Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
A |
T |
11: 110,107,481 (GRCm39) |
S711R |
possibly damaging |
Het |
Adnp |
C |
A |
2: 168,026,580 (GRCm39) |
Q238H |
possibly damaging |
Het |
Akap13 |
A |
G |
7: 75,259,229 (GRCm39) |
T618A |
probably benign |
Het |
Ankfn1 |
G |
A |
11: 89,302,845 (GRCm39) |
R58W |
probably damaging |
Het |
Atp8b5 |
A |
G |
4: 43,308,493 (GRCm39) |
|
probably benign |
Het |
Borcs5 |
G |
T |
6: 134,618,108 (GRCm39) |
|
probably benign |
Het |
C1s1 |
T |
C |
6: 124,517,906 (GRCm39) |
M25V |
possibly damaging |
Het |
Canx |
A |
T |
11: 50,188,162 (GRCm39) |
D527E |
probably benign |
Het |
Ccdc154 |
G |
A |
17: 25,382,152 (GRCm39) |
D24N |
probably damaging |
Het |
Ccnt1 |
G |
A |
15: 98,441,159 (GRCm39) |
T703I |
probably benign |
Het |
Cd46 |
T |
C |
1: 194,774,479 (GRCm39) |
S19G |
possibly damaging |
Het |
Cdc25b |
G |
A |
2: 131,034,564 (GRCm39) |
E264K |
possibly damaging |
Het |
Cdhr17 |
A |
T |
5: 17,040,916 (GRCm39) |
|
probably null |
Het |
Cog5 |
A |
C |
12: 31,710,810 (GRCm39) |
K63N |
possibly damaging |
Het |
Col28a1 |
G |
A |
6: 8,022,765 (GRCm39) |
T726I |
probably benign |
Het |
Dhx40 |
A |
G |
11: 86,690,365 (GRCm39) |
S219P |
probably damaging |
Het |
Dnah12 |
T |
A |
14: 26,536,569 (GRCm39) |
W2162R |
probably damaging |
Het |
Eef1a2 |
A |
G |
2: 180,789,774 (GRCm39) |
*464R |
probably null |
Het |
Eif1a |
T |
A |
18: 46,741,036 (GRCm39) |
D90E |
probably damaging |
Het |
Fasn |
C |
T |
11: 120,706,496 (GRCm39) |
R996Q |
possibly damaging |
Het |
Foxred2 |
A |
G |
15: 77,839,787 (GRCm39) |
|
probably null |
Het |
Frat2 |
A |
G |
19: 41,835,806 (GRCm39) |
L182P |
probably damaging |
Het |
Fxyd2 |
G |
T |
9: 45,319,609 (GRCm39) |
V24F |
probably damaging |
Het |
Gabrd |
C |
T |
4: 155,470,496 (GRCm39) |
V319I |
probably damaging |
Het |
H13 |
T |
G |
2: 152,533,788 (GRCm39) |
V267G |
possibly damaging |
Het |
Hnf4g |
T |
C |
3: 3,573,378 (GRCm39) |
|
probably benign |
Het |
Iglon5 |
T |
A |
7: 43,125,421 (GRCm39) |
T272S |
possibly damaging |
Het |
Iqgap2 |
T |
A |
13: 95,844,547 (GRCm39) |
M454L |
probably benign |
Het |
Irf8 |
T |
C |
8: 121,480,400 (GRCm39) |
C304R |
probably benign |
Het |
Itga2 |
A |
G |
13: 115,001,941 (GRCm39) |
F614L |
probably benign |
Het |
Itgb4 |
A |
C |
11: 115,874,879 (GRCm39) |
H412P |
probably benign |
Het |
Jarid2 |
T |
C |
13: 45,064,678 (GRCm39) |
F921S |
probably damaging |
Het |
Kctd13 |
A |
G |
7: 126,541,327 (GRCm39) |
D189G |
probably damaging |
Het |
Meis2 |
G |
T |
2: 115,697,756 (GRCm39) |
P381T |
probably benign |
Het |
Mertk |
G |
T |
2: 128,624,487 (GRCm39) |
A633S |
probably damaging |
Het |
Morn5 |
A |
G |
2: 35,942,993 (GRCm39) |
Y31C |
probably damaging |
Het |
Mug2 |
A |
T |
6: 122,017,627 (GRCm39) |
T455S |
possibly damaging |
Het |
Myo3a |
A |
G |
2: 22,404,744 (GRCm39) |
N700S |
probably benign |
Het |
Nisch |
T |
C |
14: 30,896,782 (GRCm39) |
T807A |
unknown |
Het |
Nkx1-1 |
A |
T |
5: 33,588,703 (GRCm39) |
V195E |
unknown |
Het |
Numa1 |
A |
G |
7: 101,649,118 (GRCm39) |
T950A |
probably benign |
Het |
Nup160 |
A |
G |
2: 90,514,429 (GRCm39) |
T126A |
possibly damaging |
Het |
Oca2 |
C |
T |
7: 55,943,586 (GRCm39) |
T253I |
probably benign |
Het |
Odad2 |
T |
C |
18: 7,286,733 (GRCm39) |
K166R |
possibly damaging |
Het |
Or6c209 |
T |
A |
10: 129,483,306 (GRCm39) |
I103N |
possibly damaging |
Het |
P4ha1 |
A |
G |
10: 59,203,112 (GRCm39) |
K435R |
probably damaging |
Het |
Pcdhgb4 |
T |
A |
18: 37,854,131 (GRCm39) |
N175K |
possibly damaging |
Het |
Phactr3 |
A |
T |
2: 177,925,739 (GRCm39) |
E338V |
possibly damaging |
Het |
Plec |
G |
T |
15: 76,064,725 (GRCm39) |
R1782S |
unknown |
Het |
Prpf39 |
A |
T |
12: 65,106,671 (GRCm39) |
Q593L |
probably damaging |
Het |
Ptprq |
T |
C |
10: 107,416,126 (GRCm39) |
Y1724C |
probably damaging |
Het |
Pygo1 |
T |
A |
9: 72,852,143 (GRCm39) |
V110D |
possibly damaging |
Het |
Rasgrf1 |
T |
A |
9: 89,826,790 (GRCm39) |
L133Q |
probably damaging |
Het |
Rgs10 |
G |
A |
7: 127,975,733 (GRCm39) |
R145C |
probably damaging |
Het |
Secisbp2 |
A |
G |
13: 51,833,855 (GRCm39) |
Y665C |
possibly damaging |
Het |
Sel1l3 |
T |
A |
5: 53,293,188 (GRCm39) |
T843S |
probably benign |
Het |
Senp7 |
G |
A |
16: 56,006,486 (GRCm39) |
V964I |
probably benign |
Het |
Setd4 |
T |
A |
16: 93,384,722 (GRCm39) |
D322V |
possibly damaging |
Het |
Sftpc |
T |
A |
14: 70,759,650 (GRCm39) |
T90S |
probably benign |
Het |
Shq1 |
A |
T |
6: 100,588,738 (GRCm39) |
D382E |
probably damaging |
Het |
Sim1 |
A |
G |
10: 50,772,029 (GRCm39) |
R13G |
probably damaging |
Het |
Slc12a1 |
T |
G |
2: 125,002,989 (GRCm39) |
|
probably benign |
Het |
Slc27a6 |
T |
C |
18: 58,731,805 (GRCm39) |
F385S |
probably benign |
Het |
Stk38l |
A |
G |
6: 146,660,048 (GRCm39) |
T27A |
probably benign |
Het |
Tasp1 |
A |
G |
2: 139,899,327 (GRCm39) |
S9P |
probably damaging |
Het |
Tcstv1a |
T |
A |
13: 120,355,290 (GRCm39) |
D114V |
probably damaging |
Het |
Tmigd1 |
A |
T |
11: 76,795,468 (GRCm39) |
R25S |
probably benign |
Het |
Tnrc6a |
T |
A |
7: 122,773,519 (GRCm39) |
Y1154N |
probably damaging |
Het |
Tox2 |
T |
C |
2: 163,045,091 (GRCm39) |
V3A |
|
Het |
Ubr1 |
A |
T |
2: 120,756,469 (GRCm39) |
D719E |
probably benign |
Het |
Ubr3 |
A |
G |
2: 69,795,822 (GRCm39) |
K923R |
|
Het |
Vmn2r12 |
C |
T |
5: 109,234,203 (GRCm39) |
V670M |
probably damaging |
Het |
Zfp983 |
T |
C |
17: 21,876,522 (GRCm39) |
S9P |
probably benign |
Het |
Zfp986 |
A |
T |
4: 145,626,030 (GRCm39) |
H230L |
probably damaging |
Het |
Zscan4f |
G |
A |
7: 11,135,241 (GRCm39) |
E216K |
probably benign |
Het |
|
Other mutations in Per3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00925:Per3
|
APN |
4 |
151,098,055 (GRCm39) |
missense |
probably benign |
0.28 |
IGL02112:Per3
|
APN |
4 |
151,113,640 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02428:Per3
|
APN |
4 |
151,102,674 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02812:Per3
|
APN |
4 |
151,108,927 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03094:Per3
|
APN |
4 |
151,093,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R0119:Per3
|
UTSW |
4 |
151,109,005 (GRCm39) |
intron |
probably benign |
|
R0565:Per3
|
UTSW |
4 |
151,118,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R0671:Per3
|
UTSW |
4 |
151,113,288 (GRCm39) |
missense |
probably benign |
0.27 |
R1186:Per3
|
UTSW |
4 |
151,110,595 (GRCm39) |
missense |
probably damaging |
0.99 |
R1736:Per3
|
UTSW |
4 |
151,093,705 (GRCm39) |
critical splice donor site |
probably null |
|
R1757:Per3
|
UTSW |
4 |
151,127,249 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1900:Per3
|
UTSW |
4 |
151,125,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R1929:Per3
|
UTSW |
4 |
151,103,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R2044:Per3
|
UTSW |
4 |
151,118,395 (GRCm39) |
missense |
probably benign |
0.01 |
R2272:Per3
|
UTSW |
4 |
151,103,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R2415:Per3
|
UTSW |
4 |
151,097,147 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4771:Per3
|
UTSW |
4 |
151,093,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R5199:Per3
|
UTSW |
4 |
151,097,352 (GRCm39) |
missense |
probably benign |
0.15 |
R5298:Per3
|
UTSW |
4 |
151,113,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R5330:Per3
|
UTSW |
4 |
151,125,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R5331:Per3
|
UTSW |
4 |
151,125,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R5920:Per3
|
UTSW |
4 |
151,096,907 (GRCm39) |
missense |
probably benign |
0.05 |
R5974:Per3
|
UTSW |
4 |
151,127,194 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6498:Per3
|
UTSW |
4 |
151,113,662 (GRCm39) |
missense |
probably benign |
0.27 |
R6907:Per3
|
UTSW |
4 |
151,128,015 (GRCm39) |
critical splice donor site |
probably null |
|
R6915:Per3
|
UTSW |
4 |
151,128,106 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7269:Per3
|
UTSW |
4 |
151,116,393 (GRCm39) |
nonsense |
probably null |
|
R7454:Per3
|
UTSW |
4 |
151,097,185 (GRCm39) |
missense |
probably benign |
0.05 |
R7555:Per3
|
UTSW |
4 |
151,102,515 (GRCm39) |
nonsense |
probably null |
|
R7771:Per3
|
UTSW |
4 |
151,125,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R7771:Per3
|
UTSW |
4 |
151,110,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R8071:Per3
|
UTSW |
4 |
151,113,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R8079:Per3
|
UTSW |
4 |
151,127,135 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8099:Per3
|
UTSW |
4 |
151,097,014 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9449:Per3
|
UTSW |
4 |
151,094,945 (GRCm39) |
missense |
probably benign |
0.02 |
R9566:Per3
|
UTSW |
4 |
151,113,335 (GRCm39) |
missense |
|
|
R9585:Per3
|
UTSW |
4 |
151,097,138 (GRCm39) |
missense |
probably benign |
0.10 |
|