Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6030469F06Rik |
A |
T |
12: 31,234,622 (GRCm39) |
|
noncoding transcript |
Het |
Actn2 |
C |
T |
13: 12,305,634 (GRCm39) |
R394Q |
probably damaging |
Het |
Atg16l1 |
A |
G |
1: 87,687,842 (GRCm39) |
D62G |
probably damaging |
Het |
Atp2b1 |
A |
G |
10: 98,839,076 (GRCm39) |
T635A |
probably benign |
Het |
Chil4 |
G |
A |
3: 106,111,043 (GRCm39) |
P284S |
possibly damaging |
Het |
Dnah1 |
G |
A |
14: 31,016,792 (GRCm39) |
T1575I |
probably damaging |
Het |
Dnah7b |
A |
G |
1: 46,376,754 (GRCm39) |
|
probably null |
Het |
Dnajc12 |
A |
G |
10: 63,242,838 (GRCm39) |
T37A |
probably benign |
Het |
Efcab5 |
T |
A |
11: 76,981,284 (GRCm39) |
N1354I |
probably damaging |
Het |
Epas1 |
T |
C |
17: 87,117,091 (GRCm39) |
L218P |
probably benign |
Het |
Fbxw15 |
T |
A |
9: 109,397,300 (GRCm39) |
|
probably benign |
Het |
Filip1l |
C |
A |
16: 57,391,155 (GRCm39) |
S581* |
probably null |
Het |
Focad |
T |
A |
4: 88,104,195 (GRCm39) |
I358K |
probably damaging |
Het |
Gm382 |
T |
A |
X: 125,968,942 (GRCm39) |
S376T |
probably benign |
Het |
Gpsm1 |
C |
T |
2: 26,214,009 (GRCm39) |
R179C |
probably damaging |
Het |
Hjurp |
A |
G |
1: 88,194,283 (GRCm39) |
|
probably benign |
Het |
Homer3 |
G |
A |
8: 70,742,793 (GRCm39) |
|
probably null |
Het |
Krt39 |
C |
T |
11: 99,405,578 (GRCm39) |
A441T |
probably benign |
Het |
Nrdc |
T |
A |
4: 108,903,841 (GRCm39) |
N662K |
probably damaging |
Het |
Obox5 |
C |
T |
7: 15,491,899 (GRCm39) |
Q105* |
probably null |
Het |
Or56a3b |
T |
A |
7: 104,770,793 (GRCm39) |
M43K |
possibly damaging |
Het |
Or5af1 |
T |
A |
11: 58,722,841 (GRCm39) |
V287D |
possibly damaging |
Het |
Or8c13 |
A |
T |
9: 38,091,645 (GRCm39) |
V158D |
probably damaging |
Het |
Pcdhb5 |
T |
A |
18: 37,455,789 (GRCm39) |
L723Q |
possibly damaging |
Het |
Pou3f3 |
G |
T |
1: 42,736,618 (GRCm39) |
A105S |
unknown |
Het |
Ppp1r3d |
C |
T |
2: 178,055,880 (GRCm39) |
D41N |
probably damaging |
Het |
Ppp4r1 |
A |
G |
17: 66,131,749 (GRCm39) |
N497S |
probably benign |
Het |
Rad54b |
T |
G |
4: 11,615,570 (GRCm39) |
N859K |
probably benign |
Het |
Sh3bp2 |
C |
T |
5: 34,707,062 (GRCm39) |
S29L |
probably benign |
Het |
Smarcad1 |
A |
T |
6: 65,033,443 (GRCm39) |
N142I |
probably benign |
Het |
Stat3 |
G |
A |
11: 100,796,378 (GRCm39) |
|
probably benign |
Het |
Stmn3 |
T |
C |
2: 180,950,576 (GRCm39) |
R77G |
probably benign |
Het |
Ugt1a1 |
CAGAGAGAGAGAGA |
CAGAGAGAGAGA |
1: 88,139,706 (GRCm39) |
|
probably benign |
Het |
Vmn2r79 |
A |
G |
7: 86,651,099 (GRCm39) |
H166R |
possibly damaging |
Het |
Xlr3a |
T |
C |
X: 72,135,450 (GRCm39) |
I87V |
possibly damaging |
Het |
|
Other mutations in Sp140l1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
FR4340:Sp140l1
|
UTSW |
1 |
85,087,072 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4131001:Sp140l1
|
UTSW |
1 |
85,077,341 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4142001:Sp140l1
|
UTSW |
1 |
85,077,341 (GRCm39) |
missense |
probably benign |
0.01 |
R0602:Sp140l1
|
UTSW |
1 |
85,077,226 (GRCm39) |
missense |
probably benign |
0.00 |
R0831:Sp140l1
|
UTSW |
1 |
85,077,226 (GRCm39) |
missense |
probably benign |
0.00 |
R1147:Sp140l1
|
UTSW |
1 |
85,077,226 (GRCm39) |
missense |
probably benign |
0.00 |
R1852:Sp140l1
|
UTSW |
1 |
85,062,852 (GRCm39) |
unclassified |
probably benign |
|
R4277:Sp140l1
|
UTSW |
1 |
85,066,521 (GRCm39) |
intron |
probably benign |
|
R4385:Sp140l1
|
UTSW |
1 |
85,087,057 (GRCm39) |
critical splice donor site |
probably null |
|
R4691:Sp140l1
|
UTSW |
1 |
85,066,521 (GRCm39) |
intron |
probably benign |
|
R4863:Sp140l1
|
UTSW |
1 |
85,066,521 (GRCm39) |
intron |
probably benign |
|
R5173:Sp140l1
|
UTSW |
1 |
85,078,288 (GRCm39) |
nonsense |
probably null |
|
R5176:Sp140l1
|
UTSW |
1 |
85,066,521 (GRCm39) |
intron |
probably benign |
|
R8174:Sp140l1
|
UTSW |
1 |
85,077,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R9606:Sp140l1
|
UTSW |
1 |
85,075,344 (GRCm39) |
splice site |
probably null |
|
|