Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
T |
C |
5: 77,026,381 (GRCm39) |
|
probably benign |
Het |
Adam5 |
T |
C |
8: 25,308,758 (GRCm39) |
E39G |
probably benign |
Het |
Anapc7 |
G |
A |
5: 122,571,540 (GRCm39) |
W205* |
probably null |
Het |
Arhgap5 |
C |
T |
12: 52,565,525 (GRCm39) |
T832I |
possibly damaging |
Het |
Arhgef10 |
T |
A |
8: 14,990,378 (GRCm39) |
|
probably benign |
Het |
Atg5 |
A |
G |
10: 44,239,040 (GRCm39) |
T274A |
probably benign |
Het |
Baiap2l2 |
G |
T |
15: 79,168,765 (GRCm39) |
|
probably benign |
Het |
Brap |
T |
A |
5: 121,803,290 (GRCm39) |
M146K |
probably damaging |
Het |
Brpf1 |
T |
C |
6: 113,298,847 (GRCm39) |
S1074P |
probably benign |
Het |
Camta1 |
A |
C |
4: 151,169,058 (GRCm39) |
I231R |
probably benign |
Het |
Ccdc15 |
C |
T |
9: 37,231,709 (GRCm39) |
G205D |
probably benign |
Het |
Cd6 |
G |
T |
19: 10,773,758 (GRCm39) |
|
probably benign |
Het |
Cdh17 |
T |
G |
4: 11,783,412 (GRCm39) |
S219R |
possibly damaging |
Het |
Cgn |
G |
A |
3: 94,674,519 (GRCm39) |
R873W |
probably damaging |
Het |
Ctnna3 |
C |
T |
10: 63,373,322 (GRCm39) |
P41L |
possibly damaging |
Het |
Dmbt1 |
T |
C |
7: 130,659,888 (GRCm39) |
W484R |
probably benign |
Het |
Dmd |
A |
G |
X: 83,469,419 (GRCm39) |
|
probably null |
Het |
Dnah17 |
C |
T |
11: 117,937,987 (GRCm39) |
V3347I |
probably benign |
Het |
Fgd5 |
T |
A |
6: 91,965,440 (GRCm39) |
S400T |
possibly damaging |
Het |
Kitl |
C |
A |
10: 99,923,206 (GRCm39) |
|
probably benign |
Het |
Lamc3 |
A |
T |
2: 31,808,533 (GRCm39) |
D763V |
probably damaging |
Het |
Lgmn |
T |
C |
12: 102,364,435 (GRCm39) |
|
probably benign |
Het |
Lpcat2 |
T |
G |
8: 93,591,598 (GRCm39) |
W81G |
possibly damaging |
Het |
Myh13 |
A |
G |
11: 67,246,773 (GRCm39) |
I1165V |
probably benign |
Het |
Nf1 |
A |
G |
11: 79,456,343 (GRCm39) |
D599G |
probably damaging |
Het |
Nin |
T |
C |
12: 70,061,567 (GRCm39) |
N2099S |
probably benign |
Het |
Nlrc4 |
T |
C |
17: 74,754,985 (GRCm39) |
D77G |
probably benign |
Het |
Otub1 |
A |
G |
19: 7,181,416 (GRCm39) |
|
probably benign |
Het |
Pabir2 |
A |
T |
X: 52,334,208 (GRCm39) |
C222S |
probably damaging |
Het |
Pah |
A |
G |
10: 87,406,193 (GRCm39) |
Y174C |
probably null |
Het |
Rbbp5 |
G |
A |
1: 132,417,444 (GRCm39) |
V88I |
probably damaging |
Het |
Scn1a |
C |
T |
2: 66,155,279 (GRCm39) |
R560H |
probably benign |
Het |
Snx5 |
T |
C |
2: 144,097,485 (GRCm39) |
I217V |
probably benign |
Het |
Syne2 |
T |
C |
12: 76,036,016 (GRCm39) |
S3769P |
probably damaging |
Het |
Tent2 |
T |
C |
13: 93,322,905 (GRCm39) |
T15A |
probably benign |
Het |
Top3b |
T |
C |
16: 16,705,486 (GRCm39) |
I417T |
probably damaging |
Het |
Tspan2 |
T |
C |
3: 102,665,549 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
C |
2: 76,540,057 (GRCm39) |
T34310A |
possibly damaging |
Het |
Ush2a |
G |
A |
1: 188,643,640 (GRCm39) |
C4334Y |
possibly damaging |
Het |
Wdpcp |
A |
G |
11: 21,609,995 (GRCm39) |
D21G |
probably damaging |
Het |
Yy2 |
A |
C |
X: 156,351,207 (GRCm39) |
D186E |
probably benign |
Het |
|
Other mutations in Tmem255b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02635:Tmem255b
|
APN |
8 |
13,505,195 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02679:Tmem255b
|
APN |
8 |
13,507,055 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02945:Tmem255b
|
APN |
8 |
13,505,141 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03007:Tmem255b
|
APN |
8 |
13,507,066 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03146:Tmem255b
|
APN |
8 |
13,504,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R2278:Tmem255b
|
UTSW |
8 |
13,501,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R2410:Tmem255b
|
UTSW |
8 |
13,491,278 (GRCm39) |
missense |
probably benign |
0.22 |
R3081:Tmem255b
|
UTSW |
8 |
13,501,048 (GRCm39) |
missense |
probably damaging |
0.99 |
R4498:Tmem255b
|
UTSW |
8 |
13,505,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R4612:Tmem255b
|
UTSW |
8 |
13,504,228 (GRCm39) |
missense |
probably benign |
0.00 |
R6018:Tmem255b
|
UTSW |
8 |
13,505,138 (GRCm39) |
missense |
probably benign |
0.00 |
R6073:Tmem255b
|
UTSW |
8 |
13,506,958 (GRCm39) |
missense |
probably damaging |
0.98 |
R6240:Tmem255b
|
UTSW |
8 |
13,504,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R6737:Tmem255b
|
UTSW |
8 |
13,507,096 (GRCm39) |
critical splice donor site |
probably null |
|
R8231:Tmem255b
|
UTSW |
8 |
13,504,225 (GRCm39) |
missense |
probably damaging |
0.97 |
R9653:Tmem255b
|
UTSW |
8 |
13,506,005 (GRCm39) |
missense |
probably damaging |
1.00 |
|