Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9530002B09Rik |
A |
T |
4: 122,595,050 (GRCm39) |
H102L |
possibly damaging |
Het |
Abcb10 |
GGCCATCG |
GG |
8: 124,696,500 (GRCm39) |
|
probably benign |
Het |
Atp6v1h |
A |
G |
1: 5,194,666 (GRCm39) |
T282A |
possibly damaging |
Het |
Clasp1 |
G |
A |
1: 118,509,078 (GRCm39) |
R1027Q |
probably damaging |
Het |
D630003M21Rik |
T |
C |
2: 158,042,931 (GRCm39) |
T870A |
probably benign |
Het |
Dnah12 |
T |
A |
14: 26,495,050 (GRCm39) |
N1369K |
possibly damaging |
Het |
Dpyd |
C |
T |
3: 118,690,775 (GRCm39) |
Q295* |
probably null |
Het |
Dync2i1 |
A |
C |
12: 116,175,460 (GRCm39) |
S906A |
possibly damaging |
Het |
Erv3 |
T |
C |
2: 131,697,846 (GRCm39) |
H171R |
possibly damaging |
Het |
Fam221b |
T |
C |
4: 43,665,865 (GRCm39) |
T249A |
probably benign |
Het |
Fcgr1 |
T |
C |
3: 96,191,592 (GRCm39) |
*405W |
probably null |
Het |
Glrx3 |
A |
G |
7: 137,060,882 (GRCm39) |
H172R |
probably benign |
Het |
Gm10770 |
T |
A |
2: 150,021,404 (GRCm39) |
K38* |
probably null |
Het |
Gm4787 |
G |
A |
12: 81,424,341 (GRCm39) |
Q606* |
probably null |
Het |
Hira |
G |
A |
16: 18,713,571 (GRCm39) |
A29T |
probably damaging |
Het |
Hnrnpab |
A |
T |
11: 51,493,451 (GRCm39) |
N252K |
probably benign |
Het |
Izumo4 |
A |
T |
10: 80,539,725 (GRCm39) |
T155S |
probably benign |
Het |
Kcnb2 |
A |
G |
1: 15,780,315 (GRCm39) |
I396V |
probably benign |
Het |
Klc1 |
A |
T |
12: 111,741,006 (GRCm39) |
I161F |
probably benign |
Het |
Lpar5 |
C |
A |
6: 125,058,690 (GRCm39) |
A137E |
possibly damaging |
Het |
Lrp4 |
C |
T |
2: 91,318,863 (GRCm39) |
S900L |
possibly damaging |
Het |
Muc6 |
T |
G |
7: 141,233,880 (GRCm39) |
E808A |
probably benign |
Het |
Or10j7 |
G |
T |
1: 173,011,531 (GRCm39) |
L157I |
probably benign |
Het |
Or5p57 |
G |
T |
7: 107,665,885 (GRCm39) |
T40K |
probably benign |
Het |
Otop3 |
T |
A |
11: 115,235,664 (GRCm39) |
L432Q |
probably damaging |
Het |
Papln |
C |
T |
12: 83,825,608 (GRCm39) |
R608C |
possibly damaging |
Het |
Pelp1 |
T |
A |
11: 70,288,976 (GRCm39) |
T257S |
probably damaging |
Het |
Pik3cd |
A |
C |
4: 149,741,776 (GRCm39) |
L390R |
probably damaging |
Het |
Ppwd1 |
A |
G |
13: 104,356,745 (GRCm39) |
Y257H |
probably damaging |
Het |
Prkcb |
G |
T |
7: 122,127,699 (GRCm39) |
W274C |
probably damaging |
Het |
Rbbp8nl |
T |
A |
2: 179,920,001 (GRCm39) |
T558S |
probably benign |
Het |
Recql4 |
T |
C |
15: 76,590,369 (GRCm39) |
D705G |
possibly damaging |
Het |
Slc30a4 |
T |
A |
2: 122,531,458 (GRCm39) |
M136L |
probably benign |
Het |
Slc5a6 |
C |
T |
5: 31,199,957 (GRCm39) |
|
probably null |
Het |
Spaca1 |
T |
C |
4: 34,039,311 (GRCm39) |
E192G |
probably damaging |
Het |
Spata31 |
C |
A |
13: 65,069,462 (GRCm39) |
P537T |
probably benign |
Het |
Tmc3 |
T |
C |
7: 83,271,713 (GRCm39) |
V955A |
probably benign |
Het |
Tnrc6c |
G |
A |
11: 117,614,152 (GRCm39) |
R770H |
probably damaging |
Het |
Toe1 |
A |
T |
4: 116,663,308 (GRCm39) |
N56K |
probably damaging |
Het |
Tprkb |
A |
G |
6: 85,905,764 (GRCm39) |
K150E |
probably damaging |
Het |
Trps1 |
T |
C |
15: 50,694,973 (GRCm39) |
K150E |
probably damaging |
Het |
Tspyl3 |
A |
G |
2: 153,066,980 (GRCm39) |
V86A |
probably benign |
Het |
Vmn2r68 |
C |
T |
7: 84,871,088 (GRCm39) |
V732I |
probably benign |
Het |
Zfp292 |
C |
T |
4: 34,806,783 (GRCm39) |
C2087Y |
possibly damaging |
Het |
Zfp933 |
G |
A |
4: 147,910,927 (GRCm39) |
A223V |
probably damaging |
Het |
Zmynd8 |
G |
A |
2: 165,654,314 (GRCm39) |
R724* |
probably null |
Het |
|
Other mutations in Dnajc22 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Dnajc22
|
APN |
15 |
98,999,059 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL00922:Dnajc22
|
APN |
15 |
98,999,460 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02155:Dnajc22
|
APN |
15 |
98,998,886 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02726:Dnajc22
|
APN |
15 |
98,998,881 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03074:Dnajc22
|
APN |
15 |
98,999,403 (GRCm39) |
missense |
probably damaging |
1.00 |
F5770:Dnajc22
|
UTSW |
15 |
98,999,363 (GRCm39) |
missense |
probably damaging |
0.99 |
R1138:Dnajc22
|
UTSW |
15 |
99,002,308 (GRCm39) |
small deletion |
probably benign |
|
R1628:Dnajc22
|
UTSW |
15 |
98,998,817 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R2018:Dnajc22
|
UTSW |
15 |
98,999,114 (GRCm39) |
missense |
probably benign |
0.06 |
R2146:Dnajc22
|
UTSW |
15 |
99,002,264 (GRCm39) |
missense |
probably benign |
0.04 |
R4342:Dnajc22
|
UTSW |
15 |
99,002,345 (GRCm39) |
nonsense |
probably null |
|
R4950:Dnajc22
|
UTSW |
15 |
98,999,615 (GRCm39) |
missense |
probably benign |
0.29 |
R7123:Dnajc22
|
UTSW |
15 |
98,999,085 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7173:Dnajc22
|
UTSW |
15 |
98,999,187 (GRCm39) |
missense |
probably benign |
0.06 |
R7640:Dnajc22
|
UTSW |
15 |
98,998,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R7997:Dnajc22
|
UTSW |
15 |
98,999,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R8338:Dnajc22
|
UTSW |
15 |
98,999,022 (GRCm39) |
missense |
probably benign |
0.00 |
R8745:Dnajc22
|
UTSW |
15 |
98,999,345 (GRCm39) |
missense |
probably benign |
0.01 |
V7580:Dnajc22
|
UTSW |
15 |
98,999,363 (GRCm39) |
missense |
probably damaging |
0.99 |
V7582:Dnajc22
|
UTSW |
15 |
98,999,363 (GRCm39) |
missense |
probably damaging |
0.99 |
V7583:Dnajc22
|
UTSW |
15 |
98,999,363 (GRCm39) |
missense |
probably damaging |
0.99 |
|