Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
C |
T |
13: 81,567,349 (GRCm39) |
G5275S |
probably benign |
Het |
Akap11 |
A |
G |
14: 78,747,699 (GRCm39) |
S1563P |
probably damaging |
Het |
Ankrd50 |
A |
G |
3: 38,511,680 (GRCm39) |
V229A |
probably damaging |
Het |
AW112010 |
A |
G |
19: 11,027,757 (GRCm39) |
|
noncoding transcript |
Het |
Ccdc158 |
A |
G |
5: 92,781,187 (GRCm39) |
S873P |
probably benign |
Het |
Cep350 |
A |
G |
1: 155,802,214 (GRCm39) |
V1104A |
probably benign |
Het |
Chil4 |
G |
A |
3: 106,121,678 (GRCm39) |
A57V |
probably damaging |
Het |
Cpa5 |
A |
G |
6: 30,624,625 (GRCm39) |
E155G |
probably damaging |
Het |
Ctsq |
T |
C |
13: 61,186,726 (GRCm39) |
I93V |
probably benign |
Het |
Dbi |
A |
T |
1: 120,048,535 (GRCm39) |
I37K |
probably benign |
Het |
Defa35 |
T |
C |
8: 21,555,208 (GRCm39) |
S43P |
probably damaging |
Het |
Fance |
T |
A |
17: 28,534,781 (GRCm39) |
|
probably benign |
Het |
Fbxl6 |
A |
G |
15: 76,422,129 (GRCm39) |
L180P |
probably damaging |
Het |
Fkbpl |
T |
C |
17: 34,865,269 (GRCm39) |
F346L |
probably damaging |
Het |
Gm11735 |
C |
A |
11: 116,632,101 (GRCm39) |
|
noncoding transcript |
Het |
Gm28042 |
T |
C |
2: 119,866,321 (GRCm39) |
I373T |
possibly damaging |
Het |
Golga4 |
T |
C |
9: 118,343,254 (GRCm39) |
S27P |
probably damaging |
Het |
Gstm1 |
C |
T |
3: 107,923,834 (GRCm39) |
|
probably null |
Het |
Lama3 |
T |
A |
18: 12,682,310 (GRCm39) |
I1092K |
probably benign |
Het |
Med15 |
A |
T |
16: 17,489,428 (GRCm39) |
|
probably benign |
Het |
Nlrp6 |
A |
G |
7: 140,501,694 (GRCm39) |
D87G |
probably damaging |
Het |
Parp11 |
A |
G |
6: 127,448,568 (GRCm39) |
T62A |
probably benign |
Het |
Pcnt |
A |
G |
10: 76,237,317 (GRCm39) |
L1323S |
probably damaging |
Het |
Ppp2r1a |
C |
T |
17: 21,176,072 (GRCm39) |
T98I |
probably benign |
Het |
Pramel11 |
T |
A |
4: 143,622,410 (GRCm39) |
Y315F |
probably damaging |
Het |
Prl7a2 |
T |
A |
13: 27,844,930 (GRCm39) |
H152L |
possibly damaging |
Het |
Rnf145 |
T |
C |
11: 44,455,104 (GRCm39) |
S662P |
probably benign |
Het |
Tnfaip3 |
A |
T |
10: 18,887,375 (GRCm39) |
M50K |
probably damaging |
Het |
Txlnb |
T |
TTA |
10: 17,714,745 (GRCm39) |
|
probably null |
Het |
Usp9x |
A |
G |
X: 12,987,687 (GRCm39) |
D638G |
possibly damaging |
Het |
Vmn1r30 |
A |
T |
6: 58,412,118 (GRCm39) |
V238E |
probably damaging |
Het |
Zfp507 |
A |
G |
7: 35,487,141 (GRCm39) |
|
probably null |
Het |
Zfp532 |
G |
T |
18: 65,789,636 (GRCm39) |
W1025L |
probably benign |
Het |
|
Other mutations in Rpl31-ps17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R2174:Rpl31-ps17
|
UTSW |
12 |
54,748,397 (GRCm39) |
unclassified |
noncoding transcript |
|
R3620:Rpl31-ps17
|
UTSW |
12 |
54,748,397 (GRCm39) |
unclassified |
noncoding transcript |
|
R3861:Rpl31-ps17
|
UTSW |
12 |
54,748,397 (GRCm39) |
unclassified |
noncoding transcript |
|
R4156:Rpl31-ps17
|
UTSW |
12 |
54,748,397 (GRCm39) |
unclassified |
noncoding transcript |
|
R4157:Rpl31-ps17
|
UTSW |
12 |
54,748,397 (GRCm39) |
unclassified |
noncoding transcript |
|
R4194:Rpl31-ps17
|
UTSW |
12 |
54,748,434 (GRCm39) |
unclassified |
noncoding transcript |
|
R4205:Rpl31-ps17
|
UTSW |
12 |
54,748,397 (GRCm39) |
unclassified |
noncoding transcript |
|
R4423:Rpl31-ps17
|
UTSW |
12 |
54,748,397 (GRCm39) |
unclassified |
noncoding transcript |
|
R4424:Rpl31-ps17
|
UTSW |
12 |
54,748,397 (GRCm39) |
unclassified |
noncoding transcript |
|
R4455:Rpl31-ps17
|
UTSW |
12 |
54,748,397 (GRCm39) |
unclassified |
noncoding transcript |
|
R4457:Rpl31-ps17
|
UTSW |
12 |
54,748,397 (GRCm39) |
unclassified |
noncoding transcript |
|
R4776:Rpl31-ps17
|
UTSW |
12 |
54,748,397 (GRCm39) |
unclassified |
noncoding transcript |
|
|