Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak |
A |
G |
19: 8,986,387 (GRCm39) |
E2557G |
possibly damaging |
Het |
Arid1a |
A |
G |
4: 133,414,075 (GRCm39) |
S1248P |
unknown |
Het |
C2cd3 |
T |
C |
7: 100,081,205 (GRCm39) |
L1327S |
probably damaging |
Het |
Ccnh |
T |
C |
13: 85,354,243 (GRCm39) |
|
probably benign |
Het |
Dcdc5 |
C |
A |
2: 106,202,738 (GRCm39) |
|
noncoding transcript |
Het |
Eprs1 |
T |
C |
1: 185,105,205 (GRCm39) |
F160S |
probably damaging |
Het |
F9 |
A |
G |
X: 59,064,345 (GRCm39) |
I190V |
probably benign |
Het |
Fam185a |
C |
A |
5: 21,660,804 (GRCm39) |
A273D |
probably damaging |
Het |
Fhod1 |
G |
A |
8: 106,058,270 (GRCm39) |
|
probably benign |
Het |
Gpat4 |
G |
A |
8: 23,670,171 (GRCm39) |
P286L |
probably damaging |
Het |
Hipk2 |
T |
C |
6: 38,720,029 (GRCm39) |
D534G |
probably damaging |
Het |
Ints6l |
T |
C |
X: 55,526,731 (GRCm39) |
L220S |
probably damaging |
Het |
Kat7 |
T |
C |
11: 95,182,357 (GRCm39) |
T250A |
probably benign |
Het |
Kif23 |
G |
A |
9: 61,832,274 (GRCm39) |
S623L |
probably benign |
Het |
Krt32 |
A |
G |
11: 99,978,947 (GRCm39) |
C36R |
probably benign |
Het |
Megf10 |
G |
A |
18: 57,410,177 (GRCm39) |
G653S |
probably damaging |
Het |
Mpp3 |
G |
T |
11: 101,914,193 (GRCm39) |
S134* |
probably null |
Het |
Msh6 |
G |
T |
17: 88,293,609 (GRCm39) |
R788L |
probably damaging |
Het |
Mxi1 |
C |
A |
19: 53,360,160 (GRCm39) |
A294E |
probably benign |
Het |
Naip5 |
T |
C |
13: 100,359,902 (GRCm39) |
I445V |
probably benign |
Het |
Naip5 |
T |
C |
13: 100,359,883 (GRCm39) |
E451G |
probably benign |
Het |
Nlrp1b |
T |
C |
11: 71,047,126 (GRCm39) |
|
probably benign |
Het |
Npy1r |
T |
C |
8: 67,157,502 (GRCm39) |
F271L |
possibly damaging |
Het |
Nup160 |
G |
T |
2: 90,552,420 (GRCm39) |
C1132F |
probably benign |
Het |
Or13p3 |
C |
T |
4: 118,567,351 (GRCm39) |
T249I |
probably damaging |
Het |
Or1o2 |
T |
A |
17: 37,543,121 (GRCm39) |
I47F |
probably damaging |
Het |
Pcdhga5 |
A |
G |
18: 37,828,167 (GRCm39) |
E205G |
possibly damaging |
Het |
Pdgfc |
A |
G |
3: 81,048,858 (GRCm39) |
T89A |
probably damaging |
Het |
Pecr |
A |
G |
1: 72,298,530 (GRCm39) |
F297L |
probably benign |
Het |
Pgr15l |
G |
T |
X: 96,120,747 (GRCm39) |
R181M |
probably damaging |
Het |
Pomgnt1 |
G |
A |
4: 116,011,325 (GRCm39) |
R230H |
probably damaging |
Het |
Ppm1d |
T |
C |
11: 85,227,993 (GRCm39) |
I303T |
probably damaging |
Het |
Ptprc |
T |
G |
1: 137,992,511 (GRCm39) |
Q1205H |
probably damaging |
Het |
Rnf112 |
A |
T |
11: 61,341,011 (GRCm39) |
|
probably benign |
Het |
Slc25a13 |
T |
A |
6: 6,109,288 (GRCm39) |
Q358L |
probably damaging |
Het |
Slc25a19 |
A |
G |
11: 115,506,285 (GRCm39) |
Y303H |
probably damaging |
Het |
Sympk |
T |
C |
7: 18,769,880 (GRCm39) |
F186L |
probably damaging |
Het |
Tmem59l |
A |
G |
8: 70,939,951 (GRCm39) |
L6S |
unknown |
Het |
Tnik |
T |
C |
3: 28,692,568 (GRCm39) |
Y820H |
probably damaging |
Het |
Tnrc6c |
C |
T |
11: 117,614,355 (GRCm39) |
R838W |
probably damaging |
Het |
Vmn2r29 |
C |
G |
7: 7,243,011 (GRCm39) |
D500H |
probably damaging |
Het |
|
Other mutations in Tek |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00654:Tek
|
APN |
4 |
94,715,538 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00805:Tek
|
APN |
4 |
94,686,956 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00806:Tek
|
APN |
4 |
94,686,956 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00807:Tek
|
APN |
4 |
94,686,956 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00870:Tek
|
APN |
4 |
94,761,318 (GRCm39) |
nonsense |
probably null |
|
IGL01348:Tek
|
APN |
4 |
94,747,895 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01398:Tek
|
APN |
4 |
94,738,014 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01683:Tek
|
APN |
4 |
94,747,148 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01827:Tek
|
APN |
4 |
94,627,882 (GRCm39) |
missense |
probably benign |
0.24 |
IGL02063:Tek
|
APN |
4 |
94,627,882 (GRCm39) |
missense |
probably benign |
0.24 |
IGL02218:Tek
|
APN |
4 |
94,743,574 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02502:Tek
|
APN |
4 |
94,741,818 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02852:Tek
|
APN |
4 |
94,743,561 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02995:Tek
|
APN |
4 |
94,627,877 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL03182:Tek
|
APN |
4 |
94,740,002 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03247:Tek
|
APN |
4 |
94,753,680 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03014:Tek
|
UTSW |
4 |
94,715,500 (GRCm39) |
missense |
probably benign |
0.05 |
R0022:Tek
|
UTSW |
4 |
94,725,509 (GRCm39) |
missense |
probably damaging |
0.98 |
R0373:Tek
|
UTSW |
4 |
94,692,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R0479:Tek
|
UTSW |
4 |
94,692,549 (GRCm39) |
missense |
probably benign |
0.01 |
R1178:Tek
|
UTSW |
4 |
94,692,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R1289:Tek
|
UTSW |
4 |
94,693,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R1331:Tek
|
UTSW |
4 |
94,627,943 (GRCm39) |
splice site |
probably benign |
|
R1502:Tek
|
UTSW |
4 |
94,669,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R1606:Tek
|
UTSW |
4 |
94,738,004 (GRCm39) |
missense |
probably damaging |
0.99 |
R2073:Tek
|
UTSW |
4 |
94,715,966 (GRCm39) |
missense |
probably benign |
0.01 |
R2075:Tek
|
UTSW |
4 |
94,715,966 (GRCm39) |
missense |
probably benign |
0.01 |
R2230:Tek
|
UTSW |
4 |
94,699,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R2851:Tek
|
UTSW |
4 |
94,708,461 (GRCm39) |
missense |
probably benign |
0.30 |
R2852:Tek
|
UTSW |
4 |
94,708,461 (GRCm39) |
missense |
probably benign |
0.30 |
R3845:Tek
|
UTSW |
4 |
94,693,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R4114:Tek
|
UTSW |
4 |
94,737,920 (GRCm39) |
missense |
probably damaging |
0.99 |
R4115:Tek
|
UTSW |
4 |
94,737,920 (GRCm39) |
missense |
probably damaging |
0.99 |
R4273:Tek
|
UTSW |
4 |
94,718,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R4425:Tek
|
UTSW |
4 |
94,751,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R4488:Tek
|
UTSW |
4 |
94,737,993 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4579:Tek
|
UTSW |
4 |
94,751,903 (GRCm39) |
nonsense |
probably null |
|
R4623:Tek
|
UTSW |
4 |
94,751,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R4651:Tek
|
UTSW |
4 |
94,669,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R4652:Tek
|
UTSW |
4 |
94,669,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R4723:Tek
|
UTSW |
4 |
94,687,397 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5059:Tek
|
UTSW |
4 |
94,692,551 (GRCm39) |
missense |
probably benign |
0.10 |
R5652:Tek
|
UTSW |
4 |
94,743,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R5793:Tek
|
UTSW |
4 |
94,708,333 (GRCm39) |
missense |
probably benign |
0.01 |
R5855:Tek
|
UTSW |
4 |
94,741,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R5912:Tek
|
UTSW |
4 |
94,686,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R6537:Tek
|
UTSW |
4 |
94,725,561 (GRCm39) |
missense |
probably benign |
0.19 |
R6727:Tek
|
UTSW |
4 |
94,741,732 (GRCm39) |
nonsense |
probably null |
|
R6835:Tek
|
UTSW |
4 |
94,741,671 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6883:Tek
|
UTSW |
4 |
94,725,426 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6887:Tek
|
UTSW |
4 |
94,693,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R7027:Tek
|
UTSW |
4 |
94,753,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R7108:Tek
|
UTSW |
4 |
94,741,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R7121:Tek
|
UTSW |
4 |
94,699,647 (GRCm39) |
missense |
probably benign |
0.19 |
R7220:Tek
|
UTSW |
4 |
94,692,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R7346:Tek
|
UTSW |
4 |
94,715,533 (GRCm39) |
missense |
probably benign |
|
R7417:Tek
|
UTSW |
4 |
94,699,582 (GRCm39) |
missense |
probably benign |
|
R7465:Tek
|
UTSW |
4 |
94,716,063 (GRCm39) |
critical splice donor site |
probably null |
|
R7818:Tek
|
UTSW |
4 |
94,715,953 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7917:Tek
|
UTSW |
4 |
94,708,372 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7942:Tek
|
UTSW |
4 |
94,740,111 (GRCm39) |
splice site |
probably null |
|
R7956:Tek
|
UTSW |
4 |
94,687,580 (GRCm39) |
splice site |
probably null |
|
R8098:Tek
|
UTSW |
4 |
94,715,907 (GRCm39) |
missense |
probably benign |
0.19 |
R8442:Tek
|
UTSW |
4 |
94,715,922 (GRCm39) |
missense |
probably benign |
0.04 |
R8523:Tek
|
UTSW |
4 |
94,687,403 (GRCm39) |
missense |
probably benign |
0.12 |
R8676:Tek
|
UTSW |
4 |
94,738,074 (GRCm39) |
missense |
probably benign |
|
R8787:Tek
|
UTSW |
4 |
94,738,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R9020:Tek
|
UTSW |
4 |
94,708,339 (GRCm39) |
missense |
probably benign |
0.40 |
R9172:Tek
|
UTSW |
4 |
94,692,583 (GRCm39) |
missense |
probably benign |
0.02 |
R9429:Tek
|
UTSW |
4 |
94,715,515 (GRCm39) |
missense |
probably benign |
|
R9564:Tek
|
UTSW |
4 |
94,762,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R9602:Tek
|
UTSW |
4 |
94,715,968 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9643:Tek
|
UTSW |
4 |
94,692,523 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9721:Tek
|
UTSW |
4 |
94,692,539 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9722:Tek
|
UTSW |
4 |
94,692,539 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9723:Tek
|
UTSW |
4 |
94,692,539 (GRCm39) |
missense |
possibly damaging |
0.94 |
|