Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A830035A12Rik |
T |
C |
11: 107,422,881 (GRCm39) |
|
noncoding transcript |
Het |
Bbs10 |
A |
G |
10: 111,135,720 (GRCm39) |
T278A |
probably benign |
Het |
Bcl6b |
A |
G |
11: 70,116,929 (GRCm39) |
L450P |
probably damaging |
Het |
Braf |
T |
G |
6: 39,592,654 (GRCm39) |
K674Q |
probably damaging |
Het |
Cep112 |
C |
T |
11: 108,410,027 (GRCm39) |
T481I |
possibly damaging |
Het |
Cep135 |
T |
A |
5: 76,772,514 (GRCm39) |
M633K |
probably benign |
Het |
Cpped1 |
T |
C |
16: 11,623,285 (GRCm39) |
Y278C |
probably damaging |
Het |
Depdc5 |
T |
A |
5: 33,061,878 (GRCm39) |
|
probably null |
Het |
Dolpp1 |
C |
T |
2: 30,286,464 (GRCm39) |
A128V |
possibly damaging |
Het |
E2f5 |
T |
A |
3: 14,668,823 (GRCm39) |
D238E |
probably benign |
Het |
Fat4 |
A |
T |
3: 39,012,689 (GRCm39) |
D2328V |
probably benign |
Het |
Fbln1 |
T |
A |
15: 85,115,757 (GRCm39) |
|
probably null |
Het |
Fkbp3 |
T |
C |
12: 65,116,778 (GRCm39) |
T53A |
probably damaging |
Het |
Flg2 |
G |
T |
3: 93,122,176 (GRCm39) |
G1449C |
unknown |
Het |
G530012D18Rik |
G |
C |
1: 85,504,923 (GRCm39) |
|
probably benign |
Het |
Glyctk |
A |
T |
9: 106,034,307 (GRCm39) |
|
probably benign |
Het |
Gm6430 |
T |
C |
1: 96,953,297 (GRCm39) |
|
noncoding transcript |
Het |
Golga1 |
C |
A |
2: 38,909,653 (GRCm39) |
|
probably null |
Het |
Gucy2g |
A |
T |
19: 55,226,269 (GRCm39) |
F216I |
probably benign |
Het |
L3mbtl3 |
A |
G |
10: 26,189,782 (GRCm39) |
V494A |
unknown |
Het |
Lama2 |
AATCAGACAGGAG |
A |
10: 27,088,124 (GRCm39) |
|
probably benign |
Het |
Lemd3 |
A |
T |
10: 120,761,335 (GRCm39) |
L907Q |
possibly damaging |
Het |
Lrp2 |
A |
T |
2: 69,332,861 (GRCm39) |
V1552D |
probably damaging |
Het |
Map3k12 |
T |
C |
15: 102,413,837 (GRCm39) |
T45A |
probably damaging |
Het |
Mycbp2 |
A |
T |
14: 103,524,664 (GRCm39) |
D665E |
probably damaging |
Het |
Myof |
A |
G |
19: 37,911,426 (GRCm39) |
S1502P |
probably damaging |
Het |
Or4p7 |
A |
T |
2: 88,222,427 (GRCm39) |
M279L |
probably benign |
Het |
Pcdhac2 |
G |
T |
18: 37,277,499 (GRCm39) |
V160L |
probably benign |
Het |
Pcnt |
T |
C |
10: 76,210,704 (GRCm39) |
E2473G |
possibly damaging |
Het |
Pitpnm2 |
T |
A |
5: 124,290,678 (GRCm39) |
I3L |
possibly damaging |
Het |
Prkd3 |
C |
A |
17: 79,290,987 (GRCm39) |
W176L |
probably damaging |
Het |
Prpf39 |
C |
T |
12: 65,103,040 (GRCm39) |
A438V |
probably damaging |
Het |
Rpgrip1 |
T |
A |
14: 52,384,856 (GRCm39) |
F655I |
probably damaging |
Het |
Rrp12 |
T |
C |
19: 41,880,990 (GRCm39) |
Y147C |
probably damaging |
Het |
Sec23b |
A |
T |
2: 144,416,638 (GRCm39) |
N429Y |
possibly damaging |
Het |
Slc2a10 |
T |
A |
2: 165,356,684 (GRCm39) |
S115T |
probably damaging |
Het |
Spg11 |
A |
C |
2: 121,905,813 (GRCm39) |
D1277E |
probably benign |
Het |
Sspo |
A |
G |
6: 48,437,454 (GRCm39) |
D1279G |
probably damaging |
Het |
St18 |
T |
C |
1: 6,898,061 (GRCm39) |
I621T |
probably benign |
Het |
Tbc1d31 |
T |
A |
15: 57,783,438 (GRCm39) |
D112E |
possibly damaging |
Het |
Tdpoz6 |
C |
A |
3: 93,599,419 (GRCm39) |
V317L |
probably benign |
Het |
Tgm4 |
A |
T |
9: 122,885,595 (GRCm39) |
D379V |
probably damaging |
Het |
Thyn1 |
A |
T |
9: 26,914,893 (GRCm39) |
D15V |
possibly damaging |
Het |
Timd6 |
A |
G |
11: 46,468,207 (GRCm39) |
T94A |
probably damaging |
Het |
Trim38 |
A |
C |
13: 23,975,474 (GRCm39) |
Q471P |
probably benign |
Het |
Trmt1 |
T |
A |
8: 85,424,384 (GRCm39) |
|
probably benign |
Het |
Ubqlnl |
C |
T |
7: 103,798,925 (GRCm39) |
V191M |
probably benign |
Het |
Usp9y |
T |
C |
Y: 1,336,375 (GRCm39) |
I1500V |
probably benign |
Het |
Vgll4 |
C |
T |
6: 114,867,573 (GRCm39) |
|
probably null |
Het |
Vmn1r173 |
T |
A |
7: 23,402,441 (GRCm39) |
N225K |
probably damaging |
Het |
Vmn2r22 |
C |
T |
6: 123,614,913 (GRCm39) |
G226R |
probably damaging |
Het |
Wnk3 |
C |
A |
X: 150,016,209 (GRCm39) |
P555Q |
probably benign |
Het |
Yes1 |
T |
G |
5: 32,797,929 (GRCm39) |
Y83D |
possibly damaging |
Het |
Zdhhc15 |
G |
A |
X: 103,604,294 (GRCm39) |
R322* |
probably null |
Het |
|
Other mutations in Tm4sf19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01094:Tm4sf19
|
APN |
16 |
32,224,772 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02468:Tm4sf19
|
APN |
16 |
32,226,533 (GRCm39) |
splice site |
probably benign |
|
IGL02573:Tm4sf19
|
APN |
16 |
32,226,678 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02938:Tm4sf19
|
APN |
16 |
32,224,733 (GRCm39) |
missense |
probably damaging |
0.98 |
R1306:Tm4sf19
|
UTSW |
16 |
32,226,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R1450:Tm4sf19
|
UTSW |
16 |
32,226,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R1522:Tm4sf19
|
UTSW |
16 |
32,224,820 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1895:Tm4sf19
|
UTSW |
16 |
32,226,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R5527:Tm4sf19
|
UTSW |
16 |
32,226,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R6166:Tm4sf19
|
UTSW |
16 |
32,226,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R6949:Tm4sf19
|
UTSW |
16 |
32,224,676 (GRCm39) |
missense |
probably benign |
0.01 |
R7269:Tm4sf19
|
UTSW |
16 |
32,224,814 (GRCm39) |
missense |
probably damaging |
0.98 |
R7316:Tm4sf19
|
UTSW |
16 |
32,226,466 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7993:Tm4sf19
|
UTSW |
16 |
32,226,458 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1177:Tm4sf19
|
UTSW |
16 |
32,224,741 (GRCm39) |
missense |
probably damaging |
1.00 |
|