Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam39 |
T |
C |
8: 41,278,106 (GRCm39) |
S166P |
probably damaging |
Het |
Appl1 |
T |
A |
14: 26,686,914 (GRCm39) |
T19S |
probably damaging |
Het |
Arid4b |
T |
A |
13: 14,344,594 (GRCm39) |
D557E |
probably benign |
Het |
Aven |
C |
T |
2: 112,390,120 (GRCm39) |
R8W |
probably benign |
Het |
C2cd2l |
T |
C |
9: 44,227,502 (GRCm39) |
E307G |
possibly damaging |
Het |
Cdh20 |
A |
C |
1: 110,027,832 (GRCm39) |
T526P |
probably benign |
Het |
Dchs1 |
C |
T |
7: 105,414,718 (GRCm39) |
V775M |
probably benign |
Het |
Dennd1b |
A |
G |
1: 138,969,673 (GRCm39) |
N63S |
probably benign |
Het |
Dtnb |
A |
T |
12: 3,694,056 (GRCm39) |
Y248F |
unknown |
Het |
Ehbp1l1 |
T |
A |
19: 5,770,089 (GRCm39) |
T405S |
possibly damaging |
Het |
Fam149a |
A |
G |
8: 45,803,490 (GRCm39) |
Y415H |
possibly damaging |
Het |
Fam186a |
A |
G |
15: 99,839,191 (GRCm39) |
L2351P |
unknown |
Het |
Fsip2 |
T |
G |
2: 82,819,687 (GRCm39) |
I5140S |
possibly damaging |
Het |
Gm8674 |
T |
C |
13: 50,054,262 (GRCm39) |
T749A |
noncoding transcript |
Het |
Kalrn |
A |
G |
16: 33,870,153 (GRCm39) |
V1894A |
noncoding transcript |
Het |
Lrba |
G |
A |
3: 86,449,882 (GRCm39) |
G2067D |
probably damaging |
Het |
Lrp2 |
G |
T |
2: 69,311,611 (GRCm39) |
Y2622* |
probably null |
Het |
Lrtm2 |
A |
C |
6: 119,297,778 (GRCm39) |
F88V |
probably damaging |
Het |
Mboat1 |
T |
C |
13: 30,429,333 (GRCm39) |
S454P |
probably damaging |
Het |
Nkpd1 |
C |
T |
7: 19,253,753 (GRCm39) |
P40S |
probably benign |
Het |
Or2b7 |
T |
C |
13: 21,739,788 (GRCm39) |
I135V |
probably benign |
Het |
Or4a76 |
T |
A |
2: 89,460,907 (GRCm39) |
I112F |
probably damaging |
Het |
Or8b54 |
G |
A |
9: 38,686,577 (GRCm39) |
V9M |
noncoding transcript |
Het |
Or8k27 |
C |
A |
2: 86,275,473 (GRCm39) |
M284I |
noncoding transcript |
Het |
Patj |
A |
G |
4: 98,570,308 (GRCm39) |
E1711G |
possibly damaging |
Het |
Pcdha4 |
A |
T |
18: 37,086,128 (GRCm39) |
I104F |
probably damaging |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Plekhg4 |
C |
T |
8: 106,107,546 (GRCm39) |
R990* |
probably null |
Het |
Pphln1 |
T |
C |
15: 93,386,930 (GRCm39) |
S343P |
probably benign |
Het |
Pram1 |
A |
T |
17: 33,860,241 (GRCm39) |
K269N |
probably damaging |
Het |
Psmd13 |
T |
A |
7: 140,466,450 (GRCm39) |
I79K |
probably damaging |
Het |
Ptprf |
T |
C |
4: 118,069,309 (GRCm39) |
D1586G |
possibly damaging |
Het |
Ptprh |
T |
A |
7: 4,584,090 (GRCm39) |
Q167H |
probably damaging |
Het |
Rbm46 |
C |
T |
3: 82,772,775 (GRCm39) |
R119Q |
probably benign |
Het |
Rreb1 |
T |
C |
13: 38,077,848 (GRCm39) |
M20T |
probably damaging |
Het |
Scrn2 |
T |
G |
11: 96,923,046 (GRCm39) |
L163R |
probably damaging |
Het |
Slc36a3 |
C |
T |
11: 55,022,433 (GRCm39) |
V254I |
probably benign |
Het |
Slc6a6 |
T |
C |
6: 91,701,951 (GRCm39) |
F120L |
probably benign |
Het |
Slc8a2 |
A |
T |
7: 15,879,230 (GRCm39) |
H572L |
probably benign |
Het |
Spats2 |
T |
A |
15: 99,106,776 (GRCm39) |
D357E |
probably damaging |
Het |
Speg |
A |
T |
1: 75,395,677 (GRCm39) |
N1816I |
probably damaging |
Het |
Sult2b1 |
A |
G |
7: 45,433,361 (GRCm39) |
V2A |
unknown |
Het |
Susd3 |
T |
C |
13: 49,384,731 (GRCm39) |
T231A |
probably benign |
Het |
Tamalin |
C |
T |
15: 101,128,902 (GRCm39) |
L217F |
probably damaging |
Het |
Tcp1 |
A |
G |
17: 13,139,738 (GRCm39) |
D261G |
probably benign |
Het |
Trpm2 |
C |
G |
10: 77,771,836 (GRCm39) |
S601T |
probably benign |
Het |
Ugt2b38 |
A |
T |
5: 87,571,659 (GRCm39) |
F124L |
probably benign |
Het |
Unc80 |
G |
T |
1: 66,693,178 (GRCm39) |
E2522D |
probably benign |
Het |
Usp34 |
A |
G |
11: 23,396,750 (GRCm39) |
T2365A |
|
Het |
Vmn2r92 |
G |
T |
17: 18,405,278 (GRCm39) |
M807I |
probably benign |
Het |
Vps13b |
C |
A |
15: 35,597,550 (GRCm39) |
P1030Q |
probably damaging |
Het |
Wrn |
T |
G |
8: 33,819,213 (GRCm39) |
K246N |
probably damaging |
Het |
Zer1 |
T |
A |
2: 29,991,147 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Kpna3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00226:Kpna3
|
APN |
14 |
61,611,737 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00321:Kpna3
|
APN |
14 |
61,629,302 (GRCm39) |
splice site |
probably benign |
|
IGL01013:Kpna3
|
APN |
14 |
61,607,966 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01833:Kpna3
|
APN |
14 |
61,607,894 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02661:Kpna3
|
APN |
14 |
61,610,398 (GRCm39) |
splice site |
probably benign |
|
IGL03070:Kpna3
|
APN |
14 |
61,608,231 (GRCm39) |
splice site |
probably benign |
|
R1428:Kpna3
|
UTSW |
14 |
61,620,669 (GRCm39) |
splice site |
probably benign |
|
R1719:Kpna3
|
UTSW |
14 |
61,624,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R1728:Kpna3
|
UTSW |
14 |
61,605,150 (GRCm39) |
missense |
probably benign |
0.00 |
R1760:Kpna3
|
UTSW |
14 |
61,607,990 (GRCm39) |
missense |
probably benign |
0.03 |
R1784:Kpna3
|
UTSW |
14 |
61,605,150 (GRCm39) |
missense |
probably benign |
0.00 |
R2107:Kpna3
|
UTSW |
14 |
61,607,933 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4184:Kpna3
|
UTSW |
14 |
61,605,624 (GRCm39) |
missense |
probably damaging |
0.96 |
R4952:Kpna3
|
UTSW |
14 |
61,607,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R5081:Kpna3
|
UTSW |
14 |
61,628,694 (GRCm39) |
missense |
probably damaging |
0.97 |
R5766:Kpna3
|
UTSW |
14 |
61,640,463 (GRCm39) |
missense |
probably benign |
0.07 |
R5887:Kpna3
|
UTSW |
14 |
61,640,461 (GRCm39) |
missense |
probably benign |
0.04 |
R5927:Kpna3
|
UTSW |
14 |
61,622,096 (GRCm39) |
missense |
probably damaging |
0.96 |
R7116:Kpna3
|
UTSW |
14 |
61,605,635 (GRCm39) |
missense |
probably benign |
0.32 |
R7615:Kpna3
|
UTSW |
14 |
61,610,411 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7674:Kpna3
|
UTSW |
14 |
61,605,086 (GRCm39) |
missense |
probably benign |
|
R7799:Kpna3
|
UTSW |
14 |
61,622,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R8115:Kpna3
|
UTSW |
14 |
61,608,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R8896:Kpna3
|
UTSW |
14 |
61,629,294 (GRCm39) |
missense |
probably benign |
0.11 |
R9636:Kpna3
|
UTSW |
14 |
61,624,903 (GRCm39) |
missense |
probably damaging |
1.00 |
|