Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5031439G07Rik |
G |
A |
15: 84,839,668 (GRCm39) |
H191Y |
probably damaging |
Het |
5730480H06Rik |
T |
A |
5: 48,536,769 (GRCm39) |
L155* |
probably null |
Het |
Ackr4 |
T |
C |
9: 103,976,410 (GRCm39) |
N179S |
probably benign |
Het |
Acp5 |
T |
C |
9: 22,040,902 (GRCm39) |
Y107C |
probably damaging |
Het |
Aff4 |
A |
T |
11: 53,289,084 (GRCm39) |
H411L |
probably damaging |
Het |
Atp5pb |
A |
G |
3: 105,866,502 (GRCm39) |
M1T |
probably null |
Het |
Atp8b5 |
G |
A |
4: 43,372,728 (GRCm39) |
|
probably null |
Het |
C1qtnf2 |
A |
G |
11: 43,381,775 (GRCm39) |
T166A |
possibly damaging |
Het |
Dctn2 |
A |
G |
10: 127,112,398 (GRCm39) |
D170G |
probably damaging |
Het |
Dennd3 |
T |
A |
15: 73,384,622 (GRCm39) |
S10T |
probably benign |
Het |
Ehbp1 |
T |
C |
11: 22,046,096 (GRCm39) |
Y551C |
possibly damaging |
Het |
Eif4g2 |
A |
T |
7: 110,673,639 (GRCm39) |
D743E |
possibly damaging |
Het |
Esr1 |
G |
A |
10: 4,696,808 (GRCm39) |
|
probably null |
Het |
Exo1 |
A |
T |
1: 175,728,480 (GRCm39) |
I515L |
probably benign |
Het |
Fam83h |
C |
T |
15: 75,874,886 (GRCm39) |
G817D |
probably damaging |
Het |
Flvcr2 |
GTAGTGTATA |
GTA |
12: 85,849,922 (GRCm39) |
|
probably null |
Het |
Garin1a |
T |
C |
6: 29,286,072 (GRCm39) |
I177T |
probably damaging |
Het |
Gcn1 |
G |
A |
5: 115,719,588 (GRCm39) |
S361N |
probably benign |
Het |
Gm6337 |
C |
T |
14: 6,050,613 (GRCm38) |
|
probably null |
Het |
Grk4 |
T |
A |
5: 34,826,540 (GRCm39) |
S47T |
probably benign |
Het |
Gstp2 |
C |
A |
19: 4,091,668 (GRCm39) |
M20I |
probably benign |
Het |
Harbi1 |
T |
C |
2: 91,543,237 (GRCm39) |
F233L |
probably benign |
Het |
Iqch |
C |
T |
9: 63,389,915 (GRCm39) |
V755I |
possibly damaging |
Het |
Iws1 |
T |
C |
18: 32,226,688 (GRCm39) |
F756L |
probably benign |
Het |
Kcnh6 |
T |
G |
11: 105,908,200 (GRCm39) |
V272G |
possibly damaging |
Het |
Kcnj10 |
C |
T |
1: 172,196,539 (GRCm39) |
R18C |
probably damaging |
Het |
Kmt2c |
A |
C |
5: 25,488,104 (GRCm39) |
S4670A |
probably damaging |
Het |
Krt80 |
T |
G |
15: 101,267,884 (GRCm39) |
M18L |
probably benign |
Het |
Lbx1 |
A |
G |
19: 45,223,359 (GRCm39) |
V103A |
probably benign |
Het |
Muc16 |
T |
A |
9: 18,548,315 (GRCm39) |
T5993S |
possibly damaging |
Het |
Or10ag57 |
C |
T |
2: 87,218,922 (GRCm39) |
T291I |
probably damaging |
Het |
Or1j17 |
A |
G |
2: 36,578,685 (GRCm39) |
T224A |
probably benign |
Het |
Or1o4 |
A |
G |
17: 37,590,711 (GRCm39) |
V200A |
probably benign |
Het |
Or8k17 |
C |
T |
2: 86,066,862 (GRCm39) |
V106M |
probably benign |
Het |
Pbxip1 |
A |
G |
3: 89,352,902 (GRCm39) |
I183V |
probably benign |
Het |
Pcdh20 |
T |
A |
14: 88,706,047 (GRCm39) |
I418F |
probably damaging |
Het |
Pclo |
T |
C |
5: 14,725,677 (GRCm39) |
F1512L |
unknown |
Het |
Phf2 |
G |
T |
13: 48,958,104 (GRCm39) |
T970K |
unknown |
Het |
Pidd1 |
A |
G |
7: 141,019,566 (GRCm39) |
V698A |
probably damaging |
Het |
Pik3ca |
T |
A |
3: 32,491,996 (GRCm39) |
V198D |
possibly damaging |
Het |
Pip5k1c |
T |
A |
10: 81,142,250 (GRCm39) |
D153E |
probably damaging |
Het |
Ppfia2 |
A |
G |
10: 106,699,236 (GRCm39) |
D795G |
probably benign |
Het |
Pramel12 |
A |
T |
4: 143,145,706 (GRCm39) |
I392F |
probably benign |
Het |
Prkar2a |
C |
A |
9: 108,596,448 (GRCm39) |
A131D |
possibly damaging |
Het |
Pter |
A |
G |
2: 12,985,366 (GRCm39) |
D232G |
probably damaging |
Het |
Qser1 |
C |
T |
2: 104,593,268 (GRCm39) |
R1583Q |
probably damaging |
Het |
Rasal2 |
A |
C |
1: 156,984,951 (GRCm39) |
V932G |
probably damaging |
Het |
Rasgrf2 |
G |
A |
13: 92,130,796 (GRCm39) |
A154V |
|
Het |
Rbm4 |
A |
G |
19: 4,837,444 (GRCm39) |
Y347H |
probably damaging |
Het |
Rfxank |
C |
A |
8: 70,584,085 (GRCm39) |
|
probably null |
Het |
Robo1 |
C |
G |
16: 72,786,678 (GRCm39) |
R897G |
possibly damaging |
Het |
Sash1 |
G |
A |
10: 8,627,000 (GRCm39) |
T364I |
probably damaging |
Het |
Skint6 |
T |
A |
4: 112,696,471 (GRCm39) |
|
probably null |
Het |
Slc22a4 |
T |
A |
11: 53,877,407 (GRCm39) |
M495L |
probably benign |
Het |
Slc39a8 |
G |
A |
3: 135,563,325 (GRCm39) |
V212I |
probably benign |
Het |
Slc40a1 |
A |
C |
1: 45,950,129 (GRCm39) |
V441G |
probably benign |
Het |
Slc7a11 |
A |
T |
3: 50,378,501 (GRCm39) |
Y246N |
probably damaging |
Het |
Spata9 |
T |
C |
13: 76,125,892 (GRCm39) |
V125A |
probably benign |
Het |
Svopl |
T |
A |
6: 37,991,741 (GRCm39) |
M380L |
probably benign |
Het |
Sycp2l |
T |
C |
13: 41,271,544 (GRCm39) |
Y23H |
probably damaging |
Het |
Syt11 |
A |
T |
3: 88,669,427 (GRCm39) |
V155E |
probably benign |
Het |
Syt5 |
T |
C |
7: 4,545,822 (GRCm39) |
Y147C |
probably damaging |
Het |
Thg1l |
T |
C |
11: 45,846,277 (GRCm39) |
T6A |
probably benign |
Het |
Tlr2 |
A |
G |
3: 83,745,546 (GRCm39) |
L179P |
probably damaging |
Het |
Tsn |
A |
T |
1: 118,232,984 (GRCm39) |
Y107N |
probably damaging |
Het |
Tspan32 |
A |
T |
7: 142,564,832 (GRCm39) |
Y114F |
probably benign |
Het |
Tube1 |
A |
C |
10: 39,023,375 (GRCm39) |
S341R |
possibly damaging |
Het |
Ubn2 |
T |
A |
6: 38,466,214 (GRCm39) |
V516D |
probably benign |
Het |
Vmn1r21 |
G |
T |
6: 57,820,910 (GRCm39) |
T178K |
noncoding transcript |
Het |
Vmn2r108 |
A |
G |
17: 20,683,465 (GRCm39) |
Y580H |
probably damaging |
Het |
Wdr75 |
T |
A |
1: 45,857,342 (GRCm39) |
F546L |
probably damaging |
Het |
Yy1 |
A |
G |
12: 108,759,619 (GRCm39) |
D94G |
probably benign |
Het |
Zfhx3 |
A |
G |
8: 109,677,349 (GRCm39) |
T2800A |
probably benign |
Het |
Zfy2 |
T |
C |
Y: 2,133,421 (GRCm39) |
T9A |
unknown |
Het |
|
Other mutations in Marchf8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02966:Marchf8
|
APN |
6 |
116,380,499 (GRCm39) |
missense |
probably damaging |
1.00 |
strider
|
UTSW |
6 |
116,379,004 (GRCm39) |
missense |
probably benign |
|
R0828:Marchf8
|
UTSW |
6 |
116,382,639 (GRCm39) |
missense |
probably benign |
0.36 |
R2869:Marchf8
|
UTSW |
6 |
116,378,106 (GRCm39) |
intron |
probably benign |
|
R2870:Marchf8
|
UTSW |
6 |
116,378,106 (GRCm39) |
intron |
probably benign |
|
R4963:Marchf8
|
UTSW |
6 |
116,363,232 (GRCm39) |
intron |
probably benign |
|
R5617:Marchf8
|
UTSW |
6 |
116,380,481 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6329:Marchf8
|
UTSW |
6 |
116,383,277 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6361:Marchf8
|
UTSW |
6 |
116,379,062 (GRCm39) |
missense |
probably null |
1.00 |
R6615:Marchf8
|
UTSW |
6 |
116,382,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R6771:Marchf8
|
UTSW |
6 |
116,379,004 (GRCm39) |
missense |
probably benign |
|
R7014:Marchf8
|
UTSW |
6 |
116,380,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R7014:Marchf8
|
UTSW |
6 |
116,380,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R7249:Marchf8
|
UTSW |
6 |
116,383,195 (GRCm39) |
missense |
probably benign |
0.17 |
R7558:Marchf8
|
UTSW |
6 |
116,380,526 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8671:Marchf8
|
UTSW |
6 |
116,378,815 (GRCm39) |
missense |
probably benign |
0.00 |
R9072:Marchf8
|
UTSW |
6 |
116,378,884 (GRCm39) |
missense |
probably benign |
0.00 |
R9073:Marchf8
|
UTSW |
6 |
116,378,884 (GRCm39) |
missense |
probably benign |
0.00 |
R9570:Marchf8
|
UTSW |
6 |
116,382,639 (GRCm39) |
missense |
probably benign |
0.36 |
R9571:Marchf8
|
UTSW |
6 |
116,383,237 (GRCm39) |
missense |
probably benign |
0.05 |
R9632:Marchf8
|
UTSW |
6 |
116,378,405 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9710:Marchf8
|
UTSW |
6 |
116,378,405 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9733:Marchf8
|
UTSW |
6 |
116,378,990 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Marchf8
|
UTSW |
6 |
116,315,233 (GRCm39) |
intron |
probably benign |
|
|