Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921539E11Rik |
C |
T |
4: 103,099,990 (GRCm39) |
S171N |
possibly damaging |
Het |
6030468B19Rik |
T |
G |
11: 117,688,594 (GRCm39) |
M1R |
probably null |
Het |
A730049H05Rik |
T |
C |
6: 92,804,975 (GRCm39) |
|
probably benign |
Het |
AC125199.3 |
G |
T |
16: 88,608,915 (GRCm39) |
H52Q |
possibly damaging |
Het |
Adam34 |
A |
T |
8: 44,105,642 (GRCm39) |
M1K |
probably null |
Het |
Adgrf5 |
T |
C |
17: 43,763,214 (GRCm39) |
|
probably null |
Het |
Antxr2 |
T |
C |
5: 98,108,564 (GRCm39) |
T316A |
probably benign |
Het |
Cc2d1a |
A |
T |
8: 84,861,542 (GRCm39) |
V714D |
probably damaging |
Het |
Cd96 |
A |
G |
16: 45,870,087 (GRCm39) |
S461P |
possibly damaging |
Het |
Cdc16 |
C |
A |
8: 13,809,188 (GRCm39) |
A51E |
probably benign |
Het |
Chd4 |
T |
A |
6: 125,091,339 (GRCm39) |
D1243E |
probably benign |
Het |
Cntf |
A |
T |
19: 12,742,697 (GRCm39) |
I21N |
probably damaging |
Het |
Col11a2 |
C |
T |
17: 34,266,118 (GRCm39) |
A282V |
probably benign |
Het |
Col14a1 |
T |
A |
15: 55,274,958 (GRCm39) |
|
probably null |
Het |
Cyp2b9 |
T |
C |
7: 25,900,564 (GRCm39) |
Y401H |
probably benign |
Het |
Dlgap4 |
A |
G |
2: 156,590,860 (GRCm39) |
|
probably null |
Het |
Fancd2 |
T |
C |
6: 113,547,979 (GRCm39) |
|
probably null |
Het |
Fcgbpl1 |
T |
A |
7: 27,839,608 (GRCm39) |
F474I |
probably benign |
Het |
Frem1 |
A |
G |
4: 82,858,599 (GRCm39) |
V1622A |
possibly damaging |
Het |
Golm1 |
ACTTCTTCT |
ACTTCT |
13: 59,797,390 (GRCm39) |
|
probably benign |
Het |
Gstm4 |
A |
G |
3: 107,951,981 (GRCm39) |
M3T |
possibly damaging |
Het |
Hdac10 |
T |
C |
15: 89,009,534 (GRCm39) |
D466G |
probably benign |
Het |
Hook2 |
A |
G |
8: 85,729,185 (GRCm39) |
E625G |
probably damaging |
Het |
Hspbp1 |
G |
C |
7: 4,667,714 (GRCm39) |
P260A |
probably benign |
Het |
Igdcc3 |
C |
A |
9: 65,088,853 (GRCm39) |
Q411K |
probably damaging |
Het |
Il18rap |
G |
A |
1: 40,581,195 (GRCm39) |
E356K |
probably benign |
Het |
Inpp4a |
A |
T |
1: 37,428,772 (GRCm39) |
M699L |
probably damaging |
Het |
Klhl6 |
G |
T |
16: 19,772,337 (GRCm39) |
T336N |
probably damaging |
Het |
Marchf7 |
T |
C |
2: 60,059,428 (GRCm39) |
|
probably null |
Het |
Mast4 |
C |
T |
13: 102,941,155 (GRCm39) |
V301I |
probably damaging |
Het |
Mlh3 |
T |
A |
12: 85,282,494 (GRCm39) |
N1412Y |
probably damaging |
Het |
Mrps27 |
A |
G |
13: 99,541,522 (GRCm39) |
M209V |
probably benign |
Het |
Mtor |
A |
T |
4: 148,548,932 (GRCm39) |
T572S |
probably benign |
Het |
Neurog1 |
T |
C |
13: 56,399,363 (GRCm39) |
K128R |
probably damaging |
Het |
Or10g6 |
T |
A |
9: 39,933,896 (GRCm39) |
L69* |
probably null |
Het |
Or2b4 |
T |
A |
17: 38,116,754 (GRCm39) |
N239K |
probably damaging |
Het |
Or5b122 |
A |
G |
19: 13,562,811 (GRCm39) |
I48V |
possibly damaging |
Het |
Pcdhgb1 |
A |
G |
18: 37,814,652 (GRCm39) |
K381R |
probably benign |
Het |
Pdzd2 |
T |
C |
15: 12,457,945 (GRCm39) |
D306G |
probably damaging |
Het |
Plekha5 |
C |
T |
6: 140,489,634 (GRCm39) |
T237I |
probably damaging |
Het |
Plscr1l1 |
T |
C |
9: 92,236,725 (GRCm39) |
M128T |
probably benign |
Het |
Pole |
A |
T |
5: 110,480,365 (GRCm39) |
I103F |
probably damaging |
Het |
Ppfia2 |
A |
T |
10: 106,310,715 (GRCm39) |
Q74L |
possibly damaging |
Het |
Ppm1d |
T |
C |
11: 85,223,178 (GRCm39) |
F261S |
probably damaging |
Het |
Psg21 |
A |
T |
7: 18,388,668 (GRCm39) |
|
probably null |
Het |
Ptprg |
T |
A |
14: 11,962,602 (GRCm38) |
F133L |
probably damaging |
Het |
Rom1 |
G |
A |
19: 8,906,569 (GRCm39) |
|
probably benign |
Het |
Rtn3 |
A |
G |
19: 7,412,489 (GRCm39) |
F762L |
probably damaging |
Het |
Sec23ip |
T |
C |
7: 128,367,164 (GRCm39) |
S600P |
probably benign |
Het |
Sema4b |
T |
A |
7: 79,869,900 (GRCm39) |
I396N |
probably damaging |
Het |
Serpina3k |
T |
A |
12: 104,307,366 (GRCm39) |
D199E |
probably benign |
Het |
Slc19a1 |
A |
G |
10: 76,885,540 (GRCm39) |
D480G |
possibly damaging |
Het |
Slc8b1 |
G |
A |
5: 120,665,880 (GRCm39) |
V404M |
probably damaging |
Het |
Slco1a4 |
T |
C |
6: 141,765,330 (GRCm39) |
D304G |
probably benign |
Het |
Smpdl3b |
G |
T |
4: 132,472,452 (GRCm39) |
A107D |
possibly damaging |
Het |
Tesk1 |
A |
G |
4: 43,447,006 (GRCm39) |
T465A |
probably benign |
Het |
Tmem245 |
A |
G |
4: 56,937,940 (GRCm39) |
F203L |
probably benign |
Het |
Tnip1 |
T |
A |
11: 54,809,542 (GRCm39) |
I442F |
probably benign |
Het |
Txnip |
A |
G |
3: 96,466,439 (GRCm39) |
K127R |
possibly damaging |
Het |
Usp32 |
A |
C |
11: 84,922,914 (GRCm39) |
L172R |
probably damaging |
Het |
Vmn2r66 |
A |
G |
7: 84,654,436 (GRCm39) |
S508P |
possibly damaging |
Het |
Vwa5b2 |
T |
A |
16: 20,416,952 (GRCm39) |
Y550N |
probably damaging |
Het |
Wdr81 |
G |
A |
11: 75,342,612 (GRCm39) |
A885V |
probably benign |
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 |
IGL02086:Klhdc1
|
APN |
12 |
69,329,958 (GRCm39) |
missense |
probably benign |
0.18 |
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 |
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 |
|