Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abr |
T |
C |
11: 76,310,659 (GRCm39) |
T752A |
probably damaging |
Het |
Adar |
A |
G |
3: 89,657,569 (GRCm39) |
T508A |
possibly damaging |
Het |
Atxn3 |
T |
A |
12: 101,912,159 (GRCm39) |
K85I |
probably benign |
Het |
Atxn7l1 |
G |
T |
12: 33,197,882 (GRCm39) |
W50L |
probably damaging |
Het |
Bahcc1 |
T |
C |
11: 120,165,251 (GRCm39) |
V894A |
probably damaging |
Het |
Bloc1s3 |
G |
T |
7: 19,241,324 (GRCm39) |
T68K |
probably benign |
Het |
Bmerb1 |
T |
A |
16: 13,855,877 (GRCm39) |
|
probably null |
Het |
Brd10 |
T |
C |
19: 29,731,242 (GRCm39) |
H590R |
possibly damaging |
Het |
C130073F10Rik |
C |
T |
4: 101,747,881 (GRCm39) |
|
probably null |
Het |
Cd55b |
T |
C |
1: 130,341,870 (GRCm39) |
I256V |
probably benign |
Het |
Celsr3 |
T |
A |
9: 108,703,734 (GRCm39) |
D72E |
probably benign |
Het |
Cep41 |
T |
C |
6: 30,658,891 (GRCm39) |
D152G |
probably benign |
Het |
Cip2a |
C |
T |
16: 48,821,436 (GRCm39) |
Q181* |
probably null |
Het |
Cpne8 |
C |
A |
15: 90,425,496 (GRCm39) |
K285N |
possibly damaging |
Het |
Csmd3 |
A |
T |
15: 47,813,349 (GRCm39) |
I1061K |
probably damaging |
Het |
Cym |
T |
A |
3: 107,129,025 (GRCm39) |
|
probably benign |
Het |
Cyp2d9 |
T |
C |
15: 82,336,720 (GRCm39) |
V23A |
probably damaging |
Het |
Dnah1 |
A |
T |
14: 31,005,159 (GRCm39) |
I2365K |
probably benign |
Het |
Dock5 |
C |
T |
14: 68,054,957 (GRCm39) |
|
probably null |
Het |
Dop1a |
A |
T |
9: 86,403,639 (GRCm39) |
H1613L |
probably damaging |
Het |
Dusp5 |
T |
C |
19: 53,518,113 (GRCm39) |
V122A |
possibly damaging |
Het |
Emc6 |
A |
G |
11: 73,067,399 (GRCm39) |
L44P |
probably damaging |
Het |
Fbxl6 |
G |
T |
15: 76,422,678 (GRCm39) |
T80K |
probably benign |
Het |
Frrs1 |
T |
A |
3: 116,692,822 (GRCm39) |
M32K |
possibly damaging |
Het |
Gfod1 |
A |
G |
13: 43,354,366 (GRCm39) |
V203A |
possibly damaging |
Het |
Gjc2 |
G |
A |
11: 59,067,840 (GRCm39) |
A214V |
unknown |
Het |
Gkn2 |
T |
C |
6: 87,355,135 (GRCm39) |
Y115H |
probably damaging |
Het |
Gpatch1 |
A |
C |
7: 34,976,704 (GRCm39) |
|
probably benign |
Het |
Hemgn |
G |
T |
4: 46,403,935 (GRCm39) |
P20Q |
possibly damaging |
Het |
Herc1 |
G |
T |
9: 66,415,571 (GRCm39) |
V4849L |
possibly damaging |
Het |
Hmcn2 |
A |
T |
2: 31,275,353 (GRCm39) |
|
probably null |
Het |
Htt |
C |
A |
5: 35,034,499 (GRCm39) |
T1990N |
possibly damaging |
Het |
Jrk |
C |
T |
15: 74,578,474 (GRCm39) |
W270* |
probably null |
Het |
Katnb1 |
A |
G |
8: 95,822,072 (GRCm39) |
D266G |
probably damaging |
Het |
Klhl42 |
A |
G |
6: 147,009,421 (GRCm39) |
K420R |
probably damaging |
Het |
Lamb1 |
C |
A |
12: 31,356,998 (GRCm39) |
T1035K |
probably damaging |
Het |
Laptm5 |
T |
C |
4: 130,656,079 (GRCm39) |
|
probably null |
Het |
Lilra5 |
T |
C |
7: 4,240,971 (GRCm39) |
S22P |
probably benign |
Het |
Mn1 |
A |
G |
5: 111,568,505 (GRCm39) |
N825S |
possibly damaging |
Het |
Mup17 |
C |
T |
4: 61,510,419 (GRCm39) |
|
probably null |
Het |
Ncapd3 |
T |
A |
9: 26,983,100 (GRCm39) |
D949E |
probably benign |
Het |
Ncoa7 |
T |
C |
10: 30,570,155 (GRCm39) |
E230G |
probably damaging |
Het |
Nxnl1 |
A |
G |
8: 72,015,512 (GRCm39) |
V132A |
probably damaging |
Het |
Oard1 |
A |
G |
17: 48,723,788 (GRCm39) |
I145V |
probably benign |
Het |
Pabpc4 |
T |
G |
4: 123,189,846 (GRCm39) |
L555R |
probably benign |
Het |
Ppp1r11 |
G |
T |
17: 37,260,866 (GRCm39) |
S21R |
possibly damaging |
Het |
Prr36 |
T |
C |
8: 4,263,831 (GRCm39) |
|
probably benign |
Het |
Serpina1a |
T |
A |
12: 103,822,038 (GRCm39) |
D298V |
probably benign |
Het |
Sqle |
A |
T |
15: 59,196,314 (GRCm39) |
H369L |
possibly damaging |
Het |
Stambp |
T |
C |
6: 83,538,881 (GRCm39) |
E173G |
probably damaging |
Het |
Syne1 |
T |
C |
10: 5,300,983 (GRCm39) |
N915S |
probably damaging |
Het |
Tjap1 |
C |
A |
17: 46,593,530 (GRCm39) |
|
probably benign |
Het |
Tmem62 |
A |
C |
2: 120,814,817 (GRCm39) |
K30T |
probably damaging |
Het |
Tmtc1 |
T |
C |
6: 148,327,346 (GRCm39) |
T56A |
probably benign |
Het |
Trav6-4 |
A |
T |
14: 53,691,946 (GRCm39) |
M18L |
probably benign |
Het |
Trim69 |
T |
C |
2: 121,998,490 (GRCm39) |
I154T |
possibly damaging |
Het |
Uggt1 |
T |
C |
1: 36,209,377 (GRCm39) |
|
probably null |
Het |
Usp48 |
T |
A |
4: 137,350,693 (GRCm39) |
M60K |
probably benign |
Het |
Usp7 |
A |
G |
16: 8,513,735 (GRCm39) |
S753P |
probably benign |
Het |
Vmn2r27 |
A |
C |
6: 124,169,404 (GRCm39) |
N575K |
probably damaging |
Het |
Wdfy4 |
A |
C |
14: 32,695,581 (GRCm39) |
D2672E |
probably benign |
Het |
Zdhhc17 |
G |
A |
10: 110,845,803 (GRCm39) |
P30L |
probably benign |
Het |
Zmym4 |
T |
A |
4: 126,800,905 (GRCm39) |
Y565F |
possibly damaging |
Het |
|
Other mutations in Cspg4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01074:Cspg4
|
APN |
9 |
56,806,149 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01322:Cspg4
|
APN |
9 |
56,805,872 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01922:Cspg4
|
APN |
9 |
56,795,171 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01993:Cspg4
|
APN |
9 |
56,805,762 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02379:Cspg4
|
APN |
9 |
56,799,893 (GRCm39) |
splice site |
probably benign |
|
IGL02398:Cspg4
|
APN |
9 |
56,793,970 (GRCm39) |
missense |
probably benign |
0.43 |
IGL02503:Cspg4
|
APN |
9 |
56,804,687 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02504:Cspg4
|
APN |
9 |
56,793,056 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02692:Cspg4
|
APN |
9 |
56,794,738 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02728:Cspg4
|
APN |
9 |
56,793,765 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02806:Cspg4
|
APN |
9 |
56,797,543 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL02886:Cspg4
|
APN |
9 |
56,804,672 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03005:Cspg4
|
APN |
9 |
56,795,772 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03008:Cspg4
|
APN |
9 |
56,805,759 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL03202:Cspg4
|
APN |
9 |
56,805,023 (GRCm39) |
missense |
possibly damaging |
0.93 |
chiclets
|
UTSW |
9 |
56,792,506 (GRCm39) |
splice site |
probably null |
|
R0066:Cspg4
|
UTSW |
9 |
56,795,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R0066:Cspg4
|
UTSW |
9 |
56,795,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R0254:Cspg4
|
UTSW |
9 |
56,804,694 (GRCm39) |
missense |
probably damaging |
0.98 |
R0284:Cspg4
|
UTSW |
9 |
56,793,423 (GRCm39) |
missense |
probably damaging |
0.96 |
R0513:Cspg4
|
UTSW |
9 |
56,805,375 (GRCm39) |
missense |
probably benign |
0.03 |
R0602:Cspg4
|
UTSW |
9 |
56,795,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R0747:Cspg4
|
UTSW |
9 |
56,797,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R1005:Cspg4
|
UTSW |
9 |
56,796,020 (GRCm39) |
missense |
probably benign |
0.13 |
R1421:Cspg4
|
UTSW |
9 |
56,803,910 (GRCm39) |
missense |
probably benign |
0.00 |
R1443:Cspg4
|
UTSW |
9 |
56,793,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R1481:Cspg4
|
UTSW |
9 |
56,795,094 (GRCm39) |
missense |
probably damaging |
0.98 |
R1585:Cspg4
|
UTSW |
9 |
56,806,151 (GRCm39) |
missense |
probably damaging |
0.99 |
R1624:Cspg4
|
UTSW |
9 |
56,795,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R1670:Cspg4
|
UTSW |
9 |
56,804,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R1721:Cspg4
|
UTSW |
9 |
56,796,027 (GRCm39) |
missense |
probably damaging |
0.98 |
R1728:Cspg4
|
UTSW |
9 |
56,805,821 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Cspg4
|
UTSW |
9 |
56,805,821 (GRCm39) |
missense |
probably benign |
0.00 |
R1763:Cspg4
|
UTSW |
9 |
56,794,263 (GRCm39) |
missense |
probably damaging |
0.97 |
R1772:Cspg4
|
UTSW |
9 |
56,804,776 (GRCm39) |
missense |
probably benign |
0.02 |
R1938:Cspg4
|
UTSW |
9 |
56,794,385 (GRCm39) |
missense |
probably benign |
0.00 |
R1975:Cspg4
|
UTSW |
9 |
56,797,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R2064:Cspg4
|
UTSW |
9 |
56,803,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R2185:Cspg4
|
UTSW |
9 |
56,794,256 (GRCm39) |
missense |
probably benign |
0.37 |
R2252:Cspg4
|
UTSW |
9 |
56,805,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R2291:Cspg4
|
UTSW |
9 |
56,800,027 (GRCm39) |
missense |
probably damaging |
0.96 |
R2329:Cspg4
|
UTSW |
9 |
56,795,834 (GRCm39) |
missense |
probably benign |
0.00 |
R3780:Cspg4
|
UTSW |
9 |
56,795,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R3830:Cspg4
|
UTSW |
9 |
56,804,905 (GRCm39) |
missense |
probably damaging |
0.99 |
R3944:Cspg4
|
UTSW |
9 |
56,793,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R4011:Cspg4
|
UTSW |
9 |
56,794,601 (GRCm39) |
missense |
probably benign |
0.19 |
R4115:Cspg4
|
UTSW |
9 |
56,805,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R4173:Cspg4
|
UTSW |
9 |
56,795,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R4243:Cspg4
|
UTSW |
9 |
56,795,141 (GRCm39) |
missense |
probably benign |
0.12 |
R4329:Cspg4
|
UTSW |
9 |
56,799,749 (GRCm39) |
missense |
probably damaging |
0.99 |
R4544:Cspg4
|
UTSW |
9 |
56,795,913 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4545:Cspg4
|
UTSW |
9 |
56,795,913 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4546:Cspg4
|
UTSW |
9 |
56,795,913 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4649:Cspg4
|
UTSW |
9 |
56,794,149 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4663:Cspg4
|
UTSW |
9 |
56,793,960 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4674:Cspg4
|
UTSW |
9 |
56,805,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R4779:Cspg4
|
UTSW |
9 |
56,793,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R4884:Cspg4
|
UTSW |
9 |
56,805,353 (GRCm39) |
missense |
probably benign |
0.00 |
R5021:Cspg4
|
UTSW |
9 |
56,805,014 (GRCm39) |
missense |
probably benign |
0.01 |
R5051:Cspg4
|
UTSW |
9 |
56,793,020 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5328:Cspg4
|
UTSW |
9 |
56,793,140 (GRCm39) |
missense |
probably benign |
0.01 |
R5394:Cspg4
|
UTSW |
9 |
56,797,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R5567:Cspg4
|
UTSW |
9 |
56,793,932 (GRCm39) |
missense |
probably benign |
0.00 |
R5682:Cspg4
|
UTSW |
9 |
56,793,480 (GRCm39) |
missense |
probably benign |
0.14 |
R5690:Cspg4
|
UTSW |
9 |
56,806,019 (GRCm39) |
missense |
probably benign |
0.01 |
R5715:Cspg4
|
UTSW |
9 |
56,798,335 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5717:Cspg4
|
UTSW |
9 |
56,793,082 (GRCm39) |
missense |
probably benign |
|
R5726:Cspg4
|
UTSW |
9 |
56,793,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R5898:Cspg4
|
UTSW |
9 |
56,792,506 (GRCm39) |
splice site |
probably null |
|
R6140:Cspg4
|
UTSW |
9 |
56,804,508 (GRCm39) |
missense |
probably benign |
0.35 |
R6147:Cspg4
|
UTSW |
9 |
56,796,056 (GRCm39) |
missense |
probably damaging |
0.99 |
R6239:Cspg4
|
UTSW |
9 |
56,795,466 (GRCm39) |
missense |
probably benign |
0.04 |
R6343:Cspg4
|
UTSW |
9 |
56,799,976 (GRCm39) |
missense |
probably benign |
|
R6351:Cspg4
|
UTSW |
9 |
56,799,928 (GRCm39) |
missense |
probably benign |
0.00 |
R6564:Cspg4
|
UTSW |
9 |
56,797,442 (GRCm39) |
missense |
probably benign |
0.02 |
R6814:Cspg4
|
UTSW |
9 |
56,797,624 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6928:Cspg4
|
UTSW |
9 |
56,805,164 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6967:Cspg4
|
UTSW |
9 |
56,797,420 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6981:Cspg4
|
UTSW |
9 |
56,794,385 (GRCm39) |
missense |
probably benign |
0.00 |
R7033:Cspg4
|
UTSW |
9 |
56,795,358 (GRCm39) |
missense |
probably damaging |
0.96 |
R7419:Cspg4
|
UTSW |
9 |
56,795,727 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7809:Cspg4
|
UTSW |
9 |
56,797,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R7940:Cspg4
|
UTSW |
9 |
56,795,381 (GRCm39) |
nonsense |
probably null |
|
R8078:Cspg4
|
UTSW |
9 |
56,797,543 (GRCm39) |
missense |
possibly damaging |
0.57 |
R8082:Cspg4
|
UTSW |
9 |
56,793,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R8217:Cspg4
|
UTSW |
9 |
56,797,637 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8237:Cspg4
|
UTSW |
9 |
56,799,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R8372:Cspg4
|
UTSW |
9 |
56,794,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R8691:Cspg4
|
UTSW |
9 |
56,800,280 (GRCm39) |
missense |
probably benign |
|
R8720:Cspg4
|
UTSW |
9 |
56,794,797 (GRCm39) |
missense |
probably benign |
0.25 |
R8907:Cspg4
|
UTSW |
9 |
56,790,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R9063:Cspg4
|
UTSW |
9 |
56,795,687 (GRCm39) |
missense |
probably benign |
0.03 |
R9115:Cspg4
|
UTSW |
9 |
56,797,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R9152:Cspg4
|
UTSW |
9 |
56,795,463 (GRCm39) |
missense |
probably benign |
0.26 |
R9154:Cspg4
|
UTSW |
9 |
56,798,287 (GRCm39) |
missense |
|
|
R9361:Cspg4
|
UTSW |
9 |
56,803,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R9574:Cspg4
|
UTSW |
9 |
56,797,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R9608:Cspg4
|
UTSW |
9 |
56,792,836 (GRCm39) |
missense |
probably benign |
|
R9685:Cspg4
|
UTSW |
9 |
56,797,622 (GRCm39) |
missense |
probably benign |
0.05 |
X0065:Cspg4
|
UTSW |
9 |
56,793,020 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1088:Cspg4
|
UTSW |
9 |
56,793,320 (GRCm39) |
missense |
probably damaging |
1.00 |
|