Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars1 |
T |
A |
8: 111,773,587 (GRCm39) |
V506E |
probably damaging |
Het |
Acaa2 |
G |
T |
18: 74,937,213 (GRCm39) |
V366F |
possibly damaging |
Het |
Ago1 |
G |
A |
4: 126,337,022 (GRCm39) |
R532C |
probably benign |
Het |
Ank2 |
T |
G |
3: 126,846,449 (GRCm39) |
D182A |
probably damaging |
Het |
Anxa4 |
T |
C |
6: 86,714,801 (GRCm39) |
D302G |
probably damaging |
Het |
Apoa4 |
A |
T |
9: 46,154,410 (GRCm39) |
E337V |
probably damaging |
Het |
Atf1 |
A |
G |
15: 100,152,158 (GRCm39) |
|
probably null |
Het |
Atp8b3 |
A |
C |
10: 80,355,980 (GRCm39) |
V1244G |
probably benign |
Het |
Cactin |
CCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAG |
CCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAG |
10: 81,157,152 (GRCm39) |
|
probably benign |
Het |
Camk2a |
G |
A |
18: 61,085,412 (GRCm39) |
V132M |
probably damaging |
Het |
Cdc40 |
A |
T |
10: 40,724,048 (GRCm39) |
Y247N |
probably benign |
Het |
Chd8 |
G |
A |
14: 52,474,534 (GRCm39) |
P166S |
probably benign |
Het |
Chl1 |
T |
A |
6: 103,706,086 (GRCm39) |
S1140R |
probably damaging |
Het |
Clstn3 |
G |
T |
6: 124,414,377 (GRCm39) |
S783* |
probably null |
Het |
Col6a1 |
A |
G |
10: 76,549,760 (GRCm39) |
S562P |
unknown |
Het |
Cpb2 |
G |
A |
14: 75,509,989 (GRCm39) |
V250M |
possibly damaging |
Het |
Cyp2c38 |
T |
A |
19: 39,451,368 (GRCm39) |
Q44L |
possibly damaging |
Het |
Dgat1 |
T |
C |
15: 76,387,395 (GRCm39) |
M325V |
possibly damaging |
Het |
Dnah11 |
T |
A |
12: 118,160,377 (GRCm39) |
M118L |
probably benign |
Het |
Dpy19l3 |
T |
A |
7: 35,452,106 (GRCm39) |
I13L |
probably benign |
Het |
Enkd1 |
A |
G |
8: 106,431,265 (GRCm39) |
|
probably null |
Het |
Fam241b |
A |
G |
10: 61,970,479 (GRCm39) |
|
probably benign |
Het |
Fhit |
T |
A |
14: 9,870,177 (GRCm38) |
|
probably null |
Het |
Gp6 |
T |
C |
7: 4,373,173 (GRCm39) |
E250G |
probably benign |
Het |
Hmgb1 |
T |
C |
5: 148,987,150 (GRCm39) |
E84G |
probably benign |
Het |
Hscb |
T |
A |
5: 110,977,012 (GRCm39) |
I227F |
probably damaging |
Het |
Hspg2 |
T |
A |
4: 137,292,249 (GRCm39) |
L4047Q |
probably damaging |
Het |
Hsph1 |
A |
G |
5: 149,541,901 (GRCm39) |
L775P |
probably benign |
Het |
Hydin |
A |
T |
8: 111,268,476 (GRCm39) |
S2947C |
probably benign |
Het |
Intu |
T |
C |
3: 40,652,029 (GRCm39) |
S829P |
probably benign |
Het |
Kcnn3 |
C |
A |
3: 89,516,977 (GRCm39) |
T462K |
probably damaging |
Het |
Lifr |
T |
C |
15: 7,198,723 (GRCm39) |
Y318H |
probably damaging |
Het |
Mier2 |
A |
G |
10: 79,378,543 (GRCm39) |
S332P |
probably damaging |
Het |
Mindy4 |
T |
C |
6: 55,253,598 (GRCm39) |
I489T |
possibly damaging |
Het |
Mmp8 |
A |
T |
9: 7,566,218 (GRCm39) |
Q358L |
probably benign |
Het |
Ms4a4a |
T |
A |
19: 11,367,728 (GRCm39) |
|
probably null |
Het |
Nav1 |
G |
C |
1: 135,395,483 (GRCm39) |
S962C |
probably damaging |
Het |
Nfe2l1 |
G |
A |
11: 96,710,271 (GRCm39) |
R653C |
probably damaging |
Het |
Nherf4 |
A |
T |
9: 44,161,594 (GRCm39) |
I95N |
probably damaging |
Het |
Nod2 |
A |
T |
8: 89,391,906 (GRCm39) |
I738F |
probably damaging |
Het |
Nrf1 |
G |
A |
6: 30,116,230 (GRCm39) |
V301I |
probably benign |
Het |
Oog1 |
T |
C |
12: 87,655,082 (GRCm39) |
F410S |
probably benign |
Het |
Or52a33 |
A |
G |
7: 103,289,165 (GRCm39) |
Y61H |
probably damaging |
Het |
Or6k4 |
G |
A |
1: 173,964,733 (GRCm39) |
C141Y |
probably benign |
Het |
Pcdhga8 |
G |
A |
18: 37,859,954 (GRCm39) |
V337I |
probably benign |
Het |
Pelp1 |
G |
T |
11: 70,286,260 (GRCm39) |
N572K |
probably benign |
Het |
Pikfyve |
T |
C |
1: 65,307,036 (GRCm39) |
V1808A |
possibly damaging |
Het |
Pirt |
A |
C |
11: 66,816,769 (GRCm39) |
S27R |
probably damaging |
Het |
Pramel20 |
A |
T |
4: 143,298,821 (GRCm39) |
I255L |
probably benign |
Het |
Rgs17 |
A |
T |
10: 5,791,488 (GRCm39) |
D96E |
probably benign |
Het |
Senp1 |
A |
G |
15: 97,964,679 (GRCm39) |
F206L |
probably benign |
Het |
Sh3rf1 |
T |
A |
8: 61,825,756 (GRCm39) |
S584T |
probably benign |
Het |
Tex44 |
A |
T |
1: 86,354,459 (GRCm39) |
K123* |
probably null |
Het |
Tpst2 |
C |
A |
5: 112,455,887 (GRCm39) |
T142K |
probably damaging |
Het |
Ttc28 |
G |
A |
5: 111,433,085 (GRCm39) |
G2040R |
possibly damaging |
Het |
Uggt2 |
T |
A |
14: 119,263,905 (GRCm39) |
I1042F |
probably damaging |
Het |
Vmn2r91 |
T |
C |
17: 18,325,693 (GRCm39) |
S104P |
probably damaging |
Het |
Wdfy3 |
T |
C |
5: 102,003,252 (GRCm39) |
|
probably null |
Het |
Zeb2 |
G |
A |
2: 44,892,584 (GRCm39) |
A223V |
probably damaging |
Het |
Zfp1002 |
T |
C |
2: 150,096,520 (GRCm39) |
D303G |
probably benign |
Het |
Zfp566 |
A |
G |
7: 29,777,930 (GRCm39) |
S84P |
probably benign |
Het |
Zfp994 |
T |
A |
17: 22,420,736 (GRCm39) |
H71L |
possibly damaging |
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 |
|
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 |
R9758:Kndc1
|
UTSW |
7 |
139,500,620 (GRCm39) |
missense |
possibly damaging |
0.71 |
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 |
|