Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adrm1b |
T |
C |
3: 92,335,815 (GRCm39) |
I296V |
probably benign |
Het |
Antkmt |
T |
C |
17: 26,010,613 (GRCm39) |
N67S |
possibly damaging |
Het |
Arhgap26 |
T |
A |
18: 39,243,525 (GRCm39) |
Y134* |
probably null |
Het |
Asap2 |
A |
G |
12: 21,263,191 (GRCm39) |
I269V |
probably benign |
Het |
Bean1 |
A |
T |
8: 104,941,784 (GRCm39) |
D34V |
probably damaging |
Het |
C8a |
C |
T |
4: 104,703,122 (GRCm39) |
V312M |
probably damaging |
Het |
Ccser1 |
T |
C |
6: 61,289,075 (GRCm39) |
S413P |
probably damaging |
Het |
Col4a2 |
A |
G |
8: 11,498,225 (GRCm39) |
N1678S |
probably benign |
Het |
Coq2 |
G |
A |
5: 100,805,698 (GRCm39) |
H313Y |
possibly damaging |
Het |
Dsg1a |
T |
A |
18: 20,457,071 (GRCm39) |
M148K |
possibly damaging |
Het |
Farp2 |
T |
A |
1: 93,504,140 (GRCm39) |
C306S |
probably damaging |
Het |
Frem2 |
A |
G |
3: 53,493,032 (GRCm39) |
V1828A |
probably damaging |
Het |
Gm6457 |
T |
C |
18: 14,703,174 (GRCm39) |
|
noncoding transcript |
Het |
Gmip |
T |
G |
8: 70,266,785 (GRCm39) |
V300G |
probably damaging |
Het |
Gstp3 |
A |
G |
19: 4,107,607 (GRCm39) |
S186P |
probably damaging |
Het |
Gvin-ps3 |
G |
C |
7: 105,683,181 (GRCm39) |
|
noncoding transcript |
Het |
Kl |
G |
T |
5: 150,912,616 (GRCm39) |
L788F |
probably damaging |
Het |
Lin9 |
T |
A |
1: 180,496,763 (GRCm39) |
L351I |
probably benign |
Het |
Lrp1b |
A |
C |
2: 41,002,994 (GRCm39) |
S1932A |
possibly damaging |
Het |
Lrrc36 |
A |
G |
8: 106,170,488 (GRCm39) |
T234A |
probably damaging |
Het |
Mafa |
T |
A |
15: 75,618,891 (GRCm39) |
Q294L |
possibly damaging |
Het |
Mesp2 |
C |
T |
7: 79,461,467 (GRCm39) |
T264I |
possibly damaging |
Het |
Mindy4 |
A |
G |
6: 55,201,092 (GRCm39) |
Y259C |
probably benign |
Het |
Or1e16 |
AGCGGTCGTAGGC |
AGC |
11: 73,286,480 (GRCm39) |
|
probably null |
Het |
Or2d3c |
A |
T |
7: 106,526,268 (GRCm39) |
S133T |
probably benign |
Het |
Or5as1 |
T |
C |
2: 86,980,825 (GRCm39) |
Y60C |
probably damaging |
Het |
Or5m13b |
A |
G |
2: 85,754,493 (GRCm39) |
N294D |
probably damaging |
Het |
Or8b48 |
A |
T |
9: 38,493,148 (GRCm39) |
T192S |
probably damaging |
Het |
Pcm1 |
T |
C |
8: 41,741,193 (GRCm39) |
|
probably null |
Het |
Plxna1 |
T |
C |
6: 89,297,998 (GRCm39) |
D1760G |
probably damaging |
Het |
Polq |
T |
A |
16: 36,862,540 (GRCm39) |
D345E |
probably damaging |
Het |
Ppp1r14a |
T |
A |
7: 28,988,926 (GRCm39) |
I56N |
probably damaging |
Het |
Ppp1r1a |
G |
A |
15: 103,441,477 (GRCm39) |
P79S |
probably damaging |
Het |
Ptprf |
C |
T |
4: 118,082,305 (GRCm39) |
R1010H |
probably benign |
Het |
Rai1 |
A |
G |
11: 60,081,423 (GRCm39) |
E1829G |
probably damaging |
Het |
Rmdn3 |
A |
G |
2: 118,986,935 (GRCm39) |
Y31H |
probably damaging |
Het |
Rrh |
T |
C |
3: 129,609,280 (GRCm39) |
S69G |
probably damaging |
Het |
Skint6 |
A |
T |
4: 112,752,121 (GRCm39) |
|
probably null |
Het |
Slc22a27 |
C |
G |
19: 7,843,303 (GRCm39) |
A359P |
probably damaging |
Het |
Sltm |
T |
G |
9: 70,486,685 (GRCm39) |
L450R |
probably damaging |
Het |
Sufu |
T |
C |
19: 46,439,404 (GRCm39) |
|
probably null |
Het |
Tmem68 |
T |
C |
4: 3,560,561 (GRCm39) |
T208A |
possibly damaging |
Het |
Tnc |
T |
A |
4: 63,911,534 (GRCm39) |
R1346* |
probably null |
Het |
Tpbg |
T |
C |
9: 85,726,478 (GRCm39) |
L149P |
probably damaging |
Het |
Trappc14 |
C |
T |
5: 138,260,502 (GRCm39) |
S308N |
probably benign |
Het |
Ubtf |
G |
A |
11: 102,198,816 (GRCm39) |
Q585* |
probably null |
Het |
Vmn2r68 |
A |
T |
7: 84,871,085 (GRCm39) |
C733S |
probably damaging |
Het |
Vmn2r-ps158 |
T |
A |
7: 42,672,684 (GRCm39) |
H106Q |
probably benign |
Het |
Zfp354b |
A |
C |
11: 50,813,917 (GRCm39) |
I336S |
probably benign |
Het |
Zfp462 |
T |
A |
4: 55,016,887 (GRCm39) |
V870E |
possibly damaging |
Het |
|
Other mutations in Wscd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00980:Wscd1
|
APN |
11 |
71,679,768 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01982:Wscd1
|
APN |
11 |
71,657,699 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01991:Wscd1
|
APN |
11 |
71,678,549 (GRCm39) |
nonsense |
probably null |
|
IGL02211:Wscd1
|
APN |
11 |
71,679,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R0011:Wscd1
|
UTSW |
11 |
71,679,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R0011:Wscd1
|
UTSW |
11 |
71,679,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R0359:Wscd1
|
UTSW |
11 |
71,657,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R0371:Wscd1
|
UTSW |
11 |
71,679,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R1340:Wscd1
|
UTSW |
11 |
71,659,586 (GRCm39) |
missense |
probably benign |
0.01 |
R1429:Wscd1
|
UTSW |
11 |
71,651,000 (GRCm39) |
missense |
probably damaging |
0.99 |
R1511:Wscd1
|
UTSW |
11 |
71,679,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R1823:Wscd1
|
UTSW |
11 |
71,651,044 (GRCm39) |
missense |
probably benign |
0.05 |
R4772:Wscd1
|
UTSW |
11 |
71,662,802 (GRCm39) |
critical splice donor site |
probably null |
|
R4885:Wscd1
|
UTSW |
11 |
71,650,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R5714:Wscd1
|
UTSW |
11 |
71,675,261 (GRCm39) |
critical splice donor site |
probably null |
|
R6351:Wscd1
|
UTSW |
11 |
71,650,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R7181:Wscd1
|
UTSW |
11 |
71,650,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R7184:Wscd1
|
UTSW |
11 |
71,679,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R7461:Wscd1
|
UTSW |
11 |
71,650,799 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7613:Wscd1
|
UTSW |
11 |
71,650,799 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7754:Wscd1
|
UTSW |
11 |
71,675,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R7875:Wscd1
|
UTSW |
11 |
71,679,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R8804:Wscd1
|
UTSW |
11 |
71,675,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R9103:Wscd1
|
UTSW |
11 |
71,674,245 (GRCm39) |
critical splice donor site |
probably null |
|
R9220:Wscd1
|
UTSW |
11 |
71,662,750 (GRCm39) |
missense |
probably benign |
0.01 |
R9359:Wscd1
|
UTSW |
11 |
71,650,799 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9473:Wscd1
|
UTSW |
11 |
71,679,644 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Wscd1
|
UTSW |
11 |
71,679,811 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Wscd1
|
UTSW |
11 |
71,679,626 (GRCm39) |
nonsense |
probably null |
|
|