Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aimp1 |
A |
T |
3: 132,382,904 (GRCm39) |
|
probably benign |
Het |
Arpc5 |
A |
G |
1: 152,644,658 (GRCm39) |
I64V |
probably benign |
Het |
C030048H21Rik |
G |
A |
2: 26,146,632 (GRCm39) |
R1227W |
probably damaging |
Het |
Cacnb1 |
T |
C |
11: 97,913,190 (GRCm39) |
E21G |
possibly damaging |
Het |
Catsper3 |
A |
G |
13: 55,946,635 (GRCm39) |
K111E |
possibly damaging |
Het |
Cda |
T |
C |
4: 138,095,157 (GRCm39) |
Y33C |
probably damaging |
Het |
Celsr3 |
A |
T |
9: 108,726,124 (GRCm39) |
R3118W |
probably damaging |
Het |
Clvs1 |
G |
A |
4: 9,281,939 (GRCm39) |
G128R |
probably damaging |
Het |
Col9a1 |
A |
G |
1: 24,224,306 (GRCm39) |
S163G |
unknown |
Het |
Cyp4v3 |
T |
C |
8: 45,760,040 (GRCm39) |
D64G |
probably benign |
Het |
Dst |
C |
A |
1: 34,290,920 (GRCm39) |
L837M |
probably damaging |
Het |
Eif2ak4 |
T |
A |
2: 118,294,536 (GRCm39) |
I1349N |
probably damaging |
Het |
Elob |
C |
A |
17: 24,043,954 (GRCm39) |
|
probably null |
Het |
Glipr1 |
T |
A |
10: 111,821,555 (GRCm39) |
I216L |
probably benign |
Het |
Gm3238 |
C |
T |
10: 77,607,126 (GRCm39) |
|
probably benign |
Het |
Gm43638 |
C |
T |
5: 87,608,258 (GRCm39) |
R527H |
probably damaging |
Het |
H2-M11 |
A |
G |
17: 36,858,445 (GRCm39) |
K80E |
probably benign |
Het |
Htt |
A |
G |
5: 35,053,370 (GRCm39) |
|
probably null |
Het |
Kif26a |
A |
G |
12: 112,124,066 (GRCm39) |
S224G |
probably damaging |
Het |
Mgat5b |
T |
A |
11: 116,822,488 (GRCm39) |
M74K |
probably damaging |
Het |
Ms4a7 |
A |
T |
19: 11,299,724 (GRCm39) |
V89D |
probably damaging |
Het |
Nlrx1 |
G |
A |
9: 44,175,365 (GRCm39) |
T137I |
probably benign |
Het |
Pcdhb12 |
A |
G |
18: 37,570,035 (GRCm39) |
T394A |
probably benign |
Het |
Pkhd1l1 |
T |
C |
15: 44,340,982 (GRCm39) |
I151T |
probably damaging |
Het |
Plcl1 |
T |
C |
1: 55,445,695 (GRCm39) |
V50A |
probably benign |
Het |
Prkd2 |
T |
C |
7: 16,599,787 (GRCm39) |
F750S |
probably damaging |
Het |
Psmd13 |
T |
C |
7: 140,477,534 (GRCm39) |
V311A |
probably damaging |
Het |
Rec8 |
C |
T |
14: 55,860,972 (GRCm39) |
Q334* |
probably null |
Het |
Rfx7 |
G |
A |
9: 72,514,972 (GRCm39) |
V157I |
probably damaging |
Het |
Sele |
G |
A |
1: 163,879,403 (GRCm39) |
C312Y |
probably damaging |
Het |
Sorcs3 |
A |
G |
19: 48,736,758 (GRCm39) |
T694A |
probably benign |
Het |
Vmn1r191 |
T |
C |
13: 22,362,890 (GRCm39) |
D288G |
probably damaging |
Het |
Vmn1r231 |
A |
T |
17: 21,110,828 (GRCm39) |
I29N |
possibly damaging |
Het |
Vmn2r1 |
T |
A |
3: 64,012,389 (GRCm39) |
L750* |
probably null |
Het |
|
Other mutations in Tma16 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01321:Tma16
|
APN |
8 |
66,929,512 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02022:Tma16
|
APN |
8 |
66,939,062 (GRCm39) |
critical splice donor site |
probably null |
|
R0064:Tma16
|
UTSW |
8 |
66,929,457 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3401:Tma16
|
UTSW |
8 |
66,936,823 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3402:Tma16
|
UTSW |
8 |
66,936,823 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3403:Tma16
|
UTSW |
8 |
66,936,823 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4399:Tma16
|
UTSW |
8 |
66,936,823 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4402:Tma16
|
UTSW |
8 |
66,936,823 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4421:Tma16
|
UTSW |
8 |
66,936,823 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4453:Tma16
|
UTSW |
8 |
66,936,823 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4493:Tma16
|
UTSW |
8 |
66,936,823 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4856:Tma16
|
UTSW |
8 |
66,934,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R4886:Tma16
|
UTSW |
8 |
66,934,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R5527:Tma16
|
UTSW |
8 |
66,936,776 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6312:Tma16
|
UTSW |
8 |
66,934,118 (GRCm39) |
missense |
probably damaging |
0.99 |
R8437:Tma16
|
UTSW |
8 |
66,929,448 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9229:Tma16
|
UTSW |
8 |
66,936,779 (GRCm39) |
missense |
probably benign |
0.01 |
|