Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001J03Rik |
C |
T |
5: 146,122,001 (GRCm39) |
R27H |
probably benign |
Het |
2310002L09Rik |
A |
T |
4: 73,868,845 (GRCm39) |
L31Q |
probably damaging |
Het |
Agbl1 |
G |
A |
7: 76,064,406 (GRCm39) |
D53N |
probably damaging |
Het |
Aloxe3 |
C |
T |
11: 69,033,749 (GRCm39) |
T621I |
probably damaging |
Het |
Als2cl |
A |
T |
9: 110,726,567 (GRCm39) |
|
probably null |
Het |
Atg9b |
T |
A |
5: 24,596,542 (GRCm39) |
T125S |
possibly damaging |
Het |
Casp8ap2 |
A |
G |
4: 32,645,343 (GRCm39) |
D1472G |
probably damaging |
Het |
Cd1d2 |
C |
G |
3: 86,894,987 (GRCm39) |
P158A |
probably damaging |
Het |
Cdc45 |
A |
G |
16: 18,627,543 (GRCm39) |
I94T |
probably benign |
Het |
Chd6 |
T |
G |
2: 160,809,800 (GRCm39) |
D1487A |
possibly damaging |
Het |
Edem2 |
T |
C |
2: 155,550,947 (GRCm39) |
Y340C |
probably damaging |
Het |
Fbxl12 |
C |
T |
9: 20,553,509 (GRCm39) |
R26H |
probably damaging |
Het |
Fgfr3 |
A |
G |
5: 33,891,284 (GRCm39) |
N516S |
probably damaging |
Het |
Gm5884 |
A |
G |
6: 128,622,021 (GRCm39) |
|
noncoding transcript |
Het |
Hdac1-ps |
A |
G |
17: 78,800,275 (GRCm39) |
D422G |
probably damaging |
Het |
Inpp4b |
C |
A |
8: 82,711,958 (GRCm39) |
A425E |
possibly damaging |
Het |
Kif1a |
A |
G |
1: 92,974,464 (GRCm39) |
Y964H |
probably damaging |
Het |
Lrp1b |
A |
C |
2: 41,660,911 (GRCm39) |
C66G |
probably damaging |
Het |
Lrp4 |
A |
G |
2: 91,321,075 (GRCm39) |
I1034V |
probably benign |
Het |
Mmrn2 |
T |
C |
14: 34,124,879 (GRCm39) |
V820A |
possibly damaging |
Het |
Mphosph9 |
G |
A |
5: 124,399,069 (GRCm39) |
T982I |
probably benign |
Het |
Mroh9 |
A |
C |
1: 162,884,341 (GRCm39) |
M399R |
probably damaging |
Het |
Mslnl |
G |
A |
17: 25,961,908 (GRCm39) |
V128M |
probably damaging |
Het |
N4bp2 |
G |
A |
5: 65,964,441 (GRCm39) |
G830D |
probably benign |
Het |
Nagpa |
G |
A |
16: 5,021,651 (GRCm39) |
|
probably benign |
Het |
Or52b1 |
C |
T |
7: 104,979,067 (GRCm39) |
V111M |
probably damaging |
Het |
Or5g23 |
G |
A |
2: 85,438,754 (GRCm39) |
P167S |
probably benign |
Het |
Oxgr1 |
T |
A |
14: 120,260,221 (GRCm39) |
|
probably benign |
Het |
Parp3 |
T |
A |
9: 106,350,924 (GRCm39) |
R323W |
possibly damaging |
Het |
Pfkfb3 |
C |
T |
2: 11,489,138 (GRCm39) |
V286I |
probably benign |
Het |
Pfkp |
C |
T |
13: 6,643,279 (GRCm39) |
G513D |
probably damaging |
Het |
Pla2g4d |
T |
C |
2: 120,112,108 (GRCm39) |
|
probably benign |
Het |
Rtl1 |
T |
C |
12: 109,557,582 (GRCm39) |
E1419G |
unknown |
Het |
Sdf2 |
G |
C |
11: 78,145,680 (GRCm39) |
V126L |
probably damaging |
Het |
Sgk2 |
T |
G |
2: 162,841,115 (GRCm39) |
L175R |
probably damaging |
Het |
Sgk2 |
C |
A |
2: 162,841,125 (GRCm39) |
F178L |
probably damaging |
Het |
Sim1 |
T |
C |
10: 50,785,911 (GRCm39) |
Y255H |
probably benign |
Het |
Slc13a5 |
T |
C |
11: 72,138,617 (GRCm39) |
E442G |
possibly damaging |
Het |
Slc38a3 |
A |
T |
9: 107,534,886 (GRCm39) |
I163N |
probably damaging |
Het |
Slc39a4 |
A |
G |
15: 76,500,870 (GRCm39) |
L31P |
probably damaging |
Het |
Slc5a11 |
GGTGC |
G |
7: 122,838,595 (GRCm39) |
|
probably null |
Het |
Slfnl1 |
G |
T |
4: 120,390,275 (GRCm39) |
|
probably benign |
Het |
Stradb |
G |
A |
1: 59,031,828 (GRCm39) |
V247M |
probably benign |
Het |
Styk1 |
T |
A |
6: 131,289,967 (GRCm39) |
|
probably benign |
Het |
Sult1d1 |
A |
G |
5: 87,707,614 (GRCm39) |
|
probably benign |
Het |
Syk |
C |
T |
13: 52,765,157 (GRCm39) |
P95S |
probably benign |
Het |
Taar2 |
T |
A |
10: 23,817,454 (GRCm39) |
N331K |
probably benign |
Het |
Thsd7b |
A |
G |
1: 130,117,587 (GRCm39) |
|
probably benign |
Het |
Tmbim7 |
G |
A |
5: 3,723,188 (GRCm39) |
|
probably null |
Het |
Tmem107 |
T |
C |
11: 68,962,247 (GRCm39) |
L68P |
probably damaging |
Het |
Tmem184c |
A |
T |
8: 78,331,276 (GRCm39) |
C158S |
probably damaging |
Het |
Tmpo |
A |
G |
10: 90,988,548 (GRCm39) |
I310T |
probably benign |
Het |
Ugt2b5 |
A |
G |
5: 87,273,266 (GRCm39) |
F467L |
possibly damaging |
Het |
Xirp1 |
T |
C |
9: 119,847,767 (GRCm39) |
E372G |
possibly damaging |
Het |
Zbtb5 |
T |
C |
4: 44,994,790 (GRCm39) |
E198G |
probably damaging |
Het |
Zfp804a |
A |
G |
2: 82,066,160 (GRCm39) |
N44D |
probably damaging |
Het |
|
Other mutations in Meak7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00494:Meak7
|
APN |
8 |
120,499,334 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00886:Meak7
|
APN |
8 |
120,500,007 (GRCm39) |
splice site |
probably benign |
|
IGL02679:Meak7
|
APN |
8 |
120,499,149 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02896:Meak7
|
APN |
8 |
120,489,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R0126:Meak7
|
UTSW |
8 |
120,489,089 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0456:Meak7
|
UTSW |
8 |
120,495,162 (GRCm39) |
missense |
probably damaging |
0.96 |
R1831:Meak7
|
UTSW |
8 |
120,497,992 (GRCm39) |
missense |
probably null |
0.00 |
R3114:Meak7
|
UTSW |
8 |
120,495,056 (GRCm39) |
missense |
probably benign |
|
R3116:Meak7
|
UTSW |
8 |
120,495,056 (GRCm39) |
missense |
probably benign |
|
R4763:Meak7
|
UTSW |
8 |
120,495,122 (GRCm39) |
missense |
probably benign |
0.09 |
R4796:Meak7
|
UTSW |
8 |
120,495,093 (GRCm39) |
missense |
probably benign |
0.13 |
R4858:Meak7
|
UTSW |
8 |
120,499,262 (GRCm39) |
missense |
probably benign |
0.17 |
R4976:Meak7
|
UTSW |
8 |
120,494,882 (GRCm39) |
missense |
probably damaging |
0.97 |
R5119:Meak7
|
UTSW |
8 |
120,494,882 (GRCm39) |
missense |
probably damaging |
0.97 |
R5393:Meak7
|
UTSW |
8 |
120,499,157 (GRCm39) |
missense |
probably benign |
0.13 |
R6811:Meak7
|
UTSW |
8 |
120,495,029 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6828:Meak7
|
UTSW |
8 |
120,499,306 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7237:Meak7
|
UTSW |
8 |
120,489,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R8536:Meak7
|
UTSW |
8 |
120,490,787 (GRCm39) |
missense |
probably benign |
0.01 |
R9047:Meak7
|
UTSW |
8 |
120,489,050 (GRCm39) |
missense |
probably benign |
0.00 |
R9375:Meak7
|
UTSW |
8 |
120,498,096 (GRCm39) |
missense |
probably benign |
|
R9414:Meak7
|
UTSW |
8 |
120,495,081 (GRCm39) |
missense |
probably benign |
0.01 |
R9668:Meak7
|
UTSW |
8 |
120,488,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R9731:Meak7
|
UTSW |
8 |
120,498,010 (GRCm39) |
missense |
probably benign |
0.16 |
|