Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130023H24Rik |
C |
A |
7: 127,836,353 (GRCm39) |
S80I |
probably benign |
Het |
Aak1 |
T |
C |
6: 86,959,627 (GRCm39) |
|
probably null |
Het |
Abcc6 |
A |
G |
7: 45,638,960 (GRCm39) |
|
probably null |
Het |
Acvr1 |
A |
G |
2: 58,353,157 (GRCm39) |
S268P |
probably damaging |
Het |
Apod |
T |
C |
16: 31,122,351 (GRCm39) |
|
probably null |
Het |
Atp5po |
T |
C |
16: 91,723,418 (GRCm39) |
I58V |
probably benign |
Het |
AU040320 |
C |
T |
4: 126,735,017 (GRCm39) |
T777M |
probably damaging |
Het |
Ccne2 |
A |
T |
4: 11,194,026 (GRCm39) |
N89I |
probably benign |
Het |
Dnah7a |
A |
G |
1: 53,543,228 (GRCm39) |
V2314A |
probably damaging |
Het |
Dop1b |
T |
C |
16: 93,595,808 (GRCm39) |
S1881P |
probably damaging |
Het |
E4f1 |
A |
G |
17: 24,666,336 (GRCm39) |
V24A |
possibly damaging |
Het |
Esrrg |
A |
T |
1: 187,882,451 (GRCm39) |
D236V |
probably damaging |
Het |
Fam240b |
T |
A |
13: 64,633,736 (GRCm39) |
I27F |
possibly damaging |
Het |
Fat1 |
T |
A |
8: 45,476,516 (GRCm39) |
I1854N |
probably damaging |
Het |
Fchsd2 |
T |
C |
7: 100,920,906 (GRCm39) |
Y480H |
probably damaging |
Het |
Fras1 |
A |
G |
5: 96,676,394 (GRCm39) |
N47S |
probably benign |
Het |
Gabrr3 |
T |
C |
16: 59,253,870 (GRCm39) |
S196P |
probably damaging |
Het |
Gbp8 |
T |
A |
5: 105,165,696 (GRCm39) |
D319V |
possibly damaging |
Het |
Hrh3 |
G |
T |
2: 179,745,763 (GRCm39) |
A61E |
probably damaging |
Het |
Idua |
T |
C |
5: 108,818,095 (GRCm39) |
I89T |
probably benign |
Het |
Ifitm3 |
T |
A |
7: 140,589,730 (GRCm39) |
I108F |
unknown |
Het |
Izumo4 |
T |
C |
10: 80,538,668 (GRCm39) |
F40S |
probably damaging |
Het |
Kifc2 |
A |
G |
15: 76,551,242 (GRCm39) |
R679G |
probably damaging |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
Ldha |
A |
T |
7: 46,500,314 (GRCm39) |
I171F |
possibly damaging |
Het |
Lrfn4 |
T |
C |
19: 4,662,191 (GRCm39) |
S609G |
probably benign |
Het |
Mmp15 |
T |
C |
8: 96,094,729 (GRCm39) |
F201S |
possibly damaging |
Het |
Myof |
C |
T |
19: 37,969,778 (GRCm39) |
V295I |
probably benign |
Het |
Or1n2 |
C |
T |
2: 36,797,369 (GRCm39) |
T137I |
possibly damaging |
Het |
Or2z2 |
T |
A |
11: 58,345,993 (GRCm39) |
M261L |
probably damaging |
Het |
Or5m12 |
G |
T |
2: 85,734,672 (GRCm39) |
A242D |
probably damaging |
Het |
Parp14 |
T |
C |
16: 35,655,137 (GRCm39) |
D1778G |
probably benign |
Het |
Pcnt |
A |
T |
10: 76,247,886 (GRCm39) |
D969E |
probably benign |
Het |
Pibf1 |
A |
T |
14: 99,350,428 (GRCm39) |
N192I |
probably benign |
Het |
Pitpnm3 |
A |
G |
11: 71,947,023 (GRCm39) |
F792S |
probably damaging |
Het |
Pkd2 |
T |
A |
5: 104,637,199 (GRCm39) |
I604N |
probably damaging |
Het |
Pla2g15 |
T |
C |
8: 106,887,775 (GRCm39) |
Y188H |
probably damaging |
Het |
Plxnc1 |
G |
T |
10: 94,700,636 (GRCm39) |
D643E |
probably benign |
Het |
Prrc2c |
G |
A |
1: 162,501,080 (GRCm39) |
P1241L |
probably damaging |
Het |
Ptprd |
T |
C |
4: 75,977,990 (GRCm39) |
E173G |
probably damaging |
Het |
Shank3 |
T |
C |
15: 89,416,557 (GRCm39) |
V232A |
probably damaging |
Het |
Shbg |
A |
G |
11: 69,507,564 (GRCm39) |
I171T |
probably damaging |
Het |
Slc22a14 |
A |
T |
9: 119,002,674 (GRCm39) |
F404L |
probably benign |
Het |
Slc37a3 |
C |
A |
6: 39,331,960 (GRCm39) |
G158C |
probably damaging |
Het |
Slfn9 |
C |
A |
11: 82,873,207 (GRCm39) |
L565F |
probably damaging |
Het |
Spmip10 |
G |
A |
18: 56,727,760 (GRCm39) |
|
probably benign |
Het |
Trank1 |
T |
A |
9: 111,195,180 (GRCm39) |
M1068K |
probably damaging |
Het |
Trbv15 |
A |
T |
6: 41,118,187 (GRCm39) |
I15L |
probably benign |
Het |
Ttn |
C |
T |
2: 76,569,918 (GRCm39) |
V26992M |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Ugt2b34 |
T |
A |
5: 87,054,560 (GRCm39) |
I74F |
probably damaging |
Het |
Vamp3 |
A |
G |
4: 151,135,477 (GRCm39) |
L47P |
probably damaging |
Het |
Zfp143 |
T |
A |
7: 109,682,522 (GRCm39) |
C363* |
probably null |
Het |
Zfp438 |
T |
C |
18: 5,213,761 (GRCm39) |
E399G |
probably damaging |
Het |
|
Other mutations in Cspg4b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01723:Cspg4b
|
APN |
13 |
113,504,091 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL03023:Cspg4b
|
APN |
13 |
113,488,275 (GRCm39) |
missense |
probably benign |
0.03 |
cumpleanos
|
UTSW |
13 |
113,504,870 (GRCm39) |
missense |
possibly damaging |
0.87 |
Sorpresa
|
UTSW |
13 |
113,454,725 (GRCm39) |
missense |
probably damaging |
1.00 |
P0018:Cspg4b
|
UTSW |
13 |
113,504,040 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0003:Cspg4b
|
UTSW |
13 |
113,505,310 (GRCm39) |
missense |
probably benign |
0.00 |
R0016:Cspg4b
|
UTSW |
13 |
113,502,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R0016:Cspg4b
|
UTSW |
13 |
113,502,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R0053:Cspg4b
|
UTSW |
13 |
113,505,023 (GRCm39) |
missense |
probably benign |
0.00 |
R0053:Cspg4b
|
UTSW |
13 |
113,505,023 (GRCm39) |
missense |
probably benign |
0.00 |
R0158:Cspg4b
|
UTSW |
13 |
113,505,687 (GRCm39) |
nonsense |
probably null |
|
R0281:Cspg4b
|
UTSW |
13 |
113,505,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R1212:Cspg4b
|
UTSW |
13 |
113,505,951 (GRCm39) |
intron |
probably benign |
|
R1300:Cspg4b
|
UTSW |
13 |
113,502,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R1434:Cspg4b
|
UTSW |
13 |
113,505,026 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1509:Cspg4b
|
UTSW |
13 |
113,504,790 (GRCm39) |
missense |
probably damaging |
0.99 |
R1738:Cspg4b
|
UTSW |
13 |
113,504,034 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1758:Cspg4b
|
UTSW |
13 |
113,505,266 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1828:Cspg4b
|
UTSW |
13 |
113,505,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R2061:Cspg4b
|
UTSW |
13 |
113,454,628 (GRCm39) |
missense |
probably damaging |
0.99 |
R2570:Cspg4b
|
UTSW |
13 |
113,455,121 (GRCm39) |
missense |
probably benign |
0.34 |
R2884:Cspg4b
|
UTSW |
13 |
113,457,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R2884:Cspg4b
|
UTSW |
13 |
113,505,725 (GRCm39) |
missense |
probably benign |
0.00 |
R3004:Cspg4b
|
UTSW |
13 |
113,502,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R3150:Cspg4b
|
UTSW |
13 |
113,488,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R3773:Cspg4b
|
UTSW |
13 |
113,454,743 (GRCm39) |
missense |
probably benign |
0.12 |
R3864:Cspg4b
|
UTSW |
13 |
113,459,485 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3971:Cspg4b
|
UTSW |
13 |
113,453,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R4004:Cspg4b
|
UTSW |
13 |
113,454,914 (GRCm39) |
missense |
probably benign |
0.00 |
R4271:Cspg4b
|
UTSW |
13 |
113,478,904 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4382:Cspg4b
|
UTSW |
13 |
113,459,288 (GRCm39) |
missense |
probably benign |
0.10 |
R4484:Cspg4b
|
UTSW |
13 |
113,455,733 (GRCm39) |
missense |
probably damaging |
0.98 |
R4570:Cspg4b
|
UTSW |
13 |
113,454,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R4600:Cspg4b
|
UTSW |
13 |
113,455,783 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4622:Cspg4b
|
UTSW |
13 |
113,456,615 (GRCm39) |
missense |
probably benign |
0.00 |
R4676:Cspg4b
|
UTSW |
13 |
113,505,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R4676:Cspg4b
|
UTSW |
13 |
113,505,341 (GRCm39) |
missense |
probably damaging |
0.98 |
R4677:Cspg4b
|
UTSW |
13 |
113,516,020 (GRCm39) |
missense |
unknown |
|
R4775:Cspg4b
|
UTSW |
13 |
113,454,229 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4779:Cspg4b
|
UTSW |
13 |
113,504,870 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4780:Cspg4b
|
UTSW |
13 |
113,454,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R4829:Cspg4b
|
UTSW |
13 |
113,504,696 (GRCm39) |
missense |
probably benign |
0.05 |
R4841:Cspg4b
|
UTSW |
13 |
113,502,724 (GRCm39) |
missense |
probably benign |
0.00 |
R4879:Cspg4b
|
UTSW |
13 |
113,456,321 (GRCm39) |
missense |
probably benign |
0.03 |
R4930:Cspg4b
|
UTSW |
13 |
113,464,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R4934:Cspg4b
|
UTSW |
13 |
113,504,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R4987:Cspg4b
|
UTSW |
13 |
113,454,635 (GRCm39) |
missense |
probably benign |
0.07 |
R5065:Cspg4b
|
UTSW |
13 |
113,457,453 (GRCm39) |
missense |
probably benign |
0.01 |
R5216:Cspg4b
|
UTSW |
13 |
113,478,947 (GRCm39) |
missense |
probably benign |
0.20 |
R5236:Cspg4b
|
UTSW |
13 |
113,502,754 (GRCm39) |
missense |
probably benign |
0.14 |
R5247:Cspg4b
|
UTSW |
13 |
113,455,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R5250:Cspg4b
|
UTSW |
13 |
113,456,305 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5337:Cspg4b
|
UTSW |
13 |
113,455,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R5342:Cspg4b
|
UTSW |
13 |
113,502,803 (GRCm39) |
critical splice donor site |
probably null |
|
R5426:Cspg4b
|
UTSW |
13 |
113,505,587 (GRCm39) |
missense |
probably benign |
0.01 |
R5472:Cspg4b
|
UTSW |
13 |
113,455,703 (GRCm39) |
missense |
probably benign |
0.12 |
R5526:Cspg4b
|
UTSW |
13 |
113,504,427 (GRCm39) |
missense |
probably benign |
0.22 |
R5589:Cspg4b
|
UTSW |
13 |
113,454,484 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5623:Cspg4b
|
UTSW |
13 |
113,483,168 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5668:Cspg4b
|
UTSW |
13 |
113,453,701 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5793:Cspg4b
|
UTSW |
13 |
113,457,556 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5824:Cspg4b
|
UTSW |
13 |
113,505,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R6038:Cspg4b
|
UTSW |
13 |
113,455,153 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6038:Cspg4b
|
UTSW |
13 |
113,455,153 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6053:Cspg4b
|
UTSW |
13 |
113,457,260 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6125:Cspg4b
|
UTSW |
13 |
113,454,217 (GRCm39) |
missense |
probably benign |
0.00 |
R6129:Cspg4b
|
UTSW |
13 |
113,505,340 (GRCm39) |
nonsense |
probably null |
|
R6290:Cspg4b
|
UTSW |
13 |
113,456,492 (GRCm39) |
missense |
probably damaging |
0.97 |
R6291:Cspg4b
|
UTSW |
13 |
113,456,981 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6302:Cspg4b
|
UTSW |
13 |
113,504,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R6317:Cspg4b
|
UTSW |
13 |
113,504,802 (GRCm39) |
missense |
probably benign |
0.09 |
R6395:Cspg4b
|
UTSW |
13 |
113,506,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R6673:Cspg4b
|
UTSW |
13 |
113,504,366 (GRCm39) |
nonsense |
probably null |
|
R6783:Cspg4b
|
UTSW |
13 |
113,456,743 (GRCm39) |
nonsense |
probably null |
|
R6800:Cspg4b
|
UTSW |
13 |
113,504,686 (GRCm39) |
missense |
probably benign |
0.02 |
R6857:Cspg4b
|
UTSW |
13 |
113,456,492 (GRCm39) |
missense |
probably damaging |
0.97 |
R6889:Cspg4b
|
UTSW |
13 |
113,454,912 (GRCm39) |
missense |
probably damaging |
0.99 |
R6934:Cspg4b
|
UTSW |
13 |
113,505,800 (GRCm39) |
missense |
probably benign |
|
R7019:Cspg4b
|
UTSW |
13 |
113,488,284 (GRCm39) |
missense |
probably benign |
0.01 |
R7100:Cspg4b
|
UTSW |
13 |
113,455,501 (GRCm39) |
missense |
|
|
R7115:Cspg4b
|
UTSW |
13 |
113,457,310 (GRCm39) |
missense |
|
|
R7152:Cspg4b
|
UTSW |
13 |
113,455,384 (GRCm39) |
missense |
|
|
R7195:Cspg4b
|
UTSW |
13 |
113,504,463 (GRCm39) |
missense |
|
|
R7213:Cspg4b
|
UTSW |
13 |
113,454,475 (GRCm39) |
missense |
|
|
R7250:Cspg4b
|
UTSW |
13 |
113,455,349 (GRCm39) |
missense |
|
|
R7341:Cspg4b
|
UTSW |
13 |
113,454,706 (GRCm39) |
missense |
|
|
R7358:Cspg4b
|
UTSW |
13 |
113,456,501 (GRCm39) |
missense |
|
|
R7359:Cspg4b
|
UTSW |
13 |
113,478,964 (GRCm39) |
missense |
|
|
R7396:Cspg4b
|
UTSW |
13 |
113,455,524 (GRCm39) |
missense |
|
|
R7632:Cspg4b
|
UTSW |
13 |
113,457,420 (GRCm39) |
missense |
|
|
R7689:Cspg4b
|
UTSW |
13 |
113,515,948 (GRCm39) |
missense |
|
|
R7713:Cspg4b
|
UTSW |
13 |
113,483,075 (GRCm39) |
missense |
|
|
R7892:Cspg4b
|
UTSW |
13 |
113,456,140 (GRCm39) |
missense |
|
|
R7975:Cspg4b
|
UTSW |
13 |
113,455,841 (GRCm39) |
missense |
|
|
R8017:Cspg4b
|
UTSW |
13 |
113,456,157 (GRCm39) |
missense |
|
|
R8019:Cspg4b
|
UTSW |
13 |
113,456,157 (GRCm39) |
missense |
|
|
R8034:Cspg4b
|
UTSW |
13 |
113,479,045 (GRCm39) |
missense |
|
|
R8101:Cspg4b
|
UTSW |
13 |
113,457,425 (GRCm39) |
missense |
|
|
R8104:Cspg4b
|
UTSW |
13 |
113,456,263 (GRCm39) |
missense |
|
|
R8122:Cspg4b
|
UTSW |
13 |
113,455,442 (GRCm39) |
missense |
|
|
R8126:Cspg4b
|
UTSW |
13 |
113,504,697 (GRCm39) |
missense |
|
|
R8272:Cspg4b
|
UTSW |
13 |
113,504,889 (GRCm39) |
missense |
|
|
R8679:Cspg4b
|
UTSW |
13 |
113,488,163 (GRCm39) |
missense |
|
|
R8973:Cspg4b
|
UTSW |
13 |
113,456,293 (GRCm39) |
missense |
|
|
R9123:Cspg4b
|
UTSW |
13 |
113,505,374 (GRCm39) |
missense |
|
|
R9125:Cspg4b
|
UTSW |
13 |
113,505,374 (GRCm39) |
missense |
|
|
R9182:Cspg4b
|
UTSW |
13 |
113,457,358 (GRCm39) |
missense |
|
|
R9233:Cspg4b
|
UTSW |
13 |
113,502,754 (GRCm39) |
missense |
|
|
R9264:Cspg4b
|
UTSW |
13 |
113,456,014 (GRCm39) |
missense |
|
|
R9306:Cspg4b
|
UTSW |
13 |
113,506,010 (GRCm39) |
missense |
unknown |
|
R9327:Cspg4b
|
UTSW |
13 |
113,453,710 (GRCm39) |
missense |
|
|
R9411:Cspg4b
|
UTSW |
13 |
113,504,767 (GRCm39) |
missense |
|
|
R9516:Cspg4b
|
UTSW |
13 |
113,455,649 (GRCm39) |
missense |
|
|
R9562:Cspg4b
|
UTSW |
13 |
113,504,574 (GRCm39) |
missense |
|
|
R9605:Cspg4b
|
UTSW |
13 |
113,456,503 (GRCm39) |
missense |
|
|
|