Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
A |
T |
16: 4,653,837 (GRCm39) |
K129* |
probably null |
Het |
Adamts6 |
A |
T |
13: 104,443,751 (GRCm39) |
D162V |
probably damaging |
Het |
Alms1 |
C |
A |
6: 85,597,714 (GRCm39) |
P1316T |
possibly damaging |
Het |
AU040320 |
A |
T |
4: 126,722,664 (GRCm39) |
N394I |
possibly damaging |
Het |
Cacng8 |
T |
C |
7: 3,464,096 (GRCm39) |
L416P |
possibly damaging |
Het |
Ccdc136 |
T |
A |
6: 29,419,313 (GRCm39) |
N944K |
probably damaging |
Het |
Clcn1 |
C |
T |
6: 42,290,814 (GRCm39) |
T896I |
probably benign |
Het |
Col16a1 |
A |
T |
4: 129,947,964 (GRCm39) |
Y228F |
probably damaging |
Het |
Cyfip1 |
A |
G |
7: 55,548,083 (GRCm39) |
D561G |
probably benign |
Het |
Ddr1 |
T |
A |
17: 35,993,667 (GRCm39) |
|
probably null |
Het |
Dedd2 |
A |
T |
7: 24,918,411 (GRCm39) |
L48Q |
probably damaging |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Het |
Dph3b-ps |
A |
G |
13: 106,683,558 (GRCm39) |
|
noncoding transcript |
Het |
Dppa3 |
T |
C |
6: 122,606,891 (GRCm39) |
F127S |
probably damaging |
Het |
Dpy19l4 |
C |
T |
4: 11,265,943 (GRCm39) |
|
probably null |
Het |
Flrt3 |
T |
C |
2: 140,502,177 (GRCm39) |
T484A |
probably damaging |
Het |
Gldc |
T |
C |
19: 30,128,936 (GRCm39) |
E179G |
probably damaging |
Het |
Gm6421 |
G |
A |
13: 117,494,969 (GRCm39) |
|
noncoding transcript |
Het |
Grk5 |
T |
C |
19: 61,065,122 (GRCm39) |
V262A |
probably damaging |
Het |
Grp |
A |
G |
18: 66,013,230 (GRCm39) |
Q132R |
probably benign |
Het |
Hap1 |
A |
G |
11: 100,246,537 (GRCm39) |
F123L |
probably damaging |
Het |
Hrc |
A |
G |
7: 44,986,445 (GRCm39) |
D532G |
probably damaging |
Het |
Igsf9b |
C |
A |
9: 27,228,733 (GRCm39) |
F164L |
probably benign |
Het |
Irag1 |
G |
T |
7: 110,470,700 (GRCm39) |
L672I |
probably damaging |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Kansl1 |
C |
T |
11: 104,315,168 (GRCm39) |
R290Q |
probably damaging |
Het |
Kifc2 |
T |
A |
15: 76,545,496 (GRCm39) |
L81Q |
probably damaging |
Het |
Klrc3 |
T |
C |
6: 129,616,538 (GRCm39) |
R160G |
probably damaging |
Het |
Mal |
A |
G |
2: 127,482,193 (GRCm39) |
M70T |
probably benign |
Het |
Mep1a |
T |
G |
17: 43,789,035 (GRCm39) |
R580S |
probably damaging |
Het |
Methig1 |
A |
T |
15: 100,251,130 (GRCm39) |
I14F |
probably damaging |
Het |
Mtf1 |
T |
C |
4: 124,715,101 (GRCm39) |
L242P |
probably damaging |
Het |
Nfkb1 |
C |
A |
3: 135,309,568 (GRCm39) |
A509S |
probably benign |
Het |
Or2h2b-ps1 |
C |
G |
17: 37,480,858 (GRCm39) |
S227T |
probably benign |
Het |
Or2n1b |
G |
A |
17: 38,460,003 (GRCm39) |
D175N |
probably damaging |
Het |
Or5ac24 |
A |
T |
16: 59,165,449 (GRCm39) |
I205K |
probably damaging |
Het |
Or7a36 |
G |
T |
10: 78,819,928 (GRCm39) |
M101I |
probably benign |
Het |
Or8k23 |
A |
T |
2: 86,186,318 (GRCm39) |
M136K |
probably damaging |
Het |
Pabpc2 |
A |
T |
18: 39,907,635 (GRCm39) |
N300I |
probably damaging |
Het |
Peg10 |
C |
T |
6: 4,755,864 (GRCm39) |
|
probably benign |
Het |
Ppp1r3a |
T |
A |
6: 14,719,603 (GRCm39) |
D437V |
probably damaging |
Het |
Prickle1 |
A |
G |
15: 93,398,783 (GRCm39) |
S682P |
probably damaging |
Het |
Prkab2 |
T |
C |
3: 97,580,308 (GRCm39) |
|
probably benign |
Het |
Pus3 |
T |
A |
9: 35,476,932 (GRCm39) |
L243Q |
possibly damaging |
Het |
Relch |
A |
G |
1: 105,605,905 (GRCm39) |
S182G |
probably damaging |
Het |
Rgs19 |
G |
A |
2: 181,331,336 (GRCm39) |
T99M |
possibly damaging |
Het |
Ripk2 |
A |
G |
4: 16,127,663 (GRCm39) |
S360P |
possibly damaging |
Het |
Rock1 |
A |
G |
18: 10,140,210 (GRCm39) |
I127T |
probably damaging |
Het |
Serpinb10 |
T |
G |
1: 107,469,947 (GRCm39) |
M143R |
probably damaging |
Het |
Sipa1l3 |
G |
A |
7: 29,048,000 (GRCm39) |
S247F |
probably damaging |
Het |
Skint6 |
T |
A |
4: 113,093,465 (GRCm39) |
Q226L |
probably damaging |
Het |
Slc6a19 |
T |
C |
13: 73,839,872 (GRCm39) |
M137V |
probably benign |
Het |
Supv3l1 |
A |
T |
10: 62,271,291 (GRCm39) |
N415K |
probably benign |
Het |
Tekt4 |
A |
G |
17: 25,692,749 (GRCm39) |
R192G |
probably damaging |
Het |
Trgv7 |
A |
T |
13: 19,362,598 (GRCm39) |
K96* |
probably null |
Het |
Tshz1 |
T |
C |
18: 84,032,053 (GRCm39) |
N785S |
probably benign |
Het |
Usb1 |
A |
G |
8: 96,070,679 (GRCm39) |
T202A |
probably damaging |
Het |
Utp18 |
A |
T |
11: 93,761,363 (GRCm39) |
D348E |
possibly damaging |
Het |
Vmn1r42 |
T |
G |
6: 89,821,598 (GRCm39) |
I324L |
probably benign |
Het |
Wnt8a |
A |
T |
18: 34,678,656 (GRCm39) |
R157* |
probably null |
Het |
Ypel1 |
A |
G |
16: 16,902,472 (GRCm39) |
|
probably null |
Het |
Zfp235 |
A |
G |
7: 23,836,546 (GRCm39) |
K31E |
probably damaging |
Het |
Zhx2 |
G |
C |
15: 57,686,089 (GRCm39) |
W486S |
probably damaging |
Het |
|
Other mutations in Gm14403 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01835:Gm14403
|
APN |
2 |
177,199,049 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02660:Gm14403
|
APN |
2 |
177,201,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R0492:Gm14403
|
UTSW |
2 |
177,200,359 (GRCm39) |
missense |
probably benign |
0.09 |
R0932:Gm14403
|
UTSW |
2 |
177,198,810 (GRCm39) |
missense |
probably benign |
0.01 |
R0975:Gm14403
|
UTSW |
2 |
177,201,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Gm14403
|
UTSW |
2 |
177,199,024 (GRCm39) |
splice site |
probably benign |
|
R1853:Gm14403
|
UTSW |
2 |
177,200,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R3011:Gm14403
|
UTSW |
2 |
177,200,786 (GRCm39) |
missense |
probably benign |
|
R3803:Gm14403
|
UTSW |
2 |
177,200,569 (GRCm39) |
missense |
probably benign |
0.04 |
R4589:Gm14403
|
UTSW |
2 |
177,200,428 (GRCm39) |
missense |
probably benign |
0.29 |
R4805:Gm14403
|
UTSW |
2 |
177,200,492 (GRCm39) |
missense |
probably damaging |
0.97 |
R5311:Gm14403
|
UTSW |
2 |
177,201,448 (GRCm39) |
unclassified |
probably benign |
|
R5425:Gm14403
|
UTSW |
2 |
177,201,448 (GRCm39) |
unclassified |
probably benign |
|
R5643:Gm14403
|
UTSW |
2 |
177,199,054 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5644:Gm14403
|
UTSW |
2 |
177,199,054 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5739:Gm14403
|
UTSW |
2 |
177,201,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R5982:Gm14403
|
UTSW |
2 |
177,200,345 (GRCm39) |
missense |
probably damaging |
0.98 |
R6197:Gm14403
|
UTSW |
2 |
177,201,448 (GRCm39) |
unclassified |
probably benign |
|
R6198:Gm14403
|
UTSW |
2 |
177,201,448 (GRCm39) |
unclassified |
probably benign |
|
R6892:Gm14403
|
UTSW |
2 |
177,201,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R7090:Gm14403
|
UTSW |
2 |
177,201,114 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7168:Gm14403
|
UTSW |
2 |
177,201,318 (GRCm39) |
missense |
probably damaging |
0.96 |
R7510:Gm14403
|
UTSW |
2 |
177,200,403 (GRCm39) |
missense |
probably benign |
0.01 |
R7623:Gm14403
|
UTSW |
2 |
177,200,405 (GRCm39) |
missense |
probably benign |
|
R8049:Gm14403
|
UTSW |
2 |
177,200,311 (GRCm39) |
missense |
probably benign |
0.00 |
R8557:Gm14403
|
UTSW |
2 |
177,201,354 (GRCm39) |
missense |
probably damaging |
0.99 |
R9224:Gm14403
|
UTSW |
2 |
177,200,336 (GRCm39) |
missense |
probably benign |
|
R9333:Gm14403
|
UTSW |
2 |
177,200,919 (GRCm39) |
missense |
probably benign |
0.42 |
R9632:Gm14403
|
UTSW |
2 |
177,201,421 (GRCm39) |
missense |
probably benign |
0.00 |
|