Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2200002D01Rik |
CCTTCTCCTTCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
CCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
7: 28,947,048 (GRCm39) |
|
probably benign |
Het |
Ankrd17 |
C |
T |
5: 90,416,508 (GRCm39) |
R1108Q |
probably damaging |
Het |
Ccdc136 |
C |
T |
6: 29,405,960 (GRCm39) |
A102V |
probably damaging |
Het |
Ccn4 |
G |
A |
15: 66,784,900 (GRCm39) |
R191K |
probably benign |
Het |
Ccnyl1 |
A |
G |
1: 64,753,750 (GRCm39) |
Y187C |
probably damaging |
Het |
Copa |
G |
A |
1: 171,944,831 (GRCm39) |
V882I |
probably benign |
Het |
Cyp17a1 |
C |
T |
19: 46,657,165 (GRCm39) |
R361H |
probably damaging |
Het |
Ddx49 |
T |
C |
8: 70,746,226 (GRCm39) |
T459A |
probably benign |
Het |
Depdc5 |
A |
G |
5: 33,122,076 (GRCm39) |
N1133S |
probably benign |
Het |
Dnajc18 |
T |
C |
18: 35,808,260 (GRCm39) |
D329G |
probably damaging |
Het |
Dusp16 |
G |
A |
6: 134,695,982 (GRCm39) |
P283L |
probably damaging |
Het |
Efcab12 |
A |
G |
6: 115,814,975 (GRCm39) |
V40A |
probably benign |
Het |
Emb |
G |
T |
13: 117,357,096 (GRCm39) |
|
probably benign |
Het |
Fam120b |
G |
A |
17: 15,626,020 (GRCm39) |
A458T |
possibly damaging |
Het |
Fgd4 |
G |
A |
16: 16,308,353 (GRCm39) |
T9I |
probably benign |
Het |
Hivep1 |
G |
A |
13: 42,308,251 (GRCm39) |
D164N |
possibly damaging |
Het |
Klf13 |
T |
A |
7: 63,574,609 (GRCm39) |
|
probably benign |
Het |
Lrrc47 |
T |
C |
4: 154,100,398 (GRCm39) |
S325P |
possibly damaging |
Het |
Mast3 |
C |
T |
8: 71,238,826 (GRCm39) |
V493M |
probably damaging |
Het |
Med22 |
T |
C |
2: 26,795,821 (GRCm39) |
T200A |
probably benign |
Het |
Mmel1 |
A |
G |
4: 154,976,967 (GRCm39) |
D561G |
probably null |
Het |
Ms4a4a |
G |
A |
19: 11,367,708 (GRCm39) |
M191I |
probably benign |
Het |
Mtcl3 |
G |
A |
10: 29,072,775 (GRCm39) |
R689Q |
probably damaging |
Het |
Myh11 |
T |
A |
16: 14,018,580 (GRCm39) |
N1922I |
|
Het |
Myo7b |
T |
C |
18: 32,133,413 (GRCm39) |
I371V |
probably benign |
Het |
Myo9b |
T |
C |
8: 71,808,483 (GRCm39) |
S1697P |
probably damaging |
Het |
Neurod4 |
T |
C |
10: 130,106,840 (GRCm39) |
T145A |
probably benign |
Het |
Nfx1 |
T |
C |
4: 41,023,756 (GRCm39) |
V1055A |
probably benign |
Het |
Ntng1 |
C |
T |
3: 110,042,680 (GRCm39) |
A49T |
probably damaging |
Het |
Oc90 |
G |
A |
15: 65,761,437 (GRCm39) |
P194S |
probably benign |
Het |
Opcml |
A |
C |
9: 28,814,624 (GRCm39) |
N292T |
probably damaging |
Het |
Oplah |
A |
G |
15: 76,193,787 (GRCm39) |
S57P |
probably benign |
Het |
Or1x6 |
T |
A |
11: 50,939,223 (GRCm39) |
Y96* |
probably null |
Het |
Or2a12 |
T |
A |
6: 42,904,534 (GRCm39) |
I123N |
probably damaging |
Het |
Or2aj4 |
T |
A |
16: 19,384,722 (GRCm39) |
I304F |
possibly damaging |
Het |
Or8k3b |
A |
T |
2: 86,520,575 (GRCm39) |
V248D |
possibly damaging |
Het |
Pdzd8 |
A |
T |
19: 59,333,574 (GRCm39) |
L149Q |
probably damaging |
Het |
Pid1 |
A |
G |
1: 84,137,032 (GRCm39) |
V33A |
probably benign |
Het |
Prpsap1 |
A |
G |
11: 116,385,015 (GRCm39) |
|
probably benign |
Het |
R3hdml |
T |
C |
2: 163,334,535 (GRCm39) |
W42R |
probably benign |
Het |
Rnase6 |
A |
T |
14: 51,367,862 (GRCm39) |
N85Y |
possibly damaging |
Het |
Scn3a |
T |
A |
2: 65,291,596 (GRCm39) |
M1717L |
possibly damaging |
Het |
Setbp1 |
C |
T |
18: 78,826,599 (GRCm39) |
S1338N |
probably benign |
Het |
Sh2b2 |
T |
C |
5: 136,253,006 (GRCm39) |
T389A |
probably benign |
Het |
Sh2d4a |
G |
A |
8: 68,747,018 (GRCm39) |
G82D |
probably damaging |
Het |
Skint9 |
A |
T |
4: 112,248,915 (GRCm39) |
M171K |
probably benign |
Het |
Slc5a11 |
C |
T |
7: 122,868,324 (GRCm39) |
R505W |
probably damaging |
Het |
Slx4 |
C |
A |
16: 3,805,820 (GRCm39) |
M577I |
probably benign |
Het |
Tarbp1 |
C |
T |
8: 127,177,462 (GRCm39) |
V737I |
probably benign |
Het |
Tm7sf3 |
C |
T |
6: 146,525,179 (GRCm39) |
D89N |
possibly damaging |
Het |
Tmem100 |
A |
T |
11: 89,926,533 (GRCm39) |
E120V |
probably damaging |
Het |
Trim72 |
C |
T |
7: 127,609,173 (GRCm39) |
T325M |
possibly damaging |
Het |
Trpc2 |
G |
A |
7: 101,739,819 (GRCm39) |
G581D |
possibly damaging |
Het |
Tyw1 |
G |
A |
5: 130,298,065 (GRCm39) |
R202Q |
probably damaging |
Het |
Ubn1 |
T |
C |
16: 4,888,492 (GRCm39) |
S154P |
unknown |
Het |
Uchl1 |
T |
A |
5: 66,833,649 (GRCm39) |
M6K |
probably damaging |
Het |
Vmn1r193 |
A |
T |
13: 22,403,989 (GRCm39) |
M1K |
probably null |
Het |
Zfp429 |
T |
A |
13: 67,538,531 (GRCm39) |
K304N |
probably benign |
Het |
Zfp618 |
A |
G |
4: 63,036,824 (GRCm39) |
N375D |
probably damaging |
Het |
Zfp7 |
TGCGGGAAAGGTTTCCACCTGAGCG |
TGCG |
15: 76,774,800 (GRCm39) |
|
probably benign |
Het |
Zfp78 |
A |
T |
7: 6,382,354 (GRCm39) |
D468V |
probably benign |
Het |
Zfp809 |
A |
C |
9: 22,150,394 (GRCm39) |
Y297S |
probably damaging |
Het |
|
Other mutations in Mettl15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00155:Mettl15
|
APN |
2 |
108,923,521 (GRCm39) |
nonsense |
probably null |
|
IGL00657:Mettl15
|
APN |
2 |
108,923,552 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02684:Mettl15
|
APN |
2 |
108,961,925 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03367:Mettl15
|
APN |
2 |
108,961,916 (GRCm39) |
missense |
probably benign |
0.10 |
R1433:Mettl15
|
UTSW |
2 |
108,923,266 (GRCm39) |
missense |
probably benign |
0.00 |
R1538:Mettl15
|
UTSW |
2 |
108,962,010 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3890:Mettl15
|
UTSW |
2 |
109,021,924 (GRCm39) |
missense |
probably benign |
0.03 |
R5464:Mettl15
|
UTSW |
2 |
109,021,967 (GRCm39) |
missense |
probably benign |
0.00 |
R6609:Mettl15
|
UTSW |
2 |
108,967,687 (GRCm39) |
missense |
probably null |
1.00 |
R7619:Mettl15
|
UTSW |
2 |
108,923,220 (GRCm39) |
nonsense |
probably null |
|
R7737:Mettl15
|
UTSW |
2 |
108,967,723 (GRCm39) |
missense |
probably damaging |
0.99 |
R8914:Mettl15
|
UTSW |
2 |
108,967,625 (GRCm39) |
intron |
probably benign |
|
R9121:Mettl15
|
UTSW |
2 |
109,104,948 (GRCm39) |
missense |
|
|
R9159:Mettl15
|
UTSW |
2 |
108,923,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R9192:Mettl15
|
UTSW |
2 |
109,104,810 (GRCm39) |
nonsense |
probably null |
|
R9566:Mettl15
|
UTSW |
2 |
108,923,592 (GRCm39) |
missense |
possibly damaging |
0.61 |
|