Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930533K18Rik |
T |
A |
10: 70,704,630 (GRCm39) |
|
noncoding transcript |
Het |
Alox5 |
A |
G |
6: 116,400,291 (GRCm39) |
|
probably benign |
Het |
Anxa11 |
T |
A |
14: 25,874,421 (GRCm39) |
D203E |
probably damaging |
Het |
Atp12a |
A |
T |
14: 56,611,938 (GRCm39) |
N371Y |
probably damaging |
Het |
Bloc1s6 |
A |
G |
2: 122,584,543 (GRCm39) |
I39M |
probably benign |
Het |
Celsr3 |
A |
C |
9: 108,711,854 (GRCm39) |
I1688L |
possibly damaging |
Het |
Cgn |
T |
C |
3: 94,682,204 (GRCm39) |
|
probably benign |
Het |
Chd4 |
A |
T |
6: 125,079,930 (GRCm39) |
I453F |
probably damaging |
Het |
Dbnl |
A |
G |
11: 5,747,321 (GRCm39) |
T247A |
probably benign |
Het |
Dpysl3 |
T |
C |
18: 43,571,136 (GRCm39) |
E46G |
possibly damaging |
Het |
Dsg1a |
T |
C |
18: 20,468,949 (GRCm39) |
|
probably benign |
Het |
Fbp1 |
C |
T |
13: 63,019,099 (GRCm39) |
E150K |
probably benign |
Het |
Flnb |
T |
A |
14: 7,927,352 (GRCm38) |
L1854Q |
probably damaging |
Het |
Gcn1 |
C |
T |
5: 115,727,362 (GRCm39) |
T714M |
probably benign |
Het |
Gm12216 |
A |
T |
11: 53,704,162 (GRCm39) |
|
probably benign |
Het |
Gpr82 |
T |
C |
X: 13,531,829 (GRCm39) |
S126P |
probably benign |
Het |
Hmbs |
T |
A |
9: 44,248,657 (GRCm39) |
H256L |
probably benign |
Het |
Ibsp |
A |
T |
5: 104,457,886 (GRCm39) |
|
probably null |
Het |
Ints13 |
A |
G |
6: 146,453,959 (GRCm39) |
V240A |
probably benign |
Het |
Iqca1l |
C |
T |
5: 24,754,760 (GRCm39) |
V337M |
possibly damaging |
Het |
Kalrn |
T |
C |
16: 33,852,837 (GRCm39) |
D343G |
probably damaging |
Het |
Kin |
T |
C |
2: 10,090,531 (GRCm39) |
|
probably benign |
Het |
Lpar3 |
T |
A |
3: 145,946,426 (GRCm39) |
C35S |
possibly damaging |
Het |
Lrrtm4 |
A |
G |
6: 79,998,953 (GRCm39) |
I122V |
possibly damaging |
Het |
Mfsd13a |
C |
T |
19: 46,354,943 (GRCm39) |
T40I |
probably benign |
Het |
Mgat4c |
T |
C |
10: 102,224,452 (GRCm39) |
M222T |
probably damaging |
Het |
Muc4 |
C |
A |
16: 32,570,488 (GRCm39) |
S516Y |
possibly damaging |
Het |
Myo1e |
A |
T |
9: 70,274,956 (GRCm39) |
Q703L |
probably damaging |
Het |
Neb |
A |
G |
2: 52,115,570 (GRCm39) |
|
probably benign |
Het |
Necab3 |
T |
G |
2: 154,388,223 (GRCm39) |
E239A |
probably null |
Het |
Npr1 |
G |
T |
3: 90,368,676 (GRCm39) |
N461K |
probably benign |
Het |
Or4k44 |
T |
C |
2: 111,367,972 (GRCm39) |
I221V |
probably damaging |
Het |
Pcdhb2 |
A |
G |
18: 37,428,543 (GRCm39) |
Y172C |
probably damaging |
Het |
Pcdhb7 |
A |
G |
18: 37,474,954 (GRCm39) |
D30G |
probably benign |
Het |
Phf12 |
A |
C |
11: 77,920,158 (GRCm39) |
Q898P |
probably benign |
Het |
Plekhn1 |
T |
C |
4: 156,309,821 (GRCm39) |
E132G |
possibly damaging |
Het |
Ptpn3 |
A |
G |
4: 57,270,075 (GRCm39) |
V29A |
probably benign |
Het |
Rundc3b |
T |
A |
5: 8,619,529 (GRCm39) |
I143F |
probably damaging |
Het |
Ryr3 |
T |
G |
2: 112,478,651 (GRCm39) |
|
probably benign |
Het |
Sash1 |
A |
G |
10: 8,626,901 (GRCm39) |
|
probably null |
Het |
Slc4a2 |
A |
G |
5: 24,636,257 (GRCm39) |
D201G |
probably benign |
Het |
Tecpr1 |
T |
A |
5: 144,150,871 (GRCm39) |
|
probably null |
Het |
Timm21 |
T |
C |
18: 84,967,326 (GRCm39) |
H150R |
probably damaging |
Het |
Tmem79 |
T |
C |
3: 88,240,241 (GRCm39) |
T236A |
probably damaging |
Het |
Usp34 |
G |
T |
11: 23,422,967 (GRCm39) |
V3095F |
probably damaging |
Het |
Vmn1r8 |
A |
T |
6: 57,013,573 (GRCm39) |
Q208L |
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 |
|
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 |
|