Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110059E24Rik |
C |
A |
19: 21,575,633 (GRCm39) |
C130F |
probably damaging |
Het |
Adam7 |
A |
G |
14: 68,738,970 (GRCm39) |
V744A |
probably benign |
Het |
Atr |
G |
T |
9: 95,752,096 (GRCm39) |
R571I |
possibly damaging |
Het |
C5ar1 |
A |
G |
7: 15,982,118 (GRCm39) |
Y301H |
probably damaging |
Het |
Cacna1d |
A |
G |
14: 29,829,753 (GRCm39) |
I954T |
probably damaging |
Het |
Ccdc157 |
A |
G |
11: 4,101,795 (GRCm39) |
F42S |
probably damaging |
Het |
Cfap251 |
T |
C |
5: 123,425,408 (GRCm39) |
V789A |
probably benign |
Het |
Chd2 |
A |
T |
7: 73,140,362 (GRCm39) |
L622* |
probably null |
Het |
Csmd3 |
T |
C |
15: 47,811,483 (GRCm39) |
T1203A |
probably benign |
Het |
Cxcl17 |
A |
G |
7: 25,101,636 (GRCm39) |
V67A |
possibly damaging |
Het |
Ddx4 |
T |
C |
13: 112,758,773 (GRCm39) |
T263A |
possibly damaging |
Het |
Eps8l1 |
A |
G |
7: 4,474,393 (GRCm39) |
D288G |
probably benign |
Het |
Fbxl4 |
A |
G |
4: 22,386,154 (GRCm39) |
K254E |
probably benign |
Het |
Glis1 |
T |
C |
4: 107,425,123 (GRCm39) |
S245P |
probably damaging |
Het |
Gm11111 |
T |
C |
5: 98,701,387 (GRCm39) |
|
probably benign |
Het |
Haus3 |
A |
T |
5: 34,311,397 (GRCm39) |
H544Q |
probably benign |
Het |
Hmcn1 |
A |
G |
1: 150,649,554 (GRCm39) |
V644A |
probably benign |
Het |
Lmo7 |
T |
C |
14: 102,114,264 (GRCm39) |
L2P |
probably damaging |
Het |
Lonrf2 |
G |
A |
1: 38,852,357 (GRCm39) |
P165S |
probably benign |
Het |
Mga |
A |
G |
2: 119,747,078 (GRCm39) |
T410A |
probably damaging |
Het |
Mical3 |
T |
C |
6: 121,001,740 (GRCm39) |
D584G |
probably damaging |
Het |
Miga1 |
A |
T |
3: 152,023,300 (GRCm39) |
F250L |
possibly damaging |
Het |
Mroh1 |
A |
G |
15: 76,336,463 (GRCm39) |
D1553G |
probably benign |
Het |
Myof |
T |
C |
19: 37,913,067 (GRCm39) |
Y1462C |
probably damaging |
Het |
Notch4 |
T |
C |
17: 34,784,718 (GRCm39) |
C144R |
probably damaging |
Het |
Obox1 |
T |
C |
7: 15,289,250 (GRCm39) |
V55A |
probably damaging |
Het |
Or14j8 |
T |
A |
17: 38,263,720 (GRCm39) |
H65L |
possibly damaging |
Het |
Or4a69 |
C |
T |
2: 89,312,876 (GRCm39) |
G201D |
probably benign |
Het |
Or6c69c |
T |
A |
10: 129,911,061 (GRCm39) |
S261T |
probably damaging |
Het |
Pclo |
T |
C |
5: 14,729,662 (GRCm39) |
|
probably benign |
Het |
Prr14l |
C |
T |
5: 32,985,293 (GRCm39) |
V1401I |
possibly damaging |
Het |
Rad51ap1 |
T |
C |
6: 126,905,130 (GRCm39) |
|
probably null |
Het |
Rev3l |
T |
A |
10: 39,698,818 (GRCm39) |
V1105D |
probably damaging |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Sgsm2 |
A |
T |
11: 74,744,674 (GRCm39) |
C848* |
probably null |
Het |
Slc39a10 |
A |
T |
1: 46,858,422 (GRCm39) |
V625E |
probably benign |
Het |
Spry4 |
C |
T |
18: 38,723,630 (GRCm39) |
M44I |
probably benign |
Het |
Stat5b |
A |
T |
11: 100,699,220 (GRCm39) |
|
probably null |
Het |
Tas2r126 |
T |
C |
6: 42,412,070 (GRCm39) |
I201T |
probably benign |
Het |
Tasor |
T |
C |
14: 27,202,050 (GRCm39) |
|
probably null |
Het |
Tex44 |
A |
G |
1: 86,355,368 (GRCm39) |
T426A |
probably benign |
Het |
Tln2 |
T |
C |
9: 67,179,950 (GRCm39) |
D807G |
possibly damaging |
Het |
Tlr9 |
A |
G |
9: 106,100,949 (GRCm39) |
N80S |
probably benign |
Het |
Trpm7 |
A |
C |
2: 126,672,082 (GRCm39) |
H579Q |
probably benign |
Het |
Ufd1 |
T |
C |
16: 18,633,661 (GRCm39) |
S29P |
probably damaging |
Het |
Ugt2a3 |
G |
T |
5: 87,473,457 (GRCm39) |
Q487K |
probably damaging |
Het |
Zfyve9 |
A |
G |
4: 108,552,964 (GRCm39) |
|
probably null |
Het |
|
Other mutations in 4933402N03Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01289:4933402N03Rik
|
APN |
7 |
130,740,350 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01374:4933402N03Rik
|
APN |
7 |
130,747,830 (GRCm39) |
missense |
probably benign |
0.34 |
IGL01394:4933402N03Rik
|
APN |
7 |
130,747,960 (GRCm39) |
nonsense |
probably null |
|
IGL01640:4933402N03Rik
|
APN |
7 |
130,740,848 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01713:4933402N03Rik
|
APN |
7 |
130,740,772 (GRCm39) |
missense |
possibly damaging |
0.92 |
H8786:4933402N03Rik
|
UTSW |
7 |
130,740,906 (GRCm39) |
missense |
probably damaging |
0.96 |
R0321:4933402N03Rik
|
UTSW |
7 |
130,747,956 (GRCm39) |
missense |
probably benign |
0.00 |
R0496:4933402N03Rik
|
UTSW |
7 |
130,747,860 (GRCm39) |
missense |
probably benign |
|
R0541:4933402N03Rik
|
UTSW |
7 |
130,740,872 (GRCm39) |
missense |
probably benign |
0.01 |
R1750:4933402N03Rik
|
UTSW |
7 |
130,747,859 (GRCm39) |
missense |
probably benign |
0.09 |
R2047:4933402N03Rik
|
UTSW |
7 |
130,747,836 (GRCm39) |
missense |
probably damaging |
0.96 |
R2404:4933402N03Rik
|
UTSW |
7 |
130,740,923 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3881:4933402N03Rik
|
UTSW |
7 |
130,740,823 (GRCm39) |
missense |
probably benign |
0.19 |
R4507:4933402N03Rik
|
UTSW |
7 |
130,747,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R4684:4933402N03Rik
|
UTSW |
7 |
130,740,413 (GRCm39) |
missense |
probably damaging |
0.96 |
R5368:4933402N03Rik
|
UTSW |
7 |
130,740,925 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5814:4933402N03Rik
|
UTSW |
7 |
130,740,811 (GRCm39) |
missense |
probably benign |
0.09 |
R6238:4933402N03Rik
|
UTSW |
7 |
130,747,863 (GRCm39) |
missense |
probably benign |
0.05 |
R8964:4933402N03Rik
|
UTSW |
7 |
130,740,716 (GRCm39) |
missense |
probably benign |
0.15 |
R9655:4933402N03Rik
|
UTSW |
7 |
130,740,695 (GRCm39) |
missense |
possibly damaging |
0.92 |
|