Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts7 |
G |
T |
9: 90,073,880 (GRCm39) |
|
probably benign |
Het |
Als2 |
A |
G |
1: 59,235,506 (GRCm39) |
V726A |
probably benign |
Het |
Apba1 |
G |
A |
19: 23,922,269 (GRCm39) |
G779E |
possibly damaging |
Het |
Atr |
T |
A |
9: 95,818,528 (GRCm39) |
V2167E |
probably damaging |
Het |
Bod1l |
T |
C |
5: 41,983,846 (GRCm39) |
K566E |
probably damaging |
Het |
Btd |
T |
C |
14: 31,389,319 (GRCm39) |
F347L |
probably benign |
Het |
Btg2 |
T |
C |
1: 134,006,643 (GRCm39) |
|
probably benign |
Het |
Cblb |
T |
A |
16: 52,003,672 (GRCm39) |
S717T |
probably benign |
Het |
Cep250 |
T |
A |
2: 155,825,198 (GRCm39) |
|
probably benign |
Het |
Cep350 |
T |
C |
1: 155,828,968 (GRCm39) |
N312S |
probably benign |
Het |
Clasp1 |
A |
T |
1: 118,530,107 (GRCm39) |
T1490S |
probably damaging |
Het |
Col7a1 |
T |
A |
9: 108,813,172 (GRCm39) |
C2906S |
probably benign |
Het |
Csmd1 |
C |
T |
8: 16,049,779 (GRCm39) |
|
probably null |
Het |
Cyp7b1 |
T |
A |
3: 18,126,739 (GRCm39) |
D469V |
probably damaging |
Het |
Dhh |
A |
T |
15: 98,792,192 (GRCm39) |
|
probably null |
Het |
Dhrs3 |
A |
G |
4: 144,646,642 (GRCm39) |
R231G |
probably damaging |
Het |
Disp3 |
A |
G |
4: 148,356,495 (GRCm39) |
S122P |
probably damaging |
Het |
Dnah1 |
T |
C |
14: 31,005,955 (GRCm39) |
I2275V |
probably benign |
Het |
Dock8 |
A |
C |
19: 25,109,584 (GRCm39) |
N922T |
probably benign |
Het |
Eef1d |
A |
G |
15: 75,774,945 (GRCm39) |
L154P |
probably damaging |
Het |
Eif4ebp1 |
C |
A |
8: 27,763,510 (GRCm39) |
P101Q |
possibly damaging |
Het |
Eif4g1 |
T |
G |
16: 20,505,502 (GRCm39) |
|
probably benign |
Het |
Emb |
A |
G |
13: 117,369,301 (GRCm39) |
M50V |
probably benign |
Het |
Eml4 |
T |
C |
17: 83,780,568 (GRCm39) |
|
probably null |
Het |
Fkbp10 |
G |
T |
11: 100,306,803 (GRCm39) |
R65L |
probably damaging |
Het |
Gm5878 |
T |
C |
6: 85,095,574 (GRCm39) |
N83S |
probably benign |
Het |
Gm8165 |
C |
T |
14: 43,913,694 (GRCm39) |
A57T |
unknown |
Het |
Gpr179 |
A |
G |
11: 97,228,726 (GRCm39) |
V1143A |
probably damaging |
Het |
Hat1 |
T |
C |
2: 71,251,604 (GRCm39) |
Y218H |
probably damaging |
Het |
Hfm1 |
T |
A |
5: 107,026,689 (GRCm39) |
N885I |
probably benign |
Het |
Ift70a1 |
T |
A |
2: 75,811,193 (GRCm39) |
M297L |
probably benign |
Het |
Inha |
T |
C |
1: 75,486,091 (GRCm39) |
S129P |
probably damaging |
Het |
Ints9 |
T |
C |
14: 65,230,457 (GRCm39) |
I128T |
probably damaging |
Het |
Klra9 |
T |
C |
6: 130,168,149 (GRCm39) |
|
probably null |
Het |
Lrba |
A |
G |
3: 86,683,356 (GRCm39) |
E2726G |
probably damaging |
Het |
Lrp1b |
T |
C |
2: 40,691,410 (GRCm39) |
N3356D |
probably benign |
Het |
Map3k5 |
A |
G |
10: 19,994,038 (GRCm39) |
D1008G |
possibly damaging |
Het |
Med4 |
T |
A |
14: 73,755,415 (GRCm39) |
L241Q |
possibly damaging |
Het |
Mtch1 |
A |
G |
17: 29,557,716 (GRCm39) |
V254A |
possibly damaging |
Het |
Napg |
C |
T |
18: 63,127,375 (GRCm39) |
|
probably benign |
Het |
Or1j11 |
T |
C |
2: 36,312,156 (GRCm39) |
S249P |
possibly damaging |
Het |
Or5k1 |
C |
T |
16: 58,617,843 (GRCm39) |
R122H |
probably benign |
Het |
Or7g33 |
A |
G |
9: 19,449,142 (GRCm39) |
F28S |
possibly damaging |
Het |
Or8d2 |
T |
C |
9: 38,760,222 (GRCm39) |
S271P |
probably damaging |
Het |
Or9r3 |
T |
A |
10: 129,948,487 (GRCm39) |
R57S |
probably damaging |
Het |
Pias1 |
T |
A |
9: 62,830,926 (GRCm39) |
S161C |
probably damaging |
Het |
Pias1 |
G |
T |
9: 62,830,927 (GRCm39) |
N160K |
possibly damaging |
Het |
Pigp |
G |
A |
16: 94,168,466 (GRCm39) |
P37S |
probably damaging |
Het |
Pik3c2b |
T |
A |
1: 133,020,065 (GRCm39) |
V1070E |
probably benign |
Het |
Pramel51 |
G |
T |
12: 88,142,792 (GRCm39) |
H275Q |
probably benign |
Het |
Prepl |
T |
C |
17: 85,378,010 (GRCm39) |
T457A |
probably damaging |
Het |
Psg23 |
G |
A |
7: 18,340,853 (GRCm39) |
A467V |
probably benign |
Het |
Rad54l |
T |
C |
4: 115,980,146 (GRCm39) |
R13G |
probably benign |
Het |
Rassf5 |
T |
C |
1: 131,108,336 (GRCm39) |
D248G |
probably damaging |
Het |
Rspo1 |
A |
G |
4: 124,898,955 (GRCm39) |
N92S |
probably damaging |
Het |
Scube1 |
G |
A |
15: 83,543,217 (GRCm39) |
|
probably benign |
Het |
Sec31b |
C |
A |
19: 44,511,554 (GRCm39) |
V616F |
probably damaging |
Het |
Sema3a |
T |
C |
5: 13,615,881 (GRCm39) |
V435A |
probably damaging |
Het |
Slc7a10 |
T |
A |
7: 34,897,123 (GRCm39) |
I208N |
probably damaging |
Het |
Stab2 |
A |
T |
10: 86,692,420 (GRCm39) |
M2151K |
possibly damaging |
Het |
Tacc1 |
T |
C |
8: 25,665,235 (GRCm39) |
D50G |
probably damaging |
Het |
Tas2r121 |
G |
T |
6: 132,677,480 (GRCm39) |
T164N |
probably damaging |
Het |
Tatdn2 |
T |
C |
6: 113,681,676 (GRCm39) |
W570R |
probably damaging |
Het |
Telo2 |
A |
T |
17: 25,323,628 (GRCm39) |
F600I |
probably damaging |
Het |
Trim36 |
T |
A |
18: 46,305,669 (GRCm39) |
H426L |
probably benign |
Het |
Trpm6 |
A |
T |
19: 18,787,016 (GRCm39) |
N531Y |
possibly damaging |
Het |
Ttc39a |
T |
C |
4: 109,299,920 (GRCm39) |
C470R |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,615,283 (GRCm39) |
E8485K |
probably damaging |
Het |
Ubr4 |
A |
T |
4: 139,196,122 (GRCm39) |
I1253F |
probably damaging |
Het |
Unc79 |
A |
T |
12: 103,088,688 (GRCm39) |
H1724L |
possibly damaging |
Het |
Vmn1r40 |
T |
A |
6: 89,691,998 (GRCm39) |
C89S |
probably benign |
Het |
Wdr55 |
A |
G |
18: 36,896,435 (GRCm39) |
E375G |
probably benign |
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 |
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 |
R8353:Cspg4
|
UTSW |
9 |
56,805,953 (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 |
|