Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adipoq |
T |
A |
16: 22,975,938 (GRCm39) |
V134E |
possibly damaging |
Het |
Agmat |
A |
G |
4: 141,483,273 (GRCm39) |
T236A |
probably benign |
Het |
Anxa9 |
T |
C |
3: 95,208,425 (GRCm39) |
N197S |
probably benign |
Het |
Arhgap23 |
A |
T |
11: 97,366,932 (GRCm39) |
D1071V |
probably damaging |
Het |
Axdnd1 |
G |
A |
1: 156,208,428 (GRCm39) |
T470M |
probably damaging |
Het |
C3 |
C |
T |
17: 57,512,303 (GRCm39) |
D1542N |
possibly damaging |
Het |
Cdh3 |
A |
T |
8: 107,263,606 (GRCm39) |
|
probably null |
Het |
Cep85l |
A |
T |
10: 53,167,906 (GRCm39) |
I624K |
probably benign |
Het |
Dchs1 |
A |
T |
7: 105,406,292 (GRCm39) |
D2313E |
possibly damaging |
Het |
Dock7 |
T |
C |
4: 98,859,066 (GRCm39) |
T1409A |
probably benign |
Het |
Exo1 |
C |
T |
1: 175,714,312 (GRCm39) |
P73L |
probably damaging |
Het |
Fgfrl1 |
C |
A |
5: 108,853,242 (GRCm39) |
H197Q |
possibly damaging |
Het |
Fsbp |
G |
A |
4: 11,583,706 (GRCm39) |
G135D |
probably damaging |
Het |
Herc3 |
G |
A |
6: 58,839,973 (GRCm39) |
R362H |
probably benign |
Het |
Herc3 |
T |
C |
6: 58,853,587 (GRCm39) |
F583L |
probably benign |
Het |
Ifna7 |
T |
C |
4: 88,734,964 (GRCm39) |
V167A |
probably damaging |
Het |
Ighv1-54 |
A |
G |
12: 115,157,596 (GRCm39) |
V17A |
possibly damaging |
Het |
Kcnh5 |
A |
G |
12: 75,134,350 (GRCm39) |
Y400H |
possibly damaging |
Het |
Kcnk16 |
T |
A |
14: 20,319,230 (GRCm39) |
M1L |
possibly damaging |
Het |
Kctd19 |
T |
C |
8: 106,123,112 (GRCm39) |
T101A |
probably benign |
Het |
Klf3 |
A |
G |
5: 64,984,560 (GRCm39) |
|
probably null |
Het |
Krtap12-1 |
G |
T |
10: 77,556,729 (GRCm39) |
V91L |
probably benign |
Het |
Lonp1 |
T |
C |
17: 56,928,952 (GRCm39) |
E270G |
possibly damaging |
Het |
Mgl2 |
T |
C |
11: 70,026,659 (GRCm39) |
L128P |
probably damaging |
Het |
Mrc1 |
A |
G |
2: 14,323,981 (GRCm39) |
Y1106C |
probably damaging |
Het |
Mybpc1 |
G |
T |
10: 88,406,521 (GRCm39) |
|
probably null |
Het |
Mypn |
C |
A |
10: 62,961,486 (GRCm39) |
L1035F |
possibly damaging |
Het |
Neurl1a |
T |
C |
19: 47,228,328 (GRCm39) |
L58P |
probably damaging |
Het |
Nlrp4e |
G |
T |
7: 23,039,988 (GRCm39) |
L770F |
probably damaging |
Het |
Npas3 |
A |
G |
12: 54,115,857 (GRCm39) |
*895W |
probably null |
Het |
Nphs2 |
T |
C |
1: 156,140,608 (GRCm39) |
I115T |
probably damaging |
Het |
Or1ad6 |
A |
G |
11: 50,860,385 (GRCm39) |
D180G |
probably damaging |
Het |
Or8g22 |
T |
A |
9: 38,958,707 (GRCm39) |
H47L |
unknown |
Het |
Patj |
A |
T |
4: 98,569,456 (GRCm39) |
K1128* |
probably null |
Het |
Pla2g5 |
C |
G |
4: 138,528,746 (GRCm39) |
C70S |
probably damaging |
Het |
Pole4 |
G |
A |
6: 82,599,095 (GRCm39) |
R119C |
possibly damaging |
Het |
Ppm1h |
G |
T |
10: 122,740,027 (GRCm39) |
L367F |
probably damaging |
Het |
Ppp1r13b |
G |
T |
12: 111,812,851 (GRCm39) |
R123S |
probably damaging |
Het |
Ptpru |
C |
T |
4: 131,535,735 (GRCm39) |
C414Y |
probably damaging |
Het |
Pum2 |
T |
A |
12: 8,769,076 (GRCm39) |
Y323* |
probably null |
Het |
Rhot2 |
T |
C |
17: 26,059,521 (GRCm39) |
D407G |
probably benign |
Het |
Rreb1 |
C |
T |
13: 38,113,579 (GRCm39) |
R313W |
possibly damaging |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Scn11a |
T |
A |
9: 119,613,115 (GRCm39) |
D825V |
probably damaging |
Het |
Selenoi |
A |
G |
5: 30,461,187 (GRCm39) |
Y141C |
probably damaging |
Het |
Smcr8 |
A |
G |
11: 60,670,330 (GRCm39) |
T493A |
probably benign |
Het |
Tjp2 |
A |
T |
19: 24,078,190 (GRCm39) |
I901N |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Ttc23l |
T |
A |
15: 10,530,781 (GRCm39) |
Y277F |
possibly damaging |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Wdr1 |
C |
T |
5: 38,697,882 (GRCm39) |
G228R |
probably damaging |
Het |
Xab2 |
T |
C |
8: 3,669,053 (GRCm39) |
N31S |
probably damaging |
Het |
|
Other mutations in Cplx4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00755:Cplx4
|
APN |
18 |
66,090,166 (GRCm39) |
splice site |
probably benign |
|
IGL01577:Cplx4
|
APN |
18 |
66,103,015 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02124:Cplx4
|
APN |
18 |
66,103,123 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02137:Cplx4
|
APN |
18 |
66,090,125 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02885:Cplx4
|
APN |
18 |
66,089,984 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03263:Cplx4
|
APN |
18 |
66,100,559 (GRCm39) |
missense |
probably benign |
0.04 |
R0894:Cplx4
|
UTSW |
18 |
66,090,116 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2107:Cplx4
|
UTSW |
18 |
66,089,964 (GRCm39) |
missense |
probably benign |
0.05 |
R3768:Cplx4
|
UTSW |
18 |
66,102,998 (GRCm39) |
missense |
probably benign |
0.39 |
R3769:Cplx4
|
UTSW |
18 |
66,102,998 (GRCm39) |
missense |
probably benign |
0.39 |
R4772:Cplx4
|
UTSW |
18 |
66,103,048 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5347:Cplx4
|
UTSW |
18 |
66,103,157 (GRCm39) |
start gained |
probably benign |
|
R7081:Cplx4
|
UTSW |
18 |
66,100,538 (GRCm39) |
critical splice donor site |
probably null |
|
R7231:Cplx4
|
UTSW |
18 |
66,090,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R7953:Cplx4
|
UTSW |
18 |
66,090,190 (GRCm39) |
splice site |
probably null |
|
R8043:Cplx4
|
UTSW |
18 |
66,090,190 (GRCm39) |
splice site |
probably null |
|
R8469:Cplx4
|
UTSW |
18 |
66,090,083 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9041:Cplx4
|
UTSW |
18 |
66,103,097 (GRCm39) |
missense |
probably damaging |
1.00 |
|