Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
C |
T |
6: 121,631,464 (GRCm39) |
T587I |
probably benign |
Het |
Abl1 |
T |
A |
2: 31,691,667 (GRCm39) |
M1062K |
probably benign |
Het |
Agbl4 |
G |
A |
4: 111,404,469 (GRCm39) |
D272N |
probably damaging |
Het |
Apob |
A |
T |
12: 8,058,261 (GRCm39) |
I2215F |
probably damaging |
Het |
Atp10b |
A |
T |
11: 43,109,784 (GRCm39) |
Q821H |
probably damaging |
Het |
Atp1a3 |
T |
C |
7: 24,678,729 (GRCm39) |
Y971C |
probably damaging |
Het |
Atp6ap1l |
A |
T |
13: 91,031,841 (GRCm39) |
H280Q |
probably damaging |
Het |
B4galt2 |
A |
T |
4: 117,734,164 (GRCm39) |
M291K |
probably damaging |
Het |
Cachd1 |
G |
T |
4: 100,809,315 (GRCm39) |
V267F |
possibly damaging |
Het |
Cadm2 |
G |
T |
16: 66,581,715 (GRCm39) |
L188M |
probably damaging |
Het |
Ccn6 |
C |
T |
10: 39,030,983 (GRCm39) |
G180D |
probably benign |
Het |
Ceacam19 |
T |
C |
7: 19,616,517 (GRCm39) |
N199S |
probably benign |
Het |
Chrna5 |
A |
G |
9: 54,905,347 (GRCm39) |
D53G |
probably benign |
Het |
Clca4a |
T |
A |
3: 144,663,059 (GRCm39) |
T597S |
probably benign |
Het |
Cluap1 |
T |
A |
16: 3,746,476 (GRCm39) |
M279K |
probably benign |
Het |
Cngb1 |
T |
A |
8: 95,991,052 (GRCm39) |
M717L |
probably benign |
Het |
Cp |
T |
C |
3: 20,036,186 (GRCm39) |
V777A |
probably benign |
Het |
Drosha |
A |
G |
15: 12,861,792 (GRCm39) |
D594G |
probably benign |
Het |
Exo5 |
A |
G |
4: 120,778,734 (GRCm39) |
|
probably benign |
Het |
Gm10549 |
C |
A |
18: 33,597,358 (GRCm39) |
|
probably benign |
Het |
Gprc5b |
A |
G |
7: 118,583,800 (GRCm39) |
I23T |
possibly damaging |
Het |
Ikbke |
T |
C |
1: 131,186,955 (GRCm39) |
Y579C |
probably damaging |
Het |
Ikzf2 |
T |
C |
1: 69,578,201 (GRCm39) |
Y362C |
probably damaging |
Het |
Itfg1 |
A |
G |
8: 86,466,978 (GRCm39) |
V365A |
probably benign |
Het |
Josd2 |
T |
C |
7: 44,120,578 (GRCm39) |
I105T |
probably damaging |
Het |
Mc3r |
G |
A |
2: 172,091,074 (GRCm39) |
A99T |
possibly damaging |
Het |
Mettl22 |
T |
A |
16: 8,306,755 (GRCm39) |
|
probably null |
Het |
Mgat5 |
A |
G |
1: 127,399,301 (GRCm39) |
I619V |
probably benign |
Het |
Nin |
T |
C |
12: 70,101,308 (GRCm39) |
I430V |
probably benign |
Het |
Or52n2c |
C |
A |
7: 104,574,852 (GRCm39) |
A40S |
possibly damaging |
Het |
Or5au1 |
A |
G |
14: 52,272,902 (GRCm39) |
F222S |
probably benign |
Het |
Or5j3 |
T |
C |
2: 86,128,990 (GRCm39) |
F277L |
probably benign |
Het |
Or5w22 |
C |
G |
2: 87,363,085 (GRCm39) |
A236G |
possibly damaging |
Het |
Or8k3 |
T |
A |
2: 86,058,731 (GRCm39) |
I195F |
possibly damaging |
Het |
Parvb |
T |
C |
15: 84,188,073 (GRCm39) |
L272P |
probably damaging |
Het |
Pde2a |
A |
G |
7: 101,149,649 (GRCm39) |
K180E |
possibly damaging |
Het |
Pik3c3 |
C |
T |
18: 30,457,615 (GRCm39) |
T736M |
probably damaging |
Het |
Plcb4 |
C |
T |
2: 135,814,991 (GRCm39) |
R760* |
probably null |
Het |
Pramel6 |
C |
T |
2: 87,340,766 (GRCm39) |
T366I |
probably benign |
Het |
Prr29 |
C |
T |
11: 106,266,062 (GRCm39) |
R42W |
probably damaging |
Het |
Prss12 |
A |
G |
3: 123,241,048 (GRCm39) |
I81V |
probably benign |
Het |
Ptpn13 |
A |
G |
5: 103,649,478 (GRCm39) |
T294A |
probably benign |
Het |
Ptprc |
A |
T |
1: 138,041,300 (GRCm39) |
|
probably null |
Het |
Sin3b |
T |
A |
8: 73,460,118 (GRCm39) |
|
probably null |
Het |
Slco5a1 |
T |
C |
1: 13,060,151 (GRCm39) |
Y190C |
probably damaging |
Het |
Slco6c1 |
T |
G |
1: 97,053,538 (GRCm39) |
Y121S |
probably damaging |
Het |
Srcap |
G |
T |
7: 127,121,317 (GRCm39) |
G217* |
probably null |
Het |
Ss18 |
A |
T |
18: 14,784,145 (GRCm39) |
M181K |
probably damaging |
Het |
Synm |
T |
C |
7: 67,385,809 (GRCm39) |
T176A |
probably benign |
Het |
Taf3 |
T |
C |
2: 9,955,971 (GRCm39) |
E579G |
probably damaging |
Het |
Taf7 |
A |
G |
18: 37,776,159 (GRCm39) |
I136T |
probably damaging |
Het |
Tyrp1 |
A |
G |
4: 80,759,018 (GRCm39) |
D297G |
probably null |
Het |
Uox |
C |
T |
3: 146,330,332 (GRCm39) |
R163* |
probably null |
Het |
Wwp1 |
G |
A |
4: 19,650,299 (GRCm39) |
S289L |
possibly damaging |
Het |
Xbp1 |
T |
C |
11: 5,471,005 (GRCm39) |
V4A |
probably benign |
Het |
Zbtb17 |
G |
A |
4: 141,190,694 (GRCm39) |
G171S |
probably benign |
Het |
Zbtb2 |
T |
C |
10: 4,319,711 (GRCm39) |
Y105C |
probably damaging |
Het |
Zeb2 |
T |
C |
2: 45,000,508 (GRCm39) |
|
probably benign |
Het |
Zkscan8 |
A |
T |
13: 21,709,397 (GRCm39) |
I167N |
probably benign |
Het |
|
Other mutations in Tfap2d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00484:Tfap2d
|
APN |
1 |
19,213,105 (GRCm39) |
missense |
probably benign |
0.44 |
IGL00837:Tfap2d
|
APN |
1 |
19,189,430 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01370:Tfap2d
|
APN |
1 |
19,175,009 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01470:Tfap2d
|
APN |
1 |
19,218,620 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01757:Tfap2d
|
APN |
1 |
19,174,804 (GRCm39) |
missense |
probably benign |
|
IGL01986:Tfap2d
|
APN |
1 |
19,189,383 (GRCm39) |
splice site |
probably benign |
|
IGL02613:Tfap2d
|
APN |
1 |
19,189,415 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02666:Tfap2d
|
APN |
1 |
19,174,979 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02812:Tfap2d
|
APN |
1 |
19,213,151 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02900:Tfap2d
|
APN |
1 |
19,189,474 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03184:Tfap2d
|
APN |
1 |
19,189,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R0389:Tfap2d
|
UTSW |
1 |
19,174,591 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0443:Tfap2d
|
UTSW |
1 |
19,174,591 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3962:Tfap2d
|
UTSW |
1 |
19,189,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R3977:Tfap2d
|
UTSW |
1 |
19,174,718 (GRCm39) |
missense |
possibly damaging |
0.76 |
R3980:Tfap2d
|
UTSW |
1 |
19,236,187 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4721:Tfap2d
|
UTSW |
1 |
19,174,984 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6281:Tfap2d
|
UTSW |
1 |
19,174,702 (GRCm39) |
missense |
probably benign |
0.12 |
R6283:Tfap2d
|
UTSW |
1 |
19,174,702 (GRCm39) |
missense |
probably benign |
0.12 |
R6493:Tfap2d
|
UTSW |
1 |
19,174,702 (GRCm39) |
missense |
probably benign |
0.12 |
R6751:Tfap2d
|
UTSW |
1 |
19,173,507 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7288:Tfap2d
|
UTSW |
1 |
19,189,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R7400:Tfap2d
|
UTSW |
1 |
19,213,150 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8156:Tfap2d
|
UTSW |
1 |
19,173,486 (GRCm39) |
missense |
probably benign |
|
R8551:Tfap2d
|
UTSW |
1 |
19,175,024 (GRCm39) |
missense |
probably benign |
0.08 |
R8686:Tfap2d
|
UTSW |
1 |
19,178,508 (GRCm39) |
missense |
probably benign |
0.06 |
R8838:Tfap2d
|
UTSW |
1 |
19,175,036 (GRCm39) |
missense |
possibly damaging |
0.83 |
|