Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921509C19Rik |
C |
A |
2: 151,315,227 (GRCm39) |
L150F |
probably damaging |
Het |
4930449I24Rik |
G |
A |
5: 146,441,542 (GRCm39) |
E230K |
possibly damaging |
Het |
4930449I24Rik |
A |
T |
5: 146,441,543 (GRCm39) |
E230V |
probably benign |
Het |
9430038I01Rik |
A |
G |
7: 136,989,117 (GRCm39) |
C93R |
possibly damaging |
Het |
Aoc1l2 |
G |
A |
6: 48,907,596 (GRCm39) |
A199T |
probably damaging |
Het |
Apobec1 |
T |
C |
6: 122,568,201 (GRCm39) |
|
probably benign |
Het |
Arl4c |
T |
A |
1: 88,629,097 (GRCm39) |
D97V |
probably damaging |
Het |
Ash1l |
A |
G |
3: 88,890,298 (GRCm39) |
T726A |
probably benign |
Het |
Asz1 |
A |
C |
6: 18,055,520 (GRCm39) |
F359V |
probably damaging |
Het |
Atr |
T |
A |
9: 95,809,250 (GRCm39) |
L1970H |
probably damaging |
Het |
Baz2a |
G |
T |
10: 127,959,450 (GRCm39) |
A1322S |
possibly damaging |
Het |
Cd209e |
T |
A |
8: 3,903,569 (GRCm39) |
I37F |
possibly damaging |
Het |
Cd209f |
T |
C |
8: 4,155,477 (GRCm39) |
K37R |
probably benign |
Het |
Cd5 |
G |
C |
19: 10,716,203 (GRCm39) |
S3C |
possibly damaging |
Het |
Clec16a |
A |
T |
16: 10,462,718 (GRCm39) |
I260F |
probably damaging |
Het |
Cltc |
A |
T |
11: 86,603,428 (GRCm39) |
Y799* |
probably null |
Het |
Cplane1 |
T |
C |
15: 8,216,852 (GRCm39) |
L690P |
probably damaging |
Het |
Dennd5a |
G |
T |
7: 109,500,325 (GRCm39) |
H909Q |
probably damaging |
Het |
Dnah12 |
A |
G |
14: 26,456,904 (GRCm39) |
D890G |
probably damaging |
Het |
Dnah2 |
A |
T |
11: 69,375,086 (GRCm39) |
M1379K |
probably benign |
Het |
Dpp10 |
A |
T |
1: 123,264,593 (GRCm39) |
I743N |
probably damaging |
Het |
Dpp9 |
T |
A |
17: 56,495,321 (GRCm39) |
T815S |
probably damaging |
Het |
Ears2 |
T |
C |
7: 121,647,447 (GRCm39) |
N279S |
probably damaging |
Het |
Ect2l |
A |
G |
10: 18,045,128 (GRCm39) |
|
probably null |
Het |
Eomes |
C |
G |
9: 118,310,353 (GRCm39) |
P288A |
probably damaging |
Het |
Fat3 |
T |
C |
9: 15,909,072 (GRCm39) |
D2310G |
probably damaging |
Het |
Fignl2 |
T |
C |
15: 100,951,854 (GRCm39) |
T143A |
probably benign |
Het |
Gdf9 |
A |
G |
11: 53,327,646 (GRCm39) |
K201E |
possibly damaging |
Het |
Gfra3 |
C |
T |
18: 34,828,710 (GRCm39) |
R228Q |
probably damaging |
Het |
Grin1 |
A |
T |
2: 25,185,829 (GRCm39) |
V876E |
probably damaging |
Het |
Igkv12-41 |
A |
C |
6: 69,835,635 (GRCm39) |
V39G |
probably damaging |
Het |
Kat7 |
A |
T |
11: 95,174,910 (GRCm39) |
M367K |
possibly damaging |
Het |
Ly6d |
T |
C |
15: 74,634,654 (GRCm39) |
K33E |
possibly damaging |
Het |
Lztfl1 |
T |
C |
9: 123,529,998 (GRCm39) |
N273S |
possibly damaging |
Het |
Macf1 |
T |
A |
4: 123,377,480 (GRCm39) |
I1485F |
possibly damaging |
Het |
Marchf10 |
G |
T |
11: 105,287,787 (GRCm39) |
L172I |
possibly damaging |
Het |
Mdn1 |
T |
G |
4: 32,748,614 (GRCm39) |
S4220A |
possibly damaging |
Het |
Muc16 |
A |
G |
9: 18,406,872 (GRCm39) |
V8460A |
possibly damaging |
Het |
Myh14 |
A |
G |
7: 44,282,936 (GRCm39) |
F769L |
probably damaging |
Het |
Myl10 |
G |
C |
5: 136,726,825 (GRCm39) |
V70L |
probably benign |
Het |
Mylk4 |
A |
G |
13: 32,905,998 (GRCm39) |
L395P |
probably damaging |
Het |
Nat8f6 |
A |
T |
6: 85,785,504 (GRCm39) |
L215* |
probably null |
Het |
Nell2 |
T |
C |
15: 95,244,768 (GRCm39) |
D443G |
probably damaging |
Het |
Nkx6-3 |
A |
G |
8: 23,647,632 (GRCm39) |
K197R |
probably benign |
Het |
Nt5c3 |
A |
T |
6: 56,859,958 (GRCm39) |
L293* |
probably null |
Het |
Ntrk1 |
A |
T |
3: 87,690,109 (GRCm39) |
V429D |
probably damaging |
Het |
Obscn |
A |
G |
11: 59,023,508 (GRCm39) |
V623A |
probably benign |
Het |
Or2o1 |
T |
C |
11: 49,051,186 (GRCm39) |
F115S |
probably benign |
Het |
Or4c1 |
A |
G |
2: 89,133,837 (GRCm39) |
L33S |
probably damaging |
Het |
Or5ac21 |
A |
G |
16: 59,124,142 (GRCm39) |
T209A |
probably damaging |
Het |
Or5p5 |
C |
T |
7: 107,414,271 (GRCm39) |
T160I |
probably benign |
Het |
Or6c74 |
T |
C |
10: 129,870,178 (GRCm39) |
S228P |
probably damaging |
Het |
Or8k22 |
A |
T |
2: 86,163,295 (GRCm39) |
I135N |
probably damaging |
Het |
Pate3 |
T |
A |
9: 35,557,969 (GRCm39) |
D33V |
probably damaging |
Het |
Pcnx1 |
T |
A |
12: 82,034,747 (GRCm39) |
I1843N |
probably damaging |
Het |
Pla2g4f |
A |
T |
2: 120,134,077 (GRCm39) |
I503N |
probably benign |
Het |
Prkg1 |
C |
A |
19: 30,602,174 (GRCm39) |
E361* |
probably null |
Het |
Proca1 |
A |
G |
11: 78,085,613 (GRCm39) |
|
probably benign |
Het |
Prss38 |
G |
T |
11: 59,263,850 (GRCm39) |
H287Q |
probably benign |
Het |
Ptpdc1 |
T |
C |
13: 48,744,114 (GRCm39) |
E169G |
probably benign |
Het |
Ptpn21 |
T |
C |
12: 98,681,440 (GRCm39) |
S65G |
probably damaging |
Het |
Rfx6 |
A |
T |
10: 51,592,135 (GRCm39) |
H177L |
probably damaging |
Het |
Slc20a2 |
G |
A |
8: 23,050,609 (GRCm39) |
G276D |
possibly damaging |
Het |
Spag6l |
A |
T |
16: 16,601,802 (GRCm39) |
L159I |
probably damaging |
Het |
Spata31f1a |
G |
A |
4: 42,850,291 (GRCm39) |
P622S |
probably benign |
Het |
St3gal1 |
A |
G |
15: 66,983,195 (GRCm39) |
V187A |
possibly damaging |
Het |
Stk33 |
T |
A |
7: 108,935,269 (GRCm39) |
E174D |
possibly damaging |
Het |
Stxbp5 |
A |
T |
10: 9,660,105 (GRCm39) |
V730E |
probably benign |
Het |
Tmprss15 |
A |
T |
16: 78,872,702 (GRCm39) |
L168* |
probably null |
Het |
Tnrc18 |
A |
T |
5: 142,745,804 (GRCm39) |
M1323K |
unknown |
Het |
Tpr |
T |
C |
1: 150,312,598 (GRCm39) |
V1932A |
probably benign |
Het |
Trak2 |
A |
G |
1: 58,950,892 (GRCm39) |
S432P |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,738,534 (GRCm39) |
F4002I |
probably benign |
Het |
Txndc11 |
G |
A |
16: 10,906,009 (GRCm39) |
T507I |
probably damaging |
Het |
Usp12 |
G |
A |
5: 146,691,349 (GRCm39) |
T135I |
possibly damaging |
Het |
Vit |
T |
A |
17: 78,934,187 (GRCm39) |
Y596* |
probably null |
Het |
Vmn1r32 |
A |
T |
6: 66,530,345 (GRCm39) |
Y144N |
possibly damaging |
Het |
Vmn2r80 |
G |
T |
10: 79,005,438 (GRCm39) |
L358F |
probably benign |
Het |
Zfp382 |
T |
G |
7: 29,825,261 (GRCm39) |
S38A |
probably benign |
Het |
|
Other mutations in Csde1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01100:Csde1
|
APN |
3 |
102,947,841 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01419:Csde1
|
APN |
3 |
102,946,086 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02147:Csde1
|
APN |
3 |
102,947,250 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02161:Csde1
|
APN |
3 |
102,957,654 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02442:Csde1
|
APN |
3 |
102,962,135 (GRCm39) |
missense |
probably benign |
0.20 |
IGL03036:Csde1
|
APN |
3 |
102,951,155 (GRCm39) |
missense |
probably damaging |
0.99 |
R0526:Csde1
|
UTSW |
3 |
102,963,742 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0727:Csde1
|
UTSW |
3 |
102,950,954 (GRCm39) |
missense |
probably benign |
|
R1738:Csde1
|
UTSW |
3 |
102,936,493 (GRCm39) |
intron |
probably benign |
|
R1744:Csde1
|
UTSW |
3 |
102,957,631 (GRCm39) |
missense |
probably benign |
0.31 |
R2007:Csde1
|
UTSW |
3 |
102,952,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R4665:Csde1
|
UTSW |
3 |
102,954,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R4806:Csde1
|
UTSW |
3 |
102,963,685 (GRCm39) |
unclassified |
probably benign |
|
R5202:Csde1
|
UTSW |
3 |
102,947,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R5298:Csde1
|
UTSW |
3 |
102,954,525 (GRCm39) |
splice site |
probably null |
|
R5429:Csde1
|
UTSW |
3 |
102,960,157 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5896:Csde1
|
UTSW |
3 |
102,947,859 (GRCm39) |
intron |
probably benign |
|
R6076:Csde1
|
UTSW |
3 |
102,948,545 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6093:Csde1
|
UTSW |
3 |
102,960,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R6118:Csde1
|
UTSW |
3 |
102,962,070 (GRCm39) |
missense |
probably benign |
0.45 |
R6213:Csde1
|
UTSW |
3 |
102,947,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R6263:Csde1
|
UTSW |
3 |
102,947,333 (GRCm39) |
missense |
probably benign |
0.05 |
R6653:Csde1
|
UTSW |
3 |
102,960,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R7155:Csde1
|
UTSW |
3 |
102,947,269 (GRCm39) |
missense |
probably damaging |
0.99 |
R8253:Csde1
|
UTSW |
3 |
102,946,037 (GRCm39) |
missense |
probably damaging |
0.98 |
R8270:Csde1
|
UTSW |
3 |
102,946,071 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8307:Csde1
|
UTSW |
3 |
102,946,389 (GRCm39) |
intron |
probably benign |
|
R9036:Csde1
|
UTSW |
3 |
102,950,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R9628:Csde1
|
UTSW |
3 |
102,962,825 (GRCm39) |
missense |
probably benign |
0.05 |
|