Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
G |
A |
11: 9,224,735 (GRCm39) |
G483R |
probably benign |
Het |
Abca9 |
T |
C |
11: 110,029,155 (GRCm39) |
D801G |
probably benign |
Het |
Aldob |
T |
C |
4: 49,538,822 (GRCm39) |
N232S |
probably damaging |
Het |
Ankhd1 |
T |
C |
18: 36,787,230 (GRCm39) |
V322A |
|
Het |
Arfgef1 |
T |
C |
1: 10,243,478 (GRCm39) |
K1024E |
probably damaging |
Het |
Arhgef40 |
T |
A |
14: 52,226,226 (GRCm39) |
V90E |
probably damaging |
Het |
Cblc |
A |
T |
7: 19,519,262 (GRCm39) |
S399R |
possibly damaging |
Het |
Ccdc17 |
T |
A |
4: 116,456,211 (GRCm39) |
I368K |
possibly damaging |
Het |
Ccdc17 |
T |
A |
4: 116,456,213 (GRCm39) |
W369R |
probably damaging |
Het |
Cd276 |
G |
A |
9: 58,444,755 (GRCm39) |
T72I |
probably damaging |
Het |
Cdk14 |
C |
T |
5: 5,277,159 (GRCm39) |
|
probably null |
Het |
Cfap61 |
C |
T |
2: 145,789,095 (GRCm39) |
S33L |
probably benign |
Het |
Cmtm2a |
A |
G |
8: 105,019,670 (GRCm39) |
F7L |
probably benign |
Het |
Eif2ak4 |
T |
C |
2: 118,280,819 (GRCm39) |
I1062T |
possibly damaging |
Het |
Fcnb |
C |
T |
2: 27,968,330 (GRCm39) |
S209N |
possibly damaging |
Het |
Fxr1 |
A |
T |
3: 34,101,878 (GRCm39) |
E204V |
probably damaging |
Het |
Fzd6 |
T |
A |
15: 38,894,959 (GRCm39) |
L375Q |
probably damaging |
Het |
Ggta1 |
T |
A |
2: 35,312,279 (GRCm39) |
E33V |
probably damaging |
Het |
Gnb1l |
T |
A |
16: 18,362,965 (GRCm39) |
I119N |
probably benign |
Het |
Gpsm1 |
A |
G |
2: 26,214,929 (GRCm39) |
|
probably null |
Het |
Hecw1 |
A |
G |
13: 14,480,692 (GRCm39) |
I885T |
probably damaging |
Het |
Itgb8 |
T |
C |
12: 119,131,905 (GRCm39) |
D580G |
probably damaging |
Het |
Kbtbd12 |
T |
A |
6: 88,594,913 (GRCm39) |
T306S |
possibly damaging |
Het |
Lrrc36 |
A |
G |
8: 106,178,717 (GRCm39) |
D304G |
possibly damaging |
Het |
Lrrn2 |
A |
G |
1: 132,865,082 (GRCm39) |
E49G |
probably damaging |
Het |
Lysmd2 |
C |
A |
9: 75,533,310 (GRCm39) |
Y88* |
probably null |
Het |
Lzts3 |
A |
G |
2: 130,477,105 (GRCm39) |
S448P |
probably benign |
Het |
Meioc |
T |
A |
11: 102,565,893 (GRCm39) |
L447* |
probably null |
Het |
Mybpc1 |
A |
G |
10: 88,394,553 (GRCm39) |
I244T |
possibly damaging |
Het |
Necab3 |
G |
A |
2: 154,389,363 (GRCm39) |
A160V |
probably benign |
Het |
Nek8 |
G |
T |
11: 78,061,587 (GRCm39) |
P314Q |
possibly damaging |
Het |
Nlrp5 |
A |
G |
7: 23,112,762 (GRCm39) |
T140A |
probably benign |
Het |
Or10p21 |
T |
C |
10: 128,847,444 (GRCm39) |
C97R |
probably damaging |
Het |
Or52ac1 |
A |
T |
7: 104,246,133 (GRCm39) |
F85Y |
probably damaging |
Het |
Or7e169 |
A |
T |
9: 19,757,780 (GRCm39) |
I45N |
probably damaging |
Het |
Or8b54 |
G |
A |
9: 38,686,577 (GRCm39) |
V9M |
noncoding transcript |
Het |
Pgm3 |
G |
A |
9: 86,452,374 (GRCm39) |
R29W |
probably damaging |
Het |
Ppp2r3d |
A |
G |
9: 101,090,231 (GRCm39) |
C31R |
probably damaging |
Het |
Prom1 |
C |
T |
5: 44,194,770 (GRCm39) |
S334N |
possibly damaging |
Het |
Rai14 |
C |
T |
15: 10,575,302 (GRCm39) |
S581N |
probably benign |
Het |
Rbm46 |
C |
T |
3: 82,772,775 (GRCm39) |
R119Q |
probably benign |
Het |
Rgs16 |
T |
C |
1: 153,616,689 (GRCm39) |
F42S |
probably benign |
Het |
Slc2a6 |
T |
G |
2: 26,917,838 (GRCm39) |
E27A |
probably benign |
Het |
Slc38a1 |
G |
A |
15: 96,490,447 (GRCm39) |
S110L |
probably benign |
Het |
Sox30 |
C |
T |
11: 45,882,592 (GRCm39) |
R541C |
probably benign |
Het |
Sptbn4 |
C |
A |
7: 27,108,314 (GRCm39) |
E703* |
probably null |
Het |
Tjp1 |
A |
T |
7: 64,993,470 (GRCm39) |
F34L |
probably damaging |
Het |
Trim65 |
T |
C |
11: 116,017,037 (GRCm39) |
Q475R |
probably benign |
Het |
Ttc38 |
A |
T |
15: 85,728,716 (GRCm39) |
R223* |
probably null |
Het |
Tulp1 |
T |
C |
17: 28,583,300 (GRCm39) |
Q80R |
probably benign |
Het |
Utp23 |
T |
C |
15: 51,745,598 (GRCm39) |
F139L |
possibly damaging |
Het |
Vmn1r121 |
A |
T |
7: 20,832,228 (GRCm39) |
F71I |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Zdbf2 |
T |
C |
1: 63,343,225 (GRCm39) |
S535P |
possibly damaging |
Het |
Zfp788 |
T |
G |
7: 41,298,801 (GRCm39) |
M479R |
probably benign |
Het |
|
Other mutations in Kctd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01318:Kctd1
|
APN |
18 |
15,195,747 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL01402:Kctd1
|
APN |
18 |
15,102,610 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01404:Kctd1
|
APN |
18 |
15,102,610 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01755:Kctd1
|
APN |
18 |
15,195,694 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02606:Kctd1
|
APN |
18 |
15,195,937 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02725:Kctd1
|
APN |
18 |
15,102,667 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02946:Kctd1
|
APN |
18 |
15,107,036 (GRCm39) |
critical splice donor site |
probably null |
|
R0128:Kctd1
|
UTSW |
18 |
15,107,237 (GRCm39) |
missense |
probably benign |
0.00 |
R0598:Kctd1
|
UTSW |
18 |
15,140,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R1398:Kctd1
|
UTSW |
18 |
15,195,654 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1669:Kctd1
|
UTSW |
18 |
15,195,517 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1701:Kctd1
|
UTSW |
18 |
15,102,617 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1745:Kctd1
|
UTSW |
18 |
15,196,263 (GRCm39) |
intron |
probably benign |
|
R1779:Kctd1
|
UTSW |
18 |
15,194,839 (GRCm39) |
missense |
probably benign |
0.01 |
R2083:Kctd1
|
UTSW |
18 |
15,107,112 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2389:Kctd1
|
UTSW |
18 |
15,195,268 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3010:Kctd1
|
UTSW |
18 |
15,107,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R4576:Kctd1
|
UTSW |
18 |
15,140,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R4673:Kctd1
|
UTSW |
18 |
15,196,284 (GRCm39) |
intron |
probably benign |
|
R4884:Kctd1
|
UTSW |
18 |
15,107,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R4961:Kctd1
|
UTSW |
18 |
15,195,580 (GRCm39) |
missense |
probably damaging |
0.97 |
R5169:Kctd1
|
UTSW |
18 |
15,195,822 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5398:Kctd1
|
UTSW |
18 |
15,195,322 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5695:Kctd1
|
UTSW |
18 |
15,196,573 (GRCm39) |
intron |
probably benign |
|
R5893:Kctd1
|
UTSW |
18 |
15,102,745 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6175:Kctd1
|
UTSW |
18 |
15,102,688 (GRCm39) |
nonsense |
probably null |
|
R6767:Kctd1
|
UTSW |
18 |
15,195,232 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6852:Kctd1
|
UTSW |
18 |
15,119,401 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6889:Kctd1
|
UTSW |
18 |
15,107,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R7189:Kctd1
|
UTSW |
18 |
15,195,700 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7228:Kctd1
|
UTSW |
18 |
15,195,469 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7688:Kctd1
|
UTSW |
18 |
15,107,255 (GRCm39) |
missense |
probably benign |
0.03 |
R8085:Kctd1
|
UTSW |
18 |
15,140,901 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8496:Kctd1
|
UTSW |
18 |
15,107,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R8924:Kctd1
|
UTSW |
18 |
15,102,745 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8978:Kctd1
|
UTSW |
18 |
15,119,491 (GRCm39) |
missense |
|
|
R9094:Kctd1
|
UTSW |
18 |
15,195,369 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9255:Kctd1
|
UTSW |
18 |
15,194,853 (GRCm39) |
missense |
probably benign |
0.00 |
R9629:Kctd1
|
UTSW |
18 |
15,196,611 (GRCm39) |
missense |
unknown |
|
R9680:Kctd1
|
UTSW |
18 |
15,140,822 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Kctd1
|
UTSW |
18 |
15,196,182 (GRCm39) |
missense |
unknown |
|
|