Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ano1 |
T |
C |
7: 144,190,882 (GRCm39) |
I401V |
possibly damaging |
Het |
Ap2a2 |
A |
T |
7: 141,184,932 (GRCm39) |
|
probably benign |
Het |
Apol7c |
T |
A |
15: 77,410,637 (GRCm39) |
D103V |
probably damaging |
Het |
Atp2a1 |
A |
G |
7: 126,049,479 (GRCm39) |
V521A |
probably benign |
Het |
Ccdc88c |
G |
T |
12: 100,883,062 (GRCm39) |
D1603E |
probably benign |
Het |
Clec4f |
T |
C |
6: 83,630,182 (GRCm39) |
I125M |
probably benign |
Het |
Dsc1 |
T |
C |
18: 20,227,679 (GRCm39) |
I520V |
probably benign |
Het |
Eomes |
G |
A |
9: 118,311,334 (GRCm39) |
A386T |
probably damaging |
Het |
Gldc |
C |
T |
19: 30,135,913 (GRCm39) |
|
probably null |
Het |
Hectd4 |
G |
T |
5: 121,445,013 (GRCm39) |
M1420I |
probably benign |
Het |
Hmcn1 |
A |
T |
1: 150,508,303 (GRCm39) |
|
probably benign |
Het |
Ighv6-3 |
G |
A |
12: 114,355,335 (GRCm39) |
T118I |
possibly damaging |
Het |
Krt82 |
A |
G |
15: 101,453,958 (GRCm39) |
F250S |
probably damaging |
Het |
Ltb |
A |
G |
17: 35,413,576 (GRCm39) |
T27A |
probably benign |
Het |
Mex3b |
T |
A |
7: 82,518,911 (GRCm39) |
S409T |
probably benign |
Het |
Mki67 |
A |
T |
7: 135,315,745 (GRCm39) |
I39N |
probably damaging |
Het |
Or51a7 |
A |
G |
7: 102,615,235 (GRCm39) |
|
probably benign |
Het |
Palmd |
A |
G |
3: 116,717,922 (GRCm39) |
S192P |
probably damaging |
Het |
Pcdh20 |
A |
T |
14: 88,704,636 (GRCm39) |
M888K |
probably benign |
Het |
Pclo |
A |
T |
5: 14,731,083 (GRCm39) |
H3195L |
unknown |
Het |
Pgm2 |
A |
T |
5: 64,260,225 (GRCm39) |
I137F |
possibly damaging |
Het |
Polq |
T |
A |
16: 36,837,671 (GRCm39) |
N194K |
probably damaging |
Het |
Rmnd1 |
T |
C |
10: 4,360,793 (GRCm39) |
|
probably null |
Het |
Rnf114 |
T |
C |
2: 167,354,459 (GRCm39) |
M180T |
probably damaging |
Het |
Sap30 |
A |
G |
8: 57,938,123 (GRCm39) |
F165L |
possibly damaging |
Het |
Scgb3a2 |
T |
A |
18: 43,900,059 (GRCm39) |
|
probably benign |
Het |
Sftpa1 |
A |
T |
14: 40,854,527 (GRCm39) |
N38I |
probably benign |
Het |
Sumf1 |
A |
G |
6: 108,152,977 (GRCm39) |
F137S |
probably damaging |
Het |
Tln2 |
C |
A |
9: 67,219,093 (GRCm39) |
R284L |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,570,703 (GRCm39) |
R26730Q |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,540,808 (GRCm39) |
R25732S |
probably damaging |
Het |
Tubgcp4 |
T |
C |
2: 121,004,082 (GRCm39) |
V41A |
probably benign |
Het |
Usp53 |
T |
A |
3: 122,751,367 (GRCm39) |
Q230L |
probably damaging |
Het |
Vmn2r57 |
T |
C |
7: 41,074,467 (GRCm39) |
E532G |
probably damaging |
Het |
Vps9d1 |
G |
T |
8: 123,972,769 (GRCm39) |
N454K |
probably damaging |
Het |
Wdr55 |
T |
C |
18: 36,895,132 (GRCm39) |
|
probably null |
Het |
Zfp263 |
T |
A |
16: 3,566,776 (GRCm39) |
C76S |
probably benign |
Het |
|
Other mutations in Arid4a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00479:Arid4a
|
APN |
12 |
71,119,367 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00546:Arid4a
|
APN |
12 |
71,122,445 (GRCm39) |
missense |
probably benign |
|
IGL00553:Arid4a
|
APN |
12 |
71,122,751 (GRCm39) |
missense |
probably benign |
0.04 |
IGL00708:Arid4a
|
APN |
12 |
71,119,502 (GRCm39) |
missense |
probably benign |
0.02 |
IGL00847:Arid4a
|
APN |
12 |
71,122,492 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01456:Arid4a
|
APN |
12 |
71,114,036 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01505:Arid4a
|
APN |
12 |
71,083,889 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01555:Arid4a
|
APN |
12 |
71,108,301 (GRCm39) |
splice site |
probably benign |
|
IGL01631:Arid4a
|
APN |
12 |
71,069,036 (GRCm39) |
splice site |
probably benign |
|
IGL02958:Arid4a
|
APN |
12 |
71,144,337 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03087:Arid4a
|
APN |
12 |
71,122,019 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03111:Arid4a
|
APN |
12 |
71,086,740 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03234:Arid4a
|
APN |
12 |
71,091,834 (GRCm39) |
missense |
probably benign |
0.34 |
After_8
|
UTSW |
12 |
71,070,272 (GRCm39) |
critical splice acceptor site |
probably null |
|
ariano
|
UTSW |
12 |
71,116,634 (GRCm39) |
nonsense |
probably null |
|
Dusty
|
UTSW |
12 |
71,106,867 (GRCm39) |
missense |
probably damaging |
1.00 |
guava
|
UTSW |
12 |
71,119,406 (GRCm39) |
missense |
probably damaging |
0.99 |
limoncello
|
UTSW |
12 |
71,114,115 (GRCm39) |
splice site |
probably null |
|
Sahara
|
UTSW |
12 |
71,106,889 (GRCm39) |
nonsense |
probably null |
|
Under_8
|
UTSW |
12 |
71,109,980 (GRCm39) |
missense |
probably benign |
0.10 |
R0047:Arid4a
|
UTSW |
12 |
71,122,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R0047:Arid4a
|
UTSW |
12 |
71,122,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R0270:Arid4a
|
UTSW |
12 |
71,119,406 (GRCm39) |
missense |
probably damaging |
0.99 |
R0310:Arid4a
|
UTSW |
12 |
71,122,604 (GRCm39) |
missense |
probably benign |
0.05 |
R0504:Arid4a
|
UTSW |
12 |
71,093,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R1061:Arid4a
|
UTSW |
12 |
71,121,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1087:Arid4a
|
UTSW |
12 |
71,122,112 (GRCm39) |
missense |
probably benign |
0.01 |
R1169:Arid4a
|
UTSW |
12 |
71,122,112 (GRCm39) |
missense |
probably benign |
0.01 |
R1171:Arid4a
|
UTSW |
12 |
71,122,112 (GRCm39) |
missense |
probably benign |
0.01 |
R1531:Arid4a
|
UTSW |
12 |
71,122,779 (GRCm39) |
missense |
probably benign |
0.01 |
R1674:Arid4a
|
UTSW |
12 |
71,122,112 (GRCm39) |
missense |
probably benign |
0.01 |
R1676:Arid4a
|
UTSW |
12 |
71,122,112 (GRCm39) |
missense |
probably benign |
0.01 |
R1768:Arid4a
|
UTSW |
12 |
71,122,112 (GRCm39) |
missense |
probably benign |
0.01 |
R1833:Arid4a
|
UTSW |
12 |
71,122,240 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1878:Arid4a
|
UTSW |
12 |
71,134,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R2290:Arid4a
|
UTSW |
12 |
71,108,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R2292:Arid4a
|
UTSW |
12 |
71,108,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R2871:Arid4a
|
UTSW |
12 |
71,069,034 (GRCm39) |
critical splice donor site |
probably null |
|
R2871:Arid4a
|
UTSW |
12 |
71,069,034 (GRCm39) |
critical splice donor site |
probably null |
|
R3411:Arid4a
|
UTSW |
12 |
71,108,299 (GRCm39) |
splice site |
probably benign |
|
R3768:Arid4a
|
UTSW |
12 |
71,113,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R3838:Arid4a
|
UTSW |
12 |
71,122,559 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4320:Arid4a
|
UTSW |
12 |
71,116,769 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4589:Arid4a
|
UTSW |
12 |
71,116,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R4829:Arid4a
|
UTSW |
12 |
71,070,272 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4862:Arid4a
|
UTSW |
12 |
71,122,721 (GRCm39) |
missense |
probably damaging |
0.96 |
R4952:Arid4a
|
UTSW |
12 |
71,070,299 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5072:Arid4a
|
UTSW |
12 |
71,091,853 (GRCm39) |
missense |
probably benign |
0.08 |
R5423:Arid4a
|
UTSW |
12 |
71,116,634 (GRCm39) |
nonsense |
probably null |
|
R5767:Arid4a
|
UTSW |
12 |
71,106,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R5911:Arid4a
|
UTSW |
12 |
71,116,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R5952:Arid4a
|
UTSW |
12 |
71,109,980 (GRCm39) |
missense |
probably benign |
0.10 |
R6088:Arid4a
|
UTSW |
12 |
71,069,010 (GRCm39) |
missense |
probably damaging |
0.99 |
R6235:Arid4a
|
UTSW |
12 |
71,116,546 (GRCm39) |
splice site |
probably null |
|
R6277:Arid4a
|
UTSW |
12 |
71,086,665 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6455:Arid4a
|
UTSW |
12 |
71,121,862 (GRCm39) |
missense |
probably benign |
0.04 |
R6523:Arid4a
|
UTSW |
12 |
71,114,115 (GRCm39) |
splice site |
probably null |
|
R6701:Arid4a
|
UTSW |
12 |
71,134,286 (GRCm39) |
missense |
probably damaging |
1.00 |
R6812:Arid4a
|
UTSW |
12 |
71,094,037 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6815:Arid4a
|
UTSW |
12 |
71,063,856 (GRCm39) |
splice site |
probably null |
|
R6837:Arid4a
|
UTSW |
12 |
71,122,289 (GRCm39) |
missense |
probably benign |
|
R6858:Arid4a
|
UTSW |
12 |
71,070,283 (GRCm39) |
missense |
probably benign |
0.01 |
R6895:Arid4a
|
UTSW |
12 |
71,110,076 (GRCm39) |
missense |
probably benign |
0.18 |
R6901:Arid4a
|
UTSW |
12 |
71,113,911 (GRCm39) |
missense |
probably damaging |
0.99 |
R6905:Arid4a
|
UTSW |
12 |
71,108,318 (GRCm39) |
missense |
probably benign |
0.43 |
R7387:Arid4a
|
UTSW |
12 |
71,134,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R7570:Arid4a
|
UTSW |
12 |
71,109,916 (GRCm39) |
nonsense |
probably null |
|
R7772:Arid4a
|
UTSW |
12 |
71,108,363 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8194:Arid4a
|
UTSW |
12 |
71,106,889 (GRCm39) |
nonsense |
probably null |
|
R8206:Arid4a
|
UTSW |
12 |
71,133,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R8552:Arid4a
|
UTSW |
12 |
71,106,849 (GRCm39) |
missense |
probably benign |
|
R8696:Arid4a
|
UTSW |
12 |
71,110,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R9015:Arid4a
|
UTSW |
12 |
71,122,168 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9109:Arid4a
|
UTSW |
12 |
71,122,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R9450:Arid4a
|
UTSW |
12 |
71,119,374 (GRCm39) |
missense |
|
|
Z1176:Arid4a
|
UTSW |
12 |
71,086,694 (GRCm39) |
missense |
possibly damaging |
0.89 |
Z1177:Arid4a
|
UTSW |
12 |
71,122,411 (GRCm39) |
missense |
possibly damaging |
0.82 |
|