Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
A |
T |
11: 110,205,378 (GRCm39) |
L301Q |
probably damaging |
Het |
Adgrl4 |
T |
C |
3: 151,223,443 (GRCm39) |
L632P |
probably damaging |
Het |
Cacna2d1 |
T |
A |
5: 16,527,562 (GRCm39) |
I539N |
probably benign |
Het |
Camta1 |
T |
A |
4: 151,164,306 (GRCm39) |
H314L |
probably damaging |
Het |
Car2 |
T |
C |
3: 14,953,025 (GRCm39) |
S56P |
probably damaging |
Het |
Chrm5 |
G |
A |
2: 112,309,793 (GRCm39) |
A441V |
probably damaging |
Het |
Cspg4 |
T |
C |
9: 56,799,976 (GRCm39) |
V1580A |
probably benign |
Het |
Dcc |
A |
G |
18: 71,469,106 (GRCm39) |
L1099P |
probably damaging |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Homo |
Epha5 |
A |
T |
5: 84,254,606 (GRCm39) |
H644Q |
probably damaging |
Het |
Eya3 |
T |
C |
4: 132,400,221 (GRCm39) |
I80T |
probably damaging |
Het |
Fdft1 |
A |
T |
14: 63,388,721 (GRCm39) |
Y304N |
probably damaging |
Het |
Fiz1 |
C |
T |
7: 5,011,400 (GRCm39) |
A373T |
possibly damaging |
Het |
Gpatch2l |
T |
A |
12: 86,307,379 (GRCm39) |
Y252* |
probably null |
Het |
Hivep1 |
G |
T |
13: 42,313,147 (GRCm39) |
G1796* |
probably null |
Het |
Irf8 |
T |
C |
8: 121,480,446 (GRCm39) |
V228A |
probably damaging |
Het |
Islr |
A |
C |
9: 58,064,379 (GRCm39) |
V376G |
probably damaging |
Het |
Kdm5a |
T |
C |
6: 120,359,894 (GRCm39) |
V230A |
probably benign |
Het |
Lpgat1 |
A |
G |
1: 191,508,684 (GRCm39) |
|
probably null |
Het |
Lrp8 |
T |
C |
4: 107,726,353 (GRCm39) |
|
probably null |
Het |
Lyzl4 |
A |
C |
9: 121,407,150 (GRCm39) |
S127A |
possibly damaging |
Het |
Map4k1 |
T |
C |
7: 28,699,715 (GRCm39) |
V606A |
possibly damaging |
Het |
Mau2 |
T |
A |
8: 70,484,173 (GRCm39) |
K138N |
probably damaging |
Het |
Meikin |
T |
C |
11: 54,261,592 (GRCm39) |
L33P |
probably damaging |
Het |
Mrpl28 |
T |
C |
17: 26,345,252 (GRCm39) |
V224A |
probably benign |
Het |
Ncdn |
T |
C |
4: 126,640,964 (GRCm39) |
D512G |
possibly damaging |
Het |
Nlrp2 |
T |
A |
7: 5,303,925 (GRCm39) |
Q200L |
possibly damaging |
Het |
Nup98 |
T |
C |
7: 101,843,957 (GRCm39) |
N89S |
possibly damaging |
Het |
Ogfrl1 |
T |
G |
1: 23,408,944 (GRCm39) |
K427N |
probably benign |
Het |
Or14a258 |
T |
A |
7: 86,035,059 (GRCm39) |
R270* |
probably null |
Het |
Or52p2 |
A |
G |
7: 102,237,753 (GRCm39) |
C66R |
probably damaging |
Het |
Or5b12 |
G |
T |
19: 12,896,946 (GRCm39) |
H242Q |
probably damaging |
Het |
Or6c201 |
A |
T |
10: 128,969,535 (GRCm39) |
L34* |
probably null |
Het |
Padi3 |
C |
T |
4: 140,530,819 (GRCm39) |
V68I |
possibly damaging |
Het |
Pign |
A |
T |
1: 105,512,820 (GRCm39) |
M621K |
probably benign |
Het |
Pigv |
C |
T |
4: 133,392,547 (GRCm39) |
V208M |
probably damaging |
Het |
Ripk4 |
A |
G |
16: 97,564,726 (GRCm39) |
|
probably benign |
Het |
Rsf1 |
A |
G |
7: 97,310,124 (GRCm39) |
K285E |
probably benign |
Het |
Serpina3k |
G |
C |
12: 104,311,562 (GRCm39) |
G380A |
probably benign |
Het |
Sorbs1 |
A |
G |
19: 40,365,426 (GRCm39) |
|
probably null |
Het |
Srrd |
G |
C |
5: 112,487,866 (GRCm39) |
A104G |
probably benign |
Het |
Tbp |
T |
A |
17: 15,721,351 (GRCm39) |
|
probably null |
Het |
Tecrl |
G |
A |
5: 83,442,447 (GRCm39) |
H209Y |
probably damaging |
Het |
Tmprss11c |
A |
G |
5: 86,404,204 (GRCm39) |
L157P |
probably damaging |
Het |
Tmprss13 |
A |
T |
9: 45,254,498 (GRCm39) |
T422S |
possibly damaging |
Het |
Ttll5 |
A |
G |
12: 86,003,473 (GRCm39) |
H1103R |
probably benign |
Het |
Urb2 |
G |
T |
8: 124,757,864 (GRCm39) |
E1190D |
probably damaging |
Het |
Vldlr |
A |
G |
19: 27,223,049 (GRCm39) |
Y699C |
probably damaging |
Het |
Vmn1r22 |
T |
G |
6: 57,877,563 (GRCm39) |
N138T |
possibly damaging |
Het |
|
Other mutations in Ckap5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00508:Ckap5
|
APN |
2 |
91,436,601 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00566:Ckap5
|
APN |
2 |
91,398,972 (GRCm39) |
splice site |
probably benign |
|
IGL00585:Ckap5
|
APN |
2 |
91,450,170 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00910:Ckap5
|
APN |
2 |
91,406,395 (GRCm39) |
missense |
probably benign |
0.32 |
IGL01309:Ckap5
|
APN |
2 |
91,400,529 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01411:Ckap5
|
APN |
2 |
91,431,356 (GRCm39) |
missense |
probably benign |
0.26 |
IGL01654:Ckap5
|
APN |
2 |
91,407,954 (GRCm39) |
missense |
probably benign |
0.26 |
IGL01684:Ckap5
|
APN |
2 |
91,385,699 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02031:Ckap5
|
APN |
2 |
91,443,117 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02057:Ckap5
|
APN |
2 |
91,431,052 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02101:Ckap5
|
APN |
2 |
91,402,885 (GRCm39) |
splice site |
probably benign |
|
IGL02250:Ckap5
|
APN |
2 |
91,379,246 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02556:Ckap5
|
APN |
2 |
91,425,186 (GRCm39) |
splice site |
probably benign |
|
IGL02620:Ckap5
|
APN |
2 |
91,436,714 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02627:Ckap5
|
APN |
2 |
91,406,366 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02693:Ckap5
|
APN |
2 |
91,400,556 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02808:Ckap5
|
APN |
2 |
91,426,859 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03086:Ckap5
|
APN |
2 |
91,400,621 (GRCm39) |
splice site |
probably benign |
|
Elephantine
|
UTSW |
2 |
91,406,614 (GRCm39) |
missense |
probably damaging |
1.00 |
hardiness
|
UTSW |
2 |
91,445,445 (GRCm39) |
missense |
possibly damaging |
0.68 |
total
|
UTSW |
2 |
91,400,597 (GRCm39) |
missense |
probably damaging |
0.99 |
K7371:Ckap5
|
UTSW |
2 |
91,425,868 (GRCm39) |
splice site |
probably benign |
|
R0106:Ckap5
|
UTSW |
2 |
91,446,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R0106:Ckap5
|
UTSW |
2 |
91,408,550 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0114:Ckap5
|
UTSW |
2 |
91,450,457 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0464:Ckap5
|
UTSW |
2 |
91,409,858 (GRCm39) |
missense |
probably benign |
0.00 |
R0633:Ckap5
|
UTSW |
2 |
91,381,088 (GRCm39) |
missense |
probably damaging |
0.96 |
R0723:Ckap5
|
UTSW |
2 |
91,385,676 (GRCm39) |
missense |
probably damaging |
0.99 |
R1037:Ckap5
|
UTSW |
2 |
91,380,974 (GRCm39) |
missense |
probably benign |
0.00 |
R1139:Ckap5
|
UTSW |
2 |
91,411,488 (GRCm39) |
missense |
probably benign |
0.11 |
R1161:Ckap5
|
UTSW |
2 |
91,429,720 (GRCm39) |
missense |
probably null |
1.00 |
R1183:Ckap5
|
UTSW |
2 |
91,416,611 (GRCm39) |
missense |
probably benign |
0.01 |
R1660:Ckap5
|
UTSW |
2 |
91,393,303 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1850:Ckap5
|
UTSW |
2 |
91,426,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R1951:Ckap5
|
UTSW |
2 |
91,386,837 (GRCm39) |
splice site |
probably benign |
|
R1968:Ckap5
|
UTSW |
2 |
91,416,688 (GRCm39) |
missense |
probably benign |
0.10 |
R2004:Ckap5
|
UTSW |
2 |
91,437,891 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2143:Ckap5
|
UTSW |
2 |
91,396,090 (GRCm39) |
missense |
probably benign |
0.00 |
R2391:Ckap5
|
UTSW |
2 |
91,416,214 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2435:Ckap5
|
UTSW |
2 |
91,411,490 (GRCm39) |
missense |
probably benign |
0.01 |
R2438:Ckap5
|
UTSW |
2 |
91,425,753 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2680:Ckap5
|
UTSW |
2 |
91,419,043 (GRCm39) |
missense |
probably benign |
|
R2698:Ckap5
|
UTSW |
2 |
91,408,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R3420:Ckap5
|
UTSW |
2 |
91,400,597 (GRCm39) |
missense |
probably damaging |
0.99 |
R3422:Ckap5
|
UTSW |
2 |
91,400,597 (GRCm39) |
missense |
probably damaging |
0.99 |
R3696:Ckap5
|
UTSW |
2 |
91,450,511 (GRCm39) |
missense |
probably benign |
0.15 |
R3698:Ckap5
|
UTSW |
2 |
91,450,511 (GRCm39) |
missense |
probably benign |
0.15 |
R3877:Ckap5
|
UTSW |
2 |
91,445,495 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4453:Ckap5
|
UTSW |
2 |
91,379,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R4604:Ckap5
|
UTSW |
2 |
91,408,476 (GRCm39) |
missense |
probably benign |
0.00 |
R4605:Ckap5
|
UTSW |
2 |
91,406,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R4849:Ckap5
|
UTSW |
2 |
91,445,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R5267:Ckap5
|
UTSW |
2 |
91,422,097 (GRCm39) |
missense |
probably null |
1.00 |
R5367:Ckap5
|
UTSW |
2 |
91,445,486 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5481:Ckap5
|
UTSW |
2 |
91,402,792 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5546:Ckap5
|
UTSW |
2 |
91,425,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R5704:Ckap5
|
UTSW |
2 |
91,406,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R5786:Ckap5
|
UTSW |
2 |
91,446,641 (GRCm39) |
splice site |
probably null |
|
R5793:Ckap5
|
UTSW |
2 |
91,450,180 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5824:Ckap5
|
UTSW |
2 |
91,389,481 (GRCm39) |
missense |
probably benign |
0.34 |
R5841:Ckap5
|
UTSW |
2 |
91,431,027 (GRCm39) |
missense |
probably benign |
0.05 |
R5875:Ckap5
|
UTSW |
2 |
91,391,206 (GRCm39) |
missense |
probably benign |
|
R5935:Ckap5
|
UTSW |
2 |
91,445,445 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6008:Ckap5
|
UTSW |
2 |
91,393,334 (GRCm39) |
missense |
probably damaging |
0.99 |
R6174:Ckap5
|
UTSW |
2 |
91,398,564 (GRCm39) |
missense |
probably benign |
0.00 |
R6624:Ckap5
|
UTSW |
2 |
91,407,996 (GRCm39) |
missense |
probably benign |
0.01 |
R6786:Ckap5
|
UTSW |
2 |
91,387,920 (GRCm39) |
missense |
probably benign |
0.01 |
R6793:Ckap5
|
UTSW |
2 |
91,399,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R6841:Ckap5
|
UTSW |
2 |
91,400,597 (GRCm39) |
missense |
probably damaging |
0.99 |
R6972:Ckap5
|
UTSW |
2 |
91,436,658 (GRCm39) |
missense |
probably damaging |
0.98 |
R7044:Ckap5
|
UTSW |
2 |
91,407,946 (GRCm39) |
missense |
probably benign |
|
R7111:Ckap5
|
UTSW |
2 |
91,437,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R7790:Ckap5
|
UTSW |
2 |
91,389,455 (GRCm39) |
missense |
probably benign |
|
R7809:Ckap5
|
UTSW |
2 |
91,436,702 (GRCm39) |
missense |
probably benign |
0.28 |
R7921:Ckap5
|
UTSW |
2 |
91,379,285 (GRCm39) |
missense |
probably damaging |
0.96 |
R8125:Ckap5
|
UTSW |
2 |
91,406,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R8331:Ckap5
|
UTSW |
2 |
91,406,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R8342:Ckap5
|
UTSW |
2 |
91,436,707 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8511:Ckap5
|
UTSW |
2 |
91,445,492 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8708:Ckap5
|
UTSW |
2 |
91,425,823 (GRCm39) |
missense |
probably benign |
0.03 |
R8946:Ckap5
|
UTSW |
2 |
91,409,861 (GRCm39) |
missense |
probably benign |
0.44 |
R8982:Ckap5
|
UTSW |
2 |
91,437,923 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9113:Ckap5
|
UTSW |
2 |
91,426,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R9161:Ckap5
|
UTSW |
2 |
91,445,653 (GRCm39) |
missense |
probably benign |
|
R9238:Ckap5
|
UTSW |
2 |
91,399,027 (GRCm39) |
missense |
probably null |
0.10 |
R9339:Ckap5
|
UTSW |
2 |
91,396,100 (GRCm39) |
missense |
probably benign |
|
R9571:Ckap5
|
UTSW |
2 |
91,387,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R9718:Ckap5
|
UTSW |
2 |
91,379,177 (GRCm39) |
missense |
probably benign |
0.10 |
X0010:Ckap5
|
UTSW |
2 |
91,426,854 (GRCm39) |
missense |
possibly damaging |
0.61 |
Z1177:Ckap5
|
UTSW |
2 |
91,416,143 (GRCm39) |
missense |
probably damaging |
1.00 |
|