Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930486L24Rik |
A |
T |
13: 60,992,928 (GRCm39) |
D250E |
probably damaging |
Het |
4930571K23Rik |
A |
G |
7: 124,968,201 (GRCm39) |
|
noncoding transcript |
Het |
Acsl3 |
T |
C |
1: 78,683,114 (GRCm39) |
|
probably benign |
Het |
Acsl6 |
C |
A |
11: 54,220,792 (GRCm39) |
T244K |
probably damaging |
Het |
Adam26b |
T |
A |
8: 43,974,000 (GRCm39) |
N334I |
probably damaging |
Het |
Adgrl4 |
C |
T |
3: 151,223,248 (GRCm39) |
T608M |
probably damaging |
Het |
Aldh2 |
A |
G |
5: 121,716,404 (GRCm39) |
|
probably null |
Het |
Alms1 |
A |
G |
6: 85,599,436 (GRCm39) |
T1890A |
possibly damaging |
Het |
Capn7 |
C |
T |
14: 31,082,117 (GRCm39) |
T441M |
probably damaging |
Het |
Cd9 |
A |
T |
6: 125,441,367 (GRCm39) |
C85S |
probably damaging |
Het |
Ctif |
A |
G |
18: 75,757,376 (GRCm39) |
|
probably benign |
Het |
Dcc |
T |
A |
18: 71,503,808 (GRCm39) |
D950V |
probably damaging |
Het |
Eif4g1 |
T |
C |
16: 20,498,530 (GRCm39) |
V422A |
probably damaging |
Het |
Enthd1 |
A |
G |
15: 80,337,124 (GRCm39) |
S437P |
probably damaging |
Het |
Fads1 |
A |
G |
19: 10,171,464 (GRCm39) |
|
probably benign |
Het |
Fat3 |
T |
A |
9: 15,856,176 (GRCm39) |
I3869L |
probably benign |
Het |
Fbxw5 |
T |
A |
2: 25,392,473 (GRCm39) |
V85E |
possibly damaging |
Het |
Fcgbpl1 |
T |
A |
7: 27,853,772 (GRCm39) |
C1579S |
probably damaging |
Het |
Fem1b |
T |
C |
9: 62,704,456 (GRCm39) |
D268G |
possibly damaging |
Het |
Focad |
T |
C |
4: 88,327,225 (GRCm39) |
L1772P |
probably damaging |
Het |
Gtf3a |
C |
A |
5: 146,888,723 (GRCm39) |
Q145K |
possibly damaging |
Het |
Hacl1 |
T |
C |
14: 31,342,957 (GRCm39) |
|
probably null |
Het |
Herc2 |
T |
A |
7: 55,803,653 (GRCm39) |
F2229L |
probably benign |
Het |
Hs3st4 |
A |
T |
7: 123,996,080 (GRCm39) |
I249L |
probably benign |
Het |
Iqsec1 |
A |
T |
6: 90,786,752 (GRCm39) |
Y7* |
probably null |
Het |
Irag2 |
A |
G |
6: 145,083,341 (GRCm39) |
|
probably benign |
Het |
Klk1b1 |
T |
A |
7: 43,619,750 (GRCm39) |
M103K |
probably benign |
Het |
Krt5 |
A |
G |
15: 101,619,020 (GRCm39) |
V287A |
probably benign |
Het |
Lgals12 |
T |
A |
19: 7,581,530 (GRCm39) |
Q59L |
possibly damaging |
Het |
Loxl4 |
A |
G |
19: 42,593,379 (GRCm39) |
V264A |
possibly damaging |
Het |
Lrp1b |
T |
C |
2: 40,712,695 (GRCm39) |
D3099G |
probably damaging |
Het |
Mical3 |
G |
A |
6: 120,984,369 (GRCm39) |
T169I |
possibly damaging |
Het |
Muc21 |
A |
C |
17: 35,931,540 (GRCm39) |
|
probably benign |
Het |
Myef2l |
G |
A |
3: 10,154,613 (GRCm39) |
V461I |
possibly damaging |
Het |
Myh7b |
A |
C |
2: 155,462,054 (GRCm39) |
S317R |
probably damaging |
Het |
Nrbp1 |
T |
A |
5: 31,403,157 (GRCm39) |
I210N |
probably damaging |
Het |
Nsd1 |
A |
T |
13: 55,361,872 (GRCm39) |
|
probably null |
Het |
Nup58 |
A |
T |
14: 60,482,119 (GRCm39) |
|
probably benign |
Het |
Or1j17 |
C |
T |
2: 36,578,259 (GRCm39) |
L82F |
probably damaging |
Het |
Or2t49 |
A |
T |
11: 58,392,502 (GRCm39) |
S293R |
probably damaging |
Het |
Or5h22 |
A |
G |
16: 58,895,270 (GRCm39) |
Y58H |
probably damaging |
Het |
Or5i1 |
T |
A |
2: 87,612,929 (GRCm39) |
I15N |
possibly damaging |
Het |
Or6c2b |
T |
C |
10: 128,947,737 (GRCm39) |
T186A |
probably benign |
Het |
Pcnx2 |
A |
G |
8: 126,577,087 (GRCm39) |
Y982H |
probably damaging |
Het |
Pias3 |
T |
C |
3: 96,609,541 (GRCm39) |
L312P |
probably damaging |
Het |
Plekhm1 |
G |
A |
11: 103,267,710 (GRCm39) |
P754S |
probably damaging |
Het |
Ppp2r5c |
T |
A |
12: 110,512,057 (GRCm39) |
L145* |
probably null |
Het |
Ppp2r5c |
T |
A |
12: 110,527,906 (GRCm39) |
|
probably benign |
Het |
Pramel29 |
A |
C |
4: 143,935,162 (GRCm39) |
I193S |
probably damaging |
Het |
Proser3 |
T |
C |
7: 30,239,446 (GRCm39) |
M553V |
probably benign |
Het |
Shf |
G |
A |
2: 122,199,163 (GRCm39) |
P51S |
probably damaging |
Het |
Smurf2 |
A |
T |
11: 106,715,514 (GRCm39) |
D664E |
possibly damaging |
Het |
Spag9 |
G |
A |
11: 93,887,391 (GRCm39) |
A99T |
probably benign |
Het |
Stim1 |
T |
G |
7: 102,003,713 (GRCm39) |
C49G |
probably damaging |
Het |
Stk32c |
T |
C |
7: 138,701,740 (GRCm39) |
I238V |
probably benign |
Het |
Tenm2 |
C |
T |
11: 35,954,004 (GRCm39) |
G1236R |
possibly damaging |
Het |
Tfb2m |
T |
A |
1: 179,372,464 (GRCm39) |
E133V |
probably null |
Het |
Tmem209 |
A |
T |
6: 30,497,867 (GRCm39) |
C143S |
probably benign |
Het |
Tnr |
T |
G |
1: 159,679,600 (GRCm39) |
N191K |
probably benign |
Het |
Vars1 |
C |
T |
17: 35,217,198 (GRCm39) |
A419T |
probably benign |
Het |
Vmn2r111 |
T |
C |
17: 22,767,041 (GRCm39) |
S819G |
probably benign |
Het |
Wls |
T |
C |
3: 159,602,995 (GRCm39) |
V136A |
probably benign |
Het |
Ybx2 |
C |
T |
11: 69,830,887 (GRCm39) |
S217L |
probably benign |
Het |
Zfp82 |
T |
C |
7: 29,756,779 (GRCm39) |
D37G |
probably benign |
Het |
|
Other mutations in Chrm3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01608:Chrm3
|
APN |
13 |
9,928,634 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02266:Chrm3
|
APN |
13 |
9,927,314 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02701:Chrm3
|
APN |
13 |
9,928,500 (GRCm39) |
nonsense |
probably null |
|
IGL03085:Chrm3
|
APN |
13 |
9,927,570 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03213:Chrm3
|
APN |
13 |
9,928,220 (GRCm39) |
missense |
probably benign |
0.22 |
R0147:Chrm3
|
UTSW |
13 |
9,928,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R0408:Chrm3
|
UTSW |
13 |
9,927,969 (GRCm39) |
missense |
probably benign |
0.10 |
R0544:Chrm3
|
UTSW |
13 |
9,927,615 (GRCm39) |
missense |
probably damaging |
0.99 |
R1557:Chrm3
|
UTSW |
13 |
9,928,350 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1647:Chrm3
|
UTSW |
13 |
9,928,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R1791:Chrm3
|
UTSW |
13 |
9,927,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Chrm3
|
UTSW |
13 |
9,928,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R2049:Chrm3
|
UTSW |
13 |
9,928,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R2909:Chrm3
|
UTSW |
13 |
9,928,033 (GRCm39) |
missense |
probably benign |
0.43 |
R4212:Chrm3
|
UTSW |
13 |
9,927,791 (GRCm39) |
missense |
probably benign |
0.01 |
R4422:Chrm3
|
UTSW |
13 |
9,928,591 (GRCm39) |
nonsense |
probably null |
|
R4790:Chrm3
|
UTSW |
13 |
9,927,698 (GRCm39) |
missense |
probably benign |
0.10 |
R4934:Chrm3
|
UTSW |
13 |
9,927,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R5353:Chrm3
|
UTSW |
13 |
9,928,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R5623:Chrm3
|
UTSW |
13 |
9,927,423 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6154:Chrm3
|
UTSW |
13 |
9,928,476 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6416:Chrm3
|
UTSW |
13 |
9,927,698 (GRCm39) |
missense |
probably benign |
|
R6693:Chrm3
|
UTSW |
13 |
9,927,458 (GRCm39) |
missense |
probably benign |
0.27 |
R7135:Chrm3
|
UTSW |
13 |
9,927,837 (GRCm39) |
missense |
probably benign |
0.00 |
R7297:Chrm3
|
UTSW |
13 |
9,927,869 (GRCm39) |
missense |
probably benign |
0.01 |
R7423:Chrm3
|
UTSW |
13 |
9,928,845 (GRCm39) |
missense |
probably benign |
|
R7591:Chrm3
|
UTSW |
13 |
9,927,349 (GRCm39) |
nonsense |
probably null |
|
R8353:Chrm3
|
UTSW |
13 |
9,927,267 (GRCm39) |
makesense |
probably null |
|
R8355:Chrm3
|
UTSW |
13 |
9,928,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R8446:Chrm3
|
UTSW |
13 |
9,928,338 (GRCm39) |
missense |
probably damaging |
0.99 |
R8453:Chrm3
|
UTSW |
13 |
9,927,267 (GRCm39) |
makesense |
probably null |
|
R9227:Chrm3
|
UTSW |
13 |
9,928,479 (GRCm39) |
missense |
probably benign |
0.00 |
R9230:Chrm3
|
UTSW |
13 |
9,928,479 (GRCm39) |
missense |
probably benign |
0.00 |
R9336:Chrm3
|
UTSW |
13 |
9,928,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R9462:Chrm3
|
UTSW |
13 |
9,927,437 (GRCm39) |
missense |
|
|
R9537:Chrm3
|
UTSW |
13 |
9,927,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R9586:Chrm3
|
UTSW |
13 |
9,927,480 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Chrm3
|
UTSW |
13 |
9,927,756 (GRCm39) |
missense |
probably benign |
0.02 |
|