Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aipl1 |
T |
C |
11: 71,921,028 (GRCm39) |
|
probably benign |
Het |
Akap11 |
T |
C |
14: 78,751,253 (GRCm39) |
D378G |
possibly damaging |
Het |
Ankrd33b |
A |
T |
15: 31,325,329 (GRCm39) |
F129L |
probably damaging |
Het |
Apob |
A |
G |
12: 8,065,222 (GRCm39) |
K4064E |
probably benign |
Het |
Arhgef10l |
T |
C |
4: 140,302,656 (GRCm39) |
D506G |
probably damaging |
Het |
Arid4b |
A |
C |
13: 14,327,997 (GRCm39) |
|
probably benign |
Het |
Ccdc88c |
A |
T |
12: 100,899,570 (GRCm39) |
Y1263N |
probably damaging |
Het |
Cplane1 |
T |
C |
15: 8,209,253 (GRCm39) |
F230S |
probably damaging |
Het |
Cpxm1 |
C |
T |
2: 130,235,601 (GRCm39) |
V464M |
probably damaging |
Het |
Dhrs7c |
A |
G |
11: 67,706,715 (GRCm39) |
E291G |
probably benign |
Het |
Dst |
C |
A |
1: 34,228,998 (GRCm39) |
P1872H |
possibly damaging |
Het |
G6pc2 |
G |
A |
2: 69,053,335 (GRCm39) |
A130T |
probably benign |
Het |
Gm4847 |
A |
G |
1: 166,462,578 (GRCm39) |
V304A |
probably damaging |
Het |
Gm8267 |
T |
C |
14: 44,955,374 (GRCm39) |
D155G |
possibly damaging |
Het |
Kank1 |
G |
A |
19: 25,388,066 (GRCm39) |
V580I |
probably benign |
Het |
Kcnh4 |
A |
G |
11: 100,636,649 (GRCm39) |
S757P |
probably damaging |
Het |
Krt34 |
C |
A |
11: 99,929,849 (GRCm39) |
A216S |
possibly damaging |
Het |
Mfhas1 |
A |
T |
8: 36,056,526 (GRCm39) |
I334F |
probably damaging |
Het |
Mrgprb8 |
A |
G |
7: 48,039,087 (GRCm39) |
M253V |
probably benign |
Het |
Or52n4b |
A |
T |
7: 108,144,137 (GRCm39) |
H133L |
probably benign |
Het |
Pp2d1 |
T |
A |
17: 53,815,468 (GRCm39) |
T419S |
probably damaging |
Het |
Pprc1 |
T |
A |
19: 46,060,782 (GRCm39) |
|
probably benign |
Het |
Reln |
A |
G |
5: 22,184,014 (GRCm39) |
S1662P |
probably damaging |
Het |
Sema7a |
G |
A |
9: 57,862,423 (GRCm39) |
E209K |
possibly damaging |
Het |
Serinc2 |
C |
T |
4: 130,158,237 (GRCm39) |
W15* |
probably null |
Het |
Serpina3k |
A |
G |
12: 104,311,525 (GRCm39) |
T368A |
probably benign |
Het |
Setd3 |
A |
T |
12: 108,129,289 (GRCm39) |
W54R |
probably damaging |
Het |
Slc9c1 |
G |
A |
16: 45,419,833 (GRCm39) |
S1001N |
probably benign |
Het |
Snapc3 |
A |
G |
4: 83,336,213 (GRCm39) |
D75G |
probably benign |
Het |
Spata31e2 |
A |
G |
1: 26,724,104 (GRCm39) |
Y359H |
probably damaging |
Het |
Stard9 |
T |
C |
2: 120,532,820 (GRCm39) |
S333P |
probably benign |
Het |
Utrn |
T |
C |
10: 12,610,948 (GRCm39) |
D469G |
probably 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 |
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 |
R6343:Ckap5
|
UTSW |
2 |
91,426,819 (GRCm39) |
missense |
possibly damaging |
0.95 |
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 |
|