Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110038F14Rik |
G |
A |
15: 76,834,475 (GRCm39) |
V124I |
probably damaging |
Het |
Adam4 |
T |
C |
12: 81,468,220 (GRCm39) |
T134A |
possibly damaging |
Het |
Aen |
G |
A |
7: 78,557,050 (GRCm39) |
M299I |
probably damaging |
Het |
Cartpt |
T |
G |
13: 100,036,548 (GRCm39) |
I67L |
probably benign |
Het |
Cc2d1a |
G |
T |
8: 84,870,033 (GRCm39) |
H161N |
probably benign |
Het |
Ccer1 |
T |
C |
10: 97,530,401 (GRCm39) |
F355L |
probably benign |
Het |
Cert1 |
A |
G |
13: 96,751,310 (GRCm39) |
E320G |
probably damaging |
Het |
Cfap206 |
C |
T |
4: 34,721,562 (GRCm39) |
S162N |
probably damaging |
Het |
Cfap299 |
T |
C |
5: 98,646,240 (GRCm39) |
|
probably null |
Het |
Cfap36 |
A |
C |
11: 29,184,414 (GRCm39) |
V114G |
probably damaging |
Het |
Cyp2b9 |
G |
A |
7: 25,909,660 (GRCm39) |
G476D |
probably damaging |
Het |
Eif3l |
T |
C |
15: 78,961,120 (GRCm39) |
Y58H |
possibly damaging |
Het |
Gapvd1 |
T |
C |
2: 34,615,410 (GRCm39) |
Y411C |
probably damaging |
Het |
Gm27029 |
G |
T |
11: 101,302,786 (GRCm39) |
F236L |
possibly damaging |
Het |
Golga1 |
T |
C |
2: 38,913,484 (GRCm39) |
T501A |
probably benign |
Het |
Heg1 |
C |
T |
16: 33,547,657 (GRCm39) |
H815Y |
probably benign |
Het |
Krt1 |
A |
T |
15: 101,756,628 (GRCm39) |
D298E |
probably damaging |
Het |
Mecr |
T |
A |
4: 131,570,907 (GRCm39) |
S32T |
probably benign |
Het |
Med1 |
A |
T |
11: 98,048,812 (GRCm39) |
Y661* |
probably null |
Het |
Or10z1 |
T |
C |
1: 174,078,092 (GRCm39) |
S134G |
probably benign |
Het |
Pla2g12b |
G |
T |
10: 59,252,239 (GRCm39) |
A37S |
probably benign |
Het |
Plekha7 |
G |
T |
7: 115,744,476 (GRCm39) |
|
probably null |
Het |
Ralgapa1 |
T |
C |
12: 55,689,133 (GRCm39) |
I1989V |
probably damaging |
Het |
Ralgapa1 |
T |
C |
12: 55,689,144 (GRCm39) |
H1938R |
probably damaging |
Het |
Sanbr |
A |
T |
11: 23,545,434 (GRCm39) |
D486E |
probably damaging |
Het |
Sec31b |
A |
G |
19: 44,515,480 (GRCm39) |
F309S |
probably damaging |
Het |
Serpina3a |
T |
C |
12: 104,087,758 (GRCm39) |
I227T |
probably benign |
Het |
Slc1a3 |
A |
G |
15: 8,675,171 (GRCm39) |
I278T |
probably damaging |
Het |
Slc1a3 |
T |
C |
15: 8,680,477 (GRCm39) |
Y127C |
probably damaging |
Het |
Spen |
T |
C |
4: 141,217,212 (GRCm39) |
K449R |
unknown |
Het |
Thoc2l |
A |
G |
5: 104,665,528 (GRCm39) |
T17A |
probably benign |
Het |
Trim68 |
A |
T |
7: 102,328,348 (GRCm39) |
|
probably null |
Het |
Vdac3-ps1 |
T |
C |
13: 18,206,034 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r75 |
A |
G |
7: 85,797,240 (GRCm39) |
|
probably benign |
Het |
Zbtb9 |
G |
T |
17: 27,193,985 (GRCm39) |
|
probably benign |
Het |
Zfp568 |
T |
A |
7: 29,687,233 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Tmem130 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02808:Tmem130
|
APN |
5 |
144,680,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R0599:Tmem130
|
UTSW |
5 |
144,674,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R0714:Tmem130
|
UTSW |
5 |
144,674,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R1807:Tmem130
|
UTSW |
5 |
144,692,174 (GRCm39) |
missense |
probably benign |
0.04 |
R1858:Tmem130
|
UTSW |
5 |
144,689,093 (GRCm39) |
splice site |
probably null |
|
R1914:Tmem130
|
UTSW |
5 |
144,674,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1915:Tmem130
|
UTSW |
5 |
144,674,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R2031:Tmem130
|
UTSW |
5 |
144,689,236 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2074:Tmem130
|
UTSW |
5 |
144,692,084 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2145:Tmem130
|
UTSW |
5 |
144,680,595 (GRCm39) |
missense |
probably benign |
0.08 |
R2183:Tmem130
|
UTSW |
5 |
144,692,242 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3971:Tmem130
|
UTSW |
5 |
144,692,131 (GRCm39) |
missense |
probably benign |
0.04 |
R5092:Tmem130
|
UTSW |
5 |
144,680,528 (GRCm39) |
missense |
probably benign |
0.04 |
R5743:Tmem130
|
UTSW |
5 |
144,687,749 (GRCm39) |
missense |
probably damaging |
0.99 |
R6151:Tmem130
|
UTSW |
5 |
144,674,661 (GRCm39) |
missense |
probably benign |
0.41 |
R6499:Tmem130
|
UTSW |
5 |
144,689,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R7124:Tmem130
|
UTSW |
5 |
144,687,721 (GRCm39) |
missense |
probably damaging |
0.97 |
R7798:Tmem130
|
UTSW |
5 |
144,680,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R7984:Tmem130
|
UTSW |
5 |
144,692,237 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9131:Tmem130
|
UTSW |
5 |
144,680,529 (GRCm39) |
missense |
|
|
R9680:Tmem130
|
UTSW |
5 |
144,674,233 (GRCm39) |
missense |
probably damaging |
1.00 |
|