Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930426L09Rik |
T |
C |
2: 19,003,623 (GRCm39) |
|
probably benign |
Het |
Abi3bp |
A |
G |
16: 56,462,930 (GRCm39) |
|
probably benign |
Het |
Asb4 |
T |
C |
6: 5,398,386 (GRCm39) |
I117T |
probably benign |
Het |
Birc6 |
T |
G |
17: 74,946,822 (GRCm39) |
L2847R |
probably damaging |
Het |
C2cd2 |
A |
G |
16: 97,691,208 (GRCm39) |
|
probably benign |
Het |
Ccdc77 |
C |
A |
6: 120,316,119 (GRCm39) |
C186F |
possibly damaging |
Het |
Cd300ld2 |
T |
A |
11: 114,903,384 (GRCm39) |
|
probably benign |
Het |
Cd55b |
A |
T |
1: 130,345,919 (GRCm39) |
D166E |
probably benign |
Het |
Cfap100 |
A |
G |
6: 90,390,954 (GRCm39) |
F8L |
probably damaging |
Het |
Col2a1 |
C |
T |
15: 97,884,618 (GRCm39) |
|
probably null |
Het |
Dbf4 |
A |
G |
5: 8,453,189 (GRCm39) |
I270T |
probably benign |
Het |
Dkk3 |
T |
C |
7: 111,748,236 (GRCm39) |
S123G |
probably benign |
Het |
Ep400 |
A |
G |
5: 110,824,809 (GRCm39) |
|
probably benign |
Het |
Fam184a |
A |
G |
10: 53,575,351 (GRCm39) |
I30T |
probably damaging |
Het |
Fam20a |
T |
C |
11: 109,564,239 (GRCm39) |
I505V |
probably benign |
Het |
Fbh1 |
T |
C |
2: 11,768,938 (GRCm39) |
D285G |
probably benign |
Het |
Fcho1 |
T |
C |
8: 72,169,444 (GRCm39) |
E154G |
probably damaging |
Het |
Knl1 |
A |
T |
2: 118,931,255 (GRCm39) |
E1990D |
probably benign |
Het |
Lancl2 |
A |
G |
6: 57,711,024 (GRCm39) |
Y394C |
probably damaging |
Het |
Lgi2 |
G |
A |
5: 52,723,299 (GRCm39) |
S50F |
probably damaging |
Het |
Map2k7 |
A |
G |
8: 4,288,950 (GRCm39) |
E14G |
probably damaging |
Het |
Mga |
A |
G |
2: 119,754,517 (GRCm39) |
I1009V |
probably damaging |
Het |
Nat9 |
C |
A |
11: 115,074,234 (GRCm39) |
|
probably null |
Het |
Nek2 |
G |
A |
1: 191,563,401 (GRCm39) |
A422T |
probably benign |
Het |
Nfkbiz |
A |
T |
16: 55,636,034 (GRCm39) |
L509Q |
probably damaging |
Het |
Or56b2 |
A |
T |
7: 104,337,634 (GRCm39) |
R137S |
probably benign |
Het |
Pgap1 |
T |
A |
1: 54,587,147 (GRCm39) |
Q143L |
probably damaging |
Het |
Pkd1l3 |
C |
T |
8: 110,392,217 (GRCm39) |
T1937I |
probably damaging |
Het |
Pou1f1 |
A |
G |
16: 65,326,784 (GRCm39) |
E128G |
probably damaging |
Het |
Ppfia3 |
T |
C |
7: 44,989,996 (GRCm39) |
|
probably benign |
Het |
Prkd1 |
T |
C |
12: 50,434,046 (GRCm39) |
I566V |
probably benign |
Het |
Psd2 |
A |
G |
18: 36,138,959 (GRCm39) |
R528G |
probably damaging |
Het |
Ptprg |
G |
T |
14: 12,110,080 (GRCm38) |
E263* |
probably null |
Het |
Radil |
T |
C |
5: 142,529,576 (GRCm39) |
D40G |
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,750,442 (GRCm39) |
Y1943F |
probably damaging |
Het |
Slc30a4 |
C |
T |
2: 122,543,947 (GRCm39) |
|
probably benign |
Het |
Slc31a1 |
A |
T |
4: 62,306,241 (GRCm39) |
T120S |
possibly damaging |
Het |
Snrpe |
A |
G |
1: 133,537,487 (GRCm39) |
|
probably benign |
Het |
Stx3 |
G |
T |
19: 11,796,046 (GRCm39) |
|
probably benign |
Het |
Thoc2l |
A |
G |
5: 104,666,867 (GRCm39) |
E463G |
possibly damaging |
Het |
Ufsp1 |
T |
A |
5: 137,293,178 (GRCm39) |
C43S |
probably damaging |
Het |
Vac14 |
T |
A |
8: 111,379,950 (GRCm39) |
M416K |
possibly damaging |
Het |
Vmn1r81 |
A |
C |
7: 11,993,792 (GRCm39) |
V272G |
possibly damaging |
Het |
Vmn2r107 |
T |
A |
17: 20,578,062 (GRCm39) |
I457K |
probably benign |
Het |
Vmn2r72 |
A |
T |
7: 85,387,374 (GRCm39) |
V730E |
probably benign |
Het |
Vmn2r9 |
T |
C |
5: 108,995,433 (GRCm39) |
Y405C |
probably damaging |
Het |
Zcchc17 |
T |
C |
4: 130,210,440 (GRCm39) |
*242W |
probably null |
Het |
Zfp503 |
T |
C |
14: 22,037,354 (GRCm39) |
K83R |
possibly damaging |
Het |
|
Other mutations in Klhdc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00157:Klhdc1
|
APN |
12 |
69,288,782 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01432:Klhdc1
|
APN |
12 |
69,298,751 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02212:Klhdc1
|
APN |
12 |
69,297,540 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02548:Klhdc1
|
APN |
12 |
69,300,492 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02861:Klhdc1
|
APN |
12 |
69,298,225 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0446:Klhdc1
|
UTSW |
12 |
69,330,082 (GRCm39) |
missense |
probably benign |
|
R0656:Klhdc1
|
UTSW |
12 |
69,304,804 (GRCm39) |
missense |
probably benign |
|
R1528:Klhdc1
|
UTSW |
12 |
69,309,972 (GRCm39) |
missense |
probably benign |
0.02 |
R3001:Klhdc1
|
UTSW |
12 |
69,302,983 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3002:Klhdc1
|
UTSW |
12 |
69,302,983 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4428:Klhdc1
|
UTSW |
12 |
69,315,000 (GRCm39) |
intron |
probably benign |
|
R4738:Klhdc1
|
UTSW |
12 |
69,329,907 (GRCm39) |
missense |
probably benign |
0.07 |
R5009:Klhdc1
|
UTSW |
12 |
69,298,712 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5366:Klhdc1
|
UTSW |
12 |
69,329,924 (GRCm39) |
missense |
probably damaging |
0.99 |
R5619:Klhdc1
|
UTSW |
12 |
69,304,919 (GRCm39) |
splice site |
probably null |
|
R5662:Klhdc1
|
UTSW |
12 |
69,329,939 (GRCm39) |
missense |
probably benign |
0.07 |
R5911:Klhdc1
|
UTSW |
12 |
69,303,025 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5995:Klhdc1
|
UTSW |
12 |
69,297,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R6708:Klhdc1
|
UTSW |
12 |
69,306,304 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6992:Klhdc1
|
UTSW |
12 |
69,300,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R7224:Klhdc1
|
UTSW |
12 |
69,309,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R7597:Klhdc1
|
UTSW |
12 |
69,316,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R7833:Klhdc1
|
UTSW |
12 |
69,329,942 (GRCm39) |
missense |
probably benign |
0.12 |
R8826:Klhdc1
|
UTSW |
12 |
69,305,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R8828:Klhdc1
|
UTSW |
12 |
69,298,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R8880:Klhdc1
|
UTSW |
12 |
69,298,817 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8939:Klhdc1
|
UTSW |
12 |
69,300,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R9091:Klhdc1
|
UTSW |
12 |
69,309,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R9114:Klhdc1
|
UTSW |
12 |
69,288,783 (GRCm39) |
missense |
probably damaging |
0.99 |
R9270:Klhdc1
|
UTSW |
12 |
69,309,968 (GRCm39) |
missense |
probably damaging |
1.00 |
|