Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actc1 |
T |
C |
2: 113,879,799 (GRCm39) |
Y220C |
probably damaging |
Het |
Actmap |
T |
C |
7: 26,896,655 (GRCm39) |
S73P |
possibly damaging |
Het |
Bmper |
G |
A |
9: 23,286,902 (GRCm39) |
G276D |
possibly damaging |
Het |
C2cd5 |
A |
T |
6: 142,984,613 (GRCm39) |
M549K |
probably benign |
Het |
Caprin1 |
A |
G |
2: 103,606,283 (GRCm39) |
V319A |
possibly damaging |
Het |
Cchcr1 |
G |
A |
17: 35,839,285 (GRCm39) |
|
probably null |
Het |
Cdc42bpb |
A |
T |
12: 111,265,783 (GRCm39) |
V1383E |
possibly damaging |
Het |
Cep350 |
T |
C |
1: 155,770,433 (GRCm39) |
E1819G |
probably damaging |
Het |
Ces4a |
A |
G |
8: 105,869,054 (GRCm39) |
E163G |
possibly damaging |
Het |
Chrnd |
C |
T |
1: 87,118,792 (GRCm39) |
R50* |
probably null |
Het |
Cntn3 |
A |
G |
6: 102,183,511 (GRCm39) |
S715P |
probably damaging |
Het |
Creb1 |
A |
T |
1: 64,598,909 (GRCm39) |
R95S |
probably benign |
Het |
Ctdp1 |
T |
C |
18: 80,492,710 (GRCm39) |
Y595C |
probably damaging |
Het |
Cts7 |
C |
T |
13: 61,504,223 (GRCm39) |
E86K |
probably damaging |
Het |
Dazap1 |
A |
G |
10: 80,113,440 (GRCm39) |
N113S |
unknown |
Het |
Dhdds |
T |
C |
4: 133,727,706 (GRCm39) |
|
probably null |
Het |
Dnaaf9 |
A |
G |
2: 130,554,938 (GRCm39) |
S998P |
probably damaging |
Het |
Dnah1 |
T |
C |
14: 30,985,395 (GRCm39) |
D3832G |
probably damaging |
Het |
Drd1 |
A |
G |
13: 54,207,182 (GRCm39) |
L344P |
probably damaging |
Het |
Fam135b |
G |
A |
15: 71,324,199 (GRCm39) |
T1256I |
probably benign |
Het |
Fam234a |
A |
T |
17: 26,432,627 (GRCm39) |
D507E |
probably benign |
Het |
Fbxw16 |
A |
T |
9: 109,278,169 (GRCm39) |
I3N |
probably benign |
Het |
Foxd4 |
A |
T |
19: 24,877,670 (GRCm39) |
W177R |
probably damaging |
Het |
Fyb2 |
A |
G |
4: 104,802,961 (GRCm39) |
S288G |
probably benign |
Het |
Gadl1 |
A |
G |
9: 115,789,519 (GRCm39) |
H275R |
probably benign |
Het |
Gbp5 |
A |
G |
3: 142,206,366 (GRCm39) |
T17A |
probably benign |
Het |
Gm1110 |
A |
T |
9: 26,800,894 (GRCm39) |
Y433* |
probably null |
Het |
Gm6408 |
C |
A |
5: 146,420,628 (GRCm39) |
D169E |
probably benign |
Het |
Gramd2b |
T |
A |
18: 56,611,972 (GRCm39) |
V145E |
probably damaging |
Het |
Grip1 |
G |
A |
10: 119,874,569 (GRCm39) |
E778K |
possibly damaging |
Het |
Hcn1 |
GCA |
GCAACA |
13: 118,112,305 (GRCm39) |
|
probably benign |
Het |
Hif1an |
G |
A |
19: 44,558,378 (GRCm39) |
V293M |
probably damaging |
Het |
Hyal3 |
A |
G |
9: 107,462,347 (GRCm39) |
D127G |
probably damaging |
Het |
Ighg1 |
T |
A |
12: 113,293,252 (GRCm39) |
D146V |
possibly damaging |
Het |
Iws1 |
T |
A |
18: 32,216,347 (GRCm39) |
D362E |
probably damaging |
Het |
Kif21b |
G |
A |
1: 136,080,961 (GRCm39) |
E601K |
probably damaging |
Het |
Krtap13-1 |
C |
T |
16: 88,526,229 (GRCm39) |
T151I |
probably benign |
Het |
Ndufa10 |
A |
T |
1: 92,379,752 (GRCm39) |
I327N |
probably benign |
Het |
Or10ag53 |
A |
G |
2: 87,082,439 (GRCm39) |
I53V |
possibly damaging |
Het |
Or10z1 |
A |
G |
1: 174,077,902 (GRCm39) |
L197P |
probably damaging |
Het |
Pcdhb14 |
T |
C |
18: 37,582,040 (GRCm39) |
V382A |
probably benign |
Het |
Pex1 |
A |
T |
5: 3,685,876 (GRCm39) |
I1206F |
probably damaging |
Het |
Pi4k2b |
T |
A |
5: 52,918,331 (GRCm39) |
D386E |
probably benign |
Het |
Pik3c2a |
A |
G |
7: 115,945,427 (GRCm39) |
F1460L |
probably damaging |
Het |
Plcb2 |
A |
C |
2: 118,545,921 (GRCm39) |
M588R |
probably damaging |
Het |
Prl7d1 |
C |
A |
13: 27,893,260 (GRCm39) |
R216L |
possibly damaging |
Het |
Psg28 |
G |
T |
7: 18,156,887 (GRCm39) |
Y449* |
probably null |
Het |
Psg28 |
T |
A |
7: 18,164,602 (GRCm39) |
T37S |
probably benign |
Het |
Psmd9 |
G |
T |
5: 123,372,745 (GRCm39) |
R76M |
probably damaging |
Het |
Rfc1 |
T |
C |
5: 65,459,391 (GRCm39) |
D189G |
probably benign |
Het |
Rnf207 |
A |
G |
4: 152,397,666 (GRCm39) |
S363P |
probably benign |
Het |
Sco1 |
T |
A |
11: 66,949,250 (GRCm39) |
D239E |
probably damaging |
Het |
Sec24d |
C |
T |
3: 123,136,803 (GRCm39) |
T512M |
probably damaging |
Het |
Shkbp1 |
T |
C |
7: 27,046,442 (GRCm39) |
K441E |
probably benign |
Het |
Slc44a5 |
A |
T |
3: 153,959,322 (GRCm39) |
I338F |
probably damaging |
Het |
Slc4a3 |
A |
T |
1: 75,534,319 (GRCm39) |
I1161F |
probably damaging |
Het |
Spmip11 |
T |
A |
15: 98,483,264 (GRCm39) |
L65I |
probably damaging |
Het |
Tnfsf9 |
T |
A |
17: 57,414,355 (GRCm39) |
L261M |
probably damaging |
Het |
Trim55 |
C |
T |
3: 19,699,498 (GRCm39) |
R77C |
probably damaging |
Het |
Vmn2r27 |
A |
G |
6: 124,168,637 (GRCm39) |
I831T |
possibly damaging |
Het |
Vwa3b |
A |
G |
1: 37,081,438 (GRCm39) |
I60V |
probably benign |
Het |
Vwf |
A |
G |
6: 125,603,230 (GRCm39) |
N860S |
|
Het |
Zfp54 |
T |
A |
17: 21,654,149 (GRCm39) |
N214K |
probably benign |
Het |
Zfp707 |
T |
C |
15: 75,845,418 (GRCm39) |
I94T |
|
Het |
|
Other mutations in Kndc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00340:Kndc1
|
APN |
7 |
139,481,904 (GRCm39) |
splice site |
probably benign |
|
IGL01061:Kndc1
|
APN |
7 |
139,502,610 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01099:Kndc1
|
APN |
7 |
139,500,700 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01522:Kndc1
|
APN |
7 |
139,493,888 (GRCm39) |
splice site |
probably benign |
|
IGL01767:Kndc1
|
APN |
7 |
139,509,959 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01884:Kndc1
|
APN |
7 |
139,494,110 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01932:Kndc1
|
APN |
7 |
139,503,705 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02133:Kndc1
|
APN |
7 |
139,500,683 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02411:Kndc1
|
APN |
7 |
139,501,829 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02472:Kndc1
|
APN |
7 |
139,490,817 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02537:Kndc1
|
APN |
7 |
139,490,326 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02708:Kndc1
|
APN |
7 |
139,481,097 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03115:Kndc1
|
APN |
7 |
139,501,425 (GRCm39) |
missense |
probably benign |
0.28 |
IGL03160:Kndc1
|
APN |
7 |
139,500,605 (GRCm39) |
nonsense |
probably null |
|
IGL03138:Kndc1
|
UTSW |
7 |
139,519,791 (GRCm39) |
missense |
possibly damaging |
0.89 |
PIT4142001:Kndc1
|
UTSW |
7 |
139,503,692 (GRCm39) |
frame shift |
probably null |
|
PIT4696001:Kndc1
|
UTSW |
7 |
139,512,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R0349:Kndc1
|
UTSW |
7 |
139,490,220 (GRCm39) |
missense |
probably benign |
0.00 |
R0384:Kndc1
|
UTSW |
7 |
139,490,515 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0415:Kndc1
|
UTSW |
7 |
139,510,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R0421:Kndc1
|
UTSW |
7 |
139,488,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R0487:Kndc1
|
UTSW |
7 |
139,493,939 (GRCm39) |
missense |
probably null |
0.19 |
R0530:Kndc1
|
UTSW |
7 |
139,481,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R0905:Kndc1
|
UTSW |
7 |
139,503,651 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1434:Kndc1
|
UTSW |
7 |
139,502,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R1608:Kndc1
|
UTSW |
7 |
139,507,321 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1644:Kndc1
|
UTSW |
7 |
139,510,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R1835:Kndc1
|
UTSW |
7 |
139,507,624 (GRCm39) |
missense |
probably damaging |
0.99 |
R2012:Kndc1
|
UTSW |
7 |
139,501,196 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2102:Kndc1
|
UTSW |
7 |
139,510,674 (GRCm39) |
missense |
probably benign |
0.02 |
R2103:Kndc1
|
UTSW |
7 |
139,501,150 (GRCm39) |
missense |
probably benign |
0.01 |
R2128:Kndc1
|
UTSW |
7 |
139,510,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R2516:Kndc1
|
UTSW |
7 |
139,501,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R3030:Kndc1
|
UTSW |
7 |
139,481,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R3617:Kndc1
|
UTSW |
7 |
139,481,976 (GRCm39) |
splice site |
probably benign |
|
R3747:Kndc1
|
UTSW |
7 |
139,507,817 (GRCm39) |
critical splice donor site |
probably null |
|
R3848:Kndc1
|
UTSW |
7 |
139,488,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R4028:Kndc1
|
UTSW |
7 |
139,509,941 (GRCm39) |
missense |
probably damaging |
0.98 |
R4043:Kndc1
|
UTSW |
7 |
139,504,044 (GRCm39) |
missense |
probably benign |
0.06 |
R4044:Kndc1
|
UTSW |
7 |
139,504,044 (GRCm39) |
missense |
probably benign |
0.06 |
R4095:Kndc1
|
UTSW |
7 |
139,516,938 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4289:Kndc1
|
UTSW |
7 |
139,490,798 (GRCm39) |
missense |
probably benign |
0.01 |
R4478:Kndc1
|
UTSW |
7 |
139,500,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R4514:Kndc1
|
UTSW |
7 |
139,490,202 (GRCm39) |
missense |
probably benign |
0.00 |
R4540:Kndc1
|
UTSW |
7 |
139,501,343 (GRCm39) |
nonsense |
probably null |
|
R4584:Kndc1
|
UTSW |
7 |
139,481,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R4693:Kndc1
|
UTSW |
7 |
139,501,695 (GRCm39) |
missense |
probably benign |
0.02 |
R4705:Kndc1
|
UTSW |
7 |
139,510,036 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4773:Kndc1
|
UTSW |
7 |
139,503,946 (GRCm39) |
nonsense |
probably null |
|
R4859:Kndc1
|
UTSW |
7 |
139,501,821 (GRCm39) |
missense |
probably benign |
0.03 |
R5004:Kndc1
|
UTSW |
7 |
139,512,792 (GRCm39) |
nonsense |
probably null |
|
R5037:Kndc1
|
UTSW |
7 |
139,490,371 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5322:Kndc1
|
UTSW |
7 |
139,516,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R5428:Kndc1
|
UTSW |
7 |
139,488,878 (GRCm39) |
missense |
probably damaging |
0.99 |
R5503:Kndc1
|
UTSW |
7 |
139,511,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R5506:Kndc1
|
UTSW |
7 |
139,507,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R5525:Kndc1
|
UTSW |
7 |
139,504,026 (GRCm39) |
missense |
probably benign |
0.00 |
R5888:Kndc1
|
UTSW |
7 |
139,475,133 (GRCm39) |
missense |
probably benign |
0.00 |
R5942:Kndc1
|
UTSW |
7 |
139,516,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R5979:Kndc1
|
UTSW |
7 |
139,519,740 (GRCm39) |
missense |
probably benign |
0.05 |
R5990:Kndc1
|
UTSW |
7 |
139,507,333 (GRCm39) |
missense |
probably damaging |
0.99 |
R6038:Kndc1
|
UTSW |
7 |
139,503,691 (GRCm39) |
frame shift |
probably null |
|
R6076:Kndc1
|
UTSW |
7 |
139,481,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R6118:Kndc1
|
UTSW |
7 |
139,503,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R6151:Kndc1
|
UTSW |
7 |
139,501,129 (GRCm39) |
missense |
probably benign |
0.04 |
R6276:Kndc1
|
UTSW |
7 |
139,500,979 (GRCm39) |
missense |
probably benign |
|
R6367:Kndc1
|
UTSW |
7 |
139,493,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R6726:Kndc1
|
UTSW |
7 |
139,502,667 (GRCm39) |
critical splice donor site |
probably null |
|
R6745:Kndc1
|
UTSW |
7 |
139,500,892 (GRCm39) |
missense |
probably benign |
0.02 |
R6886:Kndc1
|
UTSW |
7 |
139,493,485 (GRCm39) |
missense |
probably benign |
0.01 |
R6912:Kndc1
|
UTSW |
7 |
139,490,194 (GRCm39) |
missense |
probably damaging |
0.99 |
R7070:Kndc1
|
UTSW |
7 |
139,501,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R7123:Kndc1
|
UTSW |
7 |
139,516,749 (GRCm39) |
missense |
probably damaging |
0.99 |
R7158:Kndc1
|
UTSW |
7 |
139,511,773 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7248:Kndc1
|
UTSW |
7 |
139,500,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R7437:Kndc1
|
UTSW |
7 |
139,488,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R7564:Kndc1
|
UTSW |
7 |
139,500,612 (GRCm39) |
missense |
probably benign |
0.01 |
R7570:Kndc1
|
UTSW |
7 |
139,503,691 (GRCm39) |
frame shift |
probably null |
|
R7625:Kndc1
|
UTSW |
7 |
139,517,930 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7629:Kndc1
|
UTSW |
7 |
139,475,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R7726:Kndc1
|
UTSW |
7 |
139,519,751 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7840:Kndc1
|
UTSW |
7 |
139,503,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R7859:Kndc1
|
UTSW |
7 |
139,500,880 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7934:Kndc1
|
UTSW |
7 |
139,501,402 (GRCm39) |
missense |
probably benign |
0.02 |
R8011:Kndc1
|
UTSW |
7 |
139,490,536 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8062:Kndc1
|
UTSW |
7 |
139,498,760 (GRCm39) |
missense |
probably benign |
0.01 |
R8134:Kndc1
|
UTSW |
7 |
139,481,285 (GRCm39) |
splice site |
probably null |
|
R8197:Kndc1
|
UTSW |
7 |
139,493,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R8350:Kndc1
|
UTSW |
7 |
139,503,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R8399:Kndc1
|
UTSW |
7 |
139,493,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R8400:Kndc1
|
UTSW |
7 |
139,493,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R8447:Kndc1
|
UTSW |
7 |
139,481,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R8534:Kndc1
|
UTSW |
7 |
139,503,669 (GRCm39) |
missense |
probably benign |
0.27 |
R8735:Kndc1
|
UTSW |
7 |
139,490,130 (GRCm39) |
missense |
probably benign |
0.00 |
R8816:Kndc1
|
UTSW |
7 |
139,517,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R8883:Kndc1
|
UTSW |
7 |
139,507,708 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8899:Kndc1
|
UTSW |
7 |
139,507,708 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8961:Kndc1
|
UTSW |
7 |
139,507,708 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8961:Kndc1
|
UTSW |
7 |
139,503,976 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9002:Kndc1
|
UTSW |
7 |
139,507,708 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9010:Kndc1
|
UTSW |
7 |
139,507,708 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9065:Kndc1
|
UTSW |
7 |
139,507,708 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9066:Kndc1
|
UTSW |
7 |
139,507,708 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9223:Kndc1
|
UTSW |
7 |
139,501,357 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9230:Kndc1
|
UTSW |
7 |
139,500,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R9291:Kndc1
|
UTSW |
7 |
139,475,140 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9441:Kndc1
|
UTSW |
7 |
139,501,392 (GRCm39) |
missense |
probably damaging |
0.99 |
R9476:Kndc1
|
UTSW |
7 |
139,510,031 (GRCm39) |
missense |
probably benign |
0.00 |
R9510:Kndc1
|
UTSW |
7 |
139,510,031 (GRCm39) |
missense |
probably benign |
0.00 |
R9518:Kndc1
|
UTSW |
7 |
139,519,827 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Kndc1
|
UTSW |
7 |
139,501,828 (GRCm39) |
missense |
possibly damaging |
0.63 |
Z1186:Kndc1
|
UTSW |
7 |
139,490,729 (GRCm39) |
missense |
probably damaging |
0.98 |
|