Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610318N02Rik |
A |
G |
16: 16,931,410 (GRCm39) |
V275A |
possibly damaging |
Het |
Adamts2 |
A |
G |
11: 50,694,528 (GRCm39) |
D1105G |
probably benign |
Het |
Adgrb3 |
T |
A |
1: 25,151,352 (GRCm39) |
M195L |
possibly damaging |
Het |
Adrm1 |
A |
G |
2: 179,817,756 (GRCm39) |
|
probably benign |
Het |
Atg13 |
T |
A |
2: 91,509,176 (GRCm39) |
I457F |
possibly damaging |
Het |
BC034090 |
T |
C |
1: 155,102,130 (GRCm39) |
N45D |
probably damaging |
Het |
C3 |
C |
T |
17: 57,516,652 (GRCm39) |
|
probably benign |
Het |
Cacna1a |
G |
A |
8: 85,249,657 (GRCm39) |
G221D |
probably damaging |
Het |
Calr |
A |
G |
8: 85,573,335 (GRCm39) |
|
probably null |
Het |
Chd3 |
C |
T |
11: 69,248,557 (GRCm39) |
V825I |
probably damaging |
Het |
Chdh |
T |
G |
14: 29,757,761 (GRCm39) |
|
probably benign |
Het |
Commd3 |
A |
G |
2: 18,677,289 (GRCm39) |
E5G |
probably benign |
Het |
Ddi1 |
T |
C |
9: 6,265,773 (GRCm39) |
R199G |
probably damaging |
Het |
Dennd4c |
A |
G |
4: 86,723,724 (GRCm39) |
|
probably benign |
Het |
Dok7 |
G |
A |
5: 35,236,912 (GRCm39) |
G293D |
possibly damaging |
Het |
Epm2aip1 |
T |
C |
9: 111,102,596 (GRCm39) |
V523A |
probably benign |
Het |
Fam171b |
C |
T |
2: 83,709,791 (GRCm39) |
Q488* |
probably null |
Het |
Gabbr1 |
G |
A |
17: 37,359,499 (GRCm39) |
|
probably null |
Het |
Gm5965 |
T |
G |
16: 88,575,219 (GRCm39) |
S131A |
possibly damaging |
Het |
Gpcpd1 |
T |
C |
2: 132,392,244 (GRCm39) |
D235G |
probably damaging |
Het |
Grip1 |
A |
T |
10: 119,767,207 (GRCm39) |
K111* |
probably null |
Het |
Itih4 |
G |
T |
14: 30,613,706 (GRCm39) |
D308Y |
probably damaging |
Het |
Kcnj6 |
A |
G |
16: 94,633,314 (GRCm39) |
Y266H |
probably damaging |
Het |
Lrrc41 |
T |
C |
4: 115,953,663 (GRCm39) |
L783P |
probably damaging |
Het |
Map4k5 |
T |
C |
12: 69,888,737 (GRCm39) |
D298G |
probably benign |
Het |
Mapkbp1 |
T |
C |
2: 119,849,423 (GRCm39) |
F712L |
probably damaging |
Het |
Mcoln2 |
T |
C |
3: 145,869,282 (GRCm39) |
|
probably benign |
Het |
Megf11 |
T |
A |
9: 64,588,698 (GRCm39) |
S532R |
probably benign |
Het |
Mkx |
T |
C |
18: 6,937,192 (GRCm39) |
D284G |
probably benign |
Het |
Mmp16 |
A |
G |
4: 18,116,185 (GRCm39) |
I596M |
probably damaging |
Het |
Msto1 |
C |
A |
3: 88,820,993 (GRCm39) |
R34L |
probably benign |
Het |
Mtmr9 |
A |
G |
14: 63,764,254 (GRCm39) |
L491P |
probably damaging |
Het |
Or4a66 |
T |
G |
2: 88,531,310 (GRCm39) |
Y121S |
probably damaging |
Het |
Or8b52 |
T |
A |
9: 38,576,289 (GRCm39) |
I284L |
probably benign |
Het |
Or9s13 |
T |
C |
1: 92,548,057 (GRCm39) |
M143T |
probably damaging |
Het |
Otor |
T |
C |
2: 142,920,532 (GRCm39) |
V38A |
possibly damaging |
Het |
Pcdhb12 |
G |
T |
18: 37,569,207 (GRCm39) |
D118Y |
probably damaging |
Het |
Prelp |
T |
C |
1: 133,842,545 (GRCm39) |
H200R |
probably benign |
Het |
Prmt5 |
T |
C |
14: 54,747,334 (GRCm39) |
Y481C |
probably damaging |
Het |
Psg23 |
T |
G |
7: 18,348,465 (GRCm39) |
D114A |
probably damaging |
Het |
Ptger4 |
A |
T |
15: 5,272,239 (GRCm39) |
Y127N |
probably damaging |
Het |
Rabgap1l |
C |
A |
1: 160,528,368 (GRCm39) |
V385L |
probably benign |
Het |
Rergl |
T |
A |
6: 139,470,256 (GRCm39) |
K191* |
probably null |
Het |
Sart3 |
A |
G |
5: 113,897,311 (GRCm39) |
F252S |
probably damaging |
Het |
Sbno1 |
A |
T |
5: 124,519,769 (GRCm39) |
S1169T |
probably benign |
Het |
Serpinb8 |
C |
T |
1: 107,532,448 (GRCm39) |
T180M |
probably damaging |
Het |
Sipa1l1 |
G |
A |
12: 82,434,470 (GRCm39) |
E747K |
probably benign |
Het |
Sptb |
T |
A |
12: 76,634,237 (GRCm39) |
D2158V |
probably benign |
Het |
Sycp2 |
T |
G |
2: 177,999,904 (GRCm39) |
D1024A |
probably benign |
Het |
Tbr1 |
T |
G |
2: 61,636,411 (GRCm39) |
N262K |
possibly damaging |
Het |
Tnrc6a |
A |
T |
7: 122,770,717 (GRCm39) |
I836F |
probably benign |
Het |
Ttn |
T |
C |
2: 76,769,091 (GRCm39) |
E2823G |
probably damaging |
Het |
Uqcrc1 |
T |
A |
9: 108,778,026 (GRCm39) |
L441Q |
possibly damaging |
Het |
Vmn1r180 |
T |
C |
7: 23,652,424 (GRCm39) |
F196L |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,787,997 (GRCm39) |
I451M |
possibly damaging |
Het |
Zcchc7 |
A |
T |
4: 44,926,060 (GRCm39) |
H353L |
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 |
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 |
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 |
|