Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9530002B09Rik |
A |
T |
4: 122,595,050 (GRCm39) |
H102L |
possibly damaging |
Het |
Abcb5 |
T |
A |
12: 118,849,914 (GRCm39) |
M950L |
probably benign |
Het |
Ahcy |
G |
A |
2: 154,906,841 (GRCm39) |
R151* |
probably null |
Het |
Arhgef38 |
T |
G |
3: 132,855,301 (GRCm39) |
H262P |
probably damaging |
Het |
Atp6v1h |
A |
G |
1: 5,194,666 (GRCm39) |
T282A |
possibly damaging |
Het |
Camk2g |
T |
C |
14: 20,789,380 (GRCm39) |
|
probably benign |
Het |
Casp8ap2 |
C |
T |
4: 32,639,944 (GRCm39) |
H333Y |
probably benign |
Het |
Cd36 |
ACTGTCTGT |
ACTGT |
5: 18,025,526 (GRCm39) |
|
probably null |
Het |
Cdc42bpb |
C |
T |
12: 111,262,825 (GRCm39) |
G1501S |
probably benign |
Het |
Cfi |
T |
A |
3: 129,648,641 (GRCm39) |
I175K |
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 |
Dcaf4 |
C |
A |
12: 83,584,475 (GRCm39) |
|
probably null |
Het |
Dnah12 |
T |
A |
14: 26,495,050 (GRCm39) |
N1369K |
possibly damaging |
Het |
Dnajc22 |
T |
A |
15: 98,999,363 (GRCm39) |
Y183N |
probably 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 |
Fbrsl1 |
C |
T |
5: 110,527,292 (GRCm39) |
A129T |
possibly damaging |
Het |
Fcgr1 |
T |
C |
3: 96,191,592 (GRCm39) |
*405W |
probably null |
Het |
Gdap1l1 |
C |
T |
2: 163,289,406 (GRCm39) |
|
probably benign |
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 |
Gm20517 |
G |
A |
17: 47,929,757 (GRCm39) |
V65M |
probably damaging |
Het |
Gm4787 |
G |
A |
12: 81,424,341 (GRCm39) |
Q606* |
probably null |
Het |
Golga4 |
A |
G |
9: 118,385,143 (GRCm39) |
E727G |
possibly damaging |
Het |
Got1 |
T |
A |
19: 43,489,000 (GRCm39) |
|
probably benign |
Het |
Heatr5a |
A |
G |
12: 51,928,061 (GRCm39) |
|
probably benign |
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 |
Ing1 |
T |
C |
8: 11,611,934 (GRCm39) |
V124A |
probably damaging |
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 |
Lrrc37a |
T |
G |
11: 103,346,338 (GRCm39) |
N3176T |
possibly damaging |
Het |
Mbd5 |
A |
G |
2: 49,206,422 (GRCm39) |
D1713G |
probably damaging |
Het |
Mctp2 |
T |
A |
7: 71,771,499 (GRCm39) |
|
probably benign |
Het |
Muc6 |
T |
G |
7: 141,233,880 (GRCm39) |
E808A |
probably benign |
Het |
Mylk |
G |
T |
16: 34,815,574 (GRCm39) |
|
probably null |
Het |
Myrfl |
T |
C |
10: 116,697,435 (GRCm39) |
T30A |
probably damaging |
Het |
Nbeal2 |
A |
G |
9: 110,467,005 (GRCm39) |
V670A |
possibly damaging |
Het |
Nphp3 |
T |
C |
9: 103,913,093 (GRCm39) |
|
probably null |
Het |
Numbl |
T |
C |
7: 26,979,027 (GRCm39) |
S379P |
probably benign |
Het |
Or10j7 |
G |
T |
1: 173,011,531 (GRCm39) |
L157I |
probably benign |
Het |
Or5an6 |
G |
A |
19: 12,371,914 (GRCm39) |
V96I |
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 |
Pigx |
T |
C |
16: 31,906,240 (GRCm39) |
D129G |
probably damaging |
Het |
Pik3cd |
A |
C |
4: 149,741,776 (GRCm39) |
L390R |
probably damaging |
Het |
Plekhb1 |
T |
C |
7: 100,303,825 (GRCm39) |
T112A |
probably benign |
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 |
Rabep1 |
T |
C |
11: 70,828,342 (GRCm39) |
|
probably benign |
Het |
Ralgapa1 |
G |
A |
12: 55,842,438 (GRCm39) |
|
probably benign |
Het |
Rasa1 |
A |
G |
13: 85,375,064 (GRCm39) |
|
probably null |
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 |
Ror1 |
A |
G |
4: 100,298,130 (GRCm39) |
Q501R |
probably damaging |
Het |
Rundc3b |
TGCCGCCGCCGCCGCCGCCGCCGCCGC |
TGCCGCCGCCGCCGCCGCCGCCGC |
5: 8,672,549 (GRCm39) |
|
probably benign |
Het |
Sirpb1b |
A |
G |
3: 15,568,243 (GRCm39) |
V366A |
probably benign |
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 |
Sptbn2 |
C |
T |
19: 4,800,660 (GRCm39) |
R2292C |
probably damaging |
Het |
Thbd |
A |
T |
2: 148,249,110 (GRCm39) |
Y253N |
probably benign |
Het |
Tiam1 |
C |
T |
16: 89,662,159 (GRCm39) |
R653H |
probably damaging |
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 |
Ttc23 |
T |
C |
7: 67,359,063 (GRCm39) |
|
probably benign |
Het |
Ttc36 |
A |
T |
9: 44,713,094 (GRCm39) |
|
probably benign |
Het |
Tubb3 |
C |
T |
8: 124,138,414 (GRCm39) |
|
probably benign |
Het |
Vmn2r68 |
C |
T |
7: 84,871,088 (GRCm39) |
V732I |
probably benign |
Het |
Vps18 |
A |
G |
2: 119,127,709 (GRCm39) |
Y844C |
probably benign |
Het |
Wdr72 |
T |
A |
9: 74,064,552 (GRCm39) |
I528N |
probably damaging |
Het |
Zfp292 |
C |
T |
4: 34,806,783 (GRCm39) |
C2087Y |
possibly damaging |
Het |
Zfp606 |
T |
G |
7: 12,215,123 (GRCm39) |
|
probably benign |
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 Fam221b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01511:Fam221b
|
APN |
4 |
43,660,135 (GRCm39) |
splice site |
probably null |
|
IGL01576:Fam221b
|
APN |
4 |
43,666,227 (GRCm39) |
missense |
probably benign |
0.21 |
IGL02126:Fam221b
|
APN |
4 |
43,666,450 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02407:Fam221b
|
APN |
4 |
43,666,309 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02425:Fam221b
|
APN |
4 |
43,660,642 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03174:Fam221b
|
APN |
4 |
43,666,542 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Fam221b
|
UTSW |
4 |
43,665,537 (GRCm39) |
missense |
probably damaging |
0.99 |
R1786:Fam221b
|
UTSW |
4 |
43,665,537 (GRCm39) |
missense |
probably damaging |
0.99 |
R1896:Fam221b
|
UTSW |
4 |
43,660,375 (GRCm39) |
missense |
probably damaging |
0.98 |
R4091:Fam221b
|
UTSW |
4 |
43,665,987 (GRCm39) |
missense |
probably benign |
0.01 |
R4695:Fam221b
|
UTSW |
4 |
43,659,622 (GRCm39) |
splice site |
probably null |
|
R5024:Fam221b
|
UTSW |
4 |
43,659,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R5778:Fam221b
|
UTSW |
4 |
43,660,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R6335:Fam221b
|
UTSW |
4 |
43,665,942 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7994:Fam221b
|
UTSW |
4 |
43,665,514 (GRCm39) |
missense |
probably damaging |
0.97 |
R8144:Fam221b
|
UTSW |
4 |
43,665,466 (GRCm39) |
missense |
probably benign |
0.44 |
R8144:Fam221b
|
UTSW |
4 |
43,665,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R8182:Fam221b
|
UTSW |
4 |
43,660,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R8356:Fam221b
|
UTSW |
4 |
43,665,519 (GRCm39) |
missense |
probably benign |
0.05 |
R9753:Fam221b
|
UTSW |
4 |
43,665,574 (GRCm39) |
missense |
probably benign |
0.40 |
V7580:Fam221b
|
UTSW |
4 |
43,665,865 (GRCm39) |
missense |
probably benign |
|
V7581:Fam221b
|
UTSW |
4 |
43,665,865 (GRCm39) |
missense |
probably benign |
|
V7582:Fam221b
|
UTSW |
4 |
43,665,865 (GRCm39) |
missense |
probably benign |
|
V7583:Fam221b
|
UTSW |
4 |
43,665,865 (GRCm39) |
missense |
probably benign |
|
Z1177:Fam221b
|
UTSW |
4 |
43,666,039 (GRCm39) |
missense |
probably benign |
0.17 |
|