Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810065E05Rik |
A |
C |
11: 58,313,008 (GRCm39) |
|
probably benign |
Het |
A630091E08Rik |
A |
G |
7: 98,192,875 (GRCm39) |
|
noncoding transcript |
Het |
Abca8a |
T |
C |
11: 109,961,306 (GRCm39) |
T539A |
probably damaging |
Het |
Arnt2 |
G |
A |
7: 83,996,738 (GRCm39) |
R63C |
probably damaging |
Het |
Cabcoco1 |
A |
T |
10: 68,369,692 (GRCm39) |
|
probably null |
Het |
Capn7 |
T |
C |
14: 31,087,561 (GRCm39) |
|
probably benign |
Het |
Cd109 |
G |
A |
9: 78,610,389 (GRCm39) |
E1145K |
probably damaging |
Het |
Celsr1 |
A |
T |
15: 85,806,399 (GRCm39) |
V2353D |
probably damaging |
Het |
Cep350 |
C |
T |
1: 155,804,372 (GRCm39) |
D904N |
probably damaging |
Het |
Chl1 |
T |
A |
6: 103,688,019 (GRCm39) |
|
probably benign |
Het |
Colec10 |
G |
A |
15: 54,302,542 (GRCm39) |
|
probably benign |
Het |
Cst11 |
T |
A |
2: 148,612,322 (GRCm39) |
Q105L |
probably damaging |
Het |
Eps8l3 |
T |
C |
3: 107,786,857 (GRCm39) |
L11S |
probably damaging |
Het |
Gsdme |
A |
G |
6: 50,198,009 (GRCm39) |
I317T |
possibly damaging |
Het |
Itgad |
T |
C |
7: 127,802,158 (GRCm39) |
S979P |
probably damaging |
Het |
Mga |
T |
C |
2: 119,791,442 (GRCm39) |
|
probably null |
Het |
Nubpl |
T |
C |
12: 52,357,470 (GRCm39) |
|
probably benign |
Het |
Or2b4 |
T |
C |
17: 38,116,891 (GRCm39) |
L285P |
probably damaging |
Het |
Or5be3 |
T |
C |
2: 86,864,118 (GRCm39) |
Y149C |
probably damaging |
Het |
Pard3b |
G |
A |
1: 61,678,474 (GRCm39) |
E25K |
probably damaging |
Het |
Phactr1 |
T |
A |
13: 42,836,197 (GRCm39) |
Y8* |
probably null |
Het |
Phf14 |
T |
C |
6: 11,953,316 (GRCm39) |
S352P |
probably damaging |
Het |
Ppp1r16a |
C |
T |
15: 76,574,999 (GRCm39) |
|
probably benign |
Het |
Prap1 |
G |
T |
7: 139,673,390 (GRCm39) |
|
probably benign |
Het |
Prdm8 |
T |
A |
5: 98,333,119 (GRCm39) |
F229I |
probably benign |
Het |
Rfx6 |
T |
C |
10: 51,553,936 (GRCm39) |
F11L |
probably benign |
Het |
Rfx8 |
T |
A |
1: 39,757,565 (GRCm39) |
|
probably benign |
Het |
Rif1 |
C |
T |
2: 52,001,129 (GRCm39) |
R1528C |
probably damaging |
Het |
Ripk4 |
G |
A |
16: 97,564,718 (GRCm39) |
|
probably benign |
Het |
Satb1 |
T |
A |
17: 52,047,231 (GRCm39) |
I695F |
probably damaging |
Het |
Sema4d |
A |
G |
13: 51,859,293 (GRCm39) |
|
probably benign |
Het |
Slc30a4 |
T |
A |
2: 122,527,104 (GRCm39) |
T381S |
probably benign |
Het |
Suv39h2 |
T |
C |
2: 3,465,953 (GRCm39) |
Y134C |
probably damaging |
Het |
Tcerg1 |
C |
T |
18: 42,657,073 (GRCm39) |
A185V |
unknown |
Het |
Tep1 |
T |
A |
14: 51,103,486 (GRCm39) |
D268V |
probably damaging |
Het |
Tmem89 |
T |
A |
9: 108,744,485 (GRCm39) |
V126D |
probably damaging |
Het |
Trf |
T |
C |
9: 103,098,121 (GRCm39) |
T46A |
probably benign |
Het |
Trmt6 |
C |
T |
2: 132,648,689 (GRCm39) |
R415Q |
possibly damaging |
Het |
Trp53bp1 |
T |
C |
2: 121,035,006 (GRCm39) |
K1625E |
probably damaging |
Het |
Zcchc4 |
T |
A |
5: 52,964,420 (GRCm39) |
I292N |
possibly damaging |
Het |
|
Other mutations in Ankrd60 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01980:Ankrd60
|
APN |
2 |
173,412,996 (GRCm39) |
missense |
probably benign |
0.33 |
R0060:Ankrd60
|
UTSW |
2 |
173,414,406 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R0569:Ankrd60
|
UTSW |
2 |
173,412,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R0587:Ankrd60
|
UTSW |
2 |
173,410,644 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2941:Ankrd60
|
UTSW |
2 |
173,410,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R4549:Ankrd60
|
UTSW |
2 |
173,414,395 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5322:Ankrd60
|
UTSW |
2 |
173,410,610 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5763:Ankrd60
|
UTSW |
2 |
173,419,882 (GRCm39) |
frame shift |
probably null |
|
R5786:Ankrd60
|
UTSW |
2 |
173,419,882 (GRCm39) |
frame shift |
probably null |
|
R5787:Ankrd60
|
UTSW |
2 |
173,419,882 (GRCm39) |
frame shift |
probably null |
|
R5788:Ankrd60
|
UTSW |
2 |
173,419,882 (GRCm39) |
frame shift |
probably null |
|
R7527:Ankrd60
|
UTSW |
2 |
173,419,966 (GRCm39) |
missense |
probably benign |
0.00 |
R7618:Ankrd60
|
UTSW |
2 |
173,412,834 (GRCm39) |
splice site |
probably null |
|
R7756:Ankrd60
|
UTSW |
2 |
173,410,562 (GRCm39) |
makesense |
probably null |
|
R7758:Ankrd60
|
UTSW |
2 |
173,410,562 (GRCm39) |
makesense |
probably null |
|
R8039:Ankrd60
|
UTSW |
2 |
173,414,284 (GRCm39) |
critical splice donor site |
probably null |
|
R9345:Ankrd60
|
UTSW |
2 |
173,410,610 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9573:Ankrd60
|
UTSW |
2 |
173,410,791 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9604:Ankrd60
|
UTSW |
2 |
173,412,987 (GRCm39) |
missense |
probably benign |
0.14 |
|