Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700093K21Rik |
T |
A |
11: 23,468,066 (GRCm39) |
M76L |
probably benign |
Het |
Adrm1b |
T |
A |
3: 92,336,112 (GRCm39) |
|
probably benign |
Het |
Alg1 |
T |
A |
16: 5,053,086 (GRCm39) |
W116R |
probably benign |
Het |
Ano3 |
A |
T |
2: 110,715,340 (GRCm39) |
S33T |
probably damaging |
Het |
Atp2b2 |
T |
C |
6: 113,751,400 (GRCm39) |
E556G |
possibly damaging |
Het |
Brca2 |
T |
A |
5: 150,480,597 (GRCm39) |
I2761K |
possibly damaging |
Het |
Ccdc68 |
G |
A |
18: 70,079,577 (GRCm39) |
G141E |
probably benign |
Het |
Cckbr |
T |
C |
7: 105,083,732 (GRCm39) |
V220A |
probably damaging |
Het |
Ccnd3 |
G |
A |
17: 47,909,544 (GRCm39) |
R45Q |
probably damaging |
Het |
Cdh24 |
G |
T |
14: 54,874,832 (GRCm39) |
T391N |
probably damaging |
Het |
Cldn11 |
A |
G |
3: 31,204,395 (GRCm39) |
T33A |
probably damaging |
Het |
Clec2e |
T |
A |
6: 129,075,391 (GRCm39) |
Y50F |
probably benign |
Het |
Cntnap1 |
A |
G |
11: 101,075,944 (GRCm39) |
N943D |
probably benign |
Het |
Dmgdh |
T |
C |
13: 93,813,665 (GRCm39) |
V70A |
probably damaging |
Het |
Gm14496 |
C |
A |
2: 181,637,674 (GRCm39) |
Y249* |
probably null |
Het |
Gmnc |
T |
A |
16: 26,781,714 (GRCm39) |
H105L |
probably damaging |
Het |
Gpt2 |
A |
G |
8: 86,219,740 (GRCm39) |
Y62C |
probably damaging |
Het |
Ift80 |
T |
C |
3: 68,838,233 (GRCm39) |
R413G |
probably damaging |
Het |
Kctd16 |
C |
A |
18: 40,392,061 (GRCm39) |
D216E |
probably damaging |
Het |
Kif26b |
T |
C |
1: 178,743,864 (GRCm39) |
V873A |
probably benign |
Het |
Klra4 |
G |
T |
6: 130,039,117 (GRCm39) |
Q92K |
probably benign |
Het |
L1td1 |
C |
A |
4: 98,626,341 (GRCm39) |
N845K |
possibly damaging |
Het |
Lama3 |
C |
T |
18: 12,605,277 (GRCm39) |
T1077I |
possibly damaging |
Het |
Loxhd1 |
T |
C |
18: 77,429,751 (GRCm39) |
I230T |
possibly damaging |
Het |
Lsg1 |
T |
C |
16: 30,399,819 (GRCm39) |
N160S |
probably damaging |
Het |
Lyzl4 |
G |
A |
9: 121,413,469 (GRCm39) |
R24C |
probably damaging |
Het |
Mib1 |
A |
G |
18: 10,794,488 (GRCm39) |
N658S |
probably benign |
Het |
Mmp8 |
T |
C |
9: 7,566,275 (GRCm39) |
I377T |
probably damaging |
Het |
Mtmr14 |
T |
C |
6: 113,238,243 (GRCm39) |
|
probably null |
Het |
Myo1c |
A |
G |
11: 75,548,414 (GRCm39) |
T58A |
possibly damaging |
Het |
Myo9a |
C |
T |
9: 59,802,527 (GRCm39) |
Q2005* |
probably null |
Het |
Neu3 |
G |
T |
7: 99,472,636 (GRCm39) |
P34T |
probably benign |
Het |
Nlrp4b |
G |
A |
7: 10,449,512 (GRCm39) |
V205I |
probably benign |
Het |
Or4b1b |
C |
T |
2: 90,112,313 (GRCm39) |
G202D |
probably damaging |
Het |
Or4k38 |
T |
C |
2: 111,165,850 (GRCm39) |
N191S |
possibly damaging |
Het |
Or5h23 |
A |
T |
16: 58,906,334 (GRCm39) |
S171T |
probably benign |
Het |
Or5t15 |
A |
G |
2: 86,681,118 (GRCm39) |
I308T |
unknown |
Het |
Or6c66 |
T |
G |
10: 129,461,319 (GRCm39) |
T204P |
probably damaging |
Het |
Or9m1 |
T |
C |
2: 87,733,691 (GRCm39) |
T110A |
probably benign |
Het |
Pcsk6 |
T |
C |
7: 65,578,933 (GRCm39) |
|
probably null |
Het |
Pik3c2a |
A |
G |
7: 116,016,893 (GRCm39) |
V288A |
probably benign |
Het |
Plcd3 |
T |
C |
11: 102,968,629 (GRCm39) |
D354G |
probably benign |
Het |
Prkdc |
C |
A |
16: 15,524,655 (GRCm39) |
N1219K |
probably benign |
Het |
Prl3d1 |
T |
A |
13: 27,278,927 (GRCm39) |
Y41N |
probably damaging |
Het |
Qrich2 |
C |
T |
11: 116,332,234 (GRCm39) |
G2321R |
probably damaging |
Het |
Rrbp1 |
T |
C |
2: 143,831,886 (GRCm39) |
I94V |
probably benign |
Het |
Serinc1 |
C |
A |
10: 57,399,262 (GRCm39) |
V214L |
probably benign |
Het |
Serpina9 |
G |
T |
12: 103,967,728 (GRCm39) |
N222K |
probably benign |
Het |
Smchd1 |
A |
G |
17: 71,747,956 (GRCm39) |
Y429H |
probably damaging |
Het |
Smyd1 |
C |
T |
6: 71,239,164 (GRCm39) |
V9M |
probably damaging |
Het |
Sostdc1 |
C |
T |
12: 36,367,246 (GRCm39) |
Q141* |
probably null |
Het |
Spam1 |
C |
T |
6: 24,796,109 (GRCm39) |
T20I |
probably benign |
Het |
Tex47 |
T |
C |
5: 7,354,834 (GRCm39) |
V5A |
probably benign |
Het |
Thbs4 |
T |
C |
13: 92,912,582 (GRCm39) |
|
probably null |
Het |
Trim45 |
C |
T |
3: 100,837,257 (GRCm39) |
P531L |
probably damaging |
Het |
Tshb |
A |
T |
3: 102,685,478 (GRCm39) |
Y50* |
probably null |
Het |
Ttn |
T |
C |
2: 76,599,320 (GRCm39) |
I19230V |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Uba6 |
G |
A |
5: 86,270,288 (GRCm39) |
T832I |
probably damaging |
Het |
Unc13d |
A |
T |
11: 115,960,579 (GRCm39) |
V497D |
probably damaging |
Het |
Usp13 |
T |
C |
3: 32,892,007 (GRCm39) |
V62A |
probably damaging |
Het |
Vmn1r215 |
A |
C |
13: 23,260,189 (GRCm39) |
L76F |
probably damaging |
Het |
Vmn1r215 |
G |
T |
13: 23,260,190 (GRCm39) |
G77C |
probably damaging |
Het |
Vmn2r5 |
T |
C |
3: 64,411,497 (GRCm39) |
D357G |
probably damaging |
Het |
Zbtb40 |
T |
C |
4: 136,722,594 (GRCm39) |
D828G |
probably damaging |
Het |
Zfp74 |
A |
T |
7: 29,633,990 (GRCm39) |
C573S |
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 |
R5543:Cspg4b
|
UTSW |
13 |
113,457,407 (GRCm39) |
missense |
probably damaging |
0.96 |
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 |
|
|
|