Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acta2 |
G |
A |
19: 34,229,931 (GRCm39) |
T8I |
probably benign |
Het |
Adcy8 |
C |
T |
15: 64,792,882 (GRCm39) |
G25S |
probably benign |
Het |
Ahnak2 |
G |
T |
12: 112,751,749 (GRCm39) |
D35E |
|
Het |
Birc6 |
T |
C |
17: 74,969,713 (GRCm39) |
M4261T |
probably damaging |
Het |
Caln1 |
T |
G |
5: 130,534,918 (GRCm39) |
F45V |
probably damaging |
Het |
Camta2 |
A |
T |
11: 70,572,372 (GRCm39) |
I313N |
possibly damaging |
Het |
Capns1 |
T |
A |
7: 29,889,539 (GRCm39) |
E220V |
probably damaging |
Het |
Carmil1 |
C |
A |
13: 24,197,315 (GRCm39) |
V1374L |
probably benign |
Het |
Casp2 |
T |
G |
6: 42,250,972 (GRCm39) |
L290R |
possibly damaging |
Het |
Cdkn2b |
C |
A |
4: 89,228,980 (GRCm39) |
V19L |
probably benign |
Het |
Ces1c |
T |
C |
8: 93,851,139 (GRCm39) |
N162D |
probably benign |
Het |
Cfap96 |
A |
G |
8: 46,423,488 (GRCm39) |
Y75H |
probably damaging |
Het |
Chd9 |
T |
C |
8: 91,763,017 (GRCm39) |
S2281P |
probably damaging |
Het |
Ckap2l |
G |
T |
2: 129,127,600 (GRCm39) |
P193T |
possibly damaging |
Het |
Clca4b |
T |
A |
3: 144,627,757 (GRCm39) |
T405S |
probably benign |
Het |
Cmah |
T |
C |
13: 24,619,630 (GRCm39) |
V265A |
probably benign |
Het |
Cyp3a11 |
A |
T |
5: 145,797,191 (GRCm39) |
M396K |
probably benign |
Het |
Ddr2 |
A |
T |
1: 169,825,727 (GRCm39) |
M291K |
possibly damaging |
Het |
Ddx43 |
T |
A |
9: 78,309,635 (GRCm39) |
I145N |
probably benign |
Het |
Ephb2 |
T |
A |
4: 136,388,212 (GRCm39) |
|
probably null |
Het |
Fgfr1 |
A |
T |
8: 26,048,221 (GRCm39) |
K106* |
probably null |
Het |
Gpr6 |
A |
G |
10: 40,946,875 (GRCm39) |
F236L |
probably benign |
Het |
Grin2c |
A |
G |
11: 115,143,511 (GRCm39) |
S750P |
probably damaging |
Het |
Hecw2 |
A |
G |
1: 53,952,459 (GRCm39) |
S925P |
probably damaging |
Het |
Hivep3 |
CGG |
CG |
4: 119,955,108 (GRCm39) |
1141 |
probably null |
Het |
Hmg20b |
T |
A |
10: 81,185,432 (GRCm39) |
|
probably benign |
Het |
Kcnk10 |
T |
A |
12: 98,484,899 (GRCm39) |
Y79F |
probably damaging |
Het |
Lrrc30 |
A |
T |
17: 67,939,424 (GRCm39) |
F52Y |
probably damaging |
Het |
Lrriq1 |
T |
C |
10: 103,036,432 (GRCm39) |
K907R |
possibly damaging |
Het |
Mbd3 |
T |
C |
10: 80,231,352 (GRCm39) |
D63G |
probably damaging |
Het |
Mettl21a |
C |
T |
1: 64,654,266 (GRCm39) |
A84T |
probably benign |
Het |
Mmp19 |
A |
G |
10: 128,634,857 (GRCm39) |
D491G |
probably benign |
Het |
Mug1 |
A |
T |
6: 121,852,387 (GRCm39) |
|
probably null |
Het |
Myh1 |
A |
T |
11: 67,101,243 (GRCm39) |
H673L |
possibly damaging |
Het |
Nlrc5 |
T |
C |
8: 95,239,276 (GRCm39) |
|
probably null |
Het |
Nme9 |
T |
A |
9: 99,352,843 (GRCm39) |
S264R |
probably benign |
Het |
Nup153 |
T |
C |
13: 46,840,798 (GRCm39) |
T937A |
probably benign |
Het |
Obsl1 |
T |
C |
1: 75,482,024 (GRCm39) |
E282G |
probably damaging |
Het |
Or1o3 |
A |
G |
17: 37,573,745 (GRCm39) |
V270A |
probably benign |
Het |
Or2w2 |
A |
G |
13: 21,758,488 (GRCm39) |
V46A |
probably benign |
Het |
Or4l15 |
C |
A |
14: 50,198,368 (GRCm39) |
A54S |
probably benign |
Het |
Or5an10 |
T |
A |
19: 12,276,242 (GRCm39) |
M85L |
probably damaging |
Het |
Or5b99 |
T |
A |
19: 12,976,431 (GRCm39) |
I27N |
possibly damaging |
Het |
Or5m5 |
T |
A |
2: 85,814,407 (GRCm39) |
C74* |
probably null |
Het |
Or8k30 |
T |
A |
2: 86,339,397 (GRCm39) |
I198K |
possibly damaging |
Het |
Pcdhga12 |
T |
C |
18: 37,901,478 (GRCm39) |
F770S |
possibly damaging |
Het |
Pfkp |
T |
A |
13: 6,655,119 (GRCm39) |
|
probably null |
Het |
Prr29 |
C |
G |
11: 106,267,158 (GRCm39) |
H58D |
probably damaging |
Het |
Ptprz1 |
T |
A |
6: 23,001,219 (GRCm39) |
M1103K |
probably benign |
Het |
Rigi |
T |
C |
4: 40,225,651 (GRCm39) |
E250G |
probably damaging |
Het |
Rsph4a |
C |
T |
10: 33,781,473 (GRCm39) |
P108S |
probably benign |
Het |
Setd1b |
A |
C |
5: 123,290,657 (GRCm39) |
M875L |
unknown |
Het |
Slc15a2 |
A |
G |
16: 36,576,673 (GRCm39) |
S485P |
probably benign |
Het |
Smoc1 |
A |
G |
12: 81,226,444 (GRCm39) |
D423G |
probably damaging |
Het |
Spast |
T |
A |
17: 74,676,198 (GRCm39) |
V337D |
probably damaging |
Het |
Spesp1 |
T |
C |
9: 62,179,987 (GRCm39) |
K307R |
possibly damaging |
Het |
Sulf1 |
A |
G |
1: 12,906,467 (GRCm39) |
E503G |
probably benign |
Het |
Susd6 |
T |
C |
12: 80,921,341 (GRCm39) |
Y313H |
probably damaging |
Het |
Them4 |
A |
T |
3: 94,238,865 (GRCm39) |
D224V |
possibly damaging |
Het |
Tpsg1 |
G |
T |
17: 25,592,184 (GRCm39) |
G86V |
probably damaging |
Het |
Tspear |
A |
T |
10: 77,717,049 (GRCm39) |
T575S |
probably benign |
Het |
Usp21 |
A |
T |
1: 171,113,142 (GRCm39) |
H211Q |
probably benign |
Het |
Vmn1r189 |
T |
C |
13: 22,286,322 (GRCm39) |
S172G |
probably benign |
Het |
Vmn2r114 |
T |
C |
17: 23,515,944 (GRCm39) |
S516G |
probably damaging |
Het |
Vmn2r28 |
T |
A |
7: 5,484,255 (GRCm39) |
R648S |
probably benign |
Het |
Vmn2r6 |
C |
A |
3: 64,472,563 (GRCm39) |
V53F |
probably damaging |
Het |
Vmn2r76 |
A |
G |
7: 85,879,388 (GRCm39) |
I304T |
probably benign |
Het |
Vmn2r88 |
A |
C |
14: 51,651,454 (GRCm39) |
Y256S |
|
Het |
Zfhx4 |
A |
T |
3: 5,468,831 (GRCm39) |
K3021N |
probably damaging |
Het |
Zfp647 |
T |
C |
15: 76,795,988 (GRCm39) |
H224R |
probably damaging |
Het |
Zfp865 |
A |
G |
7: 5,034,130 (GRCm39) |
E705G |
probably damaging |
Het |
|
Other mutations in Chst13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03264:Chst13
|
APN |
6 |
90,286,193 (GRCm39) |
nonsense |
probably null |
|
E0374:Chst13
|
UTSW |
6 |
90,286,174 (GRCm39) |
nonsense |
probably null |
|
PIT4520001:Chst13
|
UTSW |
6 |
90,286,167 (GRCm39) |
missense |
probably benign |
0.19 |
R2301:Chst13
|
UTSW |
6 |
90,295,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R2849:Chst13
|
UTSW |
6 |
90,286,140 (GRCm39) |
missense |
probably benign |
0.00 |
R3522:Chst13
|
UTSW |
6 |
90,295,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R5068:Chst13
|
UTSW |
6 |
90,286,551 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5560:Chst13
|
UTSW |
6 |
90,295,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R5888:Chst13
|
UTSW |
6 |
90,286,554 (GRCm39) |
missense |
probably benign |
0.37 |
R6306:Chst13
|
UTSW |
6 |
90,286,260 (GRCm39) |
missense |
probably damaging |
0.99 |
R6393:Chst13
|
UTSW |
6 |
90,302,063 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6572:Chst13
|
UTSW |
6 |
90,286,588 (GRCm39) |
missense |
probably benign |
0.00 |
R7767:Chst13
|
UTSW |
6 |
90,286,566 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7880:Chst13
|
UTSW |
6 |
90,302,062 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9002:Chst13
|
UTSW |
6 |
90,286,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R9010:Chst13
|
UTSW |
6 |
90,286,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R9288:Chst13
|
UTSW |
6 |
90,286,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R9295:Chst13
|
UTSW |
6 |
90,286,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R9296:Chst13
|
UTSW |
6 |
90,286,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R9318:Chst13
|
UTSW |
6 |
90,286,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R9319:Chst13
|
UTSW |
6 |
90,286,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R9397:Chst13
|
UTSW |
6 |
90,286,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R9461:Chst13
|
UTSW |
6 |
90,286,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R9480:Chst13
|
UTSW |
6 |
90,286,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R9481:Chst13
|
UTSW |
6 |
90,286,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R9521:Chst13
|
UTSW |
6 |
90,286,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R9522:Chst13
|
UTSW |
6 |
90,286,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R9749:Chst13
|
UTSW |
6 |
90,295,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R9787:Chst13
|
UTSW |
6 |
90,286,074 (GRCm39) |
missense |
probably benign |
0.02 |
|