Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aass |
T |
A |
6: 23,091,328 (GRCm39) |
Y629F |
probably benign |
Het |
Abcb5 |
T |
A |
12: 118,836,668 (GRCm39) |
D1081V |
probably damaging |
Het |
Afdn |
A |
G |
17: 14,108,671 (GRCm39) |
E1398G |
probably damaging |
Het |
Atp8b5 |
T |
C |
4: 43,368,055 (GRCm39) |
C893R |
probably damaging |
Het |
Avl9 |
C |
T |
6: 56,713,812 (GRCm39) |
H357Y |
probably benign |
Het |
Bclaf1 |
C |
T |
10: 20,201,143 (GRCm39) |
T423I |
possibly damaging |
Het |
Btbd19 |
A |
T |
4: 116,977,789 (GRCm39) |
|
probably benign |
Het |
Cap1 |
A |
G |
4: 122,758,419 (GRCm39) |
S254P |
probably damaging |
Het |
Cdc42ep1 |
T |
C |
15: 78,731,629 (GRCm39) |
S25P |
probably benign |
Het |
Cln6 |
T |
C |
9: 62,754,252 (GRCm39) |
I98T |
possibly damaging |
Het |
Cul9 |
T |
C |
17: 46,814,957 (GRCm39) |
|
probably null |
Het |
Dcx |
T |
C |
X: 142,660,240 (GRCm39) |
E268G |
possibly damaging |
Het |
Ddias |
G |
A |
7: 92,509,366 (GRCm39) |
P183L |
probably benign |
Het |
Dnase2b |
A |
T |
3: 146,299,326 (GRCm39) |
Y42* |
probably null |
Het |
Dusp16 |
C |
T |
6: 134,738,082 (GRCm39) |
|
probably benign |
Het |
Egfr |
T |
C |
11: 16,821,881 (GRCm39) |
|
probably benign |
Het |
Fam171a1 |
T |
C |
2: 3,227,393 (GRCm39) |
V842A |
probably benign |
Het |
Folr1 |
T |
C |
7: 101,507,745 (GRCm39) |
S232G |
probably benign |
Het |
Foxj3 |
T |
C |
4: 119,473,839 (GRCm39) |
|
probably benign |
Het |
Fpr-rs6 |
T |
C |
17: 20,403,137 (GRCm39) |
M75V |
probably benign |
Het |
Fxyd5 |
G |
T |
7: 30,735,864 (GRCm39) |
L128M |
possibly damaging |
Het |
Gigyf2 |
T |
C |
1: 87,349,238 (GRCm39) |
S500P |
possibly damaging |
Het |
Inppl1 |
A |
G |
7: 101,481,275 (GRCm39) |
L268P |
probably damaging |
Het |
Klk1b24 |
A |
T |
7: 43,841,243 (GRCm39) |
H192L |
probably benign |
Het |
Llgl1 |
T |
G |
11: 60,597,828 (GRCm39) |
Y316D |
probably damaging |
Het |
Lmbrd1 |
T |
A |
1: 24,801,374 (GRCm39) |
*143R |
probably null |
Het |
Map3k15 |
T |
A |
X: 158,905,568 (GRCm39) |
N1295K |
possibly damaging |
Het |
Mcm3ap |
A |
G |
10: 76,318,513 (GRCm39) |
E678G |
probably damaging |
Het |
Mrpl44 |
T |
A |
1: 79,757,366 (GRCm39) |
Y270* |
probably null |
Het |
Nav1 |
T |
A |
1: 135,395,382 (GRCm39) |
I996L |
probably benign |
Het |
Neb |
T |
C |
2: 52,027,397 (GRCm39) |
E6868G |
probably damaging |
Het |
Nexmif |
A |
T |
X: 103,131,213 (GRCm39) |
Y235N |
probably damaging |
Het |
Nup50 |
C |
T |
15: 84,823,994 (GRCm39) |
T449M |
probably damaging |
Het |
Or14a256 |
G |
A |
7: 86,265,686 (GRCm39) |
P56S |
probably damaging |
Het |
Or2b6 |
A |
G |
13: 21,823,508 (GRCm39) |
F62L |
probably damaging |
Het |
Or51aa2 |
T |
C |
7: 103,188,274 (GRCm39) |
T56A |
probably benign |
Het |
Or52e8b |
A |
G |
7: 104,673,902 (GRCm39) |
L95P |
probably damaging |
Het |
Or52n2 |
T |
C |
7: 104,542,724 (GRCm39) |
Y37C |
possibly damaging |
Het |
Pald1 |
A |
T |
10: 61,191,587 (GRCm39) |
|
probably null |
Het |
Pde11a |
T |
A |
2: 76,121,510 (GRCm39) |
K357I |
probably damaging |
Het |
Ric3 |
A |
G |
7: 108,637,817 (GRCm39) |
V312A |
possibly damaging |
Het |
Scaper |
C |
T |
9: 55,791,205 (GRCm39) |
G231D |
probably benign |
Het |
Smc1b |
T |
A |
15: 85,001,464 (GRCm39) |
|
probably benign |
Het |
Smcr8 |
A |
G |
11: 60,668,854 (GRCm39) |
M1V |
probably null |
Het |
Smtn |
T |
C |
11: 3,477,687 (GRCm39) |
|
probably benign |
Het |
Spatc1 |
A |
T |
15: 76,152,495 (GRCm39) |
K42* |
probably null |
Het |
Taf7l |
A |
T |
X: 133,365,074 (GRCm39) |
I449K |
probably damaging |
Het |
Tram2 |
T |
A |
1: 21,075,824 (GRCm39) |
Y198F |
probably damaging |
Het |
Ttn |
C |
G |
2: 76,629,588 (GRCm39) |
W14284C |
probably damaging |
Het |
Ube3a |
A |
G |
7: 58,926,547 (GRCm39) |
K442E |
probably damaging |
Het |
Vmn2r116 |
T |
A |
17: 23,603,798 (GRCm39) |
F8I |
unknown |
Het |
Vmn2r59 |
A |
G |
7: 41,661,370 (GRCm39) |
F815S |
possibly damaging |
Het |
Zap70 |
T |
C |
1: 36,820,493 (GRCm39) |
C563R |
probably damaging |
Het |
Zfp579 |
T |
C |
7: 4,997,719 (GRCm39) |
H64R |
probably damaging |
Het |
|
Other mutations in Tex47 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00163:Tex47
|
APN |
5 |
7,355,468 (GRCm39) |
nonsense |
probably null |
|
IGL00673:Tex47
|
APN |
5 |
7,355,211 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4495001:Tex47
|
UTSW |
5 |
7,355,011 (GRCm39) |
missense |
probably benign |
0.34 |
R0648:Tex47
|
UTSW |
5 |
7,355,215 (GRCm39) |
missense |
probably benign |
0.04 |
R1911:Tex47
|
UTSW |
5 |
7,355,022 (GRCm39) |
missense |
probably damaging |
0.98 |
R2163:Tex47
|
UTSW |
5 |
7,355,022 (GRCm39) |
missense |
probably damaging |
0.98 |
R3762:Tex47
|
UTSW |
5 |
7,355,529 (GRCm39) |
missense |
probably benign |
0.01 |
R4423:Tex47
|
UTSW |
5 |
7,355,364 (GRCm39) |
missense |
probably benign |
0.10 |
R4424:Tex47
|
UTSW |
5 |
7,355,364 (GRCm39) |
missense |
probably benign |
0.10 |
R5107:Tex47
|
UTSW |
5 |
7,354,842 (GRCm39) |
missense |
probably benign |
0.01 |
R5379:Tex47
|
UTSW |
5 |
7,354,843 (GRCm39) |
missense |
probably null |
0.01 |
R5589:Tex47
|
UTSW |
5 |
7,354,834 (GRCm39) |
missense |
probably benign |
|
R6265:Tex47
|
UTSW |
5 |
7,355,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R6325:Tex47
|
UTSW |
5 |
7,354,935 (GRCm39) |
nonsense |
probably null |
|
R6580:Tex47
|
UTSW |
5 |
7,355,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R8390:Tex47
|
UTSW |
5 |
7,355,301 (GRCm39) |
missense |
probably benign |
0.00 |
R8889:Tex47
|
UTSW |
5 |
7,355,115 (GRCm39) |
missense |
probably damaging |
0.99 |
R8892:Tex47
|
UTSW |
5 |
7,355,115 (GRCm39) |
missense |
probably damaging |
0.99 |
R9416:Tex47
|
UTSW |
5 |
7,355,194 (GRCm39) |
missense |
possibly damaging |
0.48 |
|