Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933409G03Rik |
A |
T |
2: 68,445,491 (GRCm39) |
|
probably benign |
Het |
Aimp1 |
A |
T |
3: 132,373,253 (GRCm39) |
L229Q |
probably benign |
Het |
Ankrd16 |
T |
A |
2: 11,789,215 (GRCm39) |
D267E |
possibly damaging |
Het |
Apol11b |
A |
G |
15: 77,522,133 (GRCm39) |
|
probably null |
Het |
Arfgap1 |
C |
A |
2: 180,622,869 (GRCm39) |
D327E |
probably benign |
Het |
Arid3b |
A |
T |
9: 57,741,151 (GRCm39) |
D98E |
probably benign |
Het |
Atp5f1a |
T |
A |
18: 77,867,766 (GRCm39) |
|
probably benign |
Het |
Carmil3 |
A |
G |
14: 55,738,928 (GRCm39) |
T861A |
probably benign |
Het |
Cep164 |
A |
T |
9: 45,691,002 (GRCm39) |
F1259L |
possibly damaging |
Het |
Cfap91 |
G |
T |
16: 38,140,727 (GRCm39) |
P409T |
probably damaging |
Het |
Chrnd |
T |
C |
1: 87,123,512 (GRCm39) |
V350A |
probably benign |
Het |
Clcn7 |
T |
C |
17: 25,379,150 (GRCm39) |
L744P |
probably damaging |
Het |
Csl |
T |
A |
10: 99,594,453 (GRCm39) |
D204V |
possibly damaging |
Het |
Cstdc3 |
A |
G |
16: 36,132,951 (GRCm39) |
D76G |
probably null |
Het |
Cyp2c29 |
G |
T |
19: 39,275,620 (GRCm39) |
W20L |
probably damaging |
Het |
Dhrs13 |
G |
T |
11: 77,927,951 (GRCm39) |
G266* |
probably null |
Het |
Dll3 |
T |
C |
7: 27,995,716 (GRCm39) |
N362D |
probably damaging |
Het |
Efcab3 |
T |
G |
11: 104,626,940 (GRCm39) |
|
probably null |
Het |
Fanca |
A |
G |
8: 124,015,532 (GRCm39) |
V715A |
probably benign |
Het |
Fhod1 |
T |
C |
8: 106,063,983 (GRCm39) |
|
probably benign |
Het |
Fpr2 |
C |
T |
17: 18,113,394 (GRCm39) |
P130L |
probably damaging |
Het |
Glce |
A |
G |
9: 61,967,535 (GRCm39) |
Y539H |
probably damaging |
Het |
Hfe |
A |
T |
13: 23,890,866 (GRCm39) |
V91E |
probably benign |
Het |
Hoxd13 |
A |
T |
2: 74,500,301 (GRCm39) |
K281* |
probably null |
Het |
Ighv1-66 |
A |
T |
12: 115,557,157 (GRCm39) |
W3R |
probably damaging |
Het |
Impg2 |
G |
A |
16: 56,080,388 (GRCm39) |
V622I |
possibly damaging |
Het |
Jun |
A |
G |
4: 94,939,084 (GRCm39) |
M142T |
probably benign |
Het |
Krt78 |
T |
C |
15: 101,856,375 (GRCm39) |
T479A |
probably benign |
Het |
Lama3 |
T |
A |
18: 12,652,929 (GRCm39) |
C216* |
probably null |
Het |
Lin54 |
G |
T |
5: 100,594,419 (GRCm39) |
T582K |
probably damaging |
Het |
Mapk11 |
A |
G |
15: 89,029,576 (GRCm39) |
|
probably null |
Het |
Mindy3 |
A |
G |
2: 12,353,010 (GRCm39) |
M397T |
probably benign |
Het |
Mrpl41 |
T |
C |
2: 24,864,418 (GRCm39) |
T85A |
possibly damaging |
Het |
Msh6 |
T |
A |
17: 88,298,217 (GRCm39) |
L1354* |
probably null |
Het |
Mtmr12 |
T |
C |
15: 12,230,400 (GRCm39) |
V41A |
probably damaging |
Het |
Myh2 |
A |
T |
11: 67,083,551 (GRCm39) |
Q1478L |
probably benign |
Het |
Myo6 |
A |
G |
9: 80,195,320 (GRCm39) |
K897E |
probably benign |
Het |
Naprt |
G |
T |
15: 75,764,605 (GRCm39) |
|
probably null |
Het |
Nrl |
G |
A |
14: 55,759,675 (GRCm39) |
S84L |
probably benign |
Het |
Nxf1 |
A |
G |
19: 8,744,128 (GRCm39) |
|
probably benign |
Het |
Or8g2b |
A |
T |
9: 39,751,652 (GRCm39) |
R307S |
possibly damaging |
Het |
Panx2 |
G |
T |
15: 88,952,423 (GRCm39) |
V305F |
probably benign |
Het |
Pcdhga1 |
T |
C |
18: 37,795,632 (GRCm39) |
L212P |
probably damaging |
Het |
Pik3ap1 |
G |
A |
19: 41,364,320 (GRCm39) |
T133I |
probably benign |
Het |
Ppat |
A |
G |
5: 77,063,061 (GRCm39) |
W517R |
probably damaging |
Het |
Ppp1r16b |
C |
T |
2: 158,599,174 (GRCm39) |
T382I |
probably benign |
Het |
Prkdc |
G |
A |
16: 15,653,946 (GRCm39) |
R3901H |
probably damaging |
Het |
Prkdc |
A |
G |
16: 15,591,603 (GRCm39) |
K2694E |
probably damaging |
Het |
Psma8 |
A |
G |
18: 14,854,247 (GRCm39) |
I42M |
probably damaging |
Het |
Ptprd |
A |
T |
4: 76,021,200 (GRCm39) |
M599K |
probably benign |
Het |
Rnmt |
A |
G |
18: 68,444,742 (GRCm39) |
D237G |
probably null |
Het |
Rpl31-ps17 |
C |
T |
12: 54,748,397 (GRCm39) |
|
noncoding transcript |
Het |
Scaf11 |
G |
A |
15: 96,316,309 (GRCm39) |
T1085I |
possibly damaging |
Het |
Sec14l3 |
G |
A |
11: 4,016,210 (GRCm39) |
R43Q |
probably damaging |
Het |
Shc4 |
G |
T |
2: 125,494,442 (GRCm39) |
T131K |
probably benign |
Het |
Snx27 |
A |
G |
3: 94,469,330 (GRCm39) |
F4L |
probably benign |
Het |
Sorcs1 |
T |
C |
19: 50,367,379 (GRCm39) |
T228A |
probably damaging |
Het |
Spmap2l |
T |
C |
5: 77,202,383 (GRCm39) |
I268T |
possibly damaging |
Het |
Sptan1 |
C |
T |
2: 29,919,721 (GRCm39) |
|
probably benign |
Het |
Syvn1 |
C |
T |
19: 6,099,951 (GRCm39) |
|
probably benign |
Het |
Tex47 |
G |
T |
5: 7,355,364 (GRCm39) |
A182S |
probably benign |
Het |
Tpcn1 |
T |
C |
5: 120,680,583 (GRCm39) |
K549R |
probably damaging |
Het |
Upf3a |
C |
A |
8: 13,846,573 (GRCm39) |
P318T |
probably benign |
Het |
Zbtb40 |
A |
T |
4: 136,726,005 (GRCm39) |
M518K |
probably damaging |
Het |
Zcchc14 |
G |
A |
8: 122,378,680 (GRCm39) |
|
probably benign |
Het |
Zfp687 |
G |
A |
3: 94,916,439 (GRCm39) |
P861L |
probably damaging |
Het |
|
Other mutations in Art2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00551:Art2b
|
APN |
7 |
101,229,776 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03085:Art2b
|
APN |
7 |
101,229,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R1488:Art2b
|
UTSW |
7 |
101,229,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R1813:Art2b
|
UTSW |
7 |
101,229,236 (GRCm39) |
missense |
probably benign |
0.38 |
R1896:Art2b
|
UTSW |
7 |
101,229,236 (GRCm39) |
missense |
probably benign |
0.38 |
R1941:Art2b
|
UTSW |
7 |
101,229,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R1944:Art2b
|
UTSW |
7 |
101,229,153 (GRCm39) |
missense |
probably benign |
0.00 |
R1967:Art2b
|
UTSW |
7 |
101,229,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R2019:Art2b
|
UTSW |
7 |
101,229,194 (GRCm39) |
missense |
probably benign |
0.02 |
R3605:Art2b
|
UTSW |
7 |
101,229,152 (GRCm39) |
missense |
probably benign |
0.00 |
R4960:Art2b
|
UTSW |
7 |
101,229,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R5658:Art2b
|
UTSW |
7 |
101,229,569 (GRCm39) |
missense |
probably damaging |
0.99 |
R6024:Art2b
|
UTSW |
7 |
101,229,587 (GRCm39) |
missense |
probably benign |
0.03 |
R6223:Art2b
|
UTSW |
7 |
101,229,158 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6980:Art2b
|
UTSW |
7 |
101,229,680 (GRCm39) |
missense |
probably benign |
0.01 |
R7184:Art2b
|
UTSW |
7 |
101,229,658 (GRCm39) |
missense |
probably benign |
0.17 |
R8954:Art2b
|
UTSW |
7 |
101,229,110 (GRCm39) |
critical splice donor site |
probably null |
|
R8991:Art2b
|
UTSW |
7 |
101,229,590 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1176:Art2b
|
UTSW |
7 |
101,228,089 (GRCm39) |
missense |
not run |
|
|