Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm1 |
T |
A |
4: 144,248,924 (GRCm39) |
I97N |
probably damaging |
Het |
Acvrl1 |
A |
G |
15: 101,041,354 (GRCm39) |
H502R |
probably benign |
Het |
Adgrf4 |
T |
C |
17: 42,983,494 (GRCm39) |
S63G |
probably benign |
Het |
Agbl2 |
C |
A |
2: 90,621,899 (GRCm39) |
L129I |
probably damaging |
Het |
Ankrd11 |
C |
A |
8: 123,614,145 (GRCm39) |
A2542S |
probably damaging |
Het |
Armc9 |
A |
G |
1: 86,203,400 (GRCm39) |
K818R |
probably damaging |
Het |
Arsj |
T |
A |
3: 126,231,885 (GRCm39) |
C210* |
probably null |
Het |
Aspscr1 |
C |
T |
11: 120,563,926 (GRCm39) |
A11V |
unknown |
Het |
Bicc1 |
G |
T |
10: 70,792,121 (GRCm39) |
Q296K |
possibly damaging |
Het |
Borcs5 |
A |
C |
6: 134,662,942 (GRCm39) |
Q73P |
probably benign |
Het |
Capn15 |
G |
T |
17: 26,182,406 (GRCm39) |
D567E |
probably damaging |
Het |
Catsperg1 |
A |
C |
7: 28,889,239 (GRCm39) |
I866S |
probably damaging |
Het |
Ccdc27 |
G |
T |
4: 154,126,274 (GRCm39) |
H72N |
unknown |
Het |
Ccser2 |
A |
T |
14: 36,601,457 (GRCm39) |
M309K |
possibly damaging |
Het |
Cd1d2 |
A |
G |
3: 86,894,408 (GRCm39) |
S59G |
probably benign |
Het |
Chml |
G |
A |
1: 175,515,456 (GRCm39) |
P155L |
probably benign |
Het |
Csmd2 |
C |
T |
4: 128,346,251 (GRCm39) |
P1504S |
|
Het |
Dcbld2 |
A |
G |
16: 58,269,081 (GRCm39) |
|
probably null |
Het |
Ddx21 |
C |
T |
10: 62,434,022 (GRCm39) |
E246K |
probably benign |
Het |
Dhx29 |
C |
T |
13: 113,064,176 (GRCm39) |
|
probably benign |
Het |
Dis3l |
A |
C |
9: 64,219,219 (GRCm39) |
Y570* |
probably null |
Het |
Dnah14 |
T |
A |
1: 181,597,619 (GRCm39) |
Y3623N |
probably benign |
Het |
Dock8 |
A |
G |
19: 25,152,764 (GRCm39) |
D1610G |
probably damaging |
Het |
Dync1h1 |
T |
C |
12: 110,597,059 (GRCm39) |
S1669P |
probably benign |
Het |
Eif1ad12 |
A |
C |
12: 87,541,505 (GRCm39) |
K5N |
unknown |
Het |
Eif2ak4 |
T |
A |
2: 118,247,764 (GRCm39) |
I267N |
possibly damaging |
Het |
Ern2 |
A |
T |
7: 121,769,464 (GRCm39) |
V854E |
probably damaging |
Het |
Fuca2 |
G |
A |
10: 13,383,174 (GRCm39) |
|
probably null |
Het |
Gbp10 |
G |
A |
5: 105,384,015 (GRCm39) |
|
probably benign |
Het |
Gm1110 |
T |
A |
9: 26,804,924 (GRCm39) |
T380S |
probably benign |
Het |
Golga2 |
G |
A |
2: 32,178,178 (GRCm39) |
R29H |
probably benign |
Het |
Grik5 |
T |
C |
7: 24,760,022 (GRCm39) |
E259G |
probably benign |
Het |
Grm3 |
T |
C |
5: 9,620,000 (GRCm39) |
T415A |
probably benign |
Het |
Gtf3c1 |
A |
G |
7: 125,244,842 (GRCm39) |
Y1731H |
probably damaging |
Het |
Hectd2 |
T |
C |
19: 36,589,803 (GRCm39) |
C643R |
probably damaging |
Het |
Hgfac |
T |
C |
5: 35,199,972 (GRCm39) |
S118P |
probably damaging |
Het |
Hmcn1 |
A |
G |
1: 150,480,625 (GRCm39) |
V4517A |
probably benign |
Het |
Hnrnpc |
A |
T |
14: 52,312,610 (GRCm39) |
L290* |
probably null |
Het |
Homer3 |
A |
G |
8: 70,742,063 (GRCm39) |
E108G |
probably damaging |
Het |
Hsd17b3 |
G |
T |
13: 64,219,816 (GRCm39) |
S141R |
probably benign |
Het |
Hspa12b |
C |
T |
2: 130,980,396 (GRCm39) |
T105I |
probably damaging |
Het |
Ifi202b |
T |
C |
1: 173,799,787 (GRCm39) |
I231M |
probably damaging |
Het |
Inhba |
T |
A |
13: 16,192,222 (GRCm39) |
N114K |
probably benign |
Het |
Kmt2b |
C |
A |
7: 30,268,835 (GRCm39) |
M2631I |
possibly damaging |
Het |
Loxhd1 |
C |
T |
18: 77,483,061 (GRCm39) |
T1214I |
probably damaging |
Het |
Lrp1 |
G |
T |
10: 127,382,731 (GRCm39) |
N3683K |
probably damaging |
Het |
Lrrc8e |
A |
G |
8: 4,284,363 (GRCm39) |
K196R |
probably benign |
Het |
Lrrn3 |
A |
T |
12: 41,502,910 (GRCm39) |
M469K |
probably benign |
Het |
Mafb |
T |
C |
2: 160,207,749 (GRCm39) |
E283G |
probably damaging |
Het |
Mapt |
C |
A |
11: 104,189,528 (GRCm39) |
P182Q |
probably benign |
Het |
Mmp14 |
G |
T |
14: 54,675,199 (GRCm39) |
R277L |
possibly damaging |
Het |
Mucl2 |
T |
A |
15: 103,927,711 (GRCm39) |
N82I |
probably benign |
Het |
Nsun6 |
T |
A |
2: 15,001,150 (GRCm39) |
T469S |
possibly damaging |
Het |
Or13p4 |
T |
C |
4: 118,546,839 (GRCm39) |
D270G |
possibly damaging |
Het |
Or5p79 |
G |
C |
7: 108,221,933 (GRCm39) |
A305P |
probably damaging |
Het |
Or8k30 |
A |
C |
2: 86,339,691 (GRCm39) |
D296A |
probably damaging |
Het |
Osbpl5 |
A |
T |
7: 143,248,670 (GRCm39) |
F631I |
possibly damaging |
Het |
Otud3 |
G |
T |
4: 138,629,196 (GRCm39) |
D190E |
possibly damaging |
Het |
Pcdhb6 |
A |
T |
18: 37,468,332 (GRCm39) |
I418F |
possibly damaging |
Het |
Per1 |
G |
A |
11: 68,997,339 (GRCm39) |
R838H |
probably damaging |
Het |
Per2 |
G |
A |
1: 91,362,857 (GRCm39) |
P395S |
probably damaging |
Het |
Pkhd1l1 |
A |
T |
15: 44,414,157 (GRCm39) |
H2808L |
possibly damaging |
Het |
Ppfia2 |
A |
G |
10: 106,763,687 (GRCm39) |
T1227A |
probably benign |
Het |
Pramel30 |
T |
C |
4: 144,059,311 (GRCm39) |
F341L |
probably benign |
Het |
Psg17 |
C |
T |
7: 18,551,019 (GRCm39) |
D279N |
probably benign |
Het |
Rnf167 |
A |
G |
11: 70,541,623 (GRCm39) |
D235G |
probably benign |
Het |
Rxfp3 |
A |
G |
15: 11,036,362 (GRCm39) |
S337P |
probably damaging |
Het |
Sall1 |
T |
C |
8: 89,759,786 (GRCm39) |
D106G |
possibly damaging |
Het |
Sema4f |
A |
G |
6: 82,891,037 (GRCm39) |
V590A |
probably benign |
Het |
Setd1b |
A |
G |
5: 123,295,820 (GRCm39) |
D1102G |
unknown |
Het |
Six2 |
C |
A |
17: 85,995,135 (GRCm39) |
K82N |
probably damaging |
Het |
Snx29 |
T |
C |
16: 11,218,806 (GRCm39) |
M214T |
probably benign |
Het |
Son |
T |
C |
16: 91,455,810 (GRCm39) |
L1519P |
probably damaging |
Het |
Speer1h |
A |
T |
5: 11,647,579 (GRCm39) |
N106Y |
probably damaging |
Het |
Spin1 |
C |
T |
13: 51,303,085 (GRCm39) |
S226L |
probably benign |
Het |
Stxbp5l |
T |
C |
16: 37,143,965 (GRCm39) |
D131G |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,069,422 (GRCm39) |
Y2788C |
probably damaging |
Het |
Tbl3 |
C |
A |
17: 24,920,950 (GRCm39) |
|
probably null |
Het |
Themis |
A |
T |
10: 28,657,698 (GRCm39) |
I242L |
possibly damaging |
Het |
Tmem203 |
G |
A |
2: 25,145,742 (GRCm39) |
V21M |
probably benign |
Het |
Trp53inp1 |
T |
C |
4: 11,169,750 (GRCm39) |
C171R |
probably benign |
Het |
Tsg101 |
A |
G |
7: 46,563,159 (GRCm39) |
Y32H |
probably damaging |
Het |
Tyw1 |
A |
G |
5: 130,303,547 (GRCm39) |
D305G |
probably damaging |
Het |
Vmn1r40 |
A |
T |
6: 89,692,026 (GRCm39) |
Y281F |
probably damaging |
Het |
Vmn2r105 |
T |
A |
17: 20,447,937 (GRCm39) |
T296S |
probably damaging |
Het |
Vmn2r13 |
T |
C |
5: 109,319,557 (GRCm39) |
|
probably null |
Het |
Zfp933 |
A |
G |
4: 147,910,589 (GRCm39) |
F336L |
probably damaging |
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 |
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 |
R9153:Per3
|
UTSW |
4 |
151,111,796 (GRCm39) |
missense |
probably benign |
0.18 |
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 |
|