Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaa2 |
A |
G |
18: 74,920,265 (GRCm39) |
D31G |
probably damaging |
Het |
Actr2 |
A |
G |
11: 20,050,939 (GRCm39) |
|
probably benign |
Het |
Adcy8 |
A |
G |
15: 64,618,862 (GRCm39) |
C764R |
probably benign |
Het |
Ago4 |
A |
C |
4: 126,410,976 (GRCm39) |
F171C |
possibly damaging |
Het |
Akt2 |
T |
C |
7: 27,336,395 (GRCm39) |
F408S |
probably damaging |
Het |
Appl1 |
A |
T |
14: 26,650,600 (GRCm39) |
M524K |
probably damaging |
Het |
Arhgef11 |
T |
A |
3: 87,635,370 (GRCm39) |
I922N |
probably damaging |
Het |
Atp5pd |
T |
C |
11: 115,308,744 (GRCm39) |
E47G |
probably damaging |
Het |
Birc6 |
A |
G |
17: 74,835,755 (GRCm39) |
D70G |
probably benign |
Het |
Bola2 |
G |
A |
7: 126,295,731 (GRCm39) |
V56M |
probably damaging |
Het |
Cd300lg |
A |
G |
11: 101,944,918 (GRCm39) |
|
probably null |
Het |
Cdc42bpb |
A |
G |
12: 111,271,393 (GRCm39) |
|
probably benign |
Het |
Ceacam20 |
A |
G |
7: 19,710,185 (GRCm39) |
N403S |
probably damaging |
Het |
Cenpf |
T |
C |
1: 189,391,847 (GRCm39) |
M662V |
probably benign |
Het |
Chd3 |
C |
A |
11: 69,239,327 (GRCm39) |
E1607* |
probably null |
Het |
Chtf18 |
A |
T |
17: 25,946,285 (GRCm39) |
Y9* |
probably null |
Het |
Clta |
A |
G |
4: 44,032,424 (GRCm39) |
N200S |
probably benign |
Het |
Csmd1 |
G |
A |
8: 16,129,956 (GRCm39) |
S1722F |
possibly damaging |
Het |
Cyria |
C |
T |
12: 12,412,350 (GRCm39) |
T204I |
probably damaging |
Het |
Dennd4a |
T |
C |
9: 64,800,576 (GRCm39) |
S905P |
probably damaging |
Het |
Dhx57 |
T |
C |
17: 80,546,343 (GRCm39) |
K1347R |
probably damaging |
Het |
Dmc1 |
A |
T |
15: 79,480,441 (GRCm39) |
|
probably benign |
Het |
Dnhd1 |
G |
T |
7: 105,370,131 (GRCm39) |
A4519S |
probably benign |
Het |
Dnmbp |
A |
G |
19: 43,838,466 (GRCm39) |
C1120R |
probably benign |
Het |
Efs |
C |
T |
14: 55,154,680 (GRCm39) |
A427T |
probably damaging |
Het |
Erich6 |
T |
C |
3: 58,531,799 (GRCm39) |
E399G |
probably damaging |
Het |
Espl1 |
A |
G |
15: 102,225,083 (GRCm39) |
T1431A |
probably benign |
Het |
Fam184b |
A |
G |
5: 45,690,120 (GRCm39) |
S830P |
probably damaging |
Het |
Herc1 |
T |
A |
9: 66,355,357 (GRCm39) |
C2203S |
probably damaging |
Het |
Itpr1 |
G |
A |
6: 108,326,637 (GRCm39) |
V120M |
probably damaging |
Het |
Kcnh7 |
G |
A |
2: 62,546,503 (GRCm39) |
T1026I |
probably benign |
Het |
Kif1b |
A |
G |
4: 149,345,658 (GRCm39) |
I394T |
probably benign |
Het |
Ldlrap1 |
A |
C |
4: 134,484,733 (GRCm39) |
V87G |
probably damaging |
Het |
Lgals12 |
C |
T |
19: 7,580,403 (GRCm39) |
V155I |
probably damaging |
Het |
Limch1 |
A |
T |
5: 67,116,933 (GRCm39) |
N116I |
probably damaging |
Het |
Lonp2 |
C |
T |
8: 87,361,518 (GRCm39) |
R232C |
probably damaging |
Het |
Lrch1 |
C |
A |
14: 75,073,186 (GRCm39) |
C151F |
probably benign |
Het |
Lrig3 |
A |
G |
10: 125,842,812 (GRCm39) |
Y579C |
probably damaging |
Het |
Macf1 |
T |
C |
4: 123,327,068 (GRCm39) |
S4808G |
probably damaging |
Het |
Mapkap1 |
A |
T |
2: 34,513,494 (GRCm39) |
K501N |
probably damaging |
Het |
Mdc1 |
G |
T |
17: 36,165,337 (GRCm39) |
R1523L |
probably benign |
Het |
Mlh3 |
C |
T |
12: 85,312,914 (GRCm39) |
|
probably benign |
Het |
Mul1 |
T |
C |
4: 138,165,032 (GRCm39) |
|
probably benign |
Het |
Mybl2 |
G |
A |
2: 162,901,411 (GRCm39) |
|
probably benign |
Het |
Notch1 |
G |
C |
2: 26,350,470 (GRCm39) |
H2223Q |
probably benign |
Het |
Notch2 |
C |
A |
3: 98,053,936 (GRCm39) |
L2200M |
probably benign |
Het |
Odad3 |
G |
T |
9: 21,904,848 (GRCm39) |
R313S |
probably damaging |
Het |
Or10ak8 |
A |
T |
4: 118,774,667 (GRCm39) |
|
probably null |
Het |
Or12k5 |
G |
A |
2: 36,895,057 (GRCm39) |
R190* |
probably null |
Het |
Or5ae2 |
T |
A |
7: 84,506,196 (GRCm39) |
F206L |
probably benign |
Het |
Or8a1b |
T |
C |
9: 37,623,236 (GRCm39) |
Y113C |
probably damaging |
Het |
Plekhs1 |
T |
C |
19: 56,465,722 (GRCm39) |
|
probably null |
Het |
Ppm1h |
G |
A |
10: 122,777,260 (GRCm39) |
G509R |
probably damaging |
Het |
Ppp2r3c |
C |
T |
12: 55,345,207 (GRCm39) |
E94K |
probably damaging |
Het |
Ppp2r5e |
T |
A |
12: 75,509,164 (GRCm39) |
I372F |
probably damaging |
Het |
Ptprt |
G |
A |
2: 162,119,990 (GRCm39) |
T159I |
probably benign |
Het |
Rab20 |
A |
G |
8: 11,504,415 (GRCm39) |
F95S |
probably damaging |
Het |
Rfc3 |
A |
C |
5: 151,574,616 (GRCm39) |
M1R |
probably null |
Het |
Skp2 |
A |
G |
15: 9,125,280 (GRCm39) |
S100P |
probably damaging |
Het |
Smg5 |
T |
C |
3: 88,256,540 (GRCm39) |
S269P |
probably benign |
Het |
Sspo |
A |
T |
6: 48,432,352 (GRCm39) |
T684S |
probably benign |
Het |
Syt3 |
A |
G |
7: 44,042,782 (GRCm39) |
K355E |
probably damaging |
Het |
Tcp10a |
A |
T |
17: 7,610,903 (GRCm39) |
K355N |
probably damaging |
Het |
Tnrc18 |
A |
G |
5: 142,750,800 (GRCm39) |
|
probably benign |
Het |
Tsfm |
A |
G |
10: 126,866,339 (GRCm39) |
L74P |
probably benign |
Het |
Ttn |
G |
C |
2: 76,564,609 (GRCm39) |
N28509K |
probably damaging |
Het |
Ube2l6 |
G |
A |
2: 84,629,252 (GRCm39) |
M1I |
probably null |
Het |
Vmn2r80 |
T |
A |
10: 79,005,330 (GRCm39) |
H322Q |
probably damaging |
Het |
Zkscan8 |
A |
T |
13: 21,706,441 (GRCm39) |
S212T |
probably benign |
Het |
|
Other mutations in Ankrd24 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00776:Ankrd24
|
APN |
10 |
81,478,979 (GRCm39) |
unclassified |
probably benign |
|
IGL00809:Ankrd24
|
APN |
10 |
81,478,901 (GRCm39) |
unclassified |
probably benign |
|
IGL01021:Ankrd24
|
APN |
10 |
81,470,995 (GRCm39) |
splice site |
probably null |
|
IGL01073:Ankrd24
|
APN |
10 |
81,475,156 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01875:Ankrd24
|
APN |
10 |
81,465,571 (GRCm39) |
unclassified |
probably benign |
|
IGL03083:Ankrd24
|
APN |
10 |
81,474,483 (GRCm39) |
missense |
probably benign |
|
IGL03335:Ankrd24
|
APN |
10 |
81,482,967 (GRCm39) |
missense |
probably benign |
0.18 |
R0243:Ankrd24
|
UTSW |
10 |
81,470,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R0522:Ankrd24
|
UTSW |
10 |
81,472,189 (GRCm39) |
splice site |
probably benign |
|
R0607:Ankrd24
|
UTSW |
10 |
81,474,142 (GRCm39) |
missense |
probably damaging |
0.98 |
R0707:Ankrd24
|
UTSW |
10 |
81,478,547 (GRCm39) |
unclassified |
probably benign |
|
R1472:Ankrd24
|
UTSW |
10 |
81,470,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R1766:Ankrd24
|
UTSW |
10 |
81,474,472 (GRCm39) |
missense |
probably benign |
0.13 |
R1852:Ankrd24
|
UTSW |
10 |
81,478,775 (GRCm39) |
unclassified |
probably benign |
|
R1891:Ankrd24
|
UTSW |
10 |
81,479,342 (GRCm39) |
unclassified |
probably benign |
|
R2137:Ankrd24
|
UTSW |
10 |
81,482,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R3790:Ankrd24
|
UTSW |
10 |
81,478,513 (GRCm39) |
unclassified |
probably benign |
|
R4798:Ankrd24
|
UTSW |
10 |
81,479,149 (GRCm39) |
unclassified |
probably benign |
|
R4952:Ankrd24
|
UTSW |
10 |
81,482,982 (GRCm39) |
missense |
probably benign |
0.01 |
R5068:Ankrd24
|
UTSW |
10 |
81,475,699 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5237:Ankrd24
|
UTSW |
10 |
81,478,379 (GRCm39) |
unclassified |
probably benign |
|
R5418:Ankrd24
|
UTSW |
10 |
81,480,776 (GRCm39) |
unclassified |
probably benign |
|
R5795:Ankrd24
|
UTSW |
10 |
81,480,937 (GRCm39) |
unclassified |
probably benign |
|
R7188:Ankrd24
|
UTSW |
10 |
81,472,224 (GRCm39) |
nonsense |
probably null |
|
R7614:Ankrd24
|
UTSW |
10 |
81,474,523 (GRCm39) |
missense |
unknown |
|
R7750:Ankrd24
|
UTSW |
10 |
81,482,628 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8004:Ankrd24
|
UTSW |
10 |
81,474,191 (GRCm39) |
missense |
unknown |
|
R8190:Ankrd24
|
UTSW |
10 |
81,474,152 (GRCm39) |
missense |
unknown |
|
R8415:Ankrd24
|
UTSW |
10 |
81,475,947 (GRCm39) |
missense |
unknown |
|
R8670:Ankrd24
|
UTSW |
10 |
81,465,526 (GRCm39) |
start gained |
probably benign |
|
R8898:Ankrd24
|
UTSW |
10 |
81,478,352 (GRCm39) |
missense |
unknown |
|
R9475:Ankrd24
|
UTSW |
10 |
81,478,133 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9593:Ankrd24
|
UTSW |
10 |
81,475,898 (GRCm39) |
missense |
unknown |
|
R9744:Ankrd24
|
UTSW |
10 |
81,482,951 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9780:Ankrd24
|
UTSW |
10 |
81,482,196 (GRCm39) |
missense |
possibly damaging |
0.73 |
RF001:Ankrd24
|
UTSW |
10 |
81,479,405 (GRCm39) |
unclassified |
probably benign |
|
RF011:Ankrd24
|
UTSW |
10 |
81,479,405 (GRCm39) |
unclassified |
probably benign |
|
RF037:Ankrd24
|
UTSW |
10 |
81,479,407 (GRCm39) |
nonsense |
probably null |
|
RF061:Ankrd24
|
UTSW |
10 |
81,479,401 (GRCm39) |
nonsense |
probably null |
|
Z1088:Ankrd24
|
UTSW |
10 |
81,474,490 (GRCm39) |
missense |
probably damaging |
1.00 |
|