Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca3 |
T |
C |
17: 24,603,500 (GRCm39) |
L564P |
probably damaging |
Het |
Arsb |
T |
A |
13: 93,998,615 (GRCm39) |
S308T |
probably benign |
Het |
Atxn10 |
A |
G |
15: 85,346,526 (GRCm39) |
D428G |
probably benign |
Het |
BB014433 |
GCACACAGCTTTGGAGGTGTACACACCCGGGTTGGGGCCTCTACACACAGCTTTGGAGGTGTACACACCCGGGTTGGGGCCTCTGCACACAGCTTTGG |
GCACACAGCTTTGGAGGTGTACACACCCGGGTTGGGGCCTCTGCACACAGCTTTGG |
8: 15,092,160 (GRCm39) |
|
probably benign |
Het |
Cd300a |
T |
C |
11: 114,784,165 (GRCm39) |
Y58H |
probably benign |
Het |
Cemip2 |
T |
A |
19: 21,809,539 (GRCm39) |
I973N |
possibly damaging |
Het |
Crkl |
T |
A |
16: 17,286,960 (GRCm39) |
M172K |
probably damaging |
Het |
Cyfip1 |
T |
C |
7: 55,549,774 (GRCm39) |
I647T |
probably damaging |
Het |
Dlgap1 |
A |
G |
17: 70,823,683 (GRCm39) |
T223A |
probably benign |
Het |
Dmtf1 |
T |
C |
5: 9,178,044 (GRCm39) |
S372G |
probably damaging |
Het |
Dock8 |
G |
A |
19: 25,160,934 (GRCm39) |
V1814M |
probably damaging |
Het |
Dusp22 |
A |
C |
13: 30,892,737 (GRCm39) |
K171N |
probably benign |
Het |
Evi2a |
T |
C |
11: 79,418,452 (GRCm39) |
S53G |
probably benign |
Het |
Ipcef1 |
T |
A |
10: 6,840,569 (GRCm39) |
D376V |
probably damaging |
Het |
Kti12 |
A |
C |
4: 108,705,443 (GRCm39) |
E119A |
probably benign |
Het |
Kti12 |
G |
T |
4: 108,705,444 (GRCm39) |
E119D |
probably benign |
Het |
Mcur1 |
G |
A |
13: 43,713,485 (GRCm39) |
R40* |
probably null |
Het |
Mgam |
T |
A |
6: 40,717,113 (GRCm39) |
N265K |
possibly damaging |
Het |
Muc6 |
G |
A |
7: 141,231,687 (GRCm39) |
T1069I |
probably damaging |
Het |
Myh2 |
T |
C |
11: 67,077,526 (GRCm39) |
L887P |
probably damaging |
Het |
Myo1d |
T |
G |
11: 80,575,203 (GRCm39) |
D171A |
probably damaging |
Het |
Nat2 |
T |
A |
8: 67,954,002 (GRCm39) |
F37L |
probably damaging |
Het |
Nkx2-2 |
A |
G |
2: 147,019,730 (GRCm39) |
C236R |
unknown |
Het |
Nrl |
G |
A |
14: 55,759,582 (GRCm39) |
S115L |
probably benign |
Het |
Nrsn1 |
A |
C |
13: 25,446,254 (GRCm39) |
S41A |
probably damaging |
Het |
Or5b12 |
T |
A |
19: 12,897,346 (GRCm39) |
E109V |
probably damaging |
Het |
Pax8 |
T |
A |
2: 24,311,567 (GRCm39) |
H456L |
possibly damaging |
Het |
Pkd1 |
T |
A |
17: 24,790,254 (GRCm39) |
I979K |
probably damaging |
Het |
Prex2 |
A |
G |
1: 11,150,274 (GRCm39) |
N149D |
probably damaging |
Het |
Psg28 |
A |
T |
7: 18,160,149 (GRCm39) |
V349D |
probably damaging |
Het |
Ptpro |
G |
A |
6: 137,369,805 (GRCm39) |
|
probably null |
Het |
Sema4d |
T |
A |
13: 51,876,387 (GRCm39) |
K94N |
probably benign |
Het |
Slc22a22 |
A |
T |
15: 57,114,348 (GRCm39) |
D326E |
probably benign |
Het |
Slc25a29 |
G |
A |
12: 108,792,756 (GRCm39) |
T274I |
probably benign |
Het |
Slc43a1 |
T |
C |
2: 84,687,220 (GRCm39) |
F374L |
possibly damaging |
Het |
Syne1 |
G |
T |
10: 5,107,683 (GRCm39) |
Q520K |
possibly damaging |
Het |
Taar4 |
T |
C |
10: 23,837,032 (GRCm39) |
V214A |
probably benign |
Het |
Tex22 |
T |
A |
12: 113,052,103 (GRCm39) |
C54S |
possibly damaging |
Het |
Tpo |
T |
A |
12: 30,150,573 (GRCm39) |
I436F |
probably damaging |
Het |
Usp53 |
T |
C |
3: 122,743,415 (GRCm39) |
H507R |
possibly damaging |
Het |
Usp54 |
T |
C |
14: 20,638,204 (GRCm39) |
E255G |
probably benign |
Het |
Vmn2r109 |
G |
T |
17: 20,761,436 (GRCm39) |
F640L |
probably damaging |
Het |
Vmn2r124 |
A |
G |
17: 18,282,212 (GRCm39) |
Y80C |
probably damaging |
Het |
Vmn2r27 |
A |
T |
6: 124,201,201 (GRCm39) |
I252K |
probably benign |
Het |
Zfp457 |
A |
G |
13: 67,454,445 (GRCm39) |
|
probably benign |
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 |
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 |
|