Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd6 |
A |
T |
14: 8,049,850 (GRCm38) |
H213L |
possibly damaging |
Het |
Adam22 |
T |
A |
5: 8,417,322 (GRCm39) |
N40I |
possibly damaging |
Het |
Ankrd42 |
A |
G |
7: 92,231,224 (GRCm39) |
|
probably benign |
Het |
Arhgap40 |
C |
T |
2: 158,369,066 (GRCm39) |
R63C |
probably benign |
Het |
Atf7ip |
T |
G |
6: 136,536,755 (GRCm39) |
|
probably null |
Het |
Atg7 |
T |
C |
6: 114,686,172 (GRCm39) |
|
probably null |
Het |
Car6 |
A |
C |
4: 150,273,713 (GRCm39) |
|
probably null |
Het |
Carmil1 |
A |
T |
13: 24,259,667 (GRCm39) |
C302* |
probably null |
Het |
Ccdc117 |
A |
T |
11: 5,484,255 (GRCm39) |
M195K |
probably benign |
Het |
Cep95 |
T |
C |
11: 106,702,023 (GRCm39) |
M383T |
probably damaging |
Het |
Col20a1 |
A |
G |
2: 180,638,643 (GRCm39) |
E419G |
probably damaging |
Het |
Cyp2d9 |
C |
G |
15: 82,339,413 (GRCm39) |
R272G |
probably damaging |
Het |
Dhx57 |
A |
T |
17: 80,546,244 (GRCm39) |
M1380K |
possibly damaging |
Het |
Dnah14 |
A |
G |
1: 181,455,517 (GRCm39) |
S881G |
probably benign |
Het |
Fcgbp |
T |
A |
7: 27,793,248 (GRCm39) |
I1084N |
probably benign |
Het |
Fgf17 |
A |
T |
14: 70,878,981 (GRCm39) |
C21* |
probably null |
Het |
Gemin4 |
A |
G |
11: 76,103,162 (GRCm39) |
L533P |
probably damaging |
Het |
Gkn3 |
T |
C |
6: 87,365,784 (GRCm39) |
R12G |
probably benign |
Het |
Gpr161 |
G |
T |
1: 165,149,188 (GRCm39) |
R519L |
possibly damaging |
Het |
Grin2a |
A |
G |
16: 9,481,092 (GRCm39) |
V535A |
possibly damaging |
Het |
Gys1 |
G |
A |
7: 45,093,059 (GRCm39) |
|
probably null |
Het |
Hfm1 |
C |
T |
5: 106,998,276 (GRCm39) |
|
probably null |
Het |
Hmcn2 |
T |
A |
2: 31,240,517 (GRCm39) |
|
probably null |
Het |
Hnrnpul2 |
T |
C |
19: 8,808,873 (GRCm39) |
Y738H |
unknown |
Het |
Hycc1 |
T |
C |
5: 24,191,133 (GRCm39) |
|
probably null |
Het |
Igsf23 |
A |
G |
7: 19,675,684 (GRCm39) |
S141P |
possibly damaging |
Het |
Lamc3 |
A |
C |
2: 31,828,081 (GRCm39) |
M1423L |
probably benign |
Het |
Lcmt2 |
T |
C |
2: 120,970,484 (GRCm39) |
T200A |
probably benign |
Het |
Lgr4 |
T |
C |
2: 109,842,784 (GRCm39) |
V899A |
probably damaging |
Het |
Macf1 |
T |
A |
4: 123,421,145 (GRCm39) |
R36S |
possibly damaging |
Het |
Mrgprb8 |
A |
G |
7: 48,038,871 (GRCm39) |
K181E |
possibly damaging |
Het |
Muc2 |
G |
A |
7: 141,284,077 (GRCm39) |
V786M |
possibly damaging |
Het |
Nacc2 |
T |
C |
2: 25,980,041 (GRCm39) |
T132A |
probably damaging |
Het |
Nsmce2 |
T |
A |
15: 59,250,774 (GRCm39) |
I15K |
probably damaging |
Het |
Or10p22 |
T |
G |
10: 128,825,960 (GRCm39) |
Y60D |
probably damaging |
Het |
Or4k15c |
A |
G |
14: 50,321,307 (GRCm39) |
I277T |
possibly damaging |
Het |
Otoa |
A |
T |
7: 120,730,724 (GRCm39) |
|
probably null |
Het |
Otogl |
A |
G |
10: 107,644,502 (GRCm39) |
I1248T |
probably damaging |
Het |
Ppp1r17 |
T |
A |
6: 56,003,007 (GRCm39) |
D32E |
probably damaging |
Het |
Relt |
A |
C |
7: 100,496,468 (GRCm39) |
V427G |
probably damaging |
Het |
Ric1 |
T |
A |
19: 29,546,788 (GRCm39) |
V256D |
probably damaging |
Het |
Samhd1 |
T |
C |
2: 156,951,403 (GRCm39) |
T445A |
probably benign |
Het |
Sepsecs |
T |
C |
5: 52,821,646 (GRCm39) |
I189V |
probably benign |
Het |
Shroom3 |
T |
A |
5: 93,112,262 (GRCm39) |
D1793E |
probably damaging |
Het |
Sim1 |
C |
T |
10: 50,784,635 (GRCm39) |
T137I |
probably benign |
Het |
Stk17b |
A |
T |
1: 53,800,218 (GRCm39) |
D253E |
possibly damaging |
Het |
Stmnd1 |
T |
C |
13: 46,452,969 (GRCm39) |
V215A |
probably benign |
Het |
Tcl1 |
A |
G |
12: 105,185,015 (GRCm39) |
L65P |
probably damaging |
Het |
Tiam2 |
A |
C |
17: 3,558,070 (GRCm39) |
K1231N |
probably damaging |
Het |
Tm9sf3 |
T |
C |
19: 41,206,717 (GRCm39) |
Y476C |
probably damaging |
Het |
Trim63 |
T |
C |
4: 134,048,572 (GRCm39) |
S194P |
probably damaging |
Het |
Ugt1a10 |
T |
A |
1: 87,983,379 (GRCm39) |
I59N |
probably damaging |
Het |
Vmn2r65 |
A |
G |
7: 84,613,198 (GRCm39) |
F7S |
probably benign |
Het |
Zfp775 |
T |
A |
6: 48,596,589 (GRCm39) |
H154Q |
probably damaging |
Het |
Zfp804b |
C |
T |
5: 6,819,902 (GRCm39) |
V1018I |
probably benign |
Het |
|
Other mutations in 1700009N14Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00688:1700009N14Rik
|
APN |
4 |
39,451,443 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4377001:1700009N14Rik
|
UTSW |
4 |
39,451,129 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0308:1700009N14Rik
|
UTSW |
4 |
39,450,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R5061:1700009N14Rik
|
UTSW |
4 |
39,450,953 (GRCm39) |
missense |
probably benign |
0.03 |
R5154:1700009N14Rik
|
UTSW |
4 |
39,450,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R5507:1700009N14Rik
|
UTSW |
4 |
39,451,084 (GRCm39) |
missense |
probably damaging |
0.96 |
R6463:1700009N14Rik
|
UTSW |
4 |
39,450,938 (GRCm39) |
missense |
probably damaging |
0.98 |
R7253:1700009N14Rik
|
UTSW |
4 |
39,451,391 (GRCm39) |
missense |
not run |
|
R7487:1700009N14Rik
|
UTSW |
4 |
39,450,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R7790:1700009N14Rik
|
UTSW |
4 |
39,451,201 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8758:1700009N14Rik
|
UTSW |
4 |
39,450,811 (GRCm39) |
missense |
probably benign |
|
R9379:1700009N14Rik
|
UTSW |
4 |
39,451,201 (GRCm39) |
missense |
possibly damaging |
0.89 |
|