Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg3 |
A |
G |
5: 105,083,920 (GRCm39) |
W617R |
probably damaging |
Het |
Adam34l |
A |
T |
8: 44,079,568 (GRCm39) |
C219S |
probably benign |
Het |
Cep83 |
A |
T |
10: 94,555,450 (GRCm39) |
|
probably benign |
Het |
Ces1e |
G |
A |
8: 93,946,149 (GRCm39) |
|
probably benign |
Het |
Clip1 |
C |
A |
5: 123,778,594 (GRCm39) |
R443L |
probably damaging |
Het |
Clmp |
A |
G |
9: 40,672,302 (GRCm39) |
D44G |
probably benign |
Het |
Cntnap2 |
G |
A |
6: 46,506,839 (GRCm39) |
Q304* |
probably null |
Het |
Cst7 |
A |
T |
2: 150,412,435 (GRCm39) |
|
probably benign |
Het |
Dclk3 |
A |
T |
9: 111,311,789 (GRCm39) |
Y677F |
probably damaging |
Het |
Dlat |
G |
T |
9: 50,548,869 (GRCm39) |
N562K |
probably damaging |
Het |
Elmod1 |
A |
T |
9: 53,833,260 (GRCm39) |
Y182N |
probably damaging |
Het |
Fzd10 |
T |
C |
5: 128,679,077 (GRCm39) |
F266L |
probably damaging |
Het |
Gm8258 |
A |
G |
5: 104,923,952 (GRCm39) |
|
noncoding transcript |
Het |
Gm9742 |
T |
A |
13: 8,080,041 (GRCm39) |
|
noncoding transcript |
Het |
Hdlbp |
T |
C |
1: 93,358,039 (GRCm39) |
|
probably benign |
Het |
Itga8 |
A |
G |
2: 12,196,627 (GRCm39) |
S597P |
probably damaging |
Het |
Kndc1 |
A |
T |
7: 139,481,153 (GRCm39) |
I80F |
probably damaging |
Het |
Ktn1 |
A |
G |
14: 47,970,700 (GRCm39) |
N1192S |
probably benign |
Het |
Ldha |
G |
A |
7: 46,503,417 (GRCm39) |
V270M |
probably damaging |
Het |
Lyst |
T |
C |
13: 13,931,891 (GRCm39) |
|
probably benign |
Het |
Map3k9 |
A |
T |
12: 81,769,256 (GRCm39) |
F954I |
probably benign |
Het |
Mroh2b |
A |
G |
15: 4,963,877 (GRCm39) |
N823S |
probably damaging |
Het |
Mycbp2 |
A |
T |
14: 103,419,895 (GRCm39) |
N2480K |
probably damaging |
Het |
Nat1 |
A |
G |
8: 67,943,977 (GRCm39) |
K121E |
probably benign |
Het |
Neurl1b |
T |
A |
17: 26,660,519 (GRCm39) |
|
probably null |
Het |
Nnt |
C |
A |
13: 119,531,257 (GRCm39) |
L163F |
probably damaging |
Het |
Or10v5 |
A |
G |
19: 11,805,556 (GRCm39) |
V278A |
probably benign |
Het |
Otog |
A |
G |
7: 45,947,668 (GRCm39) |
T2274A |
probably damaging |
Het |
Pde4b |
G |
A |
4: 102,459,848 (GRCm39) |
R561Q |
probably damaging |
Het |
Pitpnm2 |
A |
G |
5: 124,269,264 (GRCm39) |
F453L |
probably damaging |
Het |
Pms1 |
T |
C |
1: 53,235,972 (GRCm39) |
|
probably null |
Het |
Pot1a |
A |
G |
6: 25,771,540 (GRCm39) |
V227A |
possibly damaging |
Het |
Prdx6b |
A |
G |
2: 80,123,659 (GRCm39) |
N156S |
probably damaging |
Het |
Ptpn9 |
A |
G |
9: 56,968,417 (GRCm39) |
S586G |
probably benign |
Het |
Serpina6 |
A |
T |
12: 103,618,053 (GRCm39) |
N253K |
probably damaging |
Het |
Slc12a2 |
T |
A |
18: 58,052,608 (GRCm39) |
V809D |
possibly damaging |
Het |
Slc2a8 |
C |
T |
2: 32,863,696 (GRCm39) |
A449T |
probably benign |
Het |
Slc6a6 |
A |
G |
6: 91,701,939 (GRCm39) |
I116V |
probably null |
Het |
Synj2 |
T |
A |
17: 6,058,380 (GRCm39) |
S58R |
possibly damaging |
Het |
Tafa3 |
T |
C |
3: 104,679,487 (GRCm39) |
|
probably benign |
Het |
Tktl2 |
T |
C |
8: 66,965,831 (GRCm39) |
V463A |
probably damaging |
Het |
Uchl5 |
T |
C |
1: 143,670,082 (GRCm39) |
V105A |
possibly damaging |
Het |
Usp9y |
T |
C |
Y: 1,333,600 (GRCm39) |
|
probably benign |
Het |
Vmn1r200 |
T |
C |
13: 22,579,667 (GRCm39) |
S148P |
probably damaging |
Het |
Vmn2r50 |
A |
T |
7: 9,781,644 (GRCm39) |
M367K |
possibly damaging |
Het |
Vps13a |
T |
C |
19: 16,632,570 (GRCm39) |
|
probably benign |
Het |
Wdr26 |
A |
T |
1: 181,013,635 (GRCm39) |
|
probably null |
Het |
Wdr87-ps |
A |
G |
7: 29,229,545 (GRCm39) |
|
noncoding transcript |
Het |
Ythdc2 |
T |
A |
18: 44,983,465 (GRCm39) |
M544K |
probably damaging |
Het |
Zpld2 |
A |
G |
4: 133,930,221 (GRCm39) |
I28T |
probably benign |
Het |
|
Other mutations in Ckap2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01129:Ckap2
|
APN |
8 |
22,659,774 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01519:Ckap2
|
APN |
8 |
22,658,914 (GRCm39) |
missense |
probably benign |
0.00 |
R1638:Ckap2
|
UTSW |
8 |
22,665,812 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1965:Ckap2
|
UTSW |
8 |
22,665,803 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2047:Ckap2
|
UTSW |
8 |
22,658,763 (GRCm39) |
missense |
probably benign |
0.03 |
R3023:Ckap2
|
UTSW |
8 |
22,665,877 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3843:Ckap2
|
UTSW |
8 |
22,665,774 (GRCm39) |
missense |
probably damaging |
0.98 |
R4587:Ckap2
|
UTSW |
8 |
22,666,992 (GRCm39) |
missense |
probably benign |
|
R4754:Ckap2
|
UTSW |
8 |
22,658,911 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4847:Ckap2
|
UTSW |
8 |
22,665,084 (GRCm39) |
missense |
probably damaging |
0.98 |
R5354:Ckap2
|
UTSW |
8 |
22,667,581 (GRCm39) |
missense |
probably damaging |
0.96 |
R5423:Ckap2
|
UTSW |
8 |
22,667,212 (GRCm39) |
missense |
probably benign |
0.33 |
R5717:Ckap2
|
UTSW |
8 |
22,665,063 (GRCm39) |
missense |
probably damaging |
0.98 |
R6518:Ckap2
|
UTSW |
8 |
22,663,319 (GRCm39) |
missense |
probably benign |
0.41 |
R7088:Ckap2
|
UTSW |
8 |
22,659,882 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7466:Ckap2
|
UTSW |
8 |
22,667,402 (GRCm39) |
missense |
probably benign |
0.02 |
R7943:Ckap2
|
UTSW |
8 |
22,665,090 (GRCm39) |
missense |
probably damaging |
0.97 |
R8558:Ckap2
|
UTSW |
8 |
22,658,811 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9224:Ckap2
|
UTSW |
8 |
22,659,954 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9366:Ckap2
|
UTSW |
8 |
22,658,988 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9454:Ckap2
|
UTSW |
8 |
22,665,899 (GRCm39) |
nonsense |
probably null |
|
X0058:Ckap2
|
UTSW |
8 |
22,666,814 (GRCm39) |
missense |
probably benign |
|
Z1176:Ckap2
|
UTSW |
8 |
22,659,810 (GRCm39) |
missense |
probably damaging |
1.00 |
|