Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot11 |
A |
G |
4: 106,613,178 (GRCm39) |
V319A |
probably damaging |
Het |
Afap1l1 |
A |
C |
18: 61,890,795 (GRCm39) |
S53A |
possibly damaging |
Het |
Alms1 |
T |
A |
6: 85,600,125 (GRCm39) |
N1650K |
probably damaging |
Het |
Atf6b |
T |
A |
17: 34,872,507 (GRCm39) |
V553E |
possibly damaging |
Het |
Avl9 |
T |
A |
6: 56,707,634 (GRCm39) |
I193N |
probably damaging |
Het |
Ceacam3 |
A |
G |
7: 16,895,688 (GRCm39) |
N553D |
|
Het |
Dnah3 |
C |
A |
7: 119,550,216 (GRCm39) |
V389L |
probably benign |
Het |
Erich6 |
T |
C |
3: 58,537,277 (GRCm39) |
M246V |
probably benign |
Het |
Fgfr1 |
T |
A |
8: 26,060,776 (GRCm39) |
Y483N |
probably damaging |
Het |
Fmo4 |
T |
A |
1: 162,631,191 (GRCm39) |
M259L |
probably benign |
Het |
Gnat2 |
T |
A |
3: 108,002,770 (GRCm39) |
D59E |
probably benign |
Het |
Izumo3 |
T |
A |
4: 92,034,795 (GRCm39) |
Y94F |
probably damaging |
Het |
Kcnb2 |
A |
T |
1: 15,781,444 (GRCm39) |
H772L |
probably benign |
Het |
Kcnrg |
CACAACAA |
CACAA |
14: 61,845,009 (GRCm39) |
|
probably benign |
Het |
Krt6b |
C |
T |
15: 101,586,996 (GRCm39) |
V259M |
probably benign |
Het |
Lingo2 |
A |
G |
4: 35,709,885 (GRCm39) |
C32R |
|
Het |
Lrrtm4 |
C |
T |
6: 80,000,064 (GRCm39) |
T492M |
probably damaging |
Het |
Maea |
T |
A |
5: 33,526,050 (GRCm39) |
M242K |
possibly damaging |
Het |
Mdga2 |
T |
C |
12: 66,736,206 (GRCm39) |
T341A |
probably benign |
Het |
Mfsd14b |
C |
A |
13: 65,221,414 (GRCm39) |
V293L |
probably benign |
Het |
Mmadhc |
A |
T |
2: 50,178,988 (GRCm39) |
S143R |
probably benign |
Het |
Ms4a8a |
A |
G |
19: 11,056,956 (GRCm39) |
V42A |
probably benign |
Het |
N4bp2l2 |
A |
T |
5: 150,585,103 (GRCm39) |
H292Q |
probably benign |
Het |
Nkx2-2 |
A |
G |
2: 147,027,686 (GRCm39) |
Y85H |
possibly damaging |
Het |
Pramel14 |
T |
C |
4: 143,720,818 (GRCm39) |
K41R |
possibly damaging |
Het |
Psmb9 |
T |
A |
17: 34,402,119 (GRCm39) |
D159V |
probably damaging |
Het |
Rgs4 |
T |
A |
1: 169,572,843 (GRCm39) |
D31V |
possibly damaging |
Het |
Shank1 |
G |
A |
7: 43,962,342 (GRCm39) |
S71N |
unknown |
Het |
Slc22a14 |
A |
G |
9: 119,008,528 (GRCm39) |
S247P |
probably benign |
Het |
Slc26a7 |
G |
A |
4: 14,524,540 (GRCm39) |
T448I |
possibly damaging |
Het |
Slc7a14 |
T |
A |
3: 31,278,166 (GRCm39) |
T480S |
probably benign |
Het |
Spocd1 |
T |
C |
4: 129,850,463 (GRCm39) |
S830P |
unknown |
Het |
Sycp2 |
A |
G |
2: 177,998,254 (GRCm39) |
S1089P |
probably damaging |
Het |
Tcf4 |
A |
T |
18: 69,726,382 (GRCm39) |
|
probably benign |
Het |
Tktl2 |
T |
C |
8: 66,965,813 (GRCm39) |
V457A |
probably benign |
Het |
Tmem131 |
A |
T |
1: 36,847,069 (GRCm39) |
I1343N |
probably damaging |
Het |
Tnrc6c |
G |
A |
11: 117,638,009 (GRCm39) |
A1164T |
probably damaging |
Het |
Tomm5 |
G |
A |
4: 45,107,982 (GRCm39) |
R18W |
probably damaging |
Het |
Ubxn7 |
T |
C |
16: 32,200,248 (GRCm39) |
S335P |
probably benign |
Het |
Unc5c |
A |
C |
3: 141,495,654 (GRCm39) |
T508P |
probably damaging |
Het |
Upp1 |
G |
A |
11: 9,084,909 (GRCm39) |
M209I |
|
Het |
Vmn1r213 |
A |
G |
13: 23,195,519 (GRCm39) |
D34G |
unknown |
Het |
Vmn1r235 |
G |
T |
17: 21,482,330 (GRCm39) |
W218C |
possibly damaging |
Het |
Vmn1r235 |
G |
T |
17: 21,482,329 (GRCm39) |
W218L |
probably benign |
Het |
Vmn2r57 |
T |
C |
7: 41,076,006 (GRCm39) |
E502G |
probably benign |
Het |
Wwc2 |
GCC |
GCCC |
8: 48,304,959 (GRCm39) |
|
probably null |
Het |
Zfc3h1 |
T |
A |
10: 115,247,852 (GRCm39) |
H1018Q |
probably damaging |
Het |
Zfp318 |
T |
A |
17: 46,710,421 (GRCm39) |
S715T |
probably damaging |
Het |
|
Other mutations in F830016B08Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00429:F830016B08Rik
|
APN |
18 |
60,433,340 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02642:F830016B08Rik
|
APN |
18 |
60,433,058 (GRCm39) |
missense |
probably benign |
0.00 |
FR4342:F830016B08Rik
|
UTSW |
18 |
60,433,013 (GRCm39) |
small insertion |
probably benign |
|
R0172:F830016B08Rik
|
UTSW |
18 |
60,433,036 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0375:F830016B08Rik
|
UTSW |
18 |
60,433,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R1517:F830016B08Rik
|
UTSW |
18 |
60,433,970 (GRCm39) |
nonsense |
probably null |
|
R1791:F830016B08Rik
|
UTSW |
18 |
60,433,589 (GRCm39) |
missense |
probably benign |
0.01 |
R2413:F830016B08Rik
|
UTSW |
18 |
60,433,365 (GRCm39) |
nonsense |
probably null |
|
R2696:F830016B08Rik
|
UTSW |
18 |
60,433,808 (GRCm39) |
missense |
possibly damaging |
0.75 |
R3607:F830016B08Rik
|
UTSW |
18 |
60,433,780 (GRCm39) |
nonsense |
probably null |
|
R4612:F830016B08Rik
|
UTSW |
18 |
60,434,087 (GRCm39) |
missense |
probably benign |
0.42 |
R4621:F830016B08Rik
|
UTSW |
18 |
60,433,939 (GRCm39) |
missense |
probably benign |
0.01 |
R4752:F830016B08Rik
|
UTSW |
18 |
60,434,153 (GRCm39) |
missense |
probably benign |
0.00 |
R5755:F830016B08Rik
|
UTSW |
18 |
60,433,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R5909:F830016B08Rik
|
UTSW |
18 |
60,433,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R6183:F830016B08Rik
|
UTSW |
18 |
60,432,949 (GRCm39) |
missense |
probably benign |
0.00 |
R6272:F830016B08Rik
|
UTSW |
18 |
60,433,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R7076:F830016B08Rik
|
UTSW |
18 |
60,433,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R8130:F830016B08Rik
|
UTSW |
18 |
60,433,052 (GRCm39) |
missense |
probably benign |
0.00 |
R8171:F830016B08Rik
|
UTSW |
18 |
60,433,150 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8289:F830016B08Rik
|
UTSW |
18 |
60,433,360 (GRCm39) |
missense |
probably benign |
0.45 |
R9034:F830016B08Rik
|
UTSW |
18 |
60,433,141 (GRCm39) |
missense |
probably damaging |
0.96 |
R9600:F830016B08Rik
|
UTSW |
18 |
60,433,237 (GRCm39) |
missense |
probably damaging |
0.99 |
R9614:F830016B08Rik
|
UTSW |
18 |
60,433,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R9638:F830016B08Rik
|
UTSW |
18 |
60,432,956 (GRCm39) |
missense |
probably benign |
0.00 |
R9684:F830016B08Rik
|
UTSW |
18 |
60,433,043 (GRCm39) |
missense |
probably damaging |
0.97 |
R9729:F830016B08Rik
|
UTSW |
18 |
60,433,558 (GRCm39) |
missense |
possibly damaging |
0.88 |
RF044:F830016B08Rik
|
UTSW |
18 |
60,433,010 (GRCm39) |
small insertion |
probably benign |
|
RF054:F830016B08Rik
|
UTSW |
18 |
60,433,010 (GRCm39) |
small insertion |
probably benign |
|
|