Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610524H06Rik |
A |
G |
5: 114,961,372 (GRCm39) |
|
probably null |
Het |
Abcd3 |
T |
C |
3: 121,586,491 (GRCm39) |
I70V |
possibly damaging |
Het |
Acad10 |
T |
C |
5: 121,759,411 (GRCm39) |
Y1024C |
probably damaging |
Het |
Atp2b3 |
T |
G |
X: 72,588,712 (GRCm39) |
V701G |
probably damaging |
Het |
Cbfa2t2 |
T |
A |
2: 154,342,347 (GRCm39) |
M21K |
probably damaging |
Het |
Cdc25a |
C |
T |
9: 109,710,614 (GRCm39) |
T106I |
possibly damaging |
Het |
Cdhr5 |
T |
C |
7: 140,852,083 (GRCm39) |
T190A |
probably damaging |
Het |
Chl1 |
A |
G |
6: 103,685,445 (GRCm39) |
T829A |
probably benign |
Het |
Clcn6 |
T |
C |
4: 148,097,226 (GRCm39) |
T614A |
possibly damaging |
Het |
Cntln |
A |
T |
4: 84,865,823 (GRCm39) |
R160* |
probably null |
Het |
Dclk2 |
C |
T |
3: 86,712,946 (GRCm39) |
R503Q |
possibly damaging |
Het |
Dock3 |
C |
A |
9: 106,815,158 (GRCm39) |
M1236I |
possibly damaging |
Het |
Eif4g3 |
T |
A |
4: 137,847,719 (GRCm39) |
H213Q |
probably damaging |
Het |
Eya1 |
T |
A |
1: 14,279,141 (GRCm39) |
H372L |
probably damaging |
Het |
Fam13b |
A |
G |
18: 34,630,485 (GRCm39) |
V91A |
possibly damaging |
Het |
Hat1 |
T |
A |
2: 71,264,519 (GRCm39) |
I319K |
probably benign |
Het |
Kcnf1 |
T |
C |
12: 17,225,853 (GRCm39) |
N123D |
probably benign |
Het |
Kcns3 |
C |
A |
12: 11,141,551 (GRCm39) |
G383W |
probably damaging |
Het |
Kprp |
A |
T |
3: 92,732,689 (GRCm39) |
C120* |
probably null |
Het |
Lama3 |
T |
A |
18: 12,672,774 (GRCm39) |
C2456S |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 41,366,658 (GRCm39) |
D539E |
probably damaging |
Het |
Mbd3l1 |
T |
A |
9: 18,395,947 (GRCm39) |
I24N |
probably damaging |
Het |
Med10 |
T |
C |
13: 69,958,159 (GRCm39) |
L37P |
probably damaging |
Het |
Mrc1 |
A |
T |
2: 14,313,544 (GRCm39) |
H925L |
probably damaging |
Het |
Myo15a |
T |
A |
11: 60,409,290 (GRCm39) |
I3219N |
probably damaging |
Het |
Nom1 |
C |
T |
5: 29,647,633 (GRCm39) |
Q623* |
probably null |
Het |
Nrm |
T |
A |
17: 36,175,079 (GRCm39) |
W136R |
probably damaging |
Het |
Or8h8 |
A |
C |
2: 86,753,789 (GRCm39) |
V29G |
probably benign |
Het |
Pde7b |
T |
C |
10: 20,288,836 (GRCm39) |
N298S |
probably benign |
Het |
Piezo2 |
C |
T |
18: 63,277,990 (GRCm39) |
A305T |
possibly damaging |
Het |
Pimreg |
T |
C |
11: 71,936,042 (GRCm39) |
L175P |
possibly damaging |
Het |
Pkhd1l1 |
A |
G |
15: 44,390,237 (GRCm39) |
D1451G |
probably benign |
Het |
Ptpro |
A |
G |
6: 137,355,128 (GRCm39) |
S212G |
probably benign |
Het |
Rhpn1 |
C |
T |
15: 75,585,967 (GRCm39) |
R627C |
possibly damaging |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rnase4 |
T |
G |
14: 51,342,497 (GRCm39) |
F74V |
probably damaging |
Het |
Sbno2 |
A |
G |
10: 79,896,226 (GRCm39) |
|
probably null |
Het |
Selp |
T |
C |
1: 163,954,176 (GRCm39) |
Y159H |
probably damaging |
Het |
Senp6 |
A |
G |
9: 80,000,853 (GRCm39) |
T21A |
probably damaging |
Het |
Slco1a7 |
A |
T |
6: 141,700,135 (GRCm39) |
C132* |
probably null |
Het |
Slco3a1 |
T |
C |
7: 74,154,128 (GRCm39) |
D148G |
possibly damaging |
Het |
Smtn |
G |
A |
11: 3,480,102 (GRCm39) |
P373L |
probably benign |
Het |
Snx20 |
A |
T |
8: 89,356,597 (GRCm39) |
L73Q |
probably damaging |
Het |
Sobp |
A |
G |
10: 43,033,942 (GRCm39) |
V128A |
possibly damaging |
Het |
Tcerg1 |
A |
G |
18: 42,657,357 (GRCm39) |
T280A |
unknown |
Het |
Tgfbrap1 |
A |
G |
1: 43,088,973 (GRCm39) |
V810A |
probably benign |
Het |
Thbs1 |
C |
A |
2: 117,949,678 (GRCm39) |
D589E |
probably damaging |
Het |
Tjp2 |
A |
G |
19: 24,078,239 (GRCm39) |
Y885H |
probably damaging |
Het |
Tmem109 |
A |
G |
19: 10,849,993 (GRCm39) |
S100P |
probably damaging |
Het |
Trim36 |
T |
C |
18: 46,305,562 (GRCm39) |
K462E |
probably benign |
Het |
Vmn1r226 |
A |
T |
17: 20,908,538 (GRCm39) |
I257F |
probably damaging |
Het |
Vmn2r92 |
A |
G |
17: 18,372,352 (GRCm39) |
Y54C |
probably damaging |
Het |
Wdcp |
T |
A |
12: 4,901,924 (GRCm39) |
Y593* |
probably null |
Het |
Wdr59 |
T |
C |
8: 112,177,682 (GRCm39) |
S907G |
probably damaging |
Het |
|
Other mutations in Matn3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01814:Matn3
|
APN |
12 |
9,002,091 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02138:Matn3
|
APN |
12 |
9,017,638 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02442:Matn3
|
APN |
12 |
9,017,678 (GRCm39) |
nonsense |
probably null |
|
IGL02736:Matn3
|
APN |
12 |
9,005,422 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0091:Matn3
|
UTSW |
12 |
9,002,105 (GRCm39) |
missense |
probably damaging |
0.98 |
R0585:Matn3
|
UTSW |
12 |
9,011,103 (GRCm39) |
splice site |
probably benign |
|
R0615:Matn3
|
UTSW |
12 |
9,013,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R1424:Matn3
|
UTSW |
12 |
9,011,132 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1844:Matn3
|
UTSW |
12 |
9,017,662 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1865:Matn3
|
UTSW |
12 |
9,002,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R1977:Matn3
|
UTSW |
12 |
9,011,110 (GRCm39) |
splice site |
probably benign |
|
R3015:Matn3
|
UTSW |
12 |
9,002,217 (GRCm39) |
missense |
probably damaging |
0.97 |
R3018:Matn3
|
UTSW |
12 |
9,013,578 (GRCm39) |
missense |
probably benign |
0.02 |
R5180:Matn3
|
UTSW |
12 |
9,005,374 (GRCm39) |
missense |
probably benign |
0.38 |
R5308:Matn3
|
UTSW |
12 |
9,002,308 (GRCm39) |
frame shift |
probably null |
|
R5616:Matn3
|
UTSW |
12 |
8,998,195 (GRCm39) |
missense |
probably benign |
|
R5816:Matn3
|
UTSW |
12 |
9,020,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R5849:Matn3
|
UTSW |
12 |
9,008,829 (GRCm39) |
missense |
probably benign |
0.10 |
R7065:Matn3
|
UTSW |
12 |
9,002,472 (GRCm39) |
missense |
probably damaging |
0.99 |
R7206:Matn3
|
UTSW |
12 |
9,011,170 (GRCm39) |
missense |
probably benign |
0.01 |
R8512:Matn3
|
UTSW |
12 |
9,011,183 (GRCm39) |
missense |
probably benign |
0.11 |
R8737:Matn3
|
UTSW |
12 |
9,017,665 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8951:Matn3
|
UTSW |
12 |
9,002,172 (GRCm39) |
missense |
probably damaging |
0.99 |
R9022:Matn3
|
UTSW |
12 |
9,002,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R9328:Matn3
|
UTSW |
12 |
9,002,033 (GRCm39) |
missense |
possibly damaging |
0.78 |
RF001:Matn3
|
UTSW |
12 |
9,008,797 (GRCm39) |
missense |
probably benign |
0.02 |
|