Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930584F24Rik |
A |
T |
5: 26,684,776 (GRCm39) |
|
noncoding transcript |
Het |
Acvr1 |
A |
T |
2: 58,369,901 (GRCm39) |
V36E |
probably damaging |
Het |
Aldh4a1 |
A |
G |
4: 139,370,758 (GRCm39) |
I414V |
probably benign |
Het |
Alox5 |
C |
T |
6: 116,431,128 (GRCm39) |
C100Y |
probably damaging |
Het |
Ano5 |
T |
A |
7: 51,216,068 (GRCm39) |
D348E |
probably damaging |
Het |
Arhgap30 |
G |
A |
1: 171,230,839 (GRCm39) |
V199M |
probably damaging |
Het |
Arl13b |
T |
A |
16: 62,626,999 (GRCm39) |
Q234L |
probably benign |
Het |
Atxn1 |
C |
A |
13: 45,711,052 (GRCm39) |
E627* |
probably null |
Het |
Brca1 |
A |
T |
11: 101,420,638 (GRCm39) |
V190E |
possibly damaging |
Het |
Brpf1 |
T |
C |
6: 113,292,096 (GRCm39) |
W381R |
probably damaging |
Het |
Brwd1 |
A |
C |
16: 95,829,491 (GRCm39) |
|
probably null |
Het |
C1s2 |
T |
C |
6: 124,602,604 (GRCm39) |
I530V |
possibly damaging |
Het |
C2cd3 |
C |
T |
7: 100,089,397 (GRCm39) |
R1638W |
probably damaging |
Het |
Capns1 |
T |
A |
7: 29,893,511 (GRCm39) |
|
probably benign |
Het |
Cd109 |
CATTTATTTATTTATTTATTTATTTATTTATTTAT |
CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT |
9: 78,619,782 (GRCm39) |
|
probably benign |
Het |
Cep126 |
G |
A |
9: 8,100,554 (GRCm39) |
T660I |
possibly damaging |
Het |
Cep295 |
A |
C |
9: 15,246,080 (GRCm39) |
I744R |
probably damaging |
Het |
Chd3 |
T |
C |
11: 69,250,725 (GRCm39) |
E668G |
probably benign |
Het |
Chek2 |
A |
G |
5: 110,996,553 (GRCm39) |
T172A |
probably damaging |
Het |
Col6a4 |
A |
G |
9: 105,890,501 (GRCm39) |
|
probably null |
Het |
Coq3 |
G |
A |
4: 21,900,291 (GRCm39) |
V173I |
probably benign |
Het |
Cyp4x1 |
A |
T |
4: 114,970,098 (GRCm39) |
I343N |
probably damaging |
Het |
Dnah7b |
T |
A |
1: 46,176,703 (GRCm39) |
D774E |
probably benign |
Het |
Dnai3 |
T |
C |
3: 145,802,996 (GRCm39) |
D65G |
probably benign |
Het |
Ecm1 |
G |
A |
3: 95,643,275 (GRCm39) |
R342C |
probably damaging |
Het |
Esrra |
T |
C |
19: 6,890,197 (GRCm39) |
Y209C |
probably damaging |
Het |
Gpr149 |
A |
T |
3: 62,502,592 (GRCm39) |
D421E |
probably benign |
Het |
Gpr15 |
T |
C |
16: 58,538,937 (GRCm39) |
N51D |
probably damaging |
Het |
Gpr156 |
T |
C |
16: 37,812,558 (GRCm39) |
V298A |
probably damaging |
Het |
Hmcn2 |
G |
A |
2: 31,236,507 (GRCm39) |
G350D |
probably damaging |
Het |
Ifih1 |
A |
T |
2: 62,440,902 (GRCm39) |
N421K |
probably benign |
Het |
Ilvbl |
C |
A |
10: 78,412,564 (GRCm39) |
T95K |
probably damaging |
Het |
Itgb4 |
T |
A |
11: 115,890,625 (GRCm39) |
D1104E |
probably benign |
Het |
Katnip |
C |
A |
7: 125,415,743 (GRCm39) |
|
probably benign |
Het |
Lipf |
A |
T |
19: 33,942,180 (GRCm39) |
M37L |
probably benign |
Het |
Lyst |
T |
A |
13: 13,852,775 (GRCm39) |
N2258K |
probably benign |
Het |
Moxd1 |
A |
G |
10: 24,099,758 (GRCm39) |
Y86C |
probably damaging |
Het |
Muc5ac |
T |
C |
7: 141,367,629 (GRCm39) |
|
probably null |
Het |
Myo16 |
G |
A |
8: 10,610,145 (GRCm39) |
R1162H |
probably damaging |
Het |
Myo5c |
A |
T |
9: 75,208,092 (GRCm39) |
N1609Y |
probably damaging |
Het |
Nbeal1 |
T |
C |
1: 60,240,098 (GRCm39) |
F155L |
probably damaging |
Het |
Nek4 |
A |
T |
14: 30,704,290 (GRCm39) |
M602L |
possibly damaging |
Het |
Nek9 |
A |
G |
12: 85,348,622 (GRCm39) |
S971P |
probably damaging |
Het |
Nfya |
A |
T |
17: 48,700,570 (GRCm39) |
|
probably benign |
Het |
Nrxn3 |
A |
T |
12: 89,221,547 (GRCm39) |
N442I |
probably damaging |
Het |
Nup42 |
A |
C |
5: 24,383,075 (GRCm39) |
K200N |
probably benign |
Het |
Or1e26 |
T |
A |
11: 73,480,187 (GRCm39) |
I126L |
possibly damaging |
Het |
Or4c111 |
G |
A |
2: 88,843,713 (GRCm39) |
R232* |
probably null |
Het |
Or7g32 |
G |
A |
9: 19,389,423 (GRCm39) |
T38I |
probably damaging |
Het |
Pcdh15 |
T |
A |
10: 74,126,833 (GRCm39) |
I304N |
probably damaging |
Het |
Pigo |
G |
C |
4: 43,024,779 (GRCm39) |
P107A |
probably damaging |
Het |
Plce1 |
C |
T |
19: 38,693,783 (GRCm39) |
Q769* |
probably null |
Het |
Plin2 |
C |
T |
4: 86,575,481 (GRCm39) |
R356H |
probably benign |
Het |
Ppp1r9a |
G |
T |
6: 5,113,712 (GRCm39) |
E739* |
probably null |
Het |
Ppp3cc |
G |
T |
14: 70,478,397 (GRCm39) |
N268K |
probably damaging |
Het |
Prkag3 |
T |
A |
1: 74,779,919 (GRCm39) |
D472V |
probably damaging |
Het |
Ptch2 |
A |
T |
4: 116,968,046 (GRCm39) |
D846V |
probably damaging |
Het |
Rhob |
A |
T |
12: 8,549,388 (GRCm39) |
M82K |
probably damaging |
Het |
Rps6kc1 |
T |
A |
1: 190,531,672 (GRCm39) |
R777W |
possibly damaging |
Het |
Sap130 |
T |
A |
18: 31,844,380 (GRCm39) |
V850E |
probably damaging |
Het |
Sema3a |
T |
G |
5: 13,523,407 (GRCm39) |
N125K |
probably damaging |
Het |
Sema5a |
A |
G |
15: 32,460,431 (GRCm39) |
D64G |
probably damaging |
Het |
Sgo2b |
T |
A |
8: 64,384,507 (GRCm39) |
D163V |
possibly damaging |
Het |
Slc15a1 |
A |
T |
14: 121,728,651 (GRCm39) |
Y31* |
probably null |
Het |
Smchd1 |
A |
T |
17: 71,685,252 (GRCm39) |
M1392K |
probably benign |
Het |
Sobp |
T |
A |
10: 43,036,827 (GRCm39) |
N37I |
probably damaging |
Het |
Spock3 |
G |
T |
8: 63,673,739 (GRCm39) |
C142F |
probably damaging |
Het |
Stx6 |
A |
C |
1: 155,053,650 (GRCm39) |
S86R |
probably benign |
Het |
Sult2a4 |
C |
A |
7: 13,643,726 (GRCm39) |
M280I |
probably benign |
Het |
Synm |
A |
T |
7: 67,386,080 (GRCm39) |
D527E |
probably damaging |
Het |
Tax1bp1 |
C |
T |
6: 52,710,305 (GRCm39) |
R195W |
probably damaging |
Het |
Themis2 |
A |
T |
4: 132,519,796 (GRCm39) |
N76K |
possibly damaging |
Het |
Tmem8b |
A |
G |
4: 43,690,234 (GRCm39) |
T890A |
probably benign |
Het |
Traf7 |
T |
A |
17: 24,730,785 (GRCm39) |
H366L |
possibly damaging |
Het |
Trim30c |
A |
T |
7: 104,032,459 (GRCm39) |
V289D |
probably benign |
Het |
Tsr1 |
T |
A |
11: 74,792,914 (GRCm39) |
D407E |
probably damaging |
Het |
Ubap2 |
G |
T |
4: 41,235,593 (GRCm39) |
A33E |
probably damaging |
Het |
Unc13d |
C |
A |
11: 115,964,701 (GRCm39) |
R255L |
possibly damaging |
Het |
Ush2a |
G |
T |
1: 188,542,534 (GRCm39) |
G3367* |
probably null |
Het |
Vmn1r229 |
T |
C |
17: 21,034,791 (GRCm39) |
L12P |
probably damaging |
Het |
Vmn2r27 |
C |
A |
6: 124,177,474 (GRCm39) |
G510V |
probably damaging |
Het |
Vps4b |
T |
C |
1: 106,707,712 (GRCm39) |
E257G |
probably damaging |
Het |
Vps72 |
T |
C |
3: 95,026,462 (GRCm39) |
S136P |
probably damaging |
Het |
Wdr36 |
T |
C |
18: 32,976,938 (GRCm39) |
I181T |
possibly damaging |
Het |
Wfikkn1 |
C |
T |
17: 26,096,765 (GRCm39) |
A520T |
probably benign |
Het |
|
Other mutations in Bend3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00341:Bend3
|
APN |
10 |
43,387,539 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00977:Bend3
|
APN |
10 |
43,386,945 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL00980:Bend3
|
APN |
10 |
43,387,562 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02457:Bend3
|
APN |
10 |
43,385,946 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4515001:Bend3
|
UTSW |
10 |
43,386,630 (GRCm39) |
missense |
probably damaging |
0.98 |
R0148:Bend3
|
UTSW |
10 |
43,387,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R2046:Bend3
|
UTSW |
10 |
43,387,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R2098:Bend3
|
UTSW |
10 |
43,386,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R3419:Bend3
|
UTSW |
10 |
43,385,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R3854:Bend3
|
UTSW |
10 |
43,386,713 (GRCm39) |
unclassified |
probably benign |
|
R4449:Bend3
|
UTSW |
10 |
43,388,079 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4765:Bend3
|
UTSW |
10 |
43,386,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R5070:Bend3
|
UTSW |
10 |
43,369,681 (GRCm39) |
missense |
probably damaging |
0.99 |
R5299:Bend3
|
UTSW |
10 |
43,369,686 (GRCm39) |
critical splice donor site |
probably null |
|
R5456:Bend3
|
UTSW |
10 |
43,386,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R5530:Bend3
|
UTSW |
10 |
43,387,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R5976:Bend3
|
UTSW |
10 |
43,386,540 (GRCm39) |
missense |
probably benign |
0.00 |
R6173:Bend3
|
UTSW |
10 |
43,385,864 (GRCm39) |
missense |
probably benign |
0.00 |
R7227:Bend3
|
UTSW |
10 |
43,387,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R7256:Bend3
|
UTSW |
10 |
43,369,667 (GRCm39) |
missense |
probably benign |
0.12 |
R8273:Bend3
|
UTSW |
10 |
43,386,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R9328:Bend3
|
UTSW |
10 |
43,387,419 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9739:Bend3
|
UTSW |
10 |
43,385,847 (GRCm39) |
missense |
possibly damaging |
0.95 |
RF010:Bend3
|
UTSW |
10 |
43,386,180 (GRCm39) |
missense |
possibly damaging |
0.82 |
|