0242:Ambn
|
UTSW |
5 |
88,615,831 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0563:Ambn
|
UTSW |
5 |
88,611,309 (GRCm39) |
missense |
probably benign |
0.28 |
R1649:Ambn
|
UTSW |
5 |
88,612,340 (GRCm39) |
missense |
probably benign |
0.16 |
R2118:Ambn
|
UTSW |
5 |
88,608,617 (GRCm39) |
splice site |
probably benign |
|
R2121:Ambn
|
UTSW |
5 |
88,608,617 (GRCm39) |
splice site |
probably benign |
|
R2124:Ambn
|
UTSW |
5 |
88,608,617 (GRCm39) |
splice site |
probably benign |
|
R2495:Ambn
|
UTSW |
5 |
88,615,663 (GRCm39) |
missense |
probably benign |
0.05 |
R2877:Ambn
|
UTSW |
5 |
88,608,559 (GRCm39) |
splice site |
probably benign |
|
R3779:Ambn
|
UTSW |
5 |
88,613,201 (GRCm39) |
splice site |
probably benign |
|
R4760:Ambn
|
UTSW |
5 |
88,615,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R5422:Ambn
|
UTSW |
5 |
88,612,370 (GRCm39) |
critical splice donor site |
probably null |
|
R5755:Ambn
|
UTSW |
5 |
88,612,350 (GRCm39) |
splice site |
probably null |
|
R5883:Ambn
|
UTSW |
5 |
88,615,688 (GRCm39) |
nonsense |
probably null |
|
R5970:Ambn
|
UTSW |
5 |
88,615,810 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6846:Ambn
|
UTSW |
5 |
88,609,574 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7166:Ambn
|
UTSW |
5 |
88,615,387 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7500:Ambn
|
UTSW |
5 |
88,609,493 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7809:Ambn
|
UTSW |
5 |
88,615,683 (GRCm39) |
missense |
probably benign |
0.00 |
R8306:Ambn
|
UTSW |
5 |
88,607,281 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8898:Ambn
|
UTSW |
5 |
88,613,051 (GRCm39) |
critical splice donor site |
probably null |
|
R9481:Ambn
|
UTSW |
5 |
88,613,050 (GRCm39) |
critical splice donor site |
probably null |
|
|